Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9776 |
|---|---|
| ensemblid | ENSG00000175224.17 |
| hgncid | 29091 |
| symbol | ATG13 |
| name | autophagy related 13 |
| refseq_nuc | NM_001346311.2 |
| refseq_prot | NP_001333240.1 |
| ensembl_nuc | ENST00000683050.1 |
| ensembl_prot | ENSP00000507809.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 46617553 |
| end | 46674518 |
| strand | + |
| ver | v1.2 |
| region | chr11:46617553-46674518 |
| region5000 | chr11:46612553-46679518 |
| regionname0 | ATG13_chr11_46617553_46674518 |
| regionname5000 | ATG13_chr11_46612553_46679518 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 550 | 216 | 85 | 46 | 54 | 10 | 19 | 36 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0002 | 0/0 | 550 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0003 | 0/0 | 550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1653 | 204 | 77 | 45 | 53 | 10 | 17 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| c0002 | 0/0 | 1653 | 7 | 6 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| c0003 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| c0004 | 0/0 | 1653 | 2 | 0 | 0 | 0 | 0 | 2 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| c0005 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| c0006 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| c0007 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2592 | 107 | 44 | 28 | 18 | 8 | 9 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0002 | 0/0 | 2592 | 36 | 8 | 11 | 10 | 1 | 6 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0003 | 0/1 | 2592 | 24 | 0 | 3 | 17 | 0 | 3 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0004 | 0/0 | 2592 | 14 | 14 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0005 | 0/0 | 2592 | 7 | 7 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0006 | 0/0 | 2592 | 5 | 0 | 0 | 5 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0007 | 0/0 | 2592 | 3 | 3 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0008 | 0/0 | 2592 | 3 | 3 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0009 | 0/0 | 2592 | 3 | 2 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0010 | 0/0 | 2592 | 2 | 0 | 2 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0011 | 1/0 | 2594 | 2 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0012 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0013 | 0/0 | 2592 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0014 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0015 | 0/0 | 2592 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0016 | 0/0 | 2592 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0017 | 0/0 | 2592 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0018 | 0/0 | 2592 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0019 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0020 | 0/0 | 2592 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0021 | 0/0 | 2592 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0022 | 0/0 | 2592 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| t0023 | 0/0 | 2592 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1653 | 204 | 77 | 45 | 53 | 10 | 17 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0002 | 0/0 | 1653 | 7 | 6 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0003 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0004 | 0/0 | 1653 | 2 | 0 | 0 | 0 | 0 | 2 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0006 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0002c0005 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0003c0007 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4244 | 103 | 43 | 28 | 18 | 8 | 6 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0002 | 0/0 | 4244 | 36 | 8 | 11 | 10 | 1 | 6 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0003 | 0/1 | 4244 | 23 | 0 | 3 | 16 | 0 | 3 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0004 | 0/0 | 4244 | 14 | 14 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0006 | 0/0 | 4244 | 5 | 0 | 0 | 5 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0007 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0008 | 0/0 | 4244 | 3 | 3 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0009 | 0/0 | 4244 | 3 | 2 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0010 | 0/0 | 4244 | 2 | 0 | 2 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0011 | 1/0 | 4246 | 2 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0012 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0013 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0014 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0015 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0016 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0017 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0018 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0019 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0022 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0001t0023 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0002t0005 | 0/0 | 4244 | 5 | 5 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0002t0020 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0002t0021 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0003t0005 | 0/0 | 4244 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0004t0001 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0001c0006t0003 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0002c0005t0001 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| a0003c0007t0001 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | copy fasta | chr11 | 46612553 | 46679518 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0009g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0011g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0011g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0013g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0014g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0015g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0016g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0017g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0018g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0019g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0022g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0001t0023g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0002t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0002t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0002t0020g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0002t0021g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0003t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0003t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0001c0006t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0002c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| a0003c0007t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0083 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0084 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01109 | hp1 | a0001 | c0002 | t0021 | g0026 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0024 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | IBS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01516 | hp1 | a0001 | c0001 | t0018 | g0087 | EUR | IBS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0023 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | KHV | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | KHV | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | CDX | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02280 | hp1 | a0001 | c0002 | t0005 | g0216 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0065 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02615 | hp2 | a0001 | c0003 | t0005 | g0211 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02818 | hp2 | a0001 | c0002 | t0005 | g0210 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02965 | hp2 | a0001 | c0002 | t0020 | g0025 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0022 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0096 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0214 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0212 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0215 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0027 | AFR | MSL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03654 | hp1 | a0001 | c0001 | t0022 | g0165 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | STU | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG04115 | hp1 | a0001 | c0001 | t0013 | g0056 | SAS | STU | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0176 | SAS | STU | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | CHB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0192 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18971 | hp1 | a0001 | c0001 | t0017 | g0174 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18978 | hp2 | a0001 | c0001 | t0015 | g0077 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19056 | hp1 | a0001 | c0001 | t0023 | g0101 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19090 | hp2 | a0001 | c0006 | t0003 | g0187 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA19240 | hp2 | a0001 | c0002 | t0005 | g0213 | AFR | YRI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ASW | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0177 | SAS | GIH | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA20905 | hp2 | a0002 | c0005 | t0001 | g0124 | SAS | GIH | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA18955 | hp2 | a0001 | c0001 | t0016 | g0079 | EAS | JPT | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | USA | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| NA21309 | hp2 | a0003 | c0007 | t0001 | g0107 | AFR | LWK | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0129 | REF | REF | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0011 | g0102 | REF | REF | ATG13_chr11_46612553_46679518 | ATG13 | chr11 | 46612553 | 46679518 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46650250
|
A | G | 1 | a0003 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.391A>G | p.Ile131Val | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/19 | 798/4246 | 391/1653 | 131/550 | chr11 | 46650250 | ||
| chr11:46668863
|
G | A | 1 | a0002 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1399G>A | p.Gly467Arg | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 17/19 | 1806/4246 | 1399/1653 | 467/550 | chr11 | 46668863 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46645398
|
T | A | 1 | a0001c0003 | 2 | HG02615.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.129T>A | p.Ser43Ser | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 4/19 | 536/4246 | 129/1653 | 43/550 | chr11 | 46645398 | ||
| chr11:46657599
|
T | C | 1 | a0001c0004 | 2 | HG04115.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.672T>C | p.Ser224Ser | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/19 | 1079/4246 | 672/1653 | 224/550 | chr11 | 46657599 | ||
| chr11:46667788
|
C | T | 1 | a0001c0006 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.1152C>T | p.Thr384Thr | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/19 | 1559/4246 | 1152/1653 | 384/550 | chr11 | 46667788 | ||
| chr11:46667803
|
T | C | 2 | a0001c0002a0001c0003 | 9 | HG01109.hp1 HG02280.hp1 HG02615.hp2 others(6): Show |
synonymous_variant | LOW | c.1167T>C | p.Ser389Ser | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/19 | 1574/4246 | 1167/1653 | 389/550 | chr11 | 46667803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46617598
|
C | T | 1 | a0001c0001t0023 | 1 | NA19056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-362C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/19 | 26694 | chr11 | 46617598 | |||||
| chr11:46617641
|
T | C | 1 | a0001c0001t0010 | 2 | HG01069.hp2 HG01099.hp2 |
5_prime_UTR_variant | MODIFIER | c.-319T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/19 | 26651 | chr11 | 46617641 | |||||
| chr11:46617694
|
C | T | 1 | a0001c0001t0022 | 1 | HG03654.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-266C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/19 | chr11 | 46617694 | ||||||
| chr11:46672522
|
G | A | 1 | a0001c0001t0006 | 5 | HG00597.hp1 HG02040.hp2 HG02132.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*190G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 190 | chr11 | 46672522 | |||||
| chr11:46672628
|
C | T | 5 | a0001c0001t0004a0001c0001t0009a0001c0001t0019others(2): Show | 20 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*296C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 296 | chr11 | 46672628 | |||||
| chr11:46672763
|
GTC | G | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*432_*433delTC | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 432 | chr11 | 46672763 | |||||
| chr11:46672867
|
C | T | 1 | a0001c0001t0009 | 3 | HG01243.hp1 HG01884.hp2 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 535 | chr11 | 46672867 | |||||
| chr11:46672946
|
C | A | 1 | a0001c0001t0007 | 3 | HG02486.hp2 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*614C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 614 | chr11 | 46672946 | |||||
| chr11:46673008
|
T | C | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*676T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 676 | chr11 | 46673008 | |||||
| chr11:46673048
|
T | C | 1 | a0001c0001t0012 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*716T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 716 | chr11 | 46673048 | |||||
| chr11:46673385
|
