Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79607 |
|---|---|
| ensemblid | ENSG00000197798.9 |
| hgncid | 26110 |
| symbol | FAM118B |
| name | family with sequence similarity 118 member B |
| refseq_nuc | NM_024556.4 |
| refseq_prot | NP_078832.1 |
| ensembl_nuc | ENST00000533050.6 |
| ensembl_prot | ENSP00000433343.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 126211782 |
| end | 126262968 |
| strand | + |
| ver | v1.2 |
| region | chr11:126211782-126262968 |
| region5000 | chr11:126206782-126267968 |
| regionname0 | FAM118B_chr11_126211782_126262968 |
| regionname5000 | FAM118B_chr11_126206782_126267968 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 351 | 341 | 83 | 64 | 135 | 15 | 42 | 110 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0002 | 0/0 | 351 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0003 | 0/0 | 351 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0004 | 0/0 | 351 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1056 | 332 | 74 | 64 | 135 | 15 | 42 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| c0002 | 0/0 | 1056 | 6 | 6 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| c0003 | 0/0 | 1056 | 3 | 3 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| c0004 | 0/0 | 1056 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| c0005 | 0/0 | 1056 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| c0006 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| c0007 | 0/0 | 1056 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 961 | 328 | 75 | 63 | 130 | 16 | 42 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| t0002 | 0/0 | 961 | 8 | 8 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| t0003 | 0/0 | 961 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| t0004 | 0/0 | 961 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| t0005 | 0/0 | 961 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| t0006 | 0/0 | 961 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| t0007 | 0/0 | 961 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| t0008 | 0/0 | 961 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1056 | 332 | 74 | 64 | 135 | 15 | 42 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0002 | 0/0 | 1056 | 6 | 6 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0004 | 0/0 | 1056 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0005 | 0/0 | 1056 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0002c0003 | 0/0 | 1056 | 3 | 3 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0003c0006 | 0/0 | 1056 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0004c0007 | 0/0 | 1056 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2016 | 316 | 65 | 63 | 129 | 15 | 42 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0001t0002 | 0/0 | 2016 | 6 | 6 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0001t0003 | 0/0 | 2016 | 3 | 0 | 0 | 3 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0001t0004 | 0/0 | 2016 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0001t0005 | 0/0 | 2016 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0001t0006 | 0/0 | 2016 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0001t0007 | 0/0 | 2016 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0001t0008 | 0/0 | 2016 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0002t0001 | 0/0 | 2016 | 6 | 6 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0004t0002 | 0/0 | 2016 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0001c0005t0001 | 0/0 | 2016 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0002c0003t0001 | 0/0 | 2016 | 3 | 3 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0003c0006t0001 | 0/0 | 2016 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| a0004c0007t0001 | 0/0 | 2016 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | copy fasta | chr11 | 126206782 | 126267968 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0007g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0001t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0004t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0004t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0001c0005t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0002c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0002c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0002c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0003c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| a0004c0007t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0322 | EUR | FIN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | CHS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01257 | hp2 | a0001 | c0001 | t0007 | g0236 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0320 | EUR | IBS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0321 | EUR | IBS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01517 | hp2 | a0004 | c0007 | t0001 | g0044 | EUR | IBS | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02055 | hp1 | a0001 | c0004 | t0002 | g0105 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CDX | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CDX | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CDX | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02451 | hp2 | a0001 | c0005 | t0001 | g0263 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02523 | hp1 | a0003 | c0006 | t0001 | g0167 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0264 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0261 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0310 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | STU | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0313 | AFR | YRI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | YRI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0311 | AFR | LWK | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ASW | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | GIH | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0110 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0309 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0262 | AFR | USA | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0227 | AFR | USA | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | USA | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0323 | REF | REF | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | FAM118B_chr11_126206782_126267968 | FAM118B | chr11 | 126206782 | 126267968 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:126256777
|
T | A | 1 | a0003 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.907T>A | p.Tyr303Asn | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/9 | 1032/2016 | 907/1056 | 303/351 | chr11 | 126256777 | ||
| chr11:126256778
|
A | T | 1 | a0003 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.908A>T | p.Tyr303Phe | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/9 | 1033/2016 | 908/1056 | 303/351 | chr11 | 126256778 | ||
| chr11:126256779
|
T | A | 1 | a0003 | 1 | HG02523.hp1 | stop_gained | HIGH | c.909T>A | p.Tyr303* | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/9 | 1034/2016 | 909/1056 | 303/351 | chr11 | 126256779 | ||
| chr11:126256817
|
G | A | 1 | a0004 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.947G>A | p.Arg316Gln | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/9 | 1072/2016 | 947/1056 | 316/351 | chr11 | 126256817 | ||
| chr11:126261482
|
G | A | 1 | a0002 | 3 | HG02572.hp2 HG02809.hp1 HG06807.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1040G>A | p.Arg347Lys | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 8/9 | 1165/2016 | 1040/1056 | 347/351 | chr11 | 126261482 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:126240918
|
C | A | 1 | a0001c0002 | 6 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(3): Show |
synonymous_variant | LOW | c.213C>A | p.Ala71Ala | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/9 | 338/2016 | 213/1056 | 71/351 | chr11 | 126240918 | ||
| chr11:126241038
|
C | T | 1 | a0001c0004 | 2 | HG02055.hp1 HG02109.hp1 |
synonymous_variant | LOW | c.333C>T | p.Leu111Leu | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/9 | 458/2016 | 333/1056 | 111/351 | chr11 | 126241038 | ||
| chr11:126254328
|
G | A | 1 | a0001c0005 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.591G>A | p.Lys197Lys | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/9 | 716/2016 | 591/1056 | 197/351 | chr11 | 126254328 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:126211805
|
G | T | 1 | a0001c0001t0003 | 3 | HG00423.hp1 HG02083.hp2 HG02165.hp1 |
5_prime_UTR_variant | MODIFIER | c.-102G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/9 | 23197 | chr11 | 126211805 | |||||
| chr11:126229231
|
C | A | 1 | a0001c0001t0004 | 2 | HG02615.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-70C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/9 | 5771 | chr11 | 126229231 | |||||
| chr11:126262218
|
C | T | 2 | a0001c0001t0002a0001c0004t0002 | 8 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*85C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 9/9 | 85 | chr11 | 126262218 | |||||
| chr11:126262352
|
C | T | 1 | a0001c0001t0008 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 9/9 | 219 | chr11 | 126262352 | |||||
| chr11:126262690
|
C | T | 1 | a0001c0001t0007 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*557C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 9/9 | 557 | chr11 | 126262690 | |||||
| chr11:126262694
|
A | G | 1 | a0001c0001t0006 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*561A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 9/9 | 561 | chr11 | 126262694 | |||||
| chr11:126262806
|
T | G | 1 | a0001c0001t0005 | 2 | NA18950.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*673T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 9/9 | 673 | chr11 | 126262806 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:126212154
|
C | G | 1 | a0001c0001t0001g0336 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-77+324C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126212154 | ||||||
| chr11:126212258
|
C | A | 2 | a0001c0001t0004g0010a0001c0001t0004g0011 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-77+428C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126212258 | ||||||
| chr11:126212318
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 105 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-77+488G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126212318 | ||||||
| chr11:126212323
|
C | T | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0265others(72): Show | 77 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.-77+493C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126212323 | ||||||
| chr11:126212394
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-77+564T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126212394 | ||||||
| chr11:126212472
|
C | T | 4 | a0001c0005t0001g0263a0002c0003t0001g0261a0002c0003t0001g0262others(1): Show | 4 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+642C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126212472 | ||||||
| chr11:126212766
|
C | T | 35 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0001g0229others(32): Show | 35 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.-77+936C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126212766 | ||||||
| chr11:126212870
|
G | T | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-77+1040G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126212870 | ||||||
| chr11:126213131
|
A | AT | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 109 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-77+1312dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126213131 | |||||
| chr11:126213323
|
G | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 186 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-77+1493G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126213323 | ||||||
| chr11:126213344
|
T | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0265others(72): Show | 77 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.-77+1514T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126213344 | ||||||
| chr11:126213383
