Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10691 |
|---|---|
| ensemblid | ENSG00000162419.13 |
| hgncid | 4370 |
| symbol | GMEB1 |
| name | glucocorticoid modulatory element binding protein 1 |
| refseq_nuc | NM_001319674.2 |
| refseq_prot | NP_001306603.1 |
| ensembl_nuc | ENST00000373816.6 |
| ensembl_prot | ENSP00000362922.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 28668784 |
| end | 28719353 |
| strand | + |
| ver | v1.2 |
| region | chr1:28668784-28719353 |
| region5000 | chr1:28663784-28724353 |
| regionname0 | GMEB1_chr1_28668784_28719353 |
| regionname5000 | GMEB1_chr1_28663784_28724353 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1692 | 279 | 84 | 61 | 84 | 17 | 31 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| c0002 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| c0003 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| c0004 | 0/0 | 1692 | 2 | 0 | 1 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| c0005 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| c0006 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| c0007 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4666 | 83 | 38 | 21 | 8 | 7 | 9 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0002 | 0/1 | 4668 | 80 | 8 | 15 | 41 | 6 | 9 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0003 | 1/0 | 4667 | 45 | 16 | 2 | 21 | 1 | 4 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0004 | 0/0 | 4667 | 10 | 2 | 4 | 3 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0005 | 0/0 | 4669 | 4 | 0 | 4 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0006 | 0/0 | 4667 | 4 | 4 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0007 | 0/0 | 4667 | 4 | 1 | 0 | 2 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0008 | 0/0 | 4666 | 3 | 0 | 0 | 0 | 2 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0009 | 0/0 | 4669 | 3 | 2 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0010 | 0/0 | 4666 | 3 | 0 | 3 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0011 | 0/0 | 4668 | 3 | 1 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0012 | 0/0 | 4666 | 3 | 0 | 3 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0013 | 0/0 | 4665 | 3 | 0 | 1 | 0 | 2 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0014 | 0/0 | 4663 | 3 | 3 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0015 | 0/0 | 4665 | 3 | 0 | 2 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0016 | 0/0 | 4670 | 2 | 1 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0017 | 0/0 | 4669 | 2 | 0 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0018 | 0/0 | 4664 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0019 | 0/0 | 4669 | 2 | 1 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0020 | 0/0 | 4669 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0021 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0022 | 0/0 | 4666 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0023 | 0/0 | 4668 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0024 | 0/0 | 4668 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0025 | 0/0 | 4668 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0026 | 0/0 | 4669 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0027 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0028 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0029 | 0/0 | 4668 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0030 | 0/0 | 4666 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0031 | 0/0 | 4666 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0032 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0033 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0034 | 0/0 | 4654 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0035 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0036 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0037 | 0/0 | 4669 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0038 | 0/0 | 4668 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0039 | 0/0 | 4670 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0040 | 0/0 | 4669 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0041 | 0/0 | 4666 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0042 | 0/0 | 4666 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0043 | 0/0 | 4666 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0044 | 0/0 | 4666 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0045 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0046 | 0/0 | 4665 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| t0047 | 0/0 | 4663 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1692 | 279 | 84 | 61 | 84 | 17 | 31 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0002 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0003 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0004 | 0/0 | 1692 | 2 | 0 | 1 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0005 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0006 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0002c0007 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6357 | 83 | 38 | 21 | 8 | 7 | 9 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0002 | 0/1 | 6359 | 79 | 8 | 15 | 41 | 5 | 9 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0003 | 1/0 | 6358 | 43 | 16 | 1 | 21 | 1 | 3 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0004 | 0/0 | 6358 | 10 | 2 | 4 | 3 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0005 | 0/0 | 6360 | 3 | 0 | 3 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0006 | 0/0 | 6358 | 4 | 4 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0007 | 0/0 | 6358 | 4 | 1 | 0 | 2 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0008 | 0/0 | 6357 | 3 | 0 | 0 | 0 | 2 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0009 | 0/0 | 6360 | 3 | 2 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0010 | 0/0 | 6357 | 3 | 0 | 3 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0011 | 0/0 | 6359 | 3 | 1 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0012 | 0/0 | 6357 | 3 | 0 | 3 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0013 | 0/0 | 6356 | 3 | 0 | 1 | 0 | 2 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0014 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0015 | 0/0 | 6356 | 3 | 0 | 2 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0017 | 0/0 | 6360 | 2 | 0 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0018 | 0/0 | 6355 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0019 | 0/0 | 6360 | 2 | 1 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0020 | 0/0 | 6360 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0021 | 0/0 | 6358 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0022 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0023 | 0/0 | 6359 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0024 | 0/0 | 6359 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0025 | 0/0 | 6359 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0027 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0028 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0029 | 0/0 | 6359 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0030 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0031 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0032 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0033 | 0/0 | 6358 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0034 | 0/0 | 6345 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0035 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0036 | 0/0 | 6358 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0037 | 0/0 | 6360 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0039 | 0/0 | 6361 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0041 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0042 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0043 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0044 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0045 | 0/0 | 6358 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0046 | 0/0 | 6356 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0001t0047 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0002t0016 | 0/0 | 6361 | 2 | 1 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0002t0026 | 0/0 | 6360 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0003t0014 | 0/0 | 6354 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0004t0003 | 0/0 | 6358 | 2 | 0 | 1 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0005t0038 | 0/0 | 6359 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0005t0040 | 0/0 | 6360 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0001c0006t0005 | 0/0 | 6360 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| a0002c0007t0002 | 0/0 | 6359 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | copy fasta | chr1 | 28663784 | 28724353 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0007g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0008g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0011g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0011g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0012g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0013g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0013g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0014g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0015g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0015g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0017g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0018g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0019g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0019g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0020g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0021g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0022g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0023g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0024g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0025g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0027g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0028g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0029g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0030g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0031g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0032g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0033g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0034g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0035g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0036g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0037g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0039g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0041g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0042g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0043g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0044g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0045g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0046g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0001t0047g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0002t0016g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0002t0016g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0002t0026g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0003t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0003t0014g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0004t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0004t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0005t0038g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0005t0040g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0001c0006t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| a0002c0007t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0110 | EUR | GBR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0067 | EUR | GBR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0078 | EUR | GBR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00323 | hp1 | a0001 | c0001 | t0013 | g0175 | EUR | FIN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0149 | EUR | FIN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00597 | hp1 | a0001 | c0001 | t0011 | g0286 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00609 | hp1 | a0001 | c0001 | t0015 | g0156 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00639 | hp2 | a0001 | c0001 | t0022 | g0277 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0169 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG00741 | hp2 | a0001 | c0001 | t0012 | g0211 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01070 | hp2 | a0001 | c0001 | t0019 | g0136 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01074 | hp1 | a0001 | c0001 | t0010 | g0101 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01074 | hp2 | a0001 | c0001 | t0012 | g0168 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01081 | hp1 | a0001 | c0006 | t0005 | g0225 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01099 | hp1 | a0001 | c0001 | t0015 | g0253 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0239 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01106 | hp2 | a0001 | c0001 | t0021 | g0174 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01192 | hp1 | a0001 | c0001 | t0023 | g0219 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0082 | AMR | PUR | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01255 | hp1 | a0001 | c0001 | t0029 | g0073 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01255 | hp2 | a0001 | c0002 | t0016 | g0011 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01258 | hp2 | a0001 | c0004 | t0003 | g0088 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01261 | hp2 | a0001 | c0001 | t0010 | g0113 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0228 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0179 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0257 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | IBS | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0083 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01891 | hp2 | a0001 | c0005 | t0038 | g0086 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01928 | hp2 | a0001 | c0001 | t0013 | g0235 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01952 | hp1 | a0001 | c0001 | t0020 | g0227 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02055 | hp1 | a0001 | c0005 | t0040 | g0199 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | KHV | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02145 | hp1 | a0001 | c0001 | t0025 | g0005 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0202 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CDX | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CDX | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | CDX | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CDX | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02257 | hp1 | a0001 | c0001 | t0047 | g0197 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02257 | hp2 | a0001 | c0001 | t0042 | g0125 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0285 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02293 | hp2 | a0001 | c0001 | t0015 | g0241 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0217 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0273 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0275 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0042 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02738 | hp1 | a0001 | c0001 | t0028 | g0281 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02738 | hp2 | a0001 | c0001 | t0039 | g0200 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0041 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02818 | hp2 | a0001 | c0001 | t0034 | g0122 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02970 | hp1 | a0001 | c0001 | t0044 | g0095 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0119 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02976 | hp2 | a0001 | c0001 | t0041 | g0126 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03098 | hp2 | a0001 | c0003 | t0014 | g0196 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03139 | hp1 | a0001 | c0001 | t0030 | g0188 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03225 | hp1 | a0001 | c0002 | t0026 | g0084 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0092 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03239 | hp2 | a0001 | c0001 | t0045 | g0271 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | ESN | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03654 | hp2 | a0001 | c0001 | t0031 | g0272 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04115 | hp1 | a0001 | c0001 | t0032 | g0256 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0279 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04184 | hp2 | a0001 | c0001 | t0027 | g0284 | SAS | BEB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0232 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | YRI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18906 | hp2 | a0001 | c0003 | t0014 | g0043 | AFR | YRI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18939 | hp1 | a0001 | c0001 | t0007 | g0268 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18960 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18968 | hp1 | a0001 | c0001 | t0011 | g0105 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18998 | hp1 | a0001 | c0001 | t0017 | g0039 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18999 | hp1 | a0001 | c0001 | t0046 | g0157 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19012 | hp2 | a0001 | c0001 | t0033 | g0242 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0231 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19067 | hp1 | a0001 | c0001 | t0017 | g0037 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19083 | hp1 | a0001 | c0001 | t0024 | g0283 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA19083 | hp2 | a0001 | c0001 | t0037 | g0047 | EAS | JPT | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ASW | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ASW | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20752 | hp1 | a0002 | c0007 | t0002 | g0226 | EUR | TSI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20905 | hp1 | a0001 | c0001 | t0035 | g0093 | SAS | GIH | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | GIH | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG01123 | hp2 | a0001 | c0001 | t0043 | g0148 | AMR | CLM | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02109 | hp1 | a0001 | c0001 | t0036 | g0252 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | USA | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | USA | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | USA | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | USA | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| NA21309 | hp2 | a0001 | c0002 | t0016 | g0085 | AFR | LWK | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0081 | REF | REF | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0166 | REF | REF | GMEB1_chr1_28663784_28724353 | GMEB1 | chr1 | 28663784 | 28724353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28714522