C | T | 1 | a0001c0002t0021 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1053C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1053 | chr11 | 46673385 | |||||
| chr11:46673386
|
G | A | 1 | a0001c0001t0013 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1054G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1054 | chr11 | 46673386 | |||||
| chr11:46673815
|
C | T | 1 | a0001c0001t0008 | 3 | HG02280.hp2 NA19043.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1483C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1483 | chr11 | 46673815 | |||||
| chr11:46673864
|
T | C | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(12): Show | 94 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1532T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1532 | chr11 | 46673864 | |||||
| chr11:46673871
|
C | T | 1 | a0001c0001t0016 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1539C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1539 | chr11 | 46673871 | |||||
| chr11:46673933
|
G | A | 3 | a0001c0001t0002a0001c0001t0013a0001c0001t0014 | 38 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1601G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1601 | chr11 | 46673933 | |||||
| chr11:46673947
|
G | A | 1 | a0001c0001t0014 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1615G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1615 | chr11 | 46673947 | |||||
| chr11:46674001
|
G | A | 1 | a0001c0001t0014 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1669G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1669 | chr11 | 46674001 | |||||
| chr11:46674167
|
A | G | 2 | a0001c0002t0005a0001c0003t0005 | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1835A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1835 | chr11 | 46674167 | |||||
| chr11:46674278
|
G | A | 2 | a0001c0002t0020a0001c0002t0021 | 2 | HG01109.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 1946 | chr11 | 46674278 | |||||
| chr11:46674335
|
A | G | 1 | a0001c0001t0015 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 2003 | chr11 | 46674335 | |||||
| chr11:46674373
|
G | A | 1 | a0001c0001t0017 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2041G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 2041 | chr11 | 46674373 | |||||
| chr11:46674431
|
A | T | 1 | a0001c0001t0018 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2099A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 19/19 | 2099 | chr11 | 46674431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46617973
|
G | T | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+83G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46617973 | ||||||
| chr11:46618032
|
G | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(65): Show | 69 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.-70+142G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618032 | ||||||
| chr11:46618208
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-70+318G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618208 | ||||||
| chr11:46618253
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-70+363C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618253 | ||||||
| chr11:46618408
|
C | G | 1 | a0001c0001t0003g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-70+518C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618408 | ||||||
| chr11:46618468
|
T | G | 2 | a0001c0001t0007g0002a0001c0001t0007g0064 | 3 | HG02486.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-70+578T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618468 | ||||||
| chr11:46618517
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-70+627A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618517 | ||||||
| chr11:46618753
|
T | G | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG02451.hp2 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70+863T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618753 | ||||||
| chr11:46618764
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-70+874C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618764 | ||||||
| chr11:46618953
|
A | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(63): Show | 67 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.-70+1063A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46618953 | ||||||
| chr11:46619035
|
G | T | 1 | a0001c0001t0001g0205 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-70+1145G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619035 | ||||||
| chr11:46619222
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-70+1332A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619222 | ||||||
| chr11:46619372
|
C | CT | 29 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(26): Show | 29 | HG00140.hp1 HG00597.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-70+1511dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619372
|
C | CTTTTTT | 10 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(7): Show | 10 | HG02451.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70+1506_-70+1511d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619372
|
C | CTTTTTTT | 5 | a0001c0001t0004g0038a0001c0001t0004g0039a0001c0001t0004g0040others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+1505_-70+1511d others(9): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619372
|
C | CTTTTTTT others(2): Show |
10 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(7): Show | 10 | HG01257.hp1 HG01515.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70+1503_-70+1511d others(11): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619372
|
C | CTTTTTTT others(3): Show |
9 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0055others(6): Show | 9 | HG00735.hp1 HG01074.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70+1502_-70+1511d others(12): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619372
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-70+1499_-70+1511d others(15): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619372
|
CT | C | 8 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(5): Show | 8 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+1511delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619372
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-70+1501_-70+1511d others(13): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619372
|
CTTTTTTT others(5): Show |
C | 17 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(14): Show | 18 | HG01070.hp2 HG01081.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.-70+1500_-70+1511d others(14): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619372 | |||||
| chr11:46619439
|
C | T | 2 | a0001c0004t0001g0176a0001c0004t0001g0177 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-70+1549C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619439 | ||||||
| chr11:46619556
|
G | T | 1 | a0001c0001t0003g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-70+1666G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619556 | ||||||
| chr11:46619638
|
T | A | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-70+1748T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619638 | ||||||
| chr11:46619753
|
G | A | 18 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-70+1863G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619753 | ||||||
| chr11:46619866
|
A | G | 1 | a0001c0001t0002g0020 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-70+1976A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619866 | ||||||
| chr11:46619901
|
C | T | 1 | a0001c0001t0017g0174 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-70+2011C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619901 | ||||||
| chr11:46619969
|
C | CA | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+2080dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46619969 | |||||
| chr11:46619985
|
C | T | 2 | a0001c0004t0001g0176a0001c0004t0001g0177 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-70+2095C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46619985 | ||||||
| chr11:46620012
|
G | A | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+2122G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620012 | ||||||
| chr11:46620013
|
C | A | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+2123C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620013 | ||||||
| chr11:46620026
|
C | CA | 6 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0178others(3): Show | 6 | HG01192.hp1 HG01981.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+2154dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46620026 | |||||
| chr11:46620026
|
CA | C | 79 | a0001c0001t0001g0076a0001c0001t0001g0164a0001c0001t0001g0166others(76): Show | 80 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.-70+2154delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46620026 | |||||
| chr11:46620035
|
A | G | 18 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-70+2145A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620035 | ||||||
| chr11:46620104
|
T | C | 56 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(53): Show | 57 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-70+2214T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620104 | ||||||
| chr11:46620159
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0203 | 3 | HG02630.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-70+2269C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620159 | ||||||
| chr11:46620161
|
G | A | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+2271G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620161 | ||||||
| chr11:46620256
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-70+2366G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620256 | ||||||
| chr11:46620385
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+2495G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620385 | ||||||
| chr11:46620550
|
C | T | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 4 | HG00609.hp1 HG02040.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+2660C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620550 | ||||||
| chr11:46620551
|
G | A | 11 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(8): Show | 11 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.-70+2661G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620551 | ||||||
| chr11:46620644
|
G | A | 2 | a0001c0003t0005g0211a0001c0003t0005g0212 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-70+2754G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620644 | ||||||
| chr11:46620752
|
G | A | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+2862G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620752 | ||||||
| chr11:46620896
|
A | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0170 | 2 | HG01496.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-70+3006A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46620896 | ||||||
| chr11:46621099
|
C | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-70+3209C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621099 | ||||||
| chr11:46621221
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-70+3331G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621221 | ||||||
| chr11:46621302
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-70+3412C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621302 | ||||||
| chr11:46621355
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-70+3465A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621355 | ||||||
| chr11:46621363
|
T | A | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+3473T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621363 | ||||||
| chr11:46621692
|
A | G | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+3802A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621692 | ||||||
| chr11:46621757
|
A | G | 1 | a0001c0001t0011g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-70+3867A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621757 | ||||||
| chr11:46621766
|
A | G | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+3876A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621766 | ||||||
| chr11:46621849
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-70+3959C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46621849 | ||||||
| chr11:46622073
|
TTACATAT others(13): Show |
T | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-70+4186_-70+4205d others(22): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622073 | |||||
| chr11:46622076
|
C | CAT | 8 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0162others(5): Show | 8 | HG00438.hp1 HG00673.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+4237_-70+4238d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
C | CATAT | 6 | a0001c0001t0001g0095a0001c0001t0001g0158a0001c0001t0001g0161others(3): Show | 6 | HG00140.hp1 HG00673.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+4235_-70+4238d others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
C | CATATATA others(5): Show |
1 | a0001c0001t0003g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-70+4227_-70+4238d others(14): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CAT | C | 10 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0132others(7): Show | 10 | HG01993.hp1 HG02040.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70+4237_-70+4238d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATAT | C | 15 | a0001c0001t0001g0066a0001c0001t0001g0116a0001c0001t0001g0117others(12): Show | 16 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.-70+4235_-70+4238d others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATAT | C | 12 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0120others(9): Show | 12 | HG00438.hp2 HG01358.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.-70+4233_-70+4238d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(1): Show |