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-77+1553G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126213383 | ||||||
| chr11:126213442
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-77+1612A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126213442 | ||||||
| chr11:126214077
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-77+2247G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214077 | ||||||
| chr11:126214275
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-77+2445C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214275 | ||||||
| chr11:126214276
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-77+2446C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214276 | ||||||
| chr11:126214352
|
C | CA | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(99): Show | 108 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.-77+2536dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214352 | |||||
| chr11:126214388
|
C | CT | 100 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(97): Show | 102 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(99): Show |
intron_variant | MODIFIER | c.-77+2576dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214388 | |||||
| chr11:126214388
|
C | CTT | 17 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(14): Show | 17 | HG00423.hp1 HG00544.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-77+2575_-77+2576d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214388 | |||||
| chr11:126214405
|
TTC | T | 85 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0164others(82): Show | 87 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-77+2576_-77+2577d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214405 | ||||||
| chr11:126214406
|
TC | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(38): Show | 44 | HG00323.hp1 HG00738.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.-77+2578delC | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214406 | |||||
| chr11:126214407
|
C | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(143): Show | 149 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.-77+2577C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214407 | ||||||
| chr11:126214424
|
A | G | 1 | a0001c0005t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-77+2594A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214424 | ||||||
| chr11:126214433
|
C | G | 4 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0162others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+2603C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214433 | ||||||
| chr11:126214479
|
CTT | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-77+2652_-77+2653d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214479 | |||||
| chr11:126214490
|
G | GTTTTGTT others(10): Show |
1 | a0001c0001t0001g0216 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-77+2664_-77+2665i others(19): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTGTT others(12): Show |
1 | a0001c0001t0001g0180 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-77+2664_-77+2665i others(21): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTGTT others(13): Show |
1 | a0001c0001t0001g0181 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-77+2664_-77+2665i others(22): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTGTT others(16): Show |
1 | a0001c0001t0001g0336 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-77+2664_-77+2665i others(25): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-77+2663_-77+2672d others(12): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | NA18960.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-77+2662_-77+2672d others(13): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(5): Show |
6 | a0001c0001t0001g0171a0001c0001t0001g0194a0001c0001t0001g0195others(3): Show | 6 | NA18971.hp2 NA19011.hp2 NA19065.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77+2661_-77+2672d others(14): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(6): Show |
12 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(9): Show | 12 | HG01069.hp1 HG01433.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-77+2672_-77+2673i others(15): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(7): Show |
4 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0331others(1): Show | 4 | HG00741.hp2 HG01106.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+2672_-77+2673i others(16): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(8): Show |
4 | a0001c0001t0001g0172a0001c0001t0001g0211a0001c0001t0001g0212others(1): Show | 4 | HG01167.hp1 HG03831.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+2672_-77+2673i others(17): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(9): Show |
4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0213others(1): Show | 4 | HG01175.hp1 HG02145.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+2672_-77+2673i others(18): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0175 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-77+2672_-77+2673i others(19): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0214 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-77+2672_-77+2673i others(20): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214490
|
G | GTTTTTTT others(12): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0215 | 2 | HG02273.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-77+2672_-77+2673i others(21): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214490 | |||||
| chr11:126214492
|
T | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG03704.hp1 HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-77+2662T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214492 | ||||||
| chr11:126214492
|
TTTTTTTT others(4): Show |
T | 2 | a0001c0001t0001g0170a0001c0001t0001g0187 | 2 | HG03209.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-77+2684_-77+2694d others(13): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214492 | |||||
| chr11:126214492
|
TTTTTTTT others(15): Show |
T | 1 | a0001c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-77+2673_-77+2694d others(24): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214492 | |||||
| chr11:126214494
|
TTTTTTTT others(2): Show |
T | 7 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0303others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-77+2673_-77+2681d others(11): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214494 | |||||
| chr11:126214494
|
TTTTTTTT others(13): Show |
T | 1 | a0001c0001t0001g0228 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-77+2673_-77+2692d others(22): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214494 | |||||
| chr11:126214497
|
TTTTTTGT others(10): Show |
T | 1 | a0001c0001t0001g0324 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-77+2673_-77+2689d others(19): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214497 | |||||
| chr11:126214498
|
TTTTTGTT others(9): Show |
T | 2 | a0001c0001t0001g0027a0001c0001t0001g0219 | 2 | HG02071.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-77+2673_-77+2688d others(18): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214498 | |||||
| chr11:126214499
|
TTTTGTTT others(8): Show |
T | 3 | a0001c0001t0001g0185a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG03492.hp2 NA18978.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-77+2673_-77+2687d others(17): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214499 | |||||
| chr11:126214500
|
TTTGTTTT others(7): Show |
T | 12 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0024others(9): Show | 12 | HG01884.hp2 HG02293.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.-77+2673_-77+2686d others(16): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214500 | |||||
| chr11:126214501
|
TTGTTTTT others(6): Show |
T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.-77+2673_-77+2685d others(15): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214501 | |||||
| chr11:126214502
|
TGTTTTTT others(5): Show |
T | 18 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 18 | HG01099.hp1 HG01106.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.-77+2673_-77+2684d others(14): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214502 | ||||||
| chr11:126214503
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0322 | 3 | HG00323.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-77+2674_-77+2683d others(12): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214503 | |||||
| chr11:126214503
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0323 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-77+2683_-77+2684i others(14): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214503 | |||||
| chr11:126214503
|
G | T | 50 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0172others(47): Show | 50 | HG00741.hp2 HG01069.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.-77+2673G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214503 | ||||||
| chr11:126214503
|
GTTTTTTT others(6): Show |
G | 9 | a0001c0001t0001g0008a0001c0001t0001g0315a0001c0001t0001g0316others(6): Show | 10 | HG02145.hp2 HG02280.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-77+2684_-77+2696d others(15): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214503 | |||||
| chr11:126214503
|
GTTTTTTT others(7): Show |
G | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | NA18989.hp2 NA19009.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+2684_-77+2697d others(16): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214503 | |||||
| chr11:126214508
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-77+2678T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214508 | ||||||
| chr11:126214509
|
TTTTTG | T | 20 | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0272others(17): Show | 20 | HG01070.hp1 HG01978.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.-77+2684_-77+2688d others(7): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214509 | |||||
| chr11:126214510
|
TTTTG | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0289a0001c0001t0001g0290others(11): Show | 15 | HG00408.hp2 HG00639.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.-77+2684_-77+2687d others(6): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214510 | |||||
| chr11:126214511
|
T | TTTTTTGT others(8): Show |
1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-77+2683_-77+2684i others(17): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214511 | |||||
| chr11:126214511
|
T | TTTTTTTT others(8): Show |
1 | a0001c0005t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-77+2683_-77+2684i others(17): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214511 | |||||
| chr11:126214514
|
G | GTTTTTGT others(8): Show |
2 | a0002c0003t0001g0261a0002c0003t0001g0264 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77+2689_-77+2690i others(17): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126214514 | |||||
| chr11:126214514
|
G | T | 102 | a0001c0001t0001g0007a0001c0001t0001g0132a0001c0001t0001g0133others(99): Show | 103 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(100): Show |
intron_variant | MODIFIER | c.-77+2684G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214514 | ||||||
| chr11:126214515
|
T | G | 1 | a0001c0001t0001g0266 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-77+2685T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214515 | ||||||
| chr11:126214517
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-77+2687T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214517 | ||||||
| chr11:126214527
|
T | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 105 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-77+2697T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214527 | ||||||
| chr11:126214601
|
G | A | 33 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(30): Show | 33 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-77+2771G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214601 | ||||||
| chr11:126214699
|
C | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG01884.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+2869C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214699 | ||||||
| chr11:126214893