|
A | G | 1 | a0002 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1441A>G | p.Met481Val | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1527/6358 | 1441/1692 | 481/563 | chr1 | 28714522 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28683738
|
A | G | 1 | a0001c0005 | 2 | HG01891.hp2 HG02055.hp1 |
splice_region_variant&synonymous_variant | LOW | c.126A>G | p.Gln42Gln | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/10 | 212/6358 | 126/1692 | 42/563 | chr1 | 28683738 | ||
| chr1:28696972
|
A | G | 1 | a0001c0002 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.486A>G | p.Lys162Lys | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/10 | 572/6358 | 486/1692 | 162/563 | chr1 | 28696972 | ||
| chr1:28702529
|
C | A | 1 | a0001c0006 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.690C>A | p.Ala230Ala | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/10 | 776/6358 | 690/1692 | 230/563 | chr1 | 28702529 | ||
| chr1:28710632
|
T | C | 1 | a0001c0003 | 2 | HG03098.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.981T>C | p.Tyr327Tyr | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/10 | 1067/6358 | 981/1692 | 327/563 | chr1 | 28710632 | ||
| chr1:28714287
|
A | G | 1 | a0001c0004 | 2 | HG01258.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.1206A>G | p.Pro402Pro | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1292/6358 | 1206/1692 | 402/563 | chr1 | 28714287 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28668810
|
C | T | 1 | a0001c0001t0047 | 1 | HG02257.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/10 | chr1 | 28668810 | ||||||
| chr1:28714873
|
T | A | 1 | a0001c0001t0020 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 100 | chr1 | 28714873 | |||||
| chr1:28714884
|
A | C | 1 | a0001c0001t0019 | 2 | HG01070.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 111 | chr1 | 28714884 | |||||
| chr1:28714980
|
T | G | 2 | a0001c0001t0008a0001c0001t0021 | 4 | HG01106.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*207T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 207 | chr1 | 28714980 | |||||
| chr1:28715173
|
TC | T | 2 | a0001c0001t0015a0001c0001t0046 | 4 | HG00609.hp1 HG01099.hp1 HG02293.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*401delC | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 401 | chr1 | 28715173 | |||||
| chr1:28715370
|
G | A | 1 | a0001c0001t0022 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*597G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 597 | chr1 | 28715370 | |||||
| chr1:28715381
|
G | A | 1 | a0001c0001t0023 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*608G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 608 | chr1 | 28715381 | |||||
| chr1:28715450
|
AAATT | A | 4 | a0001c0001t0014a0001c0001t0018a0001c0001t0047others(1): Show | 6 | HG02257.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*679_*682delATTA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 679 | INFO_REALIGN_3_PRIME | chr1 | 28715450 | ||||
| chr1:28715603
|
C | CA | 12 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(9): Show | 24 | HG00738.hp2 HG01070.hp2 HG01081.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*850dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 851 | INFO_REALIGN_3_PRIME | chr1 | 28715603 | ||||
| chr1:28715603
|
CA | C | 5 | a0001c0001t0013a0001c0001t0014a0001c0001t0045others(2): Show | 8 | HG00323.hp1 HG00323.hp2 HG01928.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*850delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 850 | INFO_REALIGN_3_PRIME | chr1 | 28715603 | ||||
| chr1:28715840
|
C | A | 1 | a0001c0001t0029 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1067C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1067 | chr1 | 28715840 | |||||
| chr1:28715913
|
G | A | 1 | a0001c0001t0030 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1140G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1140 | chr1 | 28715913 | |||||
| chr1:28716093
|
G | A | 1 | a0001c0001t0010 | 3 | HG01074.hp1 HG01099.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1320G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1320 | chr1 | 28716093 | |||||
| chr1:28716149
|
G | T | 1 | a0001c0001t0028 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1376G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1376 | chr1 | 28716149 | |||||
| chr1:28716741
|
TG | T | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(17): Show | 127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1979delG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1979 | INFO_REALIGN_3_PRIME | chr1 | 28716741 | ||||
| chr1:28716750
|
G | C | 1 | a0001c0001t0031 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1977G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 1977 | chr1 | 28716750 | |||||
| chr1:28716888
|
C | T | 2 | a0001c0002t0016a0001c0002t0026 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2115C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2115 | chr1 | 28716888 | |||||
| chr1:28716985
|
T | C | 2 | a0001c0002t0016a0001c0002t0026 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2212T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2212 | chr1 | 28716985 | |||||
| chr1:28717185
|
G | GT | 18 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(15): Show | 112 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2428dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr1 | 28717185 | ||||
| chr1:28717185
|
G | GTT | 5 | a0001c0001t0017a0001c0001t0020a0001c0001t0039others(2): Show | 7 | HG01255.hp2 HG01952.hp1 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2427_*2428dupTT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2429 | INFO_REALIGN_3_PRIME | chr1 | 28717185 | ||||
| chr1:28717402
|
C | T | 1 | a0001c0001t0036 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2629C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2629 | chr1 | 28717402 | |||||
| chr1:28717427
|
C | T | 1 | a0001c0001t0044 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2654C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2654 | chr1 | 28717427 | |||||
| chr1:28717451
|
A | G | 2 | a0001c0005t0038a0001c0005t0040 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2678A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2678 | chr1 | 28717451 | |||||
| chr1:28717698
|
C | G | 1 | a0001c0001t0043 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2925C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 2925 | chr1 | 28717698 | |||||
| chr1:28717835
|
A | G | 1 | a0001c0001t0035 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3062A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3062 | chr1 | 28717835 | |||||
| chr1:28718100
|
T | C | 3 | a0001c0001t0012a0001c0001t0027a0001c0001t0032 | 5 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3327T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3327 | chr1 | 28718100 | |||||
| chr1:28718329
|
G | A | 1 | a0001c0001t0041 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3556G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3556 | chr1 | 28718329 | |||||
| chr1:28718434
|
T | C | 21 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(18): Show | 108 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3661T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3661 | chr1 | 28718434 | |||||
| chr1:28718469
|
C | T | 1 | a0001c0001t0046 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3696C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3696 | chr1 | 28718469 | |||||
| chr1:28718611
|
A | G | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(16): Show | 106 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*3838A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3838 | chr1 | 28718611 | |||||
| chr1:28718634
|
G | GT | 3 | a0001c0001t0011a0001c0001t0037a0001c0001t0039 | 5 | HG00597.hp1 HG02258.hp2 HG02738.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3870dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3871 | INFO_REALIGN_3_PRIME | chr1 | 28718634 | ||||
| chr1:28718682
|
AAGAATTG others(6): Show |
A | 1 | a0001c0001t0034 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3912_*3924delAATT others(9): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3912 | INFO_REALIGN_3_PRIME | chr1 | 28718682 | ||||
| chr1:28718769
|
G | A | 1 | a0001c0001t0033 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3996G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 3996 | chr1 | 28718769 | |||||
| chr1:28718837
|
G | T | 1 | a0001c0001t0020 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4064G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4064 | chr1 | 28718837 | |||||
| chr1:28718981
|
G | A | 1 | a0001c0001t0009 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4208G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4208 | chr1 | 28718981 | |||||
| chr1:28719051
|
C | T | 1 | a0001c0001t0025 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4278C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4278 | chr1 | 28719051 | |||||
| chr1:28719107
|
G | A | 1 | a0001c0001t0022 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4334G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4334 | chr1 | 28719107 | |||||
| chr1:28719224
|
G | C | 2 | a0001c0001t0006a0001c0001t0042 | 5 | HG02145.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4451G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 10/10 | 4451 | chr1 | 28719224 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28668871
|
C | CG | 4 | a0001c0001t0002g0004a0001c0001t0003g0006a0001c0001t0004g0007others(1): Show | 4 | HG01261.hp1 HG02145.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+36dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28668871 | |||||
| chr1:28668887
|
C | CG | 89 | a0001c0001t0001g0210a0001c0001t0001g0233a0001c0001t0001g0234others(86): Show | 89 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.-31+55dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28668887 | |||||
| chr1:28668887
|
C | G | 3 | a0001c0001t0001g0287a0001c0001t0004g0007a0001c0001t0011g0286 | 3 | HG00597.hp1 HG03688.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-31+48C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28668887 | ||||||
| chr1:28668901
|
C | CG | 5 | a0001c0001t0002g0198a0001c0001t0003g0006a0001c0001t0011g0285others(2): Show | 5 | HG02258.hp2 HG04184.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+67dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28668901 | |||||
| chr1:28668904
|
G | A | 1 | a0001c0005t0040g0199 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-31+65G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28668904 | ||||||
| chr1:28669034
|
C | CG | 21 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0210others(18): Show | 21 | HG00140.hp1 HG00673.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-31+202dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28669034 | |||||
| chr1:28669042
|
T | G | 6 | a0001c0001t0002g0004a0001c0001t0002g0201a0001c0001t0006g0202others(3): Show | 6 | HG00597.hp1 HG01261.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+203T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669042 | ||||||
| chr1:28669042
|
T | TG | 8 | a0001c0001t0001g0282a0001c0001t0002g0276a0001c0001t0002g0280others(5): Show | 8 | HG00639.hp2 HG01192.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+209dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28669042 | |||||
| chr1:28669062
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+223G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669062 | ||||||
| chr1:28669106
|
C | T | 1 | a0001c0001t0019g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-31+267C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669106 | ||||||
| chr1:28669158
|
T | TG | 13 | a0001c0001t0001g0274a0001c0001t0001g0282a0001c0001t0002g0193others(10): Show | 13 | HG00597.hp1 HG01167.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.-31+326dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28669158 | |||||
| chr1:28669247
|
G | C | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-31+408G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669247 | ||||||
| chr1:28669278
|
G | A | 1 | a0001c0001t0024g0283 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-31+439G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669278 | ||||||
| chr1:28669361
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-31+522C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669361 | ||||||
| chr1:28669423
|
C | G | 1 | a0001c0001t0003g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-31+584C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669423 | ||||||
| chr1:28669700
|
C | T | 1 | a0001c0001t0027g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-31+861C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28669700 | ||||||
| chr1:28670077
|
A | G | 1 | a0001c0003t0014g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-31+1238A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670077 | ||||||
| chr1:28670153
|
T | TTTTA | 4 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+1334_-31+1337d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | |||||
| chr1:28670153
|
T | TTTTATTT others(5): Show |
52 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0051others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-31+1326_-31+1337d others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | |||||
| chr1:28670153
|
T | TTTTATTT others(9): Show |
21 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0044others(18): Show | 21 | HG00597.hp2 HG00609.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+1322_-31+1337d others(18): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | |||||
| chr1:28670153
|
T | TTTTATTT others(13): Show |
17 | a0001c0001t0002g0008a0001c0001t0002g0025a0001c0001t0002g0026others(14): Show | 17 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-31+1318_-31+1337d others(22): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | |||||
| chr1:28670153
|
T | TTTTATTT others(17): Show |
5 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(2): Show | 5 | HG01433.hp2 HG02148.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+1337_-31+1338i others(26): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670153 | |||||
| chr1:28670173
|
A | ATTTATTT others(17): Show |
1 | a0001c0001t0002g0024 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-31+1337_-31+1338i others(26): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28670173 | |||||
| chr1:28670173
|
A | G | 1 | a0001c0001t0003g0016 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-31+1334A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670173 | ||||||
| chr1:28670248
|
G | C | 3 | a0001c0001t0001g0089a0001c0004t0003g0088a0001c0004t0003g0232 | 3 | HG01258.hp2 HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-31+1409G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670248 | ||||||
| chr1:28670364
|
G | A | 1 | a0001c0001t0006g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-31+1525G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670364 | ||||||
| chr1:28670388
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-31+1549C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670388 | ||||||
| chr1:28670433
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-31+1594T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670433 | ||||||
| chr1:28670509
|
A | G | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-31+1670A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670509 | ||||||
| chr1:28670619
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+1780C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670619 | ||||||
| chr1:28670650
|
T | G | 1 | a0001c0001t0003g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-31+1811T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670650 | ||||||