C | 22 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(19): Show | 22 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-70+4231_-70+4238d others(10): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(3): Show |
C | 14 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0134others(11): Show | 14 | HG00642.hp2 HG01070.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-70+4229_-70+4238d others(12): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(5): Show |
C | 5 | a0001c0001t0001g0086a0001c0001t0001g0141a0001c0001t0001g0160others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+4227_-70+4238d others(14): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(7): Show |
C | 10 | a0001c0001t0001g0063a0001c0001t0001g0076a0001c0001t0001g0092others(7): Show | 10 | HG01516.hp1 HG02165.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70+4225_-70+4238d others(16): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(9): Show |
C | 7 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(4): Show | 7 | HG00738.hp2 HG02559.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+4223_-70+4238d others(18): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(11): Show |
C | 6 | a0001c0001t0001g0067a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+4221_-70+4238d others(20): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(13): Show |
C | 5 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0152others(2): Show | 5 | HG01261.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70+4219_-70+4238d others(22): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(15): Show |
C | 1 | a0001c0001t0004g0038 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-70+4217_-70+4238d others(24): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(17): Show |
C | 22 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(19): Show | 22 | HG00099.hp2 HG01123.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-70+4215_-70+4238d others(26): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(19): Show |
C | 46 | a0001c0001t0001g0156a0001c0001t0001g0200a0001c0001t0001g0201others(43): Show | 47 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.-70+4213_-70+4238d others(28): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622076
|
CATATATA others(23): Show |
C | 2 | a0001c0001t0003g0075a0001c0001t0003g0157 | 2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-70+4209_-70+4238d others(32): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622076 | |||||
| chr11:46622092
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-70+4202T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622092 | ||||||
| chr11:46622119
|
A | T | 1 | a0001c0001t0003g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-70+4229A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622119 | ||||||
| chr11:46622120
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-70+4231_-70+4246d others(18): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622120 | ||||||
| chr11:46622122
|
TATATATT others(7): Show |
T | 1 | a0001c0001t0003g0169 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-70+4233_-70+4246d others(16): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622122 | ||||||
| chr11:46622123
|
A | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-70+4233A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622123 | ||||||
| chr11:46622123
|
ATATATT | A | 2 | a0001c0001t0001g0112a0001c0001t0003g0113 | 2 | HG00099.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.-70+4237_-70+4242d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622123 | |||||
| chr11:46622125
|
A | ATATT | 3 | a0001c0001t0001g0100a0001c0001t0015g0077a0001c0003t0005g0211 | 3 | HG01884.hp1 HG02615.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-70+4241_-70+4244d others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46622125 | |||||
| chr11:46622125
|
A | T | 14 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(11): Show | 14 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-70+4235A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622125 | ||||||
| chr11:46622129
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-70+4239T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622129 | ||||||
| chr11:46622136
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-70+4246A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622136 | ||||||
| chr11:46622512
|
A | C | 1 | a0001c0001t0001g0202 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-70+4622A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622512 | ||||||
| chr11:46622530
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0062 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-70+4640A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622530 | ||||||
| chr11:46622593
|
T | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(63): Show | 67 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.-70+4703T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46622593 | ||||||
| chr11:46623070
|
G | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+5180G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623070 | ||||||
| chr11:46623083
|
G | A | 1 | a0001c0001t0008g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-70+5193G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623083 | ||||||
| chr11:46623265
|
G | T | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-70+5375G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623265 | ||||||
| chr11:46623273
|
A | G | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-70+5383A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623273 | ||||||
| chr11:46623293
|
C | CAAAGA | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+5412_-70+5416d others(7): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46623293 | |||||
| chr11:46623563
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-70+5673G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46623563 | ||||||
| chr11:46624008
|
G | T | 1 | a0001c0001t0002g0020 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-69-6037G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624008 | ||||||
| chr11:46624010
|
A | AT | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-6021dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46624010 | |||||
| chr11:46624108
|
G | A | 1 | a0001c0001t0008g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-69-5937G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624108 | ||||||
| chr11:46624224
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-69-5821G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624224 | ||||||
| chr11:46624480
|
A | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(65): Show | 69 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.-69-5565A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624480 | ||||||
| chr11:46624487
|
G | C | 1 | a0001c0001t0011g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-69-5558G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624487 | ||||||
| chr11:46624488
|
A | AT | 9 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0115others(6): Show | 9 | HG01106.hp2 HG01109.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-69-5544dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46624488 | |||||
| chr11:46624488
|
AT | A | 5 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0038others(2): Show | 5 | HG02809.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69-5544delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46624488 | |||||
| chr11:46624499
|
T | TG | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-5546_-69-5545i others(3): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624499 | ||||||
| chr11:46624837
|
A | G | 1 | a0001c0001t0003g0081 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-69-5208A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624837 | ||||||
| chr11:46624883
|
A | G | 18 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-69-5162A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46624883 | ||||||
| chr11:46625074
|
T | C | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-69-4971T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625074 | ||||||
| chr11:46625269
|
C | CT | 28 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0108others(25): Show | 28 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-69-4752dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46625269 | |||||
| chr11:46625269
|
C | CTT | 5 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0178others(2): Show | 5 | HG02145.hp2 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69-4753_-69-4752d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46625269 | |||||
| chr11:46625269
|
CT | C | 47 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(44): Show | 48 | HG00642.hp1 HG00642.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-69-4752delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46625269 | |||||
| chr11:46625332
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-69-4713A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625332 | ||||||
| chr11:46625351
|
C | A | 1 | a0001c0003t0005g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-69-4694C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625351 | ||||||
| chr11:46625732
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-69-4313C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625732 | ||||||
| chr11:46625793
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-69-4252G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46625793 | ||||||
| chr11:46626425
|
T | C | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-3620T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46626425 | ||||||
| chr11:46626540
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-69-3505G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46626540 | ||||||
| chr11:46626882
|
G | A | 104 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(101): Show | 105 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(102): Show |
intron_variant | MODIFIER | c.-69-3163G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46626882 | ||||||
| chr11:46627026
|
G | A | 1 | a0001c0001t0014g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-69-3019G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627026 | ||||||
| chr11:46627109
|
G | A | 11 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(8): Show | 11 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-2936G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627109 | ||||||
| chr11:46627287
|
A | G | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-2758A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627287 | ||||||
| chr11:46627358
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-69-2687G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627358 | ||||||
| chr11:46627385
|
T | A | 23 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0115others(20): Show | 23 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-69-2660T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46627385 | ||||||
| chr11:46628082
|
C | CA | 27 | a0001c0001t0001g0078a0001c0001t0001g0095a0001c0001t0001g0166others(24): Show | 27 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-69-1944dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46628082 | |||||
| chr11:46628082
|
CA | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0001g0161others(2): Show | 5 | HG01496.hp1 HG01515.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-69-1944delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46628082 | |||||
| chr11:46628169
|
G | A | 12 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(9): Show | 12 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.-69-1876G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628169 | ||||||
| chr11:46628211
|
T | C | 1 | a0001c0001t0003g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-69-1834T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628211 | ||||||
| chr11:46628369
|
T | C | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-1676T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628369 | ||||||
| chr11:46628424
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-69-1621G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628424 | ||||||
| chr11:46628508
|
A | G | 1 | a0001c0001t0012g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-69-1537A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628508 | ||||||
| chr11:46628523
|
C | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-1522C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628523 | ||||||
| chr11:46628786
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-69-1259T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628786 | ||||||
| chr11:46628825
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-69-1220C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628825 | ||||||
| chr11:46628888
|
T | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(65): Show | 69 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.-69-1157T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46628888 | ||||||
| chr11:46628938
|
CT | C | 149 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-69-1092delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr11 | 46628938 | |||||
| chr11:46629004
|