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-77+3063G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214893 | ||||||
| chr11:126214939
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-77+3109G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126214939 | ||||||
| chr11:126215136
|
C | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-77+3306C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215136 | ||||||
| chr11:126215472
|
G | C | 1 | a0001c0001t0008g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-77+3642G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215472 | ||||||
| chr11:126215553
|
T | C | 60 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(57): Show | 60 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-77+3723T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215553 | ||||||
| chr11:126215694
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-77+3864C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215694 | ||||||
| chr11:126215696
|
C | CA | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-77+3886dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126215696 | |||||
| chr11:126215696
|
C | CAA | 25 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0030others(22): Show | 25 | HG00544.hp1 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-77+3885_-77+3886d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126215696 | |||||
| chr11:126215717
|
T | A | 1 | a0001c0001t0001g0333 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-77+3887T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215717 | ||||||
| chr11:126215718
|
G | T | 4 | a0001c0001t0001g0170a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG01884.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+3888G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215718 | ||||||
| chr11:126215767
|
T | C | 2 | a0002c0003t0001g0261a0002c0003t0001g0264 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77+3937T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215767 | ||||||
| chr11:126215814
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-77+3984G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215814 | ||||||
| chr11:126215816
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-77+3986C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215816 | ||||||
| chr11:126215865
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-77+4035T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215865 | ||||||
| chr11:126215991
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-77+4161G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126215991 | ||||||
| chr11:126216324
|
C | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0132others(26): Show | 30 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-77+4494C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216324 | ||||||
| chr11:126216354
|
T | G | 1 | a0001c0001t0001g0186 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-77+4524T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216354 | ||||||
| chr11:126216372
|
T | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG01884.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+4542T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216372 | ||||||
| chr11:126216376
|
C | CA | 12 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0016others(9): Show | 13 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.-77+4555dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126216376 | |||||
| chr11:126216560
|
G | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-77+4730G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216560 | ||||||
| chr11:126216806
|
A | G | 56 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171others(53): Show | 56 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-77+4976A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216806 | ||||||
| chr11:126216873
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-77+5043T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216873 | ||||||
| chr11:126216922
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-77+5092C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216922 | ||||||
| chr11:126216977
|
C | T | 4 | a0001c0001t0001g0170a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG01884.hp1 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+5147C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216977 | ||||||
| chr11:126216981
|
G | C | 1 | a0001c0001t0001g0091 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-77+5151G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126216981 | ||||||
| chr11:126217138
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-77+5308C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126217138 | ||||||
| chr11:126217143
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-77+5313A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126217143 | ||||||
| chr11:126217345
|
C | G | 3 | a0001c0001t0001g0303a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG02647.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-77+5515C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126217345 | ||||||
| chr11:126217628
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-77+5798C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126217628 | ||||||
| chr11:126217914
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.-77+6084C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126217914 | ||||||
| chr11:126218054
|
C | T | 56 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0171others(53): Show | 56 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-77+6224C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218054 | ||||||
| chr11:126218068
|
G | C | 1 | a0001c0001t0001g0268 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-77+6238G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218068 | ||||||
| chr11:126218347
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-77+6517A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218347 | ||||||
| chr11:126218420
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-77+6590C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218420 | ||||||
| chr11:126218530
|
G | GT | 42 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(39): Show | 43 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.-77+6709dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126218530 | |||||
| chr11:126218530
|
G | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(5): Show | 9 | HG02280.hp1 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-77+6700G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218530 | ||||||
| chr11:126218531
|
T | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+6701T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218531 | ||||||
| chr11:126218579
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | NA18939.hp1 NA18959.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-77+6749C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218579 | ||||||
| chr11:126218702
|
G | A | 41 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(38): Show | 42 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.-77+6872G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218702 | ||||||
| chr11:126218706
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-77+6876G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218706 | ||||||
| chr11:126218850
|
C | T | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-77+7020C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218850 | ||||||
| chr11:126218929
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 105 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-77+7099T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218929 | ||||||
| chr11:126218969
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-77+7139G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126218969 | ||||||
| chr11:126219158
|
A | G | 32 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(29): Show | 32 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-77+7328A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219158 | ||||||
| chr11:126219185
|
C | G | 57 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(54): Show | 57 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-77+7355C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219185 | ||||||
| chr11:126219215
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-77+7385C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219215 | ||||||
| chr11:126219349
|
C | CT | 9 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0152others(6): Show | 9 | HG01243.hp2 HG01515.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77+7559dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0330 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-77+7550_-77+7559d others(12): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0318 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-77+7549_-77+7559d others(13): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0327 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-77+7548_-77+7559d others(14): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0317 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-77+7547_-77+7559d others(15): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0319 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-77+7543_-77+7559d others(19): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0324a0001c0001t0001g0331 | 2 | NA18953.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-77+7541_-77+7559d others(21): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CT | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0109a0001c0001t0001g0112others(22): Show | 26 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.-77+7559delT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTT | C | 10 | a0001c0001t0001g0108a0001c0001t0001g0134a0001c0001t0001g0137others(7): Show | 10 | HG01070.hp2 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-77+7558_-77+7559d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0043a0001c0001t0001g0107a0001c0001t0001g0213others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77+7552_-77+7559d others(10): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(3): Show |
C | 13 | a0001c0001t0001g0022a0001c0001t0001g0171a0001c0001t0001g0194others(10): Show | 13 | HG00544.hp1 HG01167.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-77+7550_-77+7559d others(12): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(4): Show |
C | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(50): Show | 56 | HG00423.hp2 HG00733.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.-77+7549_-77+7559d others(13): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(5): Show |
C | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-77+7548_-77+7559d others(14): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(6): Show |
C | 8 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG02735.hp1 HG03225.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77+7547_-77+7559d others(15): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0328others(1): Show | 4 | HG02109.hp2 HG02451.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+7546_-77+7559d others(16): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(8): Show |
C | 13 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0230others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-77+7545_-77+7559d others(17): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(9): Show |
C | 69 | a0001c0001t0001g0009a0001c0001t0001g0164a0001c0001t0001g0165others(66): Show | 70 | HG00099.hp2 HG00408.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-77+7544_-77+7559d others(18): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(10): Show |
C | 13 | a0001c0001t0001g0008a0001c0001t0001g0232a0001c0001t0001g0234others(10): Show | 14 | HG00639.hp2 HG01070.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-77+7543_-77+7559d others(19): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-77+7542_-77+7559d others(20): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219349
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-77+7541_-77+7559d others(21): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219349 | |||||