| chr1:28670663
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-31+1824C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670663 | ||||||
| chr1:28670692
|
T | C | 1 | a0001c0001t0008g0092 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-31+1853T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670692 | ||||||
| chr1:28670719
|
C | T | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-31+1880C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670719 | ||||||
| chr1:28670745
|
T | C | 98 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-31+1906T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670745 | ||||||
| chr1:28670754
|
T | G | 1 | a0001c0001t0035g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-31+1915T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670754 | ||||||
| chr1:28670763
|
G | A | 1 | a0001c0001t0022g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-31+1924G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28670763 | ||||||
| chr1:28671436
|
C | T | 1 | a0001c0001t0030g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-31+2597C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28671436 | ||||||
| chr1:28671597
|
T | G | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-31+2758T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28671597 | ||||||
| chr1:28671772
|
AAAAT | A | 3 | a0001c0001t0001g0233a0001c0001t0004g0094a0001c0001t0044g0095 | 3 | HG02970.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-31+2937_-31+2940d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28671772 | |||||
| chr1:28671960
|
A | G | 1 | a0001c0001t0035g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-31+3121A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28671960 | ||||||
| chr1:28672034
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-31+3195C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672034 | ||||||
| chr1:28672112
|
C | CA | 8 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0234others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+3283dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672112 | |||||
| chr1:28672123
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-31+3284T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672123 | ||||||
| chr1:28672125
|
A | T | 1 | a0001c0001t0001g0269 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-31+3286A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672125 | ||||||
| chr1:28672164
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-31+3325G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672164 | ||||||
| chr1:28672197
|
T | TTTTA | 58 | a0001c0001t0001g0017a0001c0001t0001g0114a0001c0001t0001g0115others(55): Show | 59 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.-31+3394_-31+3397d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | |||||
| chr1:28672197
|
T | TTTTATTT others(1): Show |
22 | a0001c0001t0001g0112a0001c0001t0001g0238a0001c0001t0001g0269others(19): Show | 23 | HG00099.hp1 HG00673.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-31+3390_-31+3397d others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | |||||
| chr1:28672197
|
T | TTTTATTT others(5): Show |
3 | a0001c0001t0011g0286a0001c0005t0038g0086a0001c0005t0040g0199 | 3 | HG00597.hp1 HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-31+3386_-31+3397d others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | |||||
| chr1:28672197
|
TTTTA | T | 5 | a0001c0001t0002g0215a0001c0001t0009g0082a0001c0001t0009g0083others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+3394_-31+3397d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | |||||
| chr1:28672197
|
TTTTATTT others(1): Show |
T | 97 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-31+3390_-31+3397d others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | |||||
| chr1:28672197
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0024g0283 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-31+3382_-31+3397d others(18): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672197 | |||||
| chr1:28672306
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-31+3467C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672306 | ||||||
| chr1:28672365
|
C | G | 1 | a0001c0001t0002g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-31+3526C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672365 | ||||||
| chr1:28672384
|
A | AT | 6 | a0001c0001t0002g0049a0001c0001t0002g0203a0001c0001t0002g0221others(3): Show | 6 | HG02055.hp1 HG02738.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+3557dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672384 | |||||
| chr1:28672419
|
T | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0247 | 2 | NA18957.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-31+3580T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672419 | ||||||
| chr1:28672443
|
TC | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0114others(26): Show | 30 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-31+3606delC | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672443 | |||||
| chr1:28672487
|
T | G | 2 | a0001c0001t0006g0202a0001c0001t0006g0206 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-31+3648T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672487 | ||||||
| chr1:28672682
|
G | A | 1 | a0001c0001t0003g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-31+3843G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672682 | ||||||
| chr1:28672736
|
C | CT | 107 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-31+3916dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672736 | |||||
| chr1:28672736
|
CT | C | 6 | a0001c0001t0003g0191a0001c0001t0010g0239a0001c0001t0011g0285others(3): Show | 6 | HG01099.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+3916delT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28672736 | |||||
| chr1:28672741
|
T | C | 19 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0090others(16): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+3902T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28672741 | ||||||
| chr1:28673000
|
G | A | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-31+4161G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673000 | ||||||
| chr1:28673076
|
G | A | 1 | a0001c0001t0003g0240 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-31+4237G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673076 | ||||||
| chr1:28673136
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0230 | 2 | HG00733.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-31+4297C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673136 | ||||||
| chr1:28673319
|
C | G | 1 | a0001c0001t0002g0079 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-31+4480C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673319 | ||||||
| chr1:28673344
|
C | T | 1 | a0001c0001t0003g0016 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-31+4505C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673344 | ||||||
| chr1:28673582
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-31+4743A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673582 | ||||||
| chr1:28673711
|
T | G | 1 | a0001c0001t0002g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-31+4872T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673711 | ||||||
| chr1:28673726
|
A | G | 3 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0246 | 3 | NA18943.hp1 NA18947.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-31+4887A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673726 | ||||||
| chr1:28673876
|
C | G | 1 | a0001c0001t0001g0249 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-31+5037C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673876 | ||||||
| chr1:28673916
|
G | T | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | HG00140.hp2 HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-31+5077G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673916 | ||||||
| chr1:28673919
|
G | T | 13 | a0001c0001t0001g0100a0001c0001t0001g0142a0001c0001t0001g0184others(10): Show | 13 | HG02080.hp1 NA18939.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+5080G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28673919 | ||||||
| chr1:28674649
|
C | T | 1 | a0001c0001t0036g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-31+5810C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674649 | ||||||
| chr1:28674675
|
G | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0230 | 2 | HG00733.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-31+5836G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674675 | ||||||
| chr1:28674708
|
C | CT | 53 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0089others(50): Show | 54 | HG00099.hp1 HG00597.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31+5897dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28674708 | |||||
| chr1:28674708
|
C | CTT | 25 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0001g0139others(22): Show | 25 | HG00639.hp2 HG01070.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-31+5896_-31+5897d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28674708 | |||||
| chr1:28674708
|
CT | C | 95 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-31+5897delT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28674708 | |||||
| chr1:28674719
|
T | A | 4 | a0001c0001t0015g0156a0001c0001t0015g0241a0001c0001t0015g0253others(1): Show | 4 | HG00609.hp1 HG01099.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+5880T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674719 | ||||||
| chr1:28674773
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-31+5934C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674773 | ||||||
| chr1:28674875
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-31+6036C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674875 | ||||||
| chr1:28674876
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0030g0188 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-31+6037G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674876 | ||||||
| chr1:28674879
|
C | T | 3 | a0001c0001t0001g0129a0001c0005t0038g0086a0001c0005t0040g0199 | 3 | HG01891.hp2 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-31+6040C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28674879 | ||||||
| chr1:28675007
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0004g0094a0001c0001t0044g0095 | 3 | HG02970.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-31+6168C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675007 | ||||||
| chr1:28675008
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-31+6169C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675008 | ||||||
| chr1:28675014
|
C | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-31+6175C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675014 | ||||||
| chr1:28675018
|
C | CT | 85 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(82): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-31+6196dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28675018 | |||||
| chr1:28675068
|
A | C | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-31+6229A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675068 | ||||||
| chr1:28675296
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-31+6457C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675296 | ||||||
| chr1:28675306
|
C | T | 19 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0090others(16): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-31+6467C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675306 | ||||||
| chr1:28675309
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0269 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-31+6470G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675309 | ||||||
| chr1:28675381
|
T | C | 98 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-31+6542T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675381 | ||||||
| chr1:28675399
|
TCG | T | 3 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | HG00140.hp2 HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-31+6561_-31+6562d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675399 | ||||||
| chr1:28675401
|
G | A | 1 | a0001c0001t0002g0049 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-31+6562G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675401 | ||||||
| chr1:28675573
|
G | A | 2 | a0001c0001t0003g0016a0001c0001t0033g0242 | 2 | NA18965.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-31+6734G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675573 | ||||||
| chr1:28675679
|
C | CA | 7 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0150others(4): Show | 8 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+6856dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28675679 | |||||
| chr1:28675679
|
CA | C | 101 | a0001c0001t0001g0142a0001c0001t0002g0004a0001c0001t0002g0008others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-31+6856delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28675679 | |||||
| chr1:28675781
|
C | G | 3 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-31+6942C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675781 | ||||||
| chr1:28675880
|
G | C | 1 | a0001c0001t0002g0038 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-31+7041G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28675880 | ||||||
| chr1:28676007
|
T | C | 1 | a0001c0001t0006g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-31+7168T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676007 | ||||||
| chr1:28676030
|
T | C | 1 | a0001c0001t0003g0240 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-31+7191T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676030 | ||||||
| chr1:28676335
|
T | C | 2 | a0001c0001t0002g0048a0001c0001t0017g0039 | 2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-30-7248T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676335 | ||||||
| chr1:28676495
|
A | G | 4 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-7088A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676495 | ||||||
| chr1:28676543
|
C | T | 1 | a0001c0001t0010g0239 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-30-7040C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676543 | ||||||
| chr1:28676546
|
T | G | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-30-7037T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676546 | ||||||
| chr1:28676685
|
G | A | 138 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0189others(135): Show | 139 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-30-6898G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676685 | ||||||
| chr1:28676724
|
C | CA | 97 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-30-6850dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28676724 | |||||
| chr1:28676730
|
A | T | 18 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0144others(15): Show | 18 | HG00280.hp1 HG00639.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30-6853A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676730 | ||||||
| chr1:28676734
|
T | A | 108 | a0001c0001t0001g0100a0001c0001t0001g0160a0001c0001t0001g0173others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-30-6849T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676734 | ||||||
| chr1:28676738
|
T | A | 5 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0215others(2): Show | 5 | HG02602.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-6845T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676738 | ||||||
| chr1:28676848
|
T | C | 56 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0130others(53): Show | 57 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-30-6735T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28676848 | ||||||
| chr1:28677213
|
C | G | 1 | a0001c0001t0002g0220 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-30-6370C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28677213 | ||||||
| chr1:28677398
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-30-6185C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28677398 | ||||||
| chr1:28677842
|
T | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0234others(2): Show | 5 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-5741T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28677842 | ||||||
| chr1:28678022
|
A | G | 4 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(1): Show | 4 | HG00438.hp1 HG02155.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-5561A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678022 | ||||||
| chr1:28678234
|
A | G | 98 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-30-5349A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678234 | ||||||
| chr1:28678248
|
A | G | 3 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0246 | 3 | NA18943.hp1 NA18947.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-30-5335A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678248 | ||||||
| chr1:28678299
|
T | TTTTG | 4 | a0001c0001t0006g0202a0001c0002t0016g0011a0001c0002t0016g0085others(1): Show | 4 | HG01255.hp2 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-5260_-30-5257d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28678299 | |||||
| chr1:28678299
|
TTTTGTTT others(1): Show |
T | 4 | a0001c0001t0001g0159a0001c0001t0003g0099a0001c0001t0030g0188others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-5264_-30-5257d others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28678299 | |||||
| chr1:28678307