G | A | 1 | a0003c0007t0001g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-69-1041G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46629004 | ||||||
| chr11:46629305
|
G | C | 1 | a0001c0002t0020g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-69-740G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46629305 | ||||||
| chr11:46629842
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-69-203G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46629842 | ||||||
| chr11:46629902
|
C | T | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-69-143C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 1/18 | chr11 | 46629902 | ||||||
| chr11:46630222
|
T | C | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-14+122T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46630222 | ||||||
| chr11:46630514
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-14+414C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46630514 | ||||||
| chr11:46630568
|
C | CTTTT | 102 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(99): Show | 103 | HG00609.hp1 HG00735.hp1 HG01070.hp2 others(100): Show |
intron_variant | MODIFIER | c.-14+482_-14+485dup others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46630568 | |||||
| chr11:46630568
|
C | CTTTTT | 21 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG00673.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-14+481_-14+485dup others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46630568 | |||||
| chr11:46630768
|
A | G | 1 | a0001c0001t0019g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-14+668A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46630768 | ||||||
| chr11:46630902
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0062 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14+802G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46630902 | ||||||
| chr11:46631032
|
A | G | 56 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(53): Show | 57 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14+932A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46631032 | ||||||
| chr11:46631133
|
A | G | 215 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-14+1033A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46631133 | ||||||
| chr11:46631192
|
G | T | 12 | a0001c0001t0002g0045a0001c0001t0002g0047a0001c0001t0002g0048others(9): Show | 12 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-14+1092G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46631192 | ||||||
| chr11:46632127
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0179 | 2 | HG00738.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-14+2027G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46632127 | ||||||
| chr11:46632597
|
C | T | 1 | a0001c0002t0005g0213 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-14+2497C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46632597 | ||||||
| chr11:46632688
|
CTT | C | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+2591_-14+2592d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46632688 | |||||
| chr11:46632854
|
T | C | 38 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(35): Show | 39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+2754T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46632854 | ||||||
| chr11:46632995
|
T | TAA | 17 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(14): Show | 17 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14+2903_-14+2904d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46632995 | |||||
| chr11:46633001
|
A | T | 9 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0012others(6): Show | 9 | HG01981.hp1 NA18942.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14+2901A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633001 | ||||||
| chr11:46633003
|
A | AAT | 5 | a0001c0001t0001g0078a0001c0001t0001g0097a0001c0001t0001g0182others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+2926_-14+2927d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46633003 | |||||
| chr11:46633003
|
A | T | 34 | a0001c0001t0001g0073a0001c0001t0001g0095a0001c0001t0001g0123others(31): Show | 35 | HG00642.hp1 HG00735.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-14+2903A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633003 | ||||||
| chr11:46633005
|
T | A | 51 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0100others(48): Show | 51 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.-14+2905T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633005 | ||||||
| chr11:46633007
|
T | A | 28 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0115others(25): Show | 28 | HG01109.hp2 HG01993.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14+2907T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633007 | ||||||
| chr11:46633009
|
T | A | 5 | a0001c0001t0001g0206a0001c0002t0005g0213a0001c0002t0005g0215others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+2909T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633009 | ||||||
| chr11:46633011
|
T | A | 1 | a0001c0003t0005g0211 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-14+2911T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633011 | ||||||
| chr11:46633015
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0184 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-14+2916_-14+2926d others(13): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633015 | ||||||
| chr11:46633016
|
ATATATAT others(6): Show |
A | 22 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0115others(19): Show | 22 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-14+2918_-14+2930d others(15): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46633016 | |||||
| chr11:46633026
|
A | AT | 9 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0068others(6): Show | 9 | HG01496.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14+2941dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46633026 | |||||
| chr11:46633026
|
A | ATAT | 19 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0001t0001g0146others(16): Show | 19 | HG00735.hp1 HG01257.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14+2927_-14+2928i others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46633026 | |||||
| chr11:46633026
|
A | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0112a0001c0001t0001g0116others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14+2926A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633026 | ||||||
| chr11:46633027
|
T | TA | 2 | a0001c0001t0001g0066a0001c0001t0002g0009 | 2 | HG02818.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-14+2927_-14+2928i others(3): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633027 | ||||||
| chr11:46633027
|
T | TATA | 14 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(11): Show | 15 | HG01070.hp2 HG01081.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14+2927_-14+2928i others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633027 | ||||||
| chr11:46633028
|
T | A | 65 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-14+2928T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633028 | ||||||
| chr11:46633029
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-14+2929T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633029 | ||||||
| chr11:46633030
|
T | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0143others(2): Show | 5 | HG00140.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+2930T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633030 | ||||||
| chr11:46633051
|
G | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+2951G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633051 | ||||||
| chr11:46633129
|
A | G | 1 | a0001c0001t0004g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14+3029A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633129 | ||||||
| chr11:46633348
|
T | C | 1 | a0001c0002t0020g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-14+3248T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633348 | ||||||
| chr11:46633370
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+3270C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633370 | ||||||
| chr11:46633537
|
G | A | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-14+3437G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633537 | ||||||
| chr11:46633774
|
A | C | 1 | a0001c0001t0004g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+3674A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633774 | ||||||
| chr11:46633777
|
C | T | 1 | a0001c0001t0008g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14+3677C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633777 | ||||||
| chr11:46633830
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-14+3730C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46633830 | ||||||
| chr11:46634062
|
A | AT | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14+3963dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46634062 | |||||
| chr11:46634092
|
G | T | 3 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0055 | 3 | HG02886.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-14+3992G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634092 | ||||||
| chr11:46634265
|
T | G | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14+4165T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634265 | ||||||
| chr11:46634318
|
G | A | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14+4218G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634318 | ||||||
| chr11:46634359
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-14+4259A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634359 | ||||||
| chr11:46634407
|
CT | C | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+4320delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46634407 | |||||
| chr11:46634411
|
T | A | 38 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(35): Show | 39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-14+4311T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634411 | ||||||
| chr11:46634474
|
C | G | 1 | a0001c0001t0008g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14+4374C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634474 | ||||||
| chr11:46634502
|
G | GTCC | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(63): Show | 67 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.-14+4404_-14+4406d others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46634502 | |||||
| chr11:46634687
|
G | A | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14+4587G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634687 | ||||||
| chr11:46634875
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0203 | 3 | HG02630.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-14+4775G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634875 | ||||||
| chr11:46634900
|
A | G | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 4 | HG00609.hp1 HG02040.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+4800A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634900 | ||||||
| chr11:46634947
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14+4847C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46634947 | ||||||
| chr11:46635195
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-14+5095C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635195 | ||||||
| chr11:46635454
|
C | A | 2 | a0001c0004t0001g0176a0001c0004t0001g0177 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-14+5354C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635454 | ||||||
| chr11:46635459
|
T | G | 1 | a0001c0001t0004g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-14+5359T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635459 | ||||||
| chr11:46635727
|
C | T | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+5627C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635727 | ||||||
| chr11:46635871
|
T | C | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+5771T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635871 | ||||||
| chr11:46635880
|
T | G | 133 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(130): Show | 134 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(131): Show |
intron_variant | MODIFIER | c.-14+5780T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46635880 | ||||||
| chr11:46636055
|
G | A | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14+5955G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46636055 | ||||||
| chr11:46636384
|
C | T | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+6284C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46636384 | ||||||
| chr11:46636518
|
A | T | 7 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0115others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+6418A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46636518 | ||||||
| chr11:46636557
|
C | CA | 52 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0111others(49): Show | 53 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-14+6481dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46636557 | |||||
| chr11:46636557
|
C | CAA | 10 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0002g0006others(7): Show | 10 | HG00735.hp1 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+6480_-14+6481d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46636557 | |||||
| chr11:46636557
|
CA | C | 13 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0038others(10): Show | 13 | HG01109.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14+6481delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46636557 | |||||