| chr11:126219442
|
C | T | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-77+7612C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219442 | ||||||
| chr11:126219559
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-77+7729C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219559 | ||||||
| chr11:126219585
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-77+7755C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219585 | ||||||
| chr11:126219696
|
A | G | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-77+7866A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219696 | ||||||
| chr11:126219718
|
C | T | 58 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0168others(55): Show | 58 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.-77+7888C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219718 | ||||||
| chr11:126219775
|
C | A | 1 | a0004c0007t0001g0044 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-77+7945C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219775 | ||||||
| chr11:126219779
|
C | A | 1 | a0004c0007t0001g0044 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-77+7949C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219779 | ||||||
| chr11:126219856
|
TA | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-77+8041delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219856 | |||||
| chr11:126219856
|
TAA | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0102a0001c0001t0001g0142others(3): Show | 6 | HG01884.hp1 HG03041.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77+8040_-77+8041d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126219856 | |||||
| chr11:126219943
|
A | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.-77+8113A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219943 | ||||||
| chr11:126219948
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0282 | 2 | NA18963.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-77+8118G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126219948 | ||||||
| chr11:126220055
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-77+8225G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126220055 | ||||||
| chr11:126220370
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-77+8540T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126220370 | ||||||
| chr11:126220570
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-76-8655C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126220570 | ||||||
| chr11:126220598
|
C | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.-76-8627C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126220598 | ||||||
| chr11:126220825
|
T | A | 1 | a0001c0001t0001g0315 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-76-8400T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126220825 | ||||||
| chr11:126220977
|
A | T | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-76-8248A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126220977 | ||||||
| chr11:126220995
|
T | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0095others(1): Show | 4 | NA18953.hp2 NA18955.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-8230T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126220995 | ||||||
| chr11:126221257
|
G | T | 1 | a0001c0001t0001g0298 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-76-7968G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126221257 | ||||||
| chr11:126221631
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-76-7594G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126221631 | ||||||
| chr11:126221662
|
T | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-76-7563T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126221662 | ||||||
| chr11:126221779
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-76-7446G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126221779 | ||||||
| chr11:126221805
|
C | G | 1 | a0001c0001t0001g0252 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-76-7420C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126221805 | ||||||
| chr11:126221962
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-76-7263G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126221962 | ||||||
| chr11:126222037
|
C | T | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-76-7188C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126222037 | ||||||
| chr11:126222046
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-76-7179C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126222046 | ||||||
| chr11:126222273
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-76-6952G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126222273 | ||||||
| chr11:126222369
|
G | C | 41 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(38): Show | 42 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.-76-6856G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126222369 | ||||||
| chr11:126222669
|
A | C | 56 | a0001c0001t0001g0059a0001c0001t0001g0168a0001c0001t0001g0169others(53): Show | 56 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-76-6556A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126222669 | ||||||
| chr11:126222776
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-76-6449C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126222776 | ||||||
| chr11:126222786
|
A | G | 2 | a0001c0001t0001g0332a0001c0001t0001g0333 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-76-6439A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126222786 | ||||||
| chr11:126223005
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-76-6220A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223005 | ||||||
| chr11:126223103
|
A | G | 1 | a0001c0001t0001g0282 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-76-6122A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223103 | ||||||
| chr11:126223107
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-6118G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223107 | ||||||
| chr11:126223158
|
G | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | HG02071.hp2 HG02155.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-76-6067G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223158 | ||||||
| chr11:126223162
|
G | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-76-6063G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223162 | ||||||
| chr11:126223203
|
G | A | 31 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0108others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.-76-6022G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223203 | ||||||
| chr11:126223322
|
C | T | 31 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0108others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.-76-5903C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223322 | ||||||
| chr11:126223388
|
G | A | 1 | a0001c0001t0008g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-76-5837G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223388 | ||||||
| chr11:126223415
|
G | A | 2 | a0001c0004t0002g0105a0001c0004t0002g0110 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-76-5810G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223415 | ||||||
| chr11:126223471
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-76-5754G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223471 | ||||||
| chr11:126223515
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-5710G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223515 | ||||||
| chr11:126223522
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-5703C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223522 | ||||||
| chr11:126223575
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0001t0001g0158 | 3 | HG00642.hp2 HG01361.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-76-5650G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126223575 | ||||||
| chr11:126223583
|
G | GA | 13 | a0001c0001t0001g0143a0001c0001t0001g0159a0001c0001t0001g0168others(10): Show | 13 | HG01109.hp1 HG01257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-76-5625dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126223583 | |||||
| chr11:126223583
|
G | GAA | 83 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(80): Show | 86 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.-76-5626_-76-5625d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126223583 | |||||
| chr11:126223583
|
G | GAAA | 9 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0053others(6): Show | 9 | HG01358.hp2 HG02071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-76-5627_-76-5625d others(5): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126223583 | |||||
| chr11:126223583
|
GA | G | 14 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(11): Show | 14 | HG01099.hp1 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-76-5625delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126223583 | |||||
| chr11:126224086
|
T | A | 2 | a0002c0003t0001g0261a0002c0003t0001g0264 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-76-5139T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126224086 | ||||||
| chr11:126224183
|
A | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-76-5042A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126224183 | ||||||
| chr11:126224400
|
G | A | 21 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0180others(18): Show | 21 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-76-4825G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126224400 | ||||||
| chr11:126224475
|
CA | C | 11 | a0001c0001t0001g0166a0001c0001t0001g0228a0001c0001t0001g0249others(8): Show | 11 | HG01099.hp1 HG01106.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-76-4721delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126224475 | |||||
| chr11:126224475
|
CAA | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0094others(8): Show | 11 | HG01243.hp1 HG01358.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-76-4722_-76-4721d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126224475 | |||||
| chr11:126224475
|
CAAA | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(55): Show | 62 | HG00408.hp2 HG00639.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-76-4723_-76-4721d others(5): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126224475 | |||||
| chr11:126224475
|
CAAAA | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0036others(14): Show | 18 | HG00323.hp1 HG01433.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-76-4724_-76-4721d others(6): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126224475 | |||||
| chr11:126224475
|
CAAAAA | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-76-4725_-76-4721d others(7): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126224475 | |||||
| chr11:126224475
|
CAAAAAA | C | 60 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0041others(57): Show | 60 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-76-4726_-76-4721d others(8): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126224475 | |||||
| chr11:126224475
|
CAAAAAAA others(2): Show |
C | 29 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0108others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.-76-4729_-76-4721d others(11): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126224475 | |||||
| chr11:126224475
|
CAAAAAAA others(3): Show |
C | 31 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0120others(28): Show | 32 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-76-4730_-76-4721d others(12): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126224475 | |||||
| chr11:126224646
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-4579A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126224646 | ||||||
| chr11:126224890
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-76-4335C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126224890 | ||||||
| chr11:126224900
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-76-4325A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126224900 | ||||||
| chr11:126224909
|
A | C | 1 | a0001c0001t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-76-4316A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126224909 | ||||||
| chr11:126225320