|
G | GTT | 9 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0210others(6): Show | 9 | HG02258.hp2 HG02809.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-5274_-30-5273d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28678307 | |||||
| chr1:28678517
|
G | C | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-5066G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678517 | ||||||
| chr1:28678547
|
G | A | 10 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(7): Show | 10 | HG00280.hp1 HG01123.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30-5036G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678547 | ||||||
| chr1:28678586
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-30-4997G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678586 | ||||||
| chr1:28678682
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-4901G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678682 | ||||||
| chr1:28678822
|
A | G | 273 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-30-4761A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678822 | ||||||
| chr1:28678899
|
G | T | 2 | a0001c0001t0002g0201a0001c0001t0003g0111 | 2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-30-4684G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678899 | ||||||
| chr1:28678907
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-30-4676G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678907 | ||||||
| chr1:28678950
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0030g0188 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-30-4633C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678950 | ||||||
| chr1:28678951
|
G | A | 6 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0001g0238others(3): Show | 6 | HG01070.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-4632G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678951 | ||||||
| chr1:28678966
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-4617A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28678966 | ||||||
| chr1:28679034
|
C | T | 1 | a0001c0001t0033g0242 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-30-4549C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679034 | ||||||
| chr1:28679119
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-30-4464C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679119 | ||||||
| chr1:28679209
|
G | T | 1 | a0001c0002t0016g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30-4374G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679209 | ||||||
| chr1:28679564
|
T | C | 1 | a0001c0001t0003g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-30-4019T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679564 | ||||||
| chr1:28679658
|
A | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0096others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-30-3925A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679658 | ||||||
| chr1:28679802
|
C | CT | 11 | a0001c0001t0001g0129a0001c0001t0001g0139a0001c0001t0001g0181others(8): Show | 11 | HG01109.hp1 HG01515.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-3765dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28679802 | |||||
| chr1:28679954
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30-3629C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28679954 | ||||||
| chr1:28680182
|
A | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0114others(26): Show | 30 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-30-3401A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680182 | ||||||
| chr1:28680214
|
C | CT | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-30-3368dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28680214 | |||||
| chr1:28680598
|
G | C | 1 | a0001c0001t0009g0082 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-30-2985G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680598 | ||||||
| chr1:28680661
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30-2922G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680661 | ||||||
| chr1:28680923
|
A | G | 6 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0001g0238others(3): Show | 6 | HG01070.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-2660A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680923 | ||||||
| chr1:28680995
|
G | A | 1 | a0001c0001t0022g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-30-2588G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28680995 | ||||||
| chr1:28681089
|
G | T | 2 | a0001c0001t0003g0124a0001c0001t0008g0092 | 2 | HG02965.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-30-2494G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681089 | ||||||
| chr1:28681217
|
G | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0114others(26): Show | 30 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-30-2366G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681217 | ||||||
| chr1:28681336
|
C | T | 13 | a0001c0001t0001g0100a0001c0001t0001g0142a0001c0001t0001g0184others(10): Show | 13 | HG02080.hp1 NA18939.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-2247C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681336 | ||||||
| chr1:28681361
|
G | A | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-2222G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681361 | ||||||
| chr1:28681452
|
G | A | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-2131G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681452 | ||||||
| chr1:28681505
|
C | T | 1 | a0001c0001t0003g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-30-2078C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681505 | ||||||
| chr1:28681563
|
T | C | 1 | a0001c0001t0003g0135 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-30-2020T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681563 | ||||||
| chr1:28681745
|
C | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-1838C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681745 | ||||||
| chr1:28681790
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-30-1793C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681790 | ||||||
| chr1:28681857
|
C | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-30-1726C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28681857 | ||||||
| chr1:28682013
|
C | A | 1 | a0001c0001t0025g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-30-1570C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682013 | ||||||
| chr1:28682426
|
C | G | 3 | a0001c0001t0003g0191a0001c0001t0011g0285a0001c0001t0036g0252 | 3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-30-1157C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682426 | ||||||
| chr1:28682591
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-30-992G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682591 | ||||||
| chr1:28682619
|
C | CA | 37 | a0001c0001t0001g0259a0001c0001t0001g0265a0001c0001t0001g0287others(34): Show | 38 | HG00597.hp1 HG00673.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.-30-943dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28682619 | |||||
| chr1:28682913
|
C | T | 3 | a0001c0001t0002g0052a0001c0001t0002g0068a0001c0001t0002g0072 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-30-670C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682913 | ||||||
| chr1:28682973
|
G | A | 2 | a0001c0001t0002g0057a0001c0001t0002g0079 | 2 | HG02040.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.-30-610G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28682973 | ||||||
| chr1:28683057
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0035 | 2 | HG00673.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-30-526A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683057 | ||||||
| chr1:28683248
|
G | A | 56 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0130others(53): Show | 57 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-30-335G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683248 | ||||||
| chr1:28683302
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30-281C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683302 | ||||||
| chr1:28683388
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-30-195C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683388 | ||||||
| chr1:28683473
|
C | T | 1 | a0001c0001t0027g0284 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-30-110C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 1/9 | chr1 | 28683473 | ||||||
| chr1:28683783
|
G | C | 1 | a0001c0001t0011g0286 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.128+43G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28683783 | ||||||
| chr1:28683888
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.128+148C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28683888 | ||||||
| chr1:28683913
|
T | A | 3 | a0001c0001t0006g0119a0001c0001t0006g0208a0001c0001t0042g0125 | 3 | HG02257.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.128+173T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28683913 | ||||||
| chr1:28684289
|
T | C | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.128+549T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28684289 | ||||||
| chr1:28684517
|
C | T | 3 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.128+777C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28684517 | ||||||
| chr1:28684562
|
C | CA | 108 | a0001c0001t0001g0013a0001c0001t0001g0151a0001c0001t0001g0181others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.128+841dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28684562 | |||||
| chr1:28684640
|
C | T | 38 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0096others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.128+900C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28684640 | ||||||
| chr1:28684743
|
G | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0215 | 3 | HG01891.hp1 HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.128+1003G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28684743 | ||||||
| chr1:28685166
|
G | A | 3 | a0001c0001t0002g0052a0001c0001t0002g0068a0001c0001t0002g0072 | 3 | HG01070.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.128+1426G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685166 | ||||||
| chr1:28685204
|
G | A | 1 | a0001c0001t0003g0016 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.128+1464G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685204 | ||||||
| chr1:28685297
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.128+1557C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685297 | ||||||
| chr1:28685479
|
A | G | 1 | a0001c0001t0002g0038 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.128+1739A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685479 | ||||||
| chr1:28685674
|
T | C | 3 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.128+1934T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685674 | ||||||
| chr1:28685736
|
G | A | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.128+1996G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685736 | ||||||
| chr1:28685827
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.128+2087C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28685827 | ||||||
| chr1:28686361
|
G | A | 38 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0096others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.128+2621G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28686361 | ||||||
| chr1:28686502
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.128+2762G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28686502 | ||||||
| chr1:28686628
|
C | CA | 30 | a0001c0001t0001g0127a0001c0001t0002g0067a0001c0001t0003g0002others(27): Show | 31 | HG00099.hp2 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.128+2907dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28686628 | |||||
| chr1:28686628
|
C | CAA | 106 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0001g0190others(103): Show | 106 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.128+2906_128+2907d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28686628 | |||||
| chr1:28686628
|
C | CAAA | 6 | a0001c0001t0002g0032a0001c0001t0002g0072a0001c0001t0002g0223others(3): Show | 6 | HG01175.hp1 HG01243.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+2905_128+2907d others(5): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28686628 | |||||
| chr1:28687004
|
A | G | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.129-3100A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687004 | ||||||
| chr1:28687130
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.129-2974G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687130 | ||||||
| chr1:28687131
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.129-2973T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687131 | ||||||
| chr1:28687334
|
T | A | 31 | a0001c0001t0003g0001a0001c0001t0003g0012a0001c0001t0003g0016others(28): Show | 32 | HG00099.hp1 HG00597.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.129-2770T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687334 | ||||||
| chr1:28687334
|
TCA | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0142a0001c0001t0001g0158others(9): Show | 12 | HG00609.hp1 HG01099.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.129-2717_129-2716d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687334 | |||||
| chr1:28687334
|
TCACA | T | 11 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0170others(8): Show | 11 | HG00280.hp2 HG02109.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.129-2719_129-2716d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687334 | |||||
| chr1:28687334
|
TCACACA | T | 4 | a0001c0001t0012g0168a0001c0001t0012g0169a0001c0001t0012g0211others(1): Show | 4 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-2721_129-2716d others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687334 | |||||
| chr1:28687336
|
A | T | 3 | a0001c0001t0001g0115a0001c0001t0006g0202a0001c0001t0006g0206 | 3 | HG02145.hp2 HG02630.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.129-2768A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687336 | ||||||
| chr1:28687361
|
C | A | 1 | a0001c0001t0011g0286 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.129-2743C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687361 | ||||||
| chr1:28687373
|
C | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0238a0001c0001t0003g0111 | 3 | HG02735.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.129-2731C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687373 | ||||||
| chr1:28687373
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0182others(10): Show | 13 | HG01070.hp2 HG01109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.129-2730_129-2729i others(11): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687373 | |||||
| chr1:28687373
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0262 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.129-2730_129-2729i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687373 | |||||
| chr1:28687375
|
C | A | 23 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0137others(20): Show | 23 | HG01070.hp2 HG01109.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.129-2729C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687375 | ||||||
| chr1:28687375
|
C | CAAAAAA | 3 | a0001c0001t0001g0172a0001c0001t0002g0087a0001c0001t0003g0191 | 3 | HG03209.hp2 HG03579.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.129-2728_129-2727i others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687375 | |||||
| chr1:28687375
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0027 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.129-2728_129-2727i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687375 | |||||
| chr1:28687375
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.129-2728_129-2727i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687375 | |||||
| chr1:28687375
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.129-2728_129-2727i others(18): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687375 | |||||
| chr1:28687377
|
C | A | 35 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0137others(32): Show | 35 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.129-2727C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687377 | ||||||
| chr1:28687377
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0233a0001c0001t0002g0055a0001c0001t0002g0056others(4): Show | 7 | HG01496.hp2 HG03453.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-2726_129-2725i others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687377 | |||||
| chr1:28687377
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0198 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.129-2726_129-2725i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687377 | |||||
| chr1:28687377
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.129-2726_129-2725i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687377 | |||||
| chr1:28687379
|
C | A | 54 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0137others(51): Show | 54 | HG00597.hp2 HG00735.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.129-2725C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687379 | ||||||
| chr1:28687379
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0002g0050a0001c0001t0009g0082a0001c0001t0009g0083others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-2724_129-2723i others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | |||||