| chr11:46636810
|
C | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+6710C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46636810 | ||||||
| chr11:46637016
|
T | G | 1 | a0001c0001t0003g0157 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-14+6916T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46637016 | ||||||
| chr11:46637163
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-14+7063G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46637163 | ||||||
| chr11:46637176
|
A | T | 7 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0001t0003g0106others(4): Show | 7 | HG00438.hp1 HG01993.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+7076A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46637176 | ||||||
| chr11:46637328
|
A | G | 18 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13-6951A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46637328 | ||||||
| chr11:46638041
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-13-6238G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638041 | ||||||
| chr11:46638129
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-13-6150T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638129 | ||||||
| chr11:46638602
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-13-5677C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638602 | ||||||
| chr11:46638620
|
A | G | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13-5659A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638620 | ||||||
| chr11:46638802
|
T | A | 215 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-13-5477T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638802 | ||||||
| chr11:46638841
|
T | C | 1 | a0001c0001t0003g0183 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-13-5438T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638841 | ||||||
| chr11:46638888
|
A | C | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-5391A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638888 | ||||||
| chr11:46638902
|
G | A | 1 | a0001c0001t0019g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-13-5377G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638902 | ||||||
| chr11:46638920
|
A | C | 3 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0060 | 3 | HG02145.hp1 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-13-5359A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638920 | ||||||
| chr11:46638991
|
TA | T | 2 | a0001c0002t0005g0215a0001c0002t0005g0216 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-13-5287delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638991 | ||||||
| chr11:46638994
|
T | A | 2 | a0001c0002t0005g0215a0001c0002t0005g0216 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-13-5285T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638994 | ||||||
| chr11:46638995
|
TA | T | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02615.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-5283delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638995 | ||||||
| chr11:46638996
|
A | T | 29 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(26): Show | 29 | HG00673.hp1 HG01069.hp1 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13-5283A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46638996 | ||||||
| chr11:46639000
|
T | A | 38 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(35): Show | 39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.-13-5279T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639000 | ||||||
| chr11:46639073
|
T | C | 48 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(45): Show | 49 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.-13-5206T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639073 | ||||||
| chr11:46639074
|
G | A | 1 | a0001c0002t0021g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13-5205G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639074 | ||||||
| chr11:46639099
|
T | C | 1 | a0001c0001t0011g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-13-5180T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639099 | ||||||
| chr11:46639189
|
T | C | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13-5090T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639189 | ||||||
| chr11:46639374
|
T | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4905T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639374 | ||||||
| chr11:46639853
|
A | AT | 6 | a0001c0001t0001g0133a0001c0001t0001g0172a0001c0001t0001g0193others(3): Show | 6 | HG00609.hp1 NA18940.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-4406dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46639853 | |||||
| chr11:46639853
|
AT | A | 55 | a0001c0001t0001g0063a0001c0001t0001g0089a0001c0001t0001g0091others(52): Show | 56 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13-4406delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46639853 | |||||
| chr11:46639853
|
ATT | A | 25 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(22): Show | 25 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.-13-4407_-13-4406d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46639853 | |||||
| chr11:46639911
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13-4368T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639911 | ||||||
| chr11:46639986
|
T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-4293T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46639986 | ||||||
| chr11:46640567
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-13-3712G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46640567 | ||||||
| chr11:46640610
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-13-3669C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46640610 | ||||||
| chr11:46640939
|
G | T | 8 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0031others(5): Show | 8 | HG02647.hp1 HG02809.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-3340G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46640939 | ||||||
| chr11:46641003
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-13-3276C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641003 | ||||||
| chr11:46641279
|
C | A | 3 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0055 | 3 | HG02886.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-13-3000C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641279 | ||||||
| chr11:46641297
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-13-2982C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641297 | ||||||
| chr11:46641662
|
G | T | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-2617G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641662 | ||||||
| chr11:46641760
|
A | AT | 206 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-13-2505dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46641760 | |||||
| chr11:46641760
|
A | ATT | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-2506_-13-2505d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46641760 | |||||
| chr11:46641780
|
CAG | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0164a0001c0001t0001g0167 | 3 | HG00673.hp1 NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-13-2496_-13-2495d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46641780 | |||||
| chr11:46641888
|
C | A | 15 | a0001c0001t0001g0076a0001c0001t0001g0161a0001c0001t0001g0164others(12): Show | 15 | HG00609.hp1 HG00673.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-13-2391C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641888 | ||||||
| chr11:46641951
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13-2328T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641951 | ||||||
| chr11:46641972
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-13-2307G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46641972 | ||||||
| chr11:46642076
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13-2203G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46642076 | ||||||
| chr11:46642081
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0182 | 3 | HG00140.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-13-2198C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46642081 | ||||||
| chr11:46642304
|
G | GT | 97 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0074others(94): Show | 98 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-13-1955dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46642304 | |||||
| chr11:46642304
|
G | GTT | 20 | a0001c0001t0001g0076a0001c0001t0001g0095a0001c0001t0001g0144others(17): Show | 20 | HG00609.hp1 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13-1956_-13-1955d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46642304 | |||||
| chr11:46642304
|
GT | G | 15 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(12): Show | 15 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13-1955delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46642304 | |||||
| chr11:46642304
|
GTTTTTTT others(2): Show |
G | 37 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(34): Show | 38 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-13-1963_-13-1955d others(11): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46642304 | |||||
| chr11:46642366
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13-1913C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46642366 | ||||||
| chr11:46642370
|
A | G | 1 | a0001c0001t0008g0003 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13-1909A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46642370 | ||||||
| chr11:46643068
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13-1211C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643068 | ||||||
| chr11:46643412
|
C | CT | 4 | a0001c0001t0003g0148a0001c0001t0003g0198a0001c0001t0003g0199others(1): Show | 4 | HG00597.hp2 NA18983.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-866dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46643412 | |||||
| chr11:46643511
|
C | G | 18 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-13-768C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643511 | ||||||
| chr11:46643523
|
G | T | 1 | a0001c0001t0001g0117 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13-756G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643523 | ||||||
| chr11:46643552
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13-727G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643552 | ||||||
| chr11:46643612
|
C | CT | 17 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0122others(14): Show | 17 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13-649dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr11 | 46643612 | |||||
| chr11:46643631
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-13-648A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643631 | ||||||
| chr11:46643645
|
C | T | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13-634C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643645 | ||||||
| chr11:46643716
|
A | G | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13-563A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643716 | ||||||
| chr11:46643980
|
A | G | 1 | a0001c0001t0012g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-13-299A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46643980 | ||||||
| chr11:46644249
|
A | G | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-30A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 2/18 | chr11 | 46644249 | ||||||
| chr11:46644542
|
A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0003g0126 | 3 | HG00558.hp1 HG00558.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.69+182A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46644542 | ||||||
| chr11:46644585
|
A | AT | 34 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(31): Show | 35 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.69+239dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr11 | 46644585 | |||||
| chr11:46644585
|
A | T | 1 | a0001c0001t0014g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+225A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46644585 | ||||||
| chr11:46644586
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.69+226T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46644586 | ||||||
| chr11:46644721
|
T | G | 38 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(35): Show | 39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.69+361T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46644721 | ||||||
| chr11:46645114
|
A | G | 38 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(35): Show | 39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.70-225A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46645114 | ||||||
| chr11:46645255
|
A | T | 1 | a0001c0001t0002g0045 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.70-84A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 3/18 | chr11 | 46645255 | ||||||
| chr11:46645518
|
T | G | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150+99T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 4/18 | chr11 | 46645518 | ||||||
| chr11:46646211
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0197 | 2 | HG00738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.270+222C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646211 | ||||||
| chr11:46646217
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.270+228C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646217 | ||||||
| chr11:46646391
|
G | A | 13 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(10): Show | 13 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.270+402G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646391 | ||||||