|
A | G | 57 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(54): Show | 57 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-76-3905A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126225320 | ||||||
| chr11:126225397
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-76-3828A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126225397 | ||||||
| chr11:126225672
|
C | G | 60 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0106others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.-76-3553C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126225672 | ||||||
| chr11:126225780
|
G | C | 1 | a0001c0001t0001g0290 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-76-3445G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126225780 | ||||||
| chr11:126225825
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-76-3400C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126225825 | ||||||
| chr11:126225852
|
C | T | 31 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0108others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.-76-3373C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126225852 | ||||||
| chr11:126225875
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-76-3350G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126225875 | ||||||
| chr11:126226069
|
A | G | 138 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-76-3156A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226069 | ||||||
| chr11:126226099
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-76-3126A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226099 | ||||||
| chr11:126226100
|
A | AAGGCCAG others(181): Show |
1 | a0001c0001t0001g0014 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-76-3080_-76-3079i others(190): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(228): Show |
1 | a0001c0001t0001g0037 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-76-3080_-76-3079i others(237): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(369): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0103 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(378): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(416): Show |
2 | a0002c0003t0001g0261a0002c0003t0001g0264 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(425): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(510): Show |
2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA19055.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(519): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(557): Show |
6 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0069others(3): Show | 6 | HG00423.hp2 HG03704.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(566): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(604): Show |
1 | a0001c0001t0001g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-76-3080_-76-3079i others(613): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(698): Show |
1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-76-3080_-76-3079i others(707): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(745): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0095 | 2 | NA18955.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(754): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(604): Show |
7 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0060others(4): Show | 7 | HG01515.hp2 HG02071.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(613): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(557): Show |
58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(55): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(566): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(604): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0066others(2): Show | 5 | HG00423.hp1 HG02273.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(613): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(510): Show |
3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0093 | 3 | NA18964.hp1 NA19009.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(519): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(463): Show |
4 | a0001c0001t0001g0058a0001c0001t0001g0090a0001c0001t0001g0097others(1): Show | 4 | HG02080.hp1 NA18949.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-3080_-76-3079i others(472): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(416): Show |
1 | a0001c0001t0001g0089 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-76-3080_-76-3079i others(425): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(463): Show |
1 | a0001c0001t0001g0052 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-76-3080_-76-3079i others(472): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(40): Show |
6 | a0001c0001t0001g0107a0001c0001t0001g0137a0001c0001t0001g0161others(3): Show | 6 | HG02071.hp1 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-76-2750_-76-2704d others(49): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(87): Show |
17 | a0001c0001t0001g0007a0001c0001t0001g0132a0001c0001t0001g0138others(14): Show | 18 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-76-2797_-76-2704d others(96): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(134): Show |
11 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0275others(8): Show | 11 | HG02109.hp2 HG02135.hp2 HG03225.hp2 others(8): Show |
intron_variant | MODIFIER | c.-76-2844_-76-2704d others(143): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(181): Show |
35 | a0001c0001t0001g0009a0001c0001t0001g0133a0001c0001t0001g0154others(32): Show | 36 | HG00408.hp2 HG01070.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.-76-2891_-76-2704d others(190): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(228): Show |
10 | a0001c0001t0001g0148a0001c0001t0001g0169a0001c0001t0001g0172others(7): Show | 10 | HG02145.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-76-2938_-76-2704d others(237): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(275): Show |
21 | a0001c0001t0001g0112a0001c0001t0001g0175a0001c0001t0001g0182others(18): Show | 21 | HG00280.hp1 HG00733.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-76-2985_-76-2704d others(284): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(510): Show |
1 | a0001c0001t0001g0290 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-76-2798_-76-2797i others(519): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(322): Show |
16 | a0001c0001t0001g0155a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 16 | HG00099.hp2 HG01106.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-76-3032_-76-2704d others(331): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(369): Show |
3 | a0001c0001t0001g0168a0001c0001t0001g0248a0003c0006t0001g0167 | 3 | HG02129.hp1 HG02523.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-76-3079_-76-2704d others(378): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(463): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0315others(1): Show | 5 | HG02280.hp1 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(472): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(557): Show |
5 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0304others(2): Show | 5 | HG02451.hp1 HG02818.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(566): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(604): Show |
11 | a0001c0001t0001g0185a0001c0001t0001g0192a0001c0001t0001g0196others(8): Show | 11 | HG00544.hp1 HG02273.hp1 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(613): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(651): Show |
8 | a0001c0001t0001g0171a0001c0001t0001g0186a0001c0001t0001g0188others(5): Show | 8 | HG00741.hp1 HG01069.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(660): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(698): Show |
9 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0208others(6): Show | 9 | HG00741.hp2 HG01106.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(707): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(745): Show |
4 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0259others(1): Show | 4 | HG01099.hp1 HG02083.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(754): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(792): Show |
13 | a0001c0001t0001g0064a0001c0001t0001g0189a0001c0001t0001g0193others(10): Show | 13 | HG01257.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(801): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(839): Show |
7 | a0001c0001t0001g0059a0001c0001t0001g0181a0001c0001t0001g0220others(4): Show | 7 | HG01358.hp1 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(848): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(980): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG02258.hp2 HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(989): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(1074): Show |
1 | a0001c0001t0001g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(1083): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(1121): Show |
1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(1130): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(1168): Show |
1 | a0001c0001t0001g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(1177): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(2531): Show |
1 | a0001c0001t0001g0177 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(2540): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(2672): Show |
1 | a0001c0001t0001g0179 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(2681): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(3377): Show |
1 | a0001c0001t0001g0178 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(3386): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | AAGGCCAG others(557): Show |
1 | a0001c0001t0001g0036 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(566): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-76-3125A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226100 | ||||||
| chr11:126226100
|
AAGGCCAG others(40): Show |
A | 16 | a0001c0001t0001g0218a0001c0001t0001g0237a0001c0001t0001g0317others(13): Show | 16 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-76-2750_-76-2704d others(49): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226100
|
AAGGCCAG others(87): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-76-2797_-76-2704d others(96): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226100 | |||||
| chr11:126226121
|
G | GCAAGTTC others(510): Show |
1 | a0001c0001t0001g0054 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-76-3080_-76-3079i others(519): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226121 | |||||
| chr11:126226146
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-3079G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226146 | ||||||
| chr11:126226147
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-3078C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226147 | ||||||
| chr11:126226183
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-3042T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226183 | ||||||
| chr11:126226193
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0319 | 2 | HG01361.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-76-3032G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226193 | ||||||
| chr11:126226194
|
C | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0319 | 2 | HG01361.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-76-3031C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226194 | ||||||
| chr11:126226220
|
T | TTCCTATC others(228): Show |
1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2996_-76-2995i others(237): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226220 | |||||
| chr11:126226230
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2995T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226230 | ||||||
| chr11:126226240
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0170 | 2 | HG03017.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-76-2985G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226240 | ||||||
| chr11:126226241
|
C | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0170 | 2 | HG03017.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-76-2984C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226241 | ||||||