| chr1:28687379
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0002g0021a0001c0001t0002g0216a0001c0001t0002g0221others(3): Show | 6 | HG01433.hp2 HG02135.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2724_129-2723i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | |||||
| chr1:28687379
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0022a0001c0001t0002g0214 | 2 | HG02148.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.129-2724_129-2723i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | |||||
| chr1:28687379
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0002g0224a0001c0001t0003g0012a0001c0001t0045g0271 | 3 | HG01928.hp1 HG03239.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.129-2724_129-2723i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | |||||
| chr1:28687379
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.129-2724_129-2723i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687379 | |||||
| chr1:28687381
|
C | A | 81 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0134others(78): Show | 81 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.129-2723C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687381 | ||||||
| chr1:28687381
|
C | CA | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-2722dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAA | 3 | a0001c0001t0001g0150a0001c0001t0013g0149a0001c0001t0043g0148 | 3 | HG00323.hp2 HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.129-2722_129-2721i others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAAAA | 3 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0010g0101 | 3 | HG01074.hp1 HG01167.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.129-2722_129-2721i others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0001g0127a0001c0001t0002g0045a0001c0001t0002g0054others(2): Show | 5 | HG03491.hp2 NA18995.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-2722_129-2721i others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAAAAA others(3): Show |
10 | a0001c0001t0002g0008a0001c0001t0002g0038a0001c0001t0002g0044others(7): Show | 10 | HG00673.hp1 HG00735.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.129-2722_129-2721i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAAAAA others(4): Show |
9 | a0001c0001t0002g0193a0001c0001t0003g0001a0001c0001t0003g0102others(6): Show | 10 | HG00597.hp1 HG00673.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-2722_129-2721i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAAAAA others(5): Show |
8 | a0001c0001t0002g0004a0001c0001t0003g0106a0001c0001t0005g0009others(5): Show | 8 | HG00738.hp2 HG01081.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-2722_129-2721i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0002g0032a0001c0001t0003g0131 | 2 | HG01106.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.129-2722_129-2721i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0017g0037 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.129-2722_129-2721i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687381
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0022g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.129-2722_129-2721i others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687381 | |||||
| chr1:28687383
|
C | A | 134 | a0001c0001t0001g0013a0001c0001t0001g0112a0001c0001t0001g0127others(131): Show | 135 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.129-2721C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687383 | ||||||
| chr1:28687383
|
C | CAAAAAAA others(1): Show |
5 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0002g0029others(2): Show | 5 | HG01346.hp2 HG01361.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | |||||
| chr1:28687383
|
C | CAAAAAAA others(2): Show |
5 | a0001c0001t0003g0002a0001c0001t0003g0090a0001c0001t0003g0120others(2): Show | 6 | HG02717.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(11): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | |||||
| chr1:28687383
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0002g0067a0001c0001t0002g0204a0001c0001t0002g0220others(2): Show | 5 | HG00099.hp2 HG00609.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | |||||
| chr1:28687383
|
C | CAAAAAAA others(4): Show |
11 | a0001c0001t0002g0025a0001c0001t0002g0033a0001c0001t0002g0062others(8): Show | 11 | HG01346.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | |||||
| chr1:28687383
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0002g0053a0001c0001t0002g0058a0001c0001t0002g0061others(2): Show | 5 | HG00099.hp1 HG02615.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | |||||
| chr1:28687383
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0002g0229a0001c0001t0003g0135a0001c0001t0028g0281others(2): Show | 5 | HG02135.hp1 HG02738.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2720_129-2719i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | |||||
| chr1:28687383
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0159a0001c0001t0001g0269a0001c0001t0018g0217 | 3 | HG01884.hp1 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.129-2720_129-2719i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | |||||
| chr1:28687383
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0039g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.129-2720_129-2719i others(19): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687383 | |||||
| chr1:28687385
|
C | A | 201 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0017others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.129-2719C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687385 | ||||||
| chr1:28687385
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0144a0001c0001t0002g0024a0001c0001t0002g0046others(3): Show | 6 | HG00280.hp1 HG00733.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2718_129-2717i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | |||||
| chr1:28687385
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0002g0030a0001c0001t0004g0273a0001c0001t0006g0119others(1): Show | 4 | HG00438.hp1 HG02602.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-2718_129-2717i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | |||||
| chr1:28687385
|
C | CAAAAAAA others(5): Show |
12 | a0001c0001t0001g0151a0001c0001t0001g0189a0001c0001t0001g0190others(9): Show | 12 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.129-2718_129-2717i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | |||||
| chr1:28687385
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0002g0077a0001c0001t0003g0133a0001c0001t0006g0206 | 3 | HG01361.hp1 HG02630.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.129-2718_129-2717i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | |||||
| chr1:28687385
|
C | CAAAAAAA others(7): Show |
6 | a0001c0001t0002g0010a0001c0001t0002g0072a0001c0001t0002g0074others(3): Show | 6 | HG01175.hp1 HG01255.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2718_129-2717i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | |||||
| chr1:28687385
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0003g0016a0001c0001t0003g0108a0001c0001t0003g0132 | 3 | HG02040.hp1 HG02165.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.129-2718_129-2717i others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687385 | |||||
| chr1:28687387
|
C | A | 247 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0017others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.129-2717C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687387 | ||||||
| chr1:28687387
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0099a0001c0001t0034g0122 | 2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0248a0001c0001t0001g0287 | 2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0249a0001c0001t0002g0066a0001c0001t0002g0069 | 3 | HG01175.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0145a0001c0001t0002g0048a0001c0001t0002g0065 | 3 | HG01123.hp1 HG01943.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0002g0070a0001c0003t0014g0196 | 2 | HG03098.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.129-2710_129-2709i others(18): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CACAAAAA others(5): Show |
1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.129-2716_129-2715i others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CACAAAAA others(6): Show |
1 | a0001c0001t0002g0222 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.129-2716_129-2715i others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CACAAAAA others(7): Show |
1 | a0001c0001t0001g0146 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.129-2716_129-2715i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CACAAAAA others(8): Show |
1 | a0001c0001t0003g0128 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.129-2716_129-2715i others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CACACAAA others(7): Show |
1 | a0001c0001t0001g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.129-2716_129-2715i others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CACACACA others(18): Show |
1 | a0001c0001t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.129-2716_129-2715i others(27): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CACACACA others(21): Show |
1 | a0001c0001t0002g0068 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.129-2716_129-2715i others(30): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687387
|
C | CACACACA others(23): Show |
1 | a0001c0001t0002g0052 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.129-2716_129-2715i others(32): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28687387 | |||||
| chr1:28687515
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.129-2589G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687515 | ||||||
| chr1:28687569
|
C | G | 1 | a0001c0001t0011g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.129-2535C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687569 | ||||||
| chr1:28687816
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0234others(2): Show | 5 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-2288G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687816 | ||||||
| chr1:28687971
|
A | G | 4 | a0001c0001t0015g0156a0001c0001t0015g0241a0001c0001t0015g0253others(1): Show | 4 | HG00609.hp1 HG01099.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-2133A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687971 | ||||||
| chr1:28687988
|
C | T | 3 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.129-2116C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28687988 | ||||||
| chr1:28688112
|
C | T | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-1992C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688112 | ||||||
| chr1:28688143
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.129-1961C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688143 | ||||||
| chr1:28688154
|
A | T | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.129-1950A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688154 | ||||||
| chr1:28688278
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.129-1826C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688278 | ||||||
| chr1:28688332
|
G | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.129-1772G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688332 | ||||||
| chr1:28688522
|
C | T | 1 | a0001c0001t0003g0133 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.129-1582C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688522 | ||||||
| chr1:28688564
|
C | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0114others(15): Show | 19 | HG00323.hp2 HG00733.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.129-1540C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688564 | ||||||
| chr1:28688653
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.129-1451A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688653 | ||||||
| chr1:28688721
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.129-1383A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688721 | ||||||
| chr1:28688903
|
C | CTTTTTTT others(2): Show |
135 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0189others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.129-1195_129-1194i others(11): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28688903 | |||||
| chr1:28688903
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0198a0001c0001t0002g0222a0001c0001t0002g0223 | 3 | NA18967.hp1 NA18978.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.129-1195_129-1194i others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28688903 | |||||
| chr1:28688931
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.129-1173G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28688931 | ||||||
| chr1:28689355
|
G | A | 12 | a0001c0001t0001g0127a0001c0001t0001g0159a0001c0001t0001g0172others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.129-749G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28689355 | ||||||
| chr1:28689637
|
A | G | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-467A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28689637 | ||||||
| chr1:28689933
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.129-171A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28689933 | ||||||
| chr1:28689983
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.129-121A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 2/9 | chr1 | 28689983 | ||||||
| chr1:28690202
|
T | TG | 14 | a0001c0001t0002g0022a0001c0001t0002g0030a0001c0001t0002g0033others(11): Show | 14 | HG00438.hp1 HG00609.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+17dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 28690202 | |||||
| chr1:28690203
|
G | GT | 142 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(139): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.211+38dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 28690203 | |||||
| chr1:28690203
|
G | GTT | 16 | a0001c0001t0001g0013a0001c0001t0001g0146a0001c0001t0001g0172others(13): Show | 16 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.211+37_211+38dupTT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 28690203 | |||||
| chr1:28690204
|
T | G | 91 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.211+18T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690204 | ||||||
| chr1:28690205
|
T | G | 1 | a0001c0001t0002g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.211+19T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690205 | ||||||
| chr1:28690360
|
C | T | 1 | a0001c0001t0006g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.211+174C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690360 | ||||||
| chr1:28690369
|
A | G | 1 | a0001c0001t0003g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.211+183A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690369 | ||||||
| chr1:28690667
|
A | G | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.211+481A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690667 | ||||||
| chr1:28690766
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.211+580A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690766 | ||||||
| chr1:28690853
|
C | T | 3 | a0001c0001t0003g0191a0001c0001t0011g0285a0001c0001t0036g0252 | 3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.211+667C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690853 | ||||||
| chr1:28690905
|
G | A | 6 | a0001c0001t0014g0041a0001c0001t0018g0042a0001c0001t0018g0217others(3): Show | 6 | HG02257.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-680G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690905 | ||||||
| chr1:28690911
|
T | C | 263 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(260): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.212-674T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28690911 | ||||||
| chr1:28691147
|
C | T | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.212-438C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691147 | ||||||
| chr1:28691152
|
G | A | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.212-433G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691152 | ||||||
| chr1:28691334
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.212-251T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691334 | ||||||
| chr1:28691374
|
A | G | 3 | a0001c0001t0006g0119a0001c0001t0006g0208a0001c0001t0042g0125 | 3 | HG02257.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.212-211A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691374 | ||||||
| chr1:28691421
|
G | A | 3 | a0001c0001t0003g0191a0001c0001t0011g0285a0001c0001t0036g0252 | 3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.212-164G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 3/9 | chr1 | 28691421 | ||||||
| chr1:28691783
|
T | A | 1 | a0001c0001t0003g0135 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.336+74T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691783 | ||||||
| chr1:28691804
|
T | TTTTA | 50 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0114others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.336+139_336+142dup others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | |||||
| chr1:28691804
|
T | TTTTATTT others(1): Show |
7 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0265others(4): Show | 7 | NA18939.hp1 NA18960.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.336+135_336+142dup others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | |||||
| chr1:28691804
|