| chr11:46646457
|
TTTTTTG | T | 82 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(79): Show | 83 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.270+487_270+492del others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46646457 | |||||
| chr11:46646845
|
G | A | 38 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(35): Show | 39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.270+856G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646845 | ||||||
| chr11:46646965
|
G | T | 1 | a0001c0001t0003g0118 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.270+976G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46646965 | ||||||
| chr11:46647271
|
GTTTTTTT others(6): Show |
G | 88 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(85): Show | 89 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.270+1305_270+1317d others(15): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46647271 | |||||
| chr11:46647280
|
G | GT | 53 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(50): Show | 54 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.270+1303dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46647280 | |||||
| chr11:46647280
|
G | T | 1 | a0001c0001t0004g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.270+1291G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647280 | ||||||
| chr11:46647280
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+1303_270+1316d others(16): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46647280 | |||||
| chr11:46647283
|
T | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0137 | 2 | HG00099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.270+1294T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647283 | ||||||
| chr11:46647288
|
T | G | 3 | a0001c0001t0001g0105a0001c0001t0010g0083a0001c0001t0010g0084 | 3 | HG01069.hp1 HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.270+1299T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647288 | ||||||
| chr11:46647293
|
G | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0062 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.270+1304G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647293 | ||||||
| chr11:46647633
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-1504G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647633 | ||||||
| chr11:46647702
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0062 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.271-1435A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46647702 | ||||||
| chr11:46648107
|
C | G | 1 | a0001c0001t0002g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.271-1030C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648107 | ||||||
| chr11:46648159
|
G | A | 1 | a0001c0001t0003g0081 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.271-978G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648159 | ||||||
| chr11:46648495
|
T | TGTCAACC others(3): Show |
1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-642_271-641ins others(10): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648495 | ||||||
| chr11:46648502
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-635G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648502 | ||||||
| chr11:46648504
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-633C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648504 | ||||||
| chr11:46648512
|
C | T | 1 | a0001c0001t0006g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.271-625C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648512 | ||||||
| chr11:46648513
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-624T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648513 | ||||||
| chr11:46648514
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-623T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648514 | ||||||
| chr11:46648516
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-621C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648516 | ||||||
| chr11:46648517
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-620G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648517 | ||||||
| chr11:46648519
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-618C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648519 | ||||||
| chr11:46648523
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-614A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648523 | ||||||
| chr11:46648558
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-579C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648558 | ||||||
| chr11:46648559
|
A | C | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-578A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648559 | ||||||
| chr11:46648560
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.271-577C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648560 | ||||||
| chr11:46648611
|
A | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-526A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648611 | ||||||
| chr11:46648658
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.271-479T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648658 | ||||||
| chr11:46648777
|
T | TA | 16 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.271-338dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46648777 | |||||
| chr11:46648777
|
TA | T | 13 | a0001c0001t0001g0076a0001c0001t0001g0152a0001c0001t0002g0007others(10): Show | 13 | HG01515.hp2 HG02040.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.271-338delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr11 | 46648777 | |||||
| chr11:46648798
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.271-339A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648798 | ||||||
| chr11:46648901
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0140 | 2 | HG01106.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.271-236G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 5/18 | chr11 | 46648901 | ||||||
| chr11:46649306
|
A | G | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.317+123A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649306 | ||||||
| chr11:46649307
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0203 | 3 | HG02630.hp2 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.317+124T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649307 | ||||||
| chr11:46649484
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0062 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.317+301C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649484 | ||||||
| chr11:46649535
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.317+352C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649535 | ||||||
| chr11:46649843
|
C | T | 9 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0131others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.318-334C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46649843 | ||||||
| chr11:46650136
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.318-41G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 6/18 | chr11 | 46650136 | ||||||
| chr11:46650513
|
C | T | 2 | a0001c0001t0006g0188a0001c0001t0006g0189 | 2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.458+196C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650513 | ||||||
| chr11:46650524
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.458+207T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650524 | ||||||
| chr11:46650699
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.458+382G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650699 | ||||||
| chr11:46650812
|
G | A | 15 | a0001c0001t0001g0076a0001c0001t0001g0161a0001c0001t0001g0164others(12): Show | 15 | HG00609.hp1 HG00673.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.458+495G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650812 | ||||||
| chr11:46650826
|
G | A | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.458+509G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650826 | ||||||
| chr11:46650950
|
A | G | 1 | a0001c0001t0018g0087 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.458+633A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46650950 | ||||||
| chr11:46651092
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.458+775T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651092 | ||||||
| chr11:46651369
|
A | G | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.458+1052A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651369 | ||||||
| chr11:46651504
|
T | C | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.458+1187T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651504 | ||||||
| chr11:46651543
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.458+1226A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651543 | ||||||
| chr11:46651608
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.458+1291A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651608 | ||||||
| chr11:46651630
|
A | T | 1 | a0001c0001t0001g0168 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.458+1313A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651630 | ||||||
| chr11:46651762
|
C | A | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+1445C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651762 | ||||||
| chr11:46651794
|
C | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(65): Show | 69 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.458+1477C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46651794 | ||||||
| chr11:46652216
|
C | G | 2 | a0001c0003t0005g0211a0001c0003t0005g0212 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.458+1899C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46652216 | ||||||
| chr11:46652679
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.458+2362C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46652679 | ||||||
| chr11:46652720
|
T | C | 5 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0058others(2): Show | 5 | HG01074.hp2 HG01261.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+2403T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46652720 | ||||||
| chr11:46652915
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0111 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.458+2598G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46652915 | ||||||
| chr11:46653180
|
C | CT | 9 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.458+2880dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46653180 | |||||
| chr11:46653236
|
G | A | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.458+2919G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653236 | ||||||
| chr11:46653267
|
G | A | 2 | a0001c0001t0003g0081a0001c0001t0016g0079 | 2 | HG01192.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.458+2950G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653267 | ||||||
| chr11:46653404
|
C | A | 1 | a0001c0001t0003g0098 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.459-2829C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653404 | ||||||
| chr11:46653417
|
G | T | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.459-2816G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653417 | ||||||
| chr11:46653426
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-2807G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653426 | ||||||
| chr11:46653480
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.459-2753C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653480 | ||||||
| chr11:46653576
|
T | G | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.459-2657T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653576 | ||||||
| chr11:46653577
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.459-2656T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653577 | ||||||
| chr11:46653578
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.459-2655T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653578 | ||||||
| chr11:46653580
|
TG | T | 2 | a0001c0001t0001g0092a0001c0001t0003g0104 | 2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.459-2652delG | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653580 | ||||||
| chr11:46653805
|
A | G | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.459-2428A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653805 | ||||||
| chr11:46653868
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.459-2365G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653868 | ||||||
| chr11:46653883
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0062 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.459-2350A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46653883 | ||||||
| chr11:46654010
|
T | C | 1 | a0001c0001t0012g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459-2223T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654010 | ||||||
| chr11:46654266
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459-1967C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654266 | ||||||
| chr11:46654281
|
T | TTA | 17 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0014others(14): Show | 17 | HG02280.hp1 HG02615.hp1 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATA | 11 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0010others(8): Show | 12 | HG00735.hp1 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATA | 11 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0054others(8): Show | 11 | HG01261.hp1 HG02451.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATAT others(1): Show |