| chr11:126226277
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2948T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226277 | ||||||
| chr11:126226287
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2938G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226287 | ||||||
| chr11:126226288
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2937C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226288 | ||||||
| chr11:126226288
|
C | CAGGCCAG others(788): Show |
4 | a0001c0001t0002g0127a0001c0001t0002g0156a0001c0001t0002g0157others(1): Show | 4 | HG02258.hp1 HG02280.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(797): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226288 | |||||
| chr11:126226324
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2901T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226324 | ||||||
| chr11:126226334
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2891G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226334 | ||||||
| chr11:126226335
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2890C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226335 | ||||||
| chr11:126226335
|
C | CAGGCCAG others(600): Show |
1 | a0001c0001t0002g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(609): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226335 | |||||
| chr11:126226371
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2854T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226371 | ||||||
| chr11:126226381
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2844G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226381 | ||||||
| chr11:126226382
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2843C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226382 | ||||||
| chr11:126226382
|
C | CAGGCCAG others(788): Show |
2 | a0001c0001t0001g0126a0001c0001t0001g0130 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(797): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226382 | |||||
| chr11:126226403
|
G | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0095others(1): Show | 4 | NA18953.hp2 NA18955.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-2822G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226403 | ||||||
| chr11:126226428
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2797G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226428 | ||||||
| chr11:126226429
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2796C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226429 | ||||||
| chr11:126226429
|
C | CAGGCCAG others(271): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0128 | 2 | HG00140.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(280): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226429 | |||||
| chr11:126226429
|
C | CAGGCCAG others(412): Show |
1 | a0001c0001t0001g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-76-2704_-76-2703i others(421): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226429 | |||||
| chr11:126226429
|
C | CAGGCCAG others(741): Show |
4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0124others(1): Show | 4 | HG00738.hp2 HG01168.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(750): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226429 | |||||
| chr11:126226429
|
C | CAGGCCAG others(788): Show |
9 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0115others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(797): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226429 | |||||
| chr11:126226429
|
C | CAGGCCAG others(835): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0121 | 2 | HG00642.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(844): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226429 | |||||
| chr11:126226429
|
C | CAGGCCAG others(878): Show |
2 | a0001c0001t0001g0106a0001c0001t0001g0158 | 2 | HG01361.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-76-2704_-76-2703i others(887): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226429 | |||||
| chr11:126226475
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2750G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226475 | ||||||
| chr11:126226476
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-2749C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226476 | ||||||
| chr11:126226525
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0260 | 2 | HG04204.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-76-2700G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226525 | ||||||
| chr11:126226800
|
G | A | 11 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0137others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-76-2425G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226800 | ||||||
| chr11:126226814
|
C | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-76-2411C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226814 | ||||||
| chr11:126226841
|
T | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0315a0001c0001t0001g0316others(1): Show | 5 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-76-2384T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226841 | ||||||
| chr11:126226935
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-76-2290C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126226935 | ||||||
| chr11:126226950
|
CA | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.-76-2260delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126226950 | |||||
| chr11:126227058
|
C | CT | 78 | a0001c0001t0001g0041a0001c0001t0001g0051a0001c0001t0001g0052others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.-76-2145dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126227058 | |||||
| chr11:126227058
|
CT | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0061others(84): Show | 88 | HG00099.hp2 HG00544.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.-76-2145delT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126227058 | |||||
| chr11:126227058
|
CTT | C | 7 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0172others(4): Show | 7 | HG01257.hp1 HG01496.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-76-2146_-76-2145d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126227058 | |||||
| chr11:126227058
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-76-2157_-76-2145d others(15): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126227058 | |||||
| chr11:126227061
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-76-2164T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227061 | ||||||
| chr11:126227101
|
C | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-76-2124C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227101 | ||||||
| chr11:126227155
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-76-2070C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227155 | ||||||
| chr11:126227207
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-76-2018C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227207 | ||||||
| chr11:126227322
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-76-1903A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227322 | ||||||
| chr11:126227346
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.-76-1879G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227346 | ||||||
| chr11:126227489
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-1736C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227489 | ||||||
| chr11:126227588
|
T | G | 2 | a0001c0002t0001g0309a0001c0002t0001g0310 | 2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-76-1637T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227588 | ||||||
| chr11:126227622
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-76-1603C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227622 | ||||||
| chr11:126227664
|
A | G | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-76-1561A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227664 | ||||||
| chr11:126227665
|
T | C | 2 | a0001c0001t0001g0168a0003c0006t0001g0167 | 2 | HG02523.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-76-1560T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227665 | ||||||
| chr11:126227680
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-76-1545T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227680 | ||||||
| chr11:126227824
|
G | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-76-1401G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126227824 | ||||||
| chr11:126228047
|
T | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-76-1178T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228047 | ||||||
| chr11:126228063
|
A | G | 58 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(55): Show | 58 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.-76-1162A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228063 | ||||||
| chr11:126228098
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-76-1127A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228098 | ||||||
| chr11:126228282
|
T | A | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-76-943T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228282 | ||||||
| chr11:126228475
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0159 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-76-750C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228475 | ||||||
| chr11:126228520
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-705G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228520 | ||||||
| chr11:126228556
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-76-669G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228556 | ||||||
| chr11:126228649
|
C | T | 1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-76-576C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228649 | ||||||
| chr11:126228654
|
A | G | 58 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(55): Show | 58 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.-76-571A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228654 | ||||||
| chr11:126228704
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-76-521T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228704 | ||||||
| chr11:126228877
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-76-348G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126228877 | ||||||
| chr11:126229110
|
A | T | 1 | a0001c0001t0001g0216 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-76-115A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126229110 | ||||||
| chr11:126229154
|
T | TA | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-76-70dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 126229154 | |||||
| chr11:126229197
|
A | C | 58 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(55): Show | 58 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.-76-28A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | chr11 | 126229197 | ||||||
| chr11:126229455
|
T | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0114 | 2 | HG00280.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-8+162T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229455 | ||||||
| chr11:126229492
|
C | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-8+199C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229492 | ||||||
| chr11:126229494
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8+201G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229494 | ||||||
| chr11:126229592
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-8+299A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229592 | ||||||
| chr11:126229603
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8+310C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229603 | ||||||
| chr11:126229678
|
C | T | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8+385C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229678 | ||||||
| chr11:126229694
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-8+401G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229694 | ||||||
| chr11:126229706
|
G | A | 3 | a0001c0001t0001g0303a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG02647.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-8+413G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229706 | ||||||