TTTTA | T | 100 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.336+139_336+142del others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | |||||
| chr1:28691804
|
TTTTATTT others(1): Show |
T | 4 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0001g0254others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+135_336+142del others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | |||||
| chr1:28691804
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.336+127_336+142del others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28691804 | |||||
| chr1:28691808
|
A | T | 1 | a0001c0001t0024g0283 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.336+99A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691808 | ||||||
| chr1:28691910
|
G | A | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.336+201G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691910 | ||||||
| chr1:28691946
|
T | C | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.336+237T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691946 | ||||||
| chr1:28691958
|
A | G | 1 | a0001c0001t0002g0280 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.336+249A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28691958 | ||||||
| chr1:28692016
|
C | CT | 7 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0234others(4): Show | 7 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.336+321dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28692016 | |||||
| chr1:28692016
|
C | CTT | 9 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0210others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.336+320_336+321dup others(2): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28692016 | |||||
| chr1:28692203
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+494C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692203 | ||||||
| chr1:28692295
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.336+586G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692295 | ||||||
| chr1:28692387
|
C | G | 2 | a0001c0001t0008g0092a0001c0001t0021g0174 | 2 | HG01106.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.337-555C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692387 | ||||||
| chr1:28692405
|
G | A | 1 | a0001c0001t0002g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.337-537G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692405 | ||||||
| chr1:28692538
|
A | AAAAAAAT others(27): Show |
1 | a0001c0001t0024g0283 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.337-402_337-369dup others(34): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 28692538 | |||||
| chr1:28692561
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0030g0188 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.337-381C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692561 | ||||||
| chr1:28692737
|
G | T | 1 | a0001c0001t0003g0135 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.337-205G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 4/9 | chr1 | 28692737 | ||||||
| chr1:28693211
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.440+166C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693211 | ||||||
| chr1:28693212
|
G | A | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.440+167G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693212 | ||||||
| chr1:28693219
|
A | AT | 11 | a0001c0001t0001g0003a0001c0001t0001g0146a0001c0001t0001g0150others(8): Show | 12 | HG00323.hp2 HG00673.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.440+189dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28693219 | |||||
| chr1:28693379
|
A | G | 137 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0189others(134): Show | 138 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.440+334A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693379 | ||||||
| chr1:28693464
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.440+419A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693464 | ||||||
| chr1:28693580
|
G | A | 1 | a0001c0001t0033g0242 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.440+535G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693580 | ||||||
| chr1:28693602
|
G | C | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.440+557G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693602 | ||||||
| chr1:28693609
|
C | T | 4 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0030others(1): Show | 4 | HG00438.hp1 HG02155.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.440+564C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693609 | ||||||
| chr1:28693626
|
A | G | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.440+581A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693626 | ||||||
| chr1:28693843
|
A | C | 4 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.440+798A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28693843 | ||||||
| chr1:28694182
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.440+1137G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28694182 | ||||||
| chr1:28694190
|
A | AT | 22 | a0001c0001t0001g0018a0001c0001t0001g0176a0001c0001t0001g0181others(19): Show | 22 | HG00597.hp1 HG00741.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.440+1164dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694190 | |||||
| chr1:28694365
|
A | AT | 109 | a0001c0001t0001g0096a0001c0001t0002g0004a0001c0001t0002g0008others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.440+1330dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694365 | |||||
| chr1:28694518
|
GA | G | 100 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.440+1485delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694518 | |||||
| chr1:28694674
|
G | GT | 6 | a0001c0001t0001g0265a0001c0001t0002g0008a0001c0001t0002g0056others(3): Show | 6 | HG00673.hp1 HG04115.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.440+1641dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694674 | |||||
| chr1:28694738
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.440+1693A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28694738 | ||||||
| chr1:28694889
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.440+1844C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28694889 | ||||||
| chr1:28694905
|
G | T | 1 | a0001c0001t0012g0211 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.440+1860G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28694905 | ||||||
| chr1:28694961
|
C | CT | 58 | a0001c0001t0001g0018a0001c0001t0001g0089a0001c0001t0001g0116others(55): Show | 59 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.440+1937dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28694961 | |||||
| chr1:28695045
|
A | G | 1 | a0001c0001t0003g0278 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.441-1882A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695045 | ||||||
| chr1:28695113
|
C | T | 1 | a0001c0001t0017g0037 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.441-1814C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695113 | ||||||
| chr1:28695293
|
C | T | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.441-1634C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695293 | ||||||
| chr1:28695294
|
G | A | 1 | a0001c0001t0006g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441-1633G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695294 | ||||||
| chr1:28695666
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441-1261C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695666 | ||||||
| chr1:28695721
|
G | A | 1 | a0001c0001t0002g0044 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.441-1206G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695721 | ||||||
| chr1:28695745
|
C | T | 3 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231 | 3 | HG01243.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441-1182C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695745 | ||||||
| chr1:28695811
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.441-1116C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695811 | ||||||
| chr1:28695863
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.441-1064C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695863 | ||||||
| chr1:28695896
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.441-1031G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695896 | ||||||
| chr1:28695926
|
G | A | 3 | a0001c0001t0001g0267a0001c0005t0038g0086a0001c0005t0040g0199 | 3 | HG01891.hp2 HG02055.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.441-1001G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695926 | ||||||
| chr1:28695938
|
C | CA | 15 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0146others(12): Show | 15 | HG00609.hp1 HG01123.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.441-953dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
C | CAA | 17 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0192others(14): Show | 17 | HG00099.hp1 HG00673.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.441-954_441-953dup others(2): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
C | CAAA | 13 | a0001c0001t0001g0170a0001c0001t0001g0259a0001c0001t0003g0016others(10): Show | 13 | HG00597.hp1 HG01106.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.441-955_441-953dup others(3): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
C | CAAAA | 6 | a0001c0001t0003g0001a0001c0001t0003g0135a0001c0001t0003g0141others(3): Show | 7 | HG02083.hp2 HG02132.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.441-956_441-953dup others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
C | CAAAAA | 6 | a0001c0001t0003g0012a0001c0001t0003g0107a0001c0001t0003g0237others(3): Show | 6 | HG01258.hp2 HG02135.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.441-957_441-953dup others(5): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441-967_441-953dup others(15): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
CA | C | 42 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0096others(39): Show | 42 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.441-953delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
CAA | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.441-954_441-953del others(2): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
CAAAAAAA others(4): Show |
C | 17 | a0001c0001t0002g0008a0001c0001t0002g0023a0001c0001t0002g0030others(14): Show | 17 | HG00438.hp1 HG00673.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.441-963_441-953del others(11): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
CAAAAAAA others(5): Show |
C | 83 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0021others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.441-964_441-953del others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
CAAAAAAA others(6): Show |
C | 19 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0137others(16): Show | 19 | HG01070.hp2 HG01109.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.441-965_441-953del others(13): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695938
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0183a0001c0001t0001g0238 | 2 | HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.441-966_441-953del others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695938 | |||||
| chr1:28695942
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.441-985A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695942 | ||||||
| chr1:28695963
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0019g0275 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.441-963_441-952del others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695963 | ||||||
| chr1:28695973
|
A | T | 1 | a0001c0001t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.441-954A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695973 | ||||||
| chr1:28695974
|
A | AT | 10 | a0001c0001t0001g0089a0001c0001t0001g0150a0001c0001t0001g0172others(7): Show | 10 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-949dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28695974 | |||||
| chr1:28695974
|
A | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0114a0001c0001t0001g0115others(12): Show | 16 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.441-953A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695974 | ||||||
| chr1:28695975
|
T | A | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0003g0102others(3): Show | 6 | HG00280.hp2 HG00673.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.441-952T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28695975 | ||||||
| chr1:28696041
|
ATTGT | A | 122 | a0001c0001t0001g0129a0001c0001t0001g0139a0001c0001t0001g0150others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.441-879_441-876del others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28696041 | |||||
| chr1:28696044
|
G | GTTTA | 17 | a0001c0001t0001g0114a0001c0001t0001g0130a0001c0001t0001g0134others(14): Show | 17 | HG00280.hp1 HG01123.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.441-880_441-879ins others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28696044 | |||||
| chr1:28696048
|
G | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0112others(66): Show | 71 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.441-879G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28696048 | ||||||
| chr1:28696048
|
G | GTTTA | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0012g0169 | 3 | HG00673.hp2 HG00735.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.441-847_441-844dup others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 28696048 | |||||
| chr1:28696433
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.441-494T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28696433 | ||||||
| chr1:28696617
|
T | A | 1 | a0001c0001t0002g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.441-310T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28696617 | ||||||
| chr1:28696863
|
G | A | 19 | a0001c0001t0001g0112a0001c0001t0001g0129a0001c0001t0001g0137others(16): Show | 19 | HG01070.hp2 HG01109.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.441-64G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 5/9 | chr1 | 28696863 | ||||||
| chr1:28697152
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.598+68C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697152 | ||||||
| chr1:28697162
|
C | CAT | 27 | a0001c0001t0002g0010a0001c0001t0002g0051a0001c0001t0002g0053others(24): Show | 27 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.598+115_598+116dup others(2): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
C | CATAT | 37 | a0001c0001t0001g0018a0001c0001t0001g0254a0001c0001t0001g0255others(34): Show | 38 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.598+113_598+116dup others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
C | CATATAT | 33 | a0001c0001t0001g0114a0001c0001t0001g0129a0001c0001t0001g0162others(30): Show | 33 | HG00099.hp2 HG00738.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.598+111_598+116dup others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
C | CATATATA others(1): Show |
49 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.598+109_598+116dup others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
C | CATATATA others(3): Show |
26 | a0001c0001t0001g0089a0001c0001t0001g0115a0001c0001t0001g0160others(23): Show | 26 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.598+107_598+116dup others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
C | CATATATA others(5): Show |
3 | a0001c0001t0001g0173a0001c0001t0002g0056a0001c0001t0003g0236 | 3 | HG02896.hp1 NA18942.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.598+105_598+116dup others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
C | CATATATA others(7): Show |
3 | a0001c0001t0001g0130a0001c0001t0001g0269a0001c0001t0003g0140 | 3 | HG02809.hp1 NA18522.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.598+103_598+116dup others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
C | CATATATA others(9): Show |
3 | a0001c0001t0001g0258a0001c0001t0003g0121a0001c0001t0003g0246 | 3 | HG02572.hp1 HG02896.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.598+101_598+116dup others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
C | CATATATA others(11): Show |
1 | a0001c0001t0001g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.598+99_598+116dupA others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATAT | C | 5 | a0001c0001t0001g0144a0001c0001t0001g0161a0001c0001t0001g0287others(2): Show | 5 | HG00280.hp1 HG02630.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+113_598+116del others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATAT | C | 11 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0146others(8): Show | 11 | HG01123.hp1 HG01167.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.598+111_598+116del others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(1): Show |
C | 8 | a0001c0001t0001g0003a0001c0001t0006g0119a0001c0001t0006g0208others(5): Show | 9 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.598+109_598+116del others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(3): Show |
C | 12 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0210others(9): Show | 12 | HG01074.hp1 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+107_598+116del others(10): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(5): Show |
C | 10 | a0001c0001t0001g0015a0001c0001t0001g0159a0001c0001t0001g0267others(7): Show | 10 | HG00609.hp1 HG00639.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.598+105_598+116del others(12): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(7): Show |