5 | a0001c0001t0002g0045a0001c0001t0002g0050a0001c0001t0002g0053others(2): Show | 5 | HG01074.hp2 HG01515.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(10): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0004g0040a0001c0002t0005g0214 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.459-1951_459-1950i others(12): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0004g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459-1951_459-1950i others(18): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0004g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.459-1951_459-1950i others(20): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATAT others(15): Show |
4 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0038others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(24): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATAT others(17): Show |
4 | a0001c0001t0004g0030a0001c0001t0004g0042a0001c0001t0009g0023others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-1951_459-1950i others(26): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0009g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.459-1951_459-1950i others(28): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654281
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0004g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459-1951_459-1950i others(32): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654281 | |||||
| chr11:46654283
|
T | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0008others(58): Show | 62 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.459-1950T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654283 | ||||||
| chr11:46654283
|
T | TTA | 23 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(20): Show | 23 | HG00609.hp2 HG00642.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.459-1924_459-1923d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | |||||
| chr11:46654283
|
T | TTATA | 20 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0085others(17): Show | 20 | HG00099.hp1 HG00099.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.459-1926_459-1923d others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | |||||
| chr11:46654283
|
T | TTATATA | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG00609.hp1 HG02040.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.459-1928_459-1923d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | |||||
| chr11:46654283
|
T | TTATATAT others(3): Show |
1 | a0001c0004t0001g0177 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.459-1932_459-1923d others(12): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | |||||
| chr11:46654283
|
TTA | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0158a0001c0001t0011g0065 | 3 | HG01515.hp1 HG02451.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.459-1924_459-1923d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr11 | 46654283 | |||||
| chr11:46654325
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.459-1908C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654325 | ||||||
| chr11:46654807
|
C | T | 85 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.459-1426C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654807 | ||||||
| chr11:46654866
|
C | T | 5 | a0001c0001t0002g0009a0001c0001t0002g0012a0001c0001t0002g0013others(2): Show | 5 | NA18960.hp2 NA18978.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.459-1367C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46654866 | ||||||
| chr11:46655125
|
C | T | 18 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.459-1108C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655125 | ||||||
| chr11:46655141
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.459-1092T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655141 | ||||||
| chr11:46655260
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01261.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.459-973G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655260 | ||||||
| chr11:46655315
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0182 | 3 | HG00140.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.459-918A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655315 | ||||||
| chr11:46655616
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.459-617A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655616 | ||||||
| chr11:46655790
|
T | C | 1 | a0001c0001t0006g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.459-443T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46655790 | ||||||
| chr11:46656184
|
C | G | 13 | a0001c0001t0001g0076a0001c0001t0001g0164a0001c0001t0001g0166others(10): Show | 13 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.459-49C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 7/18 | chr11 | 46656184 | ||||||
| chr11:46656314
|
T | TCTCCTAA others(9): Show |
1 | a0001c0001t0001g0130 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.499+42_499+57dupCT others(14): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 46656314 | |||||
| chr11:46656624
|
C | G | 1 | a0001c0002t0005g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.499+351C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656624 | ||||||
| chr11:46656742
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.500-353G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656742 | ||||||
| chr11:46656773
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.500-322G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656773 | ||||||
| chr11:46656862
|
A | G | 18 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.500-233A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656862 | ||||||
| chr11:46656912
|
C | CACACAT | 57 | a0001c0001t0001g0130a0001c0001t0002g0001a0001c0001t0002g0005others(54): Show | 58 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.500-178_500-173dup others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 46656912 | |||||
| chr11:46656922
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.500-173C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | chr11 | 46656922 | ||||||
| chr11:46656928
|
T | TAC | 2 | a0001c0001t0001g0159a0001c0001t0003g0106 | 2 | HG01123.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.500-147_500-146dup others(2): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 46656928 | |||||
| chr11:46656928
|
TAC | T | 18 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(15): Show | 18 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.500-147_500-146del others(2): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr11 | 46656928 | |||||
| chr11:46657322
|
T | C | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+131T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 9/18 | chr11 | 46657322 | ||||||
| chr11:46657412
|
T | G | 2 | a0001c0003t0005g0211a0001c0003t0005g0212 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.597-112T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 9/18 | chr11 | 46657412 | ||||||
| chr11:46657431
|
G | A | 1 | a0001c0001t0011g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.597-93G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 9/18 | chr11 | 46657431 | ||||||
| chr11:46657765
|
A | G | 1 | a0001c0002t0005g0210 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.695+143A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46657765 | ||||||
| chr11:46657939
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695+317C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46657939 | ||||||
| chr11:46658021
|
A | G | 1 | a0001c0001t0014g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.695+399A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658021 | ||||||
| chr11:46658389
|
C | T | 1 | a0001c0002t0005g0213 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.695+767C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658389 | ||||||
| chr11:46658453
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.695+831T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658453 | ||||||
| chr11:46658479
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.695+857C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658479 | ||||||
| chr11:46658533
|
C | A | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.696-859C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658533 | ||||||
| chr11:46658638
|
C | G | 13 | a0001c0001t0001g0076a0001c0001t0001g0164a0001c0001t0001g0166others(10): Show | 13 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.696-754C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658638 | ||||||
| chr11:46658895
|
G | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.696-497G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46658895 | ||||||
| chr11:46659164
|
C | G | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-228C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 10/18 | chr11 | 46659164 | ||||||
| chr11:46659676
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.789+191C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46659676 | ||||||
| chr11:46659806
|
A | G | 1 | a0001c0002t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.789+321A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46659806 | ||||||
| chr11:46659865
|
A | C | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.789+380A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46659865 | ||||||
| chr11:46659952
|
T | A | 1 | a0001c0001t0003g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.789+467T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46659952 | ||||||
| chr11:46660149
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.789+664C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660149 | ||||||
| chr11:46660386
|
G | GT | 139 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(136): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.789+915dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46660386 | |||||
| chr11:46660386
|
G | GTT | 5 | a0001c0001t0001g0080a0001c0001t0001g0137a0001c0001t0001g0193others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+914_789+915dup others(2): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46660386 | |||||
| chr11:46660386
|
GT | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.789+915delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46660386 | |||||
| chr11:46660594
|
A | G | 215 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.789+1109A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660594 | ||||||
| chr11:46660667
|
C | G | 38 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(35): Show | 39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.789+1182C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660667 | ||||||
| chr11:46660704
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0003g0198 | 2 | HG03239.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.789+1219G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660704 | ||||||
| chr11:46660723
|
A | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0156a0001c0001t0001g0209 | 3 | HG01106.hp1 HG02257.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.789+1238A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660723 | ||||||
| chr11:46660882
|
T | A | 1 | a0001c0001t0003g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.789+1397T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46660882 | ||||||
| chr11:46661006
|
A | G | 2 | a0001c0001t0004g0035a0001c0001t0004g0036 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.789+1521A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661006 | ||||||
| chr11:46661035
|
T | A | 1 | a0001c0001t0004g0031 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.789+1550T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661035 | ||||||
| chr11:46661215
|
A | G | 1 | a0001c0001t0004g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.789+1730A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661215 | ||||||
| chr11:46661243
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.789+1758C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661243 | ||||||
| chr11:46661390
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.789+1905C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661390 | ||||||
| chr11:46661517
|
C | CA | 69 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.789+2050dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46661517 | |||||
| chr11:46661517
|
CA | C | 21 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0115others(18): Show | 21 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.789+2050delA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46661517 | |||||
| chr11:46661570
|
G | A | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.789+2085G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661570 | ||||||
| chr11:46661622
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.789+2137A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46661622 | ||||||
| chr11:46662034
|
C | CAT | 3 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0182 | 3 | HG00140.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.790-1960_790-1959d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46662034 | |||||
| chr11:46662034
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.790-1963C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662034 | ||||||
| chr11:46662045
|
A | C | 3 | a0001c0001t0009g0023a0001c0001t0009g0024a0001c0001t0009g0041 | 3 | HG01243.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.790-1952A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662045 | ||||||
| chr11:46662075