| chr11:126229822
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8+529T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229822 | ||||||
| chr11:126229940
|
C | A | 1 | a0001c0001t0008g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8+647C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229940 | ||||||
| chr11:126229943
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0054 | 4 | HG00099.hp1 HG00140.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+650G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229943 | ||||||
| chr11:126229944
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-8+651C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126229944 | ||||||
| chr11:126230000
|
C | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0152 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+707C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126230000 | ||||||
| chr11:126230232
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8+939T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126230232 | ||||||
| chr11:126230523
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8+1230G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126230523 | ||||||
| chr11:126230806
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8+1513A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126230806 | ||||||
| chr11:126231037
|
C | T | 57 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(54): Show | 57 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-8+1744C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126231037 | ||||||
| chr11:126231320
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-8+2027A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126231320 | ||||||
| chr11:126231410
|
A | AT | 38 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(35): Show | 38 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.-8+2126dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 126231410 | |||||
| chr11:126231864
|
A | G | 4 | a0001c0001t0001g0324a0001c0001t0001g0328a0001c0001t0001g0330others(1): Show | 4 | NA18953.hp1 NA18970.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+2571A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126231864 | ||||||
| chr11:126231929
|
C | A | 1 | a0001c0001t0001g0066 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-8+2636C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126231929 | ||||||
| chr11:126231984
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8+2691C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126231984 | ||||||
| chr11:126232389
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-2606G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126232389 | ||||||
| chr11:126232673
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-2322T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126232673 | ||||||
| chr11:126232722
|
T | A | 57 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0169others(54): Show | 57 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-7-2273T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126232722 | ||||||
| chr11:126232723
|
A | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.-7-2272A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126232723 | ||||||
| chr11:126232724
|
A | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0325 | 2 | HG01261.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-7-2271A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126232724 | ||||||
| chr11:126232729
|
A | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-2266A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126232729 | ||||||
| chr11:126232800
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-2195G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126232800 | ||||||
| chr11:126232853
|
A | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.-7-2142A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126232853 | ||||||
| chr11:126233117
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-7-1878G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126233117 | ||||||
| chr11:126233330
|
C | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0205 | 2 | NA18955.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-7-1665C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126233330 | ||||||
| chr11:126233344
|
G | A | 39 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(36): Show | 39 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.-7-1651G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126233344 | ||||||
| chr11:126233433
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.-7-1562C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126233433 | ||||||
| chr11:126233473
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-7-1522A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126233473 | ||||||
| chr11:126233484
|
TCAAAAAC others(4): Show |
T | 29 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0132others(26): Show | 30 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-7-1505_-7-1495del others(11): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 126233484 | |||||
| chr11:126233634
|
CCTAA | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0101 | 3 | NA18968.hp1 NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-7-1358_-7-1355del others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 126233634 | |||||
| chr11:126233675
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-7-1320T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126233675 | ||||||
| chr11:126233770
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-7-1225T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126233770 | ||||||
| chr11:126234009
|
G | T | 6 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-986G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234009 | ||||||
| chr11:126234014
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-7-981C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234014 | ||||||
| chr11:126234125
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-870G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234125 | ||||||
| chr11:126234231
|
A | G | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | NA18989.hp2 NA19009.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-764A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234231 | ||||||
| chr11:126234360
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-7-635C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234360 | ||||||
| chr11:126234605
|
T | G | 1 | a0001c0001t0001g0301 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-7-390T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234605 | ||||||
| chr11:126234664
|
T | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 103 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.-7-331T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234664 | ||||||
| chr11:126234680
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-7-315C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234680 | ||||||
| chr11:126234778
|
C | T | 6 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0311others(3): Show | 6 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-217C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 2/8 | chr11 | 126234778 | ||||||
| chr11:126235160
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.86+73C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235160 | ||||||
| chr11:126235324
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.86+237A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235324 | ||||||
| chr11:126235337
|
C | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.86+250C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235337 | ||||||
| chr11:126235424
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.86+337A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235424 | ||||||
| chr11:126235466
|
C | T | 1 | a0001c0002t0001g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.86+379C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235466 | ||||||
| chr11:126235485
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.86+398A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235485 | ||||||
| chr11:126235557
|
C | T | 57 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(54): Show | 57 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.86+470C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235557 | ||||||
| chr11:126235657
|
CACAGGTG others(3988): Show |
C | 1 | a0001c0001t0001g0307 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.86+578_87-1133del | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126235657 | |||||
| chr11:126235795
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.86+708A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235795 | ||||||
| chr11:126235871
|
C | CTACTTAT others(21): Show |
25 | a0001c0001t0001g0107a0001c0001t0001g0132a0001c0001t0001g0133others(22): Show | 25 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.86+784_86+785insTA others(26): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235871 | ||||||
| chr11:126235871
|
C | CTCCTTAT others(21): Show |
4 | a0001c0001t0001g0007a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 5 | HG02622.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.86+784_86+785insTC others(26): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235871 | ||||||
| chr11:126235873
|
T | TGA | 29 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0132others(26): Show | 30 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.86+786_86+787insGA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235873 | ||||||
| chr11:126235885
|
A | G | 1 | a0001c0005t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.86+798A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235885 | ||||||
| chr11:126235924
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.86+837T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235924 | ||||||
| chr11:126235952
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.86+865T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235952 | ||||||
| chr11:126235994
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.86+907A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126235994 | ||||||
| chr11:126236070
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.86+983T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236070 | ||||||
| chr11:126236110
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.86+1023G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236110 | ||||||
| chr11:126236162
|
A | G | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.86+1075A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236162 | ||||||
| chr11:126236176
|
G | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0076others(2): Show | 5 | NA18941.hp1 NA18944.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.86+1089G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236176 | ||||||
| chr11:126236194
|
T | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | NA18939.hp1 NA18959.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.86+1107T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236194 | ||||||
| chr11:126236302
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.86+1215G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236302 | ||||||
| chr11:126236403
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0297a0001c0001t0001g0308 | 4 | HG00408.hp2 NA18949.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+1316A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236403 | ||||||
| chr11:126236586
|
G | A | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.86+1499G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236586 | ||||||
| chr11:126236766
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0297a0001c0001t0001g0308 | 4 | HG00408.hp2 NA18949.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+1679T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126236766 | ||||||
| chr11:126236917
|
CT | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.86+1850delT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126236917 | |||||