C | 33 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0097others(30): Show | 33 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.598+103_598+116del others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(9): Show |
C | 6 | a0001c0001t0003g0104a0001c0001t0003g0106a0001c0001t0003g0110others(3): Show | 6 | HG00099.hp1 HG01106.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+101_598+116del others(16): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(11): Show |
C | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG00733.hp1 HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.598+99_598+116delA others(17): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(13): Show |
C | 2 | a0001c0001t0001g0171a0001c0001t0004g0152 | 2 | HG01069.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.598+97_598+116delA others(19): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(15): Show |
C | 2 | a0001c0001t0001g0164a0001c0001t0002g0218 | 2 | HG00597.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.598+95_598+116delA others(21): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697162
|
CATATATA others(17): Show |
C | 1 | a0001c0001t0002g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.598+93_598+116delA others(23): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28697162 | |||||
| chr1:28697193
|
A | G | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+109A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697193 | ||||||
| chr1:28697270
|
G | A | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.598+186G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697270 | ||||||
| chr1:28697285
|
T | C | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.598+201T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697285 | ||||||
| chr1:28697400
|
G | T | 1 | a0001c0001t0003g0103 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.598+316G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697400 | ||||||
| chr1:28697431
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.598+347C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697431 | ||||||
| chr1:28697495
|
A | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+411A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697495 | ||||||
| chr1:28697496
|
C | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+412C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697496 | ||||||
| chr1:28697617
|
C | A | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.598+533C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697617 | ||||||
| chr1:28697619
|
A | G | 3 | a0001c0001t0003g0191a0001c0001t0011g0285a0001c0001t0036g0252 | 3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.598+535A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697619 | ||||||
| chr1:28697857
|
C | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.598+773C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697857 | ||||||
| chr1:28697867
|
C | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA18939.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.598+783C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697867 | ||||||
| chr1:28697875
|
C | G | 2 | a0001c0001t0001g0115a0001c0001t0031g0272 | 2 | HG02735.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.598+791C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697875 | ||||||
| chr1:28697892
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.598+808C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28697892 | ||||||
| chr1:28698274
|
C | T | 21 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0090others(18): Show | 22 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.598+1190C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698274 | ||||||
| chr1:28698391
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0030g0188 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.598+1307G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698391 | ||||||
| chr1:28698394
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+1310G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698394 | ||||||
| chr1:28698396
|
C | T | 98 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.598+1312C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698396 | ||||||
| chr1:28698441
|
C | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+1357C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698441 | ||||||
| chr1:28698442
|
A | G | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.598+1358A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698442 | ||||||
| chr1:28698444
|
A | G | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.598+1360A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698444 | ||||||
| chr1:28698461
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.598+1377G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698461 | ||||||
| chr1:28698568
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.598+1484G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698568 | ||||||
| chr1:28698674
|
C | CA | 104 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.598+1605dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28698674 | |||||
| chr1:28698719
|
C | T | 1 | a0001c0001t0003g0240 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.598+1635C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698719 | ||||||
| chr1:28698842
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+1758G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698842 | ||||||
| chr1:28698908
|
C | A | 3 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0071 | 3 | NA18942.hp2 NA18964.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.598+1824C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28698908 | ||||||
| chr1:28699235
|
G | A | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.598+2151G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28699235 | ||||||
| chr1:28699486
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.598+2402A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28699486 | ||||||
| chr1:28699515
|
C | T | 2 | a0001c0001t0002g0070a0001c0001t0002g0222 | 2 | NA19012.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.598+2431C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28699515 | ||||||
| chr1:28699517
|
C | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.598+2433C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28699517 | ||||||
| chr1:28700058
|
C | CA | 45 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0001g0185others(42): Show | 46 | HG00673.hp1 HG01175.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.599-2357dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700058 | |||||
| chr1:28700058
|
CA | C | 24 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.599-2357delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700058 | |||||
| chr1:28700058
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0045g0271 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.599-2368_599-2357d others(14): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700058 | |||||
| chr1:28700278
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.599-2160C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700278 | ||||||
| chr1:28700279
|
G | A | 1 | a0001c0001t0004g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.599-2159G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700279 | ||||||
| chr1:28700463
|
G | A | 3 | a0001c0001t0003g0191a0001c0001t0011g0285a0001c0001t0036g0252 | 3 | HG02109.hp1 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.599-1975G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700463 | ||||||
| chr1:28700483
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.599-1955C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700483 | ||||||
| chr1:28700513
|
C | CA | 13 | a0001c0001t0001g0018a0001c0001t0001g0130a0001c0001t0001g0269others(10): Show | 13 | HG00438.hp1 HG00609.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.599-1903dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700513 | |||||
| chr1:28700513
|
CA | C | 84 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0096others(81): Show | 86 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.599-1903delA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700513 | |||||
| chr1:28700664
|
A | G | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.599-1774A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700664 | ||||||
| chr1:28700684
|
C | CA | 24 | a0001c0001t0001g0142a0001c0001t0002g0033a0001c0001t0002g0221others(21): Show | 25 | HG01255.hp2 HG02055.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.599-1738dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28700684 | |||||
| chr1:28700799
|
C | T | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.599-1639C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700799 | ||||||
| chr1:28700827
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.599-1611C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700827 | ||||||
| chr1:28700893
|
G | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1545G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700893 | ||||||
| chr1:28700933
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.599-1505T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700933 | ||||||
| chr1:28700961
|
G | A | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1477G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28700961 | ||||||
| chr1:28701142
|
A | G | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.599-1296A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701142 | ||||||
| chr1:28701268
|
C | CT | 35 | a0001c0001t0001g0248a0001c0001t0003g0001a0001c0001t0003g0012others(32): Show | 36 | HG00099.hp1 HG00597.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.599-1153dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28701268 | |||||
| chr1:28701268
|
C | CTTTTT | 15 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0090others(12): Show | 16 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.599-1157_599-1153d others(7): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28701268 | |||||
| chr1:28701268
|
C | CTTTTTT | 102 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0002g0008others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.599-1158_599-1153d others(8): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28701268 | |||||
| chr1:28701268
|
C | CTTTTTTT | 20 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0210others(17): Show | 20 | HG01261.hp1 HG01346.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-1159_599-1153d others(9): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 28701268 | |||||
| chr1:28701294
|
T | C | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1144T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701294 | ||||||
| chr1:28701387
|
A | G | 1 | a0002c0007t0002g0226 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.599-1051A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701387 | ||||||
| chr1:28701398
|
T | C | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1040T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701398 | ||||||
| chr1:28701415
|
A | G | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.599-1023A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701415 | ||||||
| chr1:28701559
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0114others(15): Show | 19 | HG00323.hp2 HG00733.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.599-879C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701559 | ||||||
| chr1:28701748
|
C | T | 2 | a0001c0001t0003g0104a0001c0001t0028g0281 | 2 | HG02738.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.599-690C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 6/9 | chr1 | 28701748 | ||||||
| chr1:28702680
|
C | T | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.730+111C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28702680 | ||||||
| chr1:28702982
|
A | G | 1 | a0001c0001t0006g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.730+413A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28702982 | ||||||
| chr1:28702986
|
C | T | 2 | a0001c0001t0002g0064a0001c0001t0002g0074 | 2 | HG00438.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.730+417C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28702986 | ||||||
| chr1:28703043
|
A | G | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.730+474A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703043 | ||||||
| chr1:28703317
|
TTTA | T | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.730+754_730+756del others(3): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 28703317 | |||||
| chr1:28703389
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0114others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.731-803C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703389 | ||||||
| chr1:28703493
|
C | A | 1 | a0001c0001t0002g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.731-699C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703493 | ||||||
| chr1:28703648
|
G | A | 2 | a0001c0001t0002g0048a0001c0001t0017g0039 | 2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.731-544G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703648 | ||||||
| chr1:28703696
|
A | C | 3 | a0001c0002t0016g0011a0001c0002t0016g0085a0001c0002t0026g0084 | 3 | HG01255.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.731-496A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703696 | ||||||
| chr1:28703714
|
C | G | 1 | a0001c0001t0002g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.731-478C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703714 | ||||||
| chr1:28703844
|
T | C | 1 | a0001c0001t0004g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.731-348T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28703844 | ||||||
| chr1:28704138
|
A | G | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.731-54A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 7/9 | chr1 | 28704138 | ||||||
| chr1:28704376
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0030g0188 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.868+47C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704376 | ||||||
| chr1:28704380
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0090a0001c0001t0003g0120 | 4 | HG02717.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+51C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704380 | ||||||
| chr1:28704608
|
A | T | 3 | a0001c0001t0003g0016a0001c0001t0018g0042a0001c0001t0018g0217 | 3 | HG02572.hp2 HG02723.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.868+279A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704608 | ||||||
| chr1:28704649
|
A | G | 1 | a0001c0001t0006g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.868+320A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704649 | ||||||
| chr1:28704666
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0269 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.868+337C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704666 | ||||||
| chr1:28704667
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0031g0272 | 2 | HG02735.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.868+338G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704667 | ||||||
| chr1:28704686
|
A | G | 2 | a0001c0001t0003g0191a0001c0001t0011g0285 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.868+357A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704686 | ||||||
| chr1:28704788
|
A | G | 4 | a0001c0001t0001g0243a0001c0001t0001g0254a0001c0001t0001g0260others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+459A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704788 | ||||||
| chr1:28704854
|
C | T | 1 | a0001c0001t0003g0278 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.868+525C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28704854 | ||||||
| chr1:28705082
|
C | CA | 21 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0001g0170others(18): Show | 21 | HG02135.hp1 HG02300.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.868+773dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28705082 | |||||
| chr1:28705102
|
A | C | 1 | a0001c0001t0003g0133 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.868+773A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705102 | ||||||
| chr1:28705161
|
G | A | 1 | a0001c0001t0004g0273 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.868+832G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705161 | ||||||
| chr1:28705206
|
T | C | 10 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(7): Show | 10 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.868+877T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705206 | ||||||
| chr1:28705298
|
G | A | 2 | a0001c0001t0002g0064a0001c0001t0002g0074 | 2 | HG00438.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.868+969G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705298 | ||||||
| chr1:28705430
|
C | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.868+1101C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705430 | ||||||
| chr1:28705445
|
C | CT | 10 | a0001c0001t0001g0150a0001c0001t0002g0032a0001c0001t0002g0033others(7): Show | 10 | HG01109.hp1 HG01261.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.868+1135dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28705445 | |||||
| chr1:28705445
|