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.790-1922G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662075 | ||||||
| chr11:46662130
|
C | T | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.790-1867C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662130 | ||||||
| chr11:46662134
|
C | CA | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.790-1863_790-1862i others(3): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662134 | ||||||
| chr11:46662407
|
A | G | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.790-1590A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662407 | ||||||
| chr11:46662419
|
A | G | 2 | a0001c0003t0005g0211a0001c0003t0005g0212 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.790-1578A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662419 | ||||||
| chr11:46662532
|
T | C | 214 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.790-1465T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662532 | ||||||
| chr11:46662974
|
A | T | 38 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(35): Show | 39 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.790-1023A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46662974 | ||||||
| chr11:46663070
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.790-927C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663070 | ||||||
| chr11:46663127
|
T | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(63): Show | 67 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.790-870T>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663127 | ||||||
| chr11:46663221
|
G | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0144 | 2 | HG00558.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.790-776G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663221 | ||||||
| chr11:46663265
|
C | CA | 176 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0069others(173): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.790-710dupA | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46663265 | |||||
| chr11:46663265
|
C | CAA | 19 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0080others(16): Show | 19 | HG00673.hp2 HG01099.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.790-711_790-710dup others(2): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46663265 | |||||
| chr11:46663265
|
CAAAAAA | C | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-715_790-710del others(6): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46663265 | |||||
| chr11:46663289
|
G | A | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-708G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663289 | ||||||
| chr11:46663426
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0164a0001c0001t0001g0167 | 3 | HG00673.hp1 NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.790-571C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | chr11 | 46663426 | ||||||
| chr11:46663945
|
C | CT | 18 | a0001c0001t0001g0082a0001c0001t0001g0127a0001c0001t0001g0162others(15): Show | 18 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.790-34dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr11 | 46663945 | |||||
| chr11:46664555
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.889-294A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 12/18 | chr11 | 46664555 | ||||||
| chr11:46664710
|
G | A | 85 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.889-139G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 12/18 | chr11 | 46664710 | ||||||
| chr11:46665053
|
C | G | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+94C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 13/18 | chr11 | 46665053 | ||||||
| chr11:46665317
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1000-66G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 13/18 | chr11 | 46665317 | ||||||
| chr11:46665677
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1136+158C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46665677 | ||||||
| chr11:46665794
|
T | TTCC | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136+277_1136+279d others(5): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665794 | |||||
| chr11:46665797
|
C | CT | 30 | a0001c0001t0001g0137a0001c0001t0001g0147a0001c0001t0001g0151others(27): Show | 30 | HG01109.hp1 HG01192.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1136+302dupT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665797 | |||||
| chr11:46665797
|
C | CTT | 5 | a0001c0001t0002g0062a0001c0001t0004g0032a0001c0001t0004g0037others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+301_1136+302d others(4): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665797 | |||||
| chr11:46665797
|
C | CTTTTT | 24 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0007others(21): Show | 25 | HG01070.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1136+298_1136+302d others(7): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665797 | |||||
| chr11:46665797
|
C | CTTTTTT | 11 | a0001c0001t0002g0006a0001c0001t0002g0015a0001c0001t0002g0017others(8): Show | 11 | HG00735.hp1 HG01361.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1136+297_1136+302d others(8): Show |
ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46665797 | |||||
| chr11:46666074
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1136+555G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666074 | ||||||
| chr11:46666137
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1136+618A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666137 | ||||||
| chr11:46666159
|
C | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0164a0001c0001t0001g0167 | 3 | HG00673.hp1 NA18747.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1136+640C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666159 | ||||||
| chr11:46666321
|
C | G | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+802C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666321 | ||||||
| chr11:46666582
|
A | C | 2 | a0001c0003t0005g0211a0001c0003t0005g0212 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1136+1063A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666582 | ||||||
| chr11:46666659
|
G | A | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-1114G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666659 | ||||||
| chr11:46666819
|
C | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0123 | 2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1137-954C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666819 | ||||||
| chr11:46666862
|
AT | A | 6 | a0001c0001t0002g0051a0001c0002t0005g0210a0001c0002t0005g0213others(3): Show | 6 | HG02280.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137-900delT | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr11 | 46666862 | |||||
| chr11:46666875
|
A | C | 1 | a0001c0001t0002g0050 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1137-898A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666875 | ||||||
| chr11:46666989
|
C | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1137-784C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46666989 | ||||||
| chr11:46667010
|
G | A | 2 | a0001c0001t0008g0003a0001c0001t0008g0004 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1137-763G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667010 | ||||||
| chr11:46667122
|
G | A | 1 | a0001c0001t0014g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1137-651G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667122 | ||||||
| chr11:46667632
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0010g0084 | 2 | HG01069.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1137-141A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667632 | ||||||
| chr11:46667674
|
T | C | 1 | a0001c0001t0008g0004 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1137-99T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667674 | ||||||
| chr11:46667724
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1137-49G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 14/18 | chr11 | 46667724 | ||||||
| chr11:46668015
|
G | T | 1 | a0001c0001t0002g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1251+128G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668015 | ||||||
| chr11:46668106
|
C | T | 24 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0004g0030others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1251+219C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668106 | ||||||
| chr11:46668181
|
T | C | 1 | a0001c0001t0008g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1251+294T>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668181 | ||||||
| chr11:46668223
|
A | G | 10 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0142others(7): Show | 10 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1252-276A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668223 | ||||||
| chr11:46668439
|
A | G | 2 | a0001c0003t0005g0211a0001c0003t0005g0212 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1252-60A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 15/18 | chr11 | 46668439 | ||||||
| chr11:46668588
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0111 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1329+12G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 16/18 | chr11 | 46668588 | ||||||
| chr11:46668704
|
A | G | 8 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(5): Show | 8 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1330-90A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 16/18 | chr11 | 46668704 | ||||||
| chr11:46669165
|
G | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1447-239G>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 17/18 | chr11 | 46669165 | ||||||
| chr11:46669217
|
C | T | 1 | a0001c0001t0019g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1447-187C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 17/18 | chr11 | 46669217 | ||||||
| chr11:46669273
|
G | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1447-131G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 17/18 | chr11 | 46669273 | ||||||
| chr11:46669542
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1575+10C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46669542 | ||||||
| chr11:46669767
|
C | A | 5 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1575+235C>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46669767 | ||||||
| chr11:46670046
|
G | T | 12 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0131others(9): Show | 12 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1575+514G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670046 | ||||||
| chr11:46670055
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1575+523A>C | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670055 | ||||||
| chr11:46670187
|
A | G | 87 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(84): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.1575+655A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670187 | ||||||
| chr11:46670495
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1575+963A>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670495 | ||||||
| chr11:46670497
|
AG | A | 23 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0115others(20): Show | 23 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1575+966delG | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670497 | ||||||
| chr11:46670862
|
A | G | 1 | a0001c0001t0003g0075 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1575+1330A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670862 | ||||||
| chr11:46670887
|
C | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0142a0001c0001t0001g0145others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1575+1355C>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46670887 | ||||||
| chr11:46671139
|
C | T | 25 | a0001c0001t0003g0075a0001c0001t0003g0081a0001c0001t0003g0093others(22): Show | 25 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1576-1116C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671139 | ||||||
| chr11:46671202
|
TC | T | 2 | a0001c0002t0020g0025a0001c0002t0021g0026 | 2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1576-1052delC | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671202 | ||||||
| chr11:46671320
|
C | T | 61 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.1576-935C>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671320 | ||||||
| chr11:46671409
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0190 | 2 | HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1576-846A>G | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671409 | ||||||
| chr11:46671514
|
G | T | 11 | a0001c0001t0002g0045a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00735.hp1 HG01074.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1576-741G>T | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671514 | ||||||
| chr11:46671610
|
G | A | 7 | a0001c0002t0005g0210a0001c0002t0005g0213a0001c0002t0005g0214others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1576-645G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671610 | ||||||
| chr11:46671619
|
G | A | 39 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(36): Show | 40 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1576-636G>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671619 | ||||||
| chr11:46671752
|
T | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0007 | 2 | NA18942.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1576-503T>A | ATG13 | ENSG00000175224.17 | transcript | ENST00000683050.1 | protein_coding | 18/18 | chr11 | 46671752 |