CT | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0096others(36): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.868+1135delT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28705445 | |||||
| chr1:28705552
|
C | T | 1 | a0001c0001t0039g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.868+1223C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705552 | ||||||
| chr1:28705595
|
G | A | 1 | a0001c0001t0003g0109 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.868+1266G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705595 | ||||||
| chr1:28705834
|
T | C | 1 | a0001c0001t0002g0025 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.868+1505T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28705834 | ||||||
| chr1:28706011
|
G | A | 19 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0090others(16): Show | 20 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.868+1682G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706011 | ||||||
| chr1:28706068
|
G | A | 10 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(7): Show | 10 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.868+1739G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706068 | ||||||
| chr1:28706071
|
A | G | 17 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0090others(14): Show | 18 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.868+1742A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706071 | ||||||
| chr1:28706086
|
A | G | 266 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0015others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.868+1757A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706086 | ||||||
| chr1:28706092
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0269 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.868+1763T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706092 | ||||||
| chr1:28706157
|
A | AAAAT | 7 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0003g0001others(4): Show | 8 | HG00639.hp1 HG02083.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.868+1856_868+1859d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706157 | |||||
| chr1:28706157
|
AAAAT | A | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.868+1856_868+1859d others(6): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706157 | |||||
| chr1:28706244
|
T | C | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.868+1915T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706244 | ||||||
| chr1:28706307
|
T | C | 1 | a0001c0001t0011g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.868+1978T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706307 | ||||||
| chr1:28706338
|
C | T | 6 | a0001c0001t0014g0041a0001c0001t0018g0042a0001c0001t0018g0217others(3): Show | 6 | HG02257.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.868+2009C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706338 | ||||||
| chr1:28706413
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.868+2084T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706413 | ||||||
| chr1:28706459
|
C | T | 1 | a0001c0001t0006g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.868+2130C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706459 | ||||||
| chr1:28706573
|
CAGCCTGG others(35): Show |
C | 10 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(7): Show | 10 | HG00280.hp1 HG01123.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.868+2246_868+2287d others(44): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706573 | |||||
| chr1:28706603
|
C | CA | 8 | a0001c0001t0002g0057a0001c0001t0002g0229a0001c0001t0006g0202others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.868+2288dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706603 | |||||
| chr1:28706910
|
A | G | 1 | a0001c0001t0003g0107 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.868+2581A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706910 | ||||||
| chr1:28706975
|
T | TG | 28 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.868+2648dupG | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706975 | |||||
| chr1:28706977
|
G | GT | 78 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0017others(75): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.868+2673dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706977 | |||||
| chr1:28706977
|
G | GTT | 19 | a0001c0001t0001g0097a0001c0001t0001g0178a0001c0001t0001g0184others(16): Show | 19 | HG01255.hp2 HG01952.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.868+2672_868+2673d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706977 | |||||
| chr1:28706977
|
GT | G | 8 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0210others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.868+2673delT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28706977 | |||||
| chr1:28706978
|
T | G | 68 | a0001c0001t0002g0004a0001c0001t0002g0024a0001c0001t0002g0025others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.868+2649T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706978 | ||||||
| chr1:28706990
|
T | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01123.hp1 HG01167.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.868+2661T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28706990 | ||||||
| chr1:28707063
|
A | G | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.868+2734A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707063 | ||||||
| chr1:28707122
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.868+2793A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707122 | ||||||
| chr1:28707196
|
G | A | 107 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.868+2867G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707196 | ||||||
| chr1:28707229
|
G | A | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.868+2900G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707229 | ||||||
| chr1:28707261
|
C | T | 4 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+2932C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28707261 | ||||||
| chr1:28708355
|
G | A | 102 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.869-2165G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708355 | ||||||
| chr1:28708607
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.869-1913A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708607 | ||||||
| chr1:28708741
|
C | T | 1 | a0001c0001t0011g0286 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.869-1779C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708741 | ||||||
| chr1:28708794
|
G | A | 1 | a0001c0001t0003g0240 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.869-1726G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708794 | ||||||
| chr1:28708897
|
C | T | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.869-1623C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708897 | ||||||
| chr1:28708899
|
A | T | 1 | a0001c0001t0030g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.869-1621A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708899 | ||||||
| chr1:28708914
|
A | G | 138 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0189others(135): Show | 139 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.869-1606A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708914 | ||||||
| chr1:28708947
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.869-1573C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28708947 | ||||||
| chr1:28709058
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.869-1462C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709058 | ||||||
| chr1:28709133
|
C | CA | 102 | a0001c0001t0001g0192a0001c0001t0001g0249a0001c0001t0001g0265others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.869-1371dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28709133 | |||||
| chr1:28709133
|
C | CAA | 7 | a0001c0001t0002g0045a0001c0001t0002g0070a0001c0001t0002g0215others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.869-1372_869-1371d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28709133 | |||||
| chr1:28709246
|
G | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0114others(26): Show | 30 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.869-1274G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709246 | ||||||
| chr1:28709260
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.869-1260T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709260 | ||||||
| chr1:28709371
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.869-1149A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709371 | ||||||
| chr1:28709502
|
G | C | 1 | a0001c0001t0004g0273 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.869-1018G>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709502 | ||||||
| chr1:28709511
|
A | G | 1 | a0001c0001t0002g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.869-1009A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709511 | ||||||
| chr1:28709584
|
A | T | 2 | a0001c0001t0010g0113a0001c0001t0010g0239 | 2 | HG01099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.869-936A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709584 | ||||||
| chr1:28709585
|
A | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0089others(51): Show | 56 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.869-935A>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709585 | ||||||
| chr1:28709586
|
T | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-934T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709586 | ||||||
| chr1:28709770
|
T | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.869-750T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709770 | ||||||
| chr1:28709929
|
A | G | 2 | a0001c0005t0038g0086a0001c0005t0040g0199 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.869-591A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709929 | ||||||
| chr1:28709933
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-587G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28709933 | ||||||
| chr1:28710424
|
A | G | 1 | a0001c0001t0039g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.869-96A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 8/9 | chr1 | 28710424 | ||||||
| chr1:28710728
|
C | CT | 136 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0189others(133): Show | 137 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.991+98dupT | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28710728 | |||||
| chr1:28710783
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.991+141G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28710783 | ||||||
| chr1:28711157
|
G | A | 1 | a0001c0001t0002g0075 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.991+515G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711157 | ||||||
| chr1:28711265
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.991+623G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711265 | ||||||
| chr1:28711267
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.991+625C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711267 | ||||||
| chr1:28711281
|
T | G | 103 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.991+639T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711281 | ||||||
| chr1:28711299
|
A | G | 1 | a0001c0001t0017g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.991+657A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711299 | ||||||
| chr1:28711300
|
G | A | 2 | a0001c0001t0002g0070a0001c0001t0017g0039 | 2 | NA18998.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.991+658G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711300 | ||||||
| chr1:28711300
|
G | GA | 104 | a0001c0001t0001g0100a0001c0001t0001g0184a0001c0001t0002g0004others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.991+667dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28711300 | |||||
| chr1:28711599
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.991+957G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711599 | ||||||
| chr1:28711647
|
G | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0139a0001c0001t0004g0138 | 3 | HG01109.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.991+1005G>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711647 | ||||||
| chr1:28711661
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.991+1019C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711661 | ||||||
| chr1:28711952
|
C | T | 5 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231others(2): Show | 5 | HG01070.hp2 HG01243.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+1310C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28711952 | ||||||
| chr1:28712098
|
G | A | 103 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.991+1456G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712098 | ||||||
| chr1:28712108
|
T | A | 1 | a0001c0001t0039g0200 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.991+1466T>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712108 | ||||||
| chr1:28712150
|
A | G | 5 | a0001c0001t0003g0109a0001c0001t0003g0140a0001c0001t0003g0141others(2): Show | 5 | NA18943.hp1 NA18947.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.991+1508A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712150 | ||||||
| chr1:28712159
|
G | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0154a0001c0001t0003g0155others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+1517G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712159 | ||||||
| chr1:28712315
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.991+1673C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712315 | ||||||
| chr1:28712332
|
A | C | 1 | a0001c0001t0003g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.991+1690A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712332 | ||||||
| chr1:28712425
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.992-1648C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712425 | ||||||
| chr1:28712560
|
C | T | 103 | a0001c0001t0002g0004a0001c0001t0002g0008a0001c0001t0002g0010others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.992-1513C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712560 | ||||||
| chr1:28712636
|
T | C | 1 | a0001c0001t0018g0217 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.992-1437T>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712636 | ||||||
| chr1:28712647
|
C | A | 1 | a0001c0001t0003g0278 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.992-1426C>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712647 | ||||||
| chr1:28712704
|
A | C | 5 | a0001c0001t0009g0082a0001c0001t0009g0083a0001c0001t0009g0231others(2): Show | 5 | HG01070.hp2 HG01243.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1369A>C | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712704 | ||||||
| chr1:28712712
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.992-1361G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712712 | ||||||
| chr1:28712858
|
A | G | 24 | a0001c0001t0001g0127a0001c0001t0001g0172a0001c0001t0001g0210others(21): Show | 25 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.992-1215A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712858 | ||||||
| chr1:28712877
|
G | A | 1 | a0001c0001t0007g0212 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.992-1196G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28712877 | ||||||
| chr1:28712995
|
C | CA | 197 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(194): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.992-1067dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28712995 | |||||
| chr1:28712995
|
C | CAA | 39 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0096others(36): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.992-1068_992-1067d others(4): Show |
GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28712995 | |||||
| chr1:28713012
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0269 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.992-1061G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713012 | ||||||
| chr1:28713019
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0018g0042 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.992-1054G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713019 | ||||||
| chr1:28713020
|
C | T | 1 | a0001c0001t0043g0148 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.992-1053C>T | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713020 | ||||||
| chr1:28713035
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.992-1038G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713035 | ||||||
| chr1:28713037
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.992-1036A>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713037 | ||||||
| chr1:28713157
|
C | CA | 50 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(47): Show | 51 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.992-898dupA | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28713157 | |||||
| chr1:28713384
|
G | A | 1 | a0001c0001t0007g0212 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.992-689G>A | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713384 | ||||||
| chr1:28713921
|
C | G | 2 | a0001c0001t0019g0136a0001c0001t0019g0275 | 2 | HG01070.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.992-152C>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28713921 | ||||||
| chr1:28714038
|
T | G | 1 | a0001c0001t0002g0074 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.992-35T>G | GMEB1 | ENSG00000162419.13 | transcript | ENST00000373816.6 | protein_coding | 9/9 | chr1 | 28714038 |