| chr11:126236917
|
CTT | C | 44 | a0001c0001t0001g0009a0001c0001t0001g0187a0001c0001t0001g0201others(41): Show | 45 | HG00408.hp2 HG00639.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.86+1849_86+1850del others(2): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126236917 | |||||
| chr11:126237009
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.86+1922C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237009 | ||||||
| chr11:126237061
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.86+1974C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237061 | ||||||
| chr11:126237083
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.86+1996A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237083 | ||||||
| chr11:126237215
|
C | CT | 118 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0018others(115): Show | 120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.86+2151dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237215 | |||||
| chr11:126237215
|
C | CTT | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.86+2150_86+2151dup others(2): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237215 | |||||
| chr11:126237215
|
C | CTTT | 17 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.86+2149_86+2151dup others(3): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237215 | |||||
| chr11:126237215
|
C | CTTTT | 47 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0075others(44): Show | 47 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.86+2148_86+2151dup others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237215 | |||||
| chr11:126237215
|
C | CTTTTT | 7 | a0001c0001t0001g0169a0001c0001t0001g0175a0001c0001t0001g0181others(4): Show | 7 | HG00741.hp2 HG01358.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.86+2147_86+2151dup others(5): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237215 | |||||
| chr11:126237215
|
CT | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(10): Show | 14 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.86+2151delT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237215 | |||||
| chr11:126237216
|
T | A | 3 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0002t0001g0310 | 3 | HG02615.hp1 HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.86+2129T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237216 | ||||||
| chr11:126237217
|
T | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(10): Show | 14 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.86+2130T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237217 | ||||||
| chr11:126237410
|
A | AT | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.86+2329dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237410 | |||||
| chr11:126237458
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.86+2371A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237458 | ||||||
| chr11:126237633
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.86+2546G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237633 | ||||||
| chr11:126237680
|
TAAA | T | 39 | a0001c0001t0001g0076a0001c0001t0001g0093a0001c0001t0001g0104others(36): Show | 39 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.86+2618_86+2620del others(3): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237680 | |||||
| chr11:126237680
|
TAAAA | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.86+2617_86+2620del others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237680 | |||||
| chr11:126237680
|
TAAAAA | T | 11 | a0001c0001t0001g0020a0001c0001t0001g0048a0001c0001t0001g0052others(8): Show | 11 | HG01081.hp2 HG01167.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.86+2616_86+2620del others(5): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237680 | |||||
| chr11:126237716
|
G | T | 1 | a0001c0001t0008g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.86+2629G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237716 | ||||||
| chr11:126237726
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0304others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+2639G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237726 | ||||||
| chr11:126237779
|
C | T | 2 | a0001c0001t0001g0168a0003c0006t0001g0167 | 2 | HG02523.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.86+2692C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237779 | ||||||
| chr11:126237851
|
G | A | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.86+2764G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237851 | ||||||
| chr11:126237856
|
C | CA | 6 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0052others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.86+2786dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237856 | |||||
| chr11:126237856
|
CA | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.86+2786delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126237856 | |||||
| chr11:126237967
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.87-2825T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126237967 | ||||||
| chr11:126238016
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.87-2776A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126238016 | ||||||
| chr11:126238287
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.87-2505A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126238287 | ||||||
| chr11:126238376
|
T | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 103 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.87-2416T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126238376 | ||||||
| chr11:126238516
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.87-2276T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126238516 | ||||||
| chr11:126238616
|
G | A | 2 | a0001c0001t0001g0303a0001c0001t0001g0306 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.87-2176G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126238616 | ||||||
| chr11:126238882
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.87-1910G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126238882 | ||||||
| chr11:126238960
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.87-1832T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126238960 | ||||||
| chr11:126238972
|
C | CT | 39 | a0001c0001t0001g0058a0001c0001t0001g0074a0001c0001t0001g0164others(36): Show | 39 | HG00733.hp1 HG01081.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.87-1803dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126238972 | |||||
| chr11:126238972
|
C | CTT | 7 | a0001c0001t0001g0194a0001c0001t0001g0228a0001c0001t0001g0237others(4): Show | 7 | HG00099.hp2 HG01192.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.87-1804_87-1803dup others(2): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126238972 | |||||
| chr11:126239120
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.87-1672C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239120 | ||||||
| chr11:126239151
|
G | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.87-1641G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239151 | ||||||
| chr11:126239165
|
G | A | 39 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(36): Show | 39 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.87-1627G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239165 | ||||||
| chr11:126239252
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.87-1540T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239252 | ||||||
| chr11:126239367
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.87-1425T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239367 | ||||||
| chr11:126239568
|
T | G | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.87-1224T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239568 | ||||||
| chr11:126239592
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.87-1200C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239592 | ||||||
| chr11:126239653
|
A | G | 72 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(69): Show | 72 | HG00323.hp1 HG00544.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.87-1139A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239653 | ||||||
| chr11:126239674
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.87-1118C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239674 | ||||||
| chr11:126239698
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.87-1094G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239698 | ||||||
| chr11:126239793
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.87-999C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239793 | ||||||
| chr11:126239934
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | NA18939.hp1 NA18959.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.87-858G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126239934 | ||||||
| chr11:126240077
|
AAG | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG02647.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.87-710_87-709delAG | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126240077 | |||||
| chr11:126240117
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.87-675C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126240117 | ||||||
| chr11:126240381
|
C | T | 4 | a0001c0001t0001g0265a0001c0001t0001g0281a0001c0001t0001g0283others(1): Show | 4 | HG02602.hp1 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.87-411C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126240381 | ||||||
| chr11:126240410
|
A | G | 1 | a0001c0001t0001g0308 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.87-382A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126240410 | ||||||
| chr11:126240420
|
C | T | 1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.87-372C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126240420 | ||||||
| chr11:126240423
|
C | T | 49 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(46): Show | 49 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.87-369C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126240423 | ||||||
| chr11:126240481
|
G | GCTATA | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.87-310_87-306dupCT others(3): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126240481 | |||||
| chr11:126240551
|
A | C | 1 | a0001c0001t0001g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.87-241A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126240551 | ||||||
| chr11:126240657
|
GGT | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0054 | 4 | HG00099.hp1 HG00140.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.87-132_87-131delGT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 126240657 | |||||
| chr11:126240692
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0103 | 2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.87-100A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 3/8 | chr11 | 126240692 | ||||||
| chr11:126241061
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.339+17G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241061 | ||||||
| chr11:126241083
|
C | A | 47 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0169others(44): Show | 47 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.339+39C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241083 | ||||||
| chr11:126241093
|
A | C | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.339+49A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241093 | ||||||
| chr11:126241109
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.339+65T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241109 | ||||||
| chr11:126241129
|
GCATGCCA others(3): Show |
G | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.339+86_339+95delCA others(8): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241129 | ||||||
| chr11:126241196
|
G | A | 34 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(31): Show | 34 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.339+152G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241196 | ||||||
| chr11:126241199
|
A | G | 47 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0169others(44): Show | 47 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.339+155A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241199 | ||||||
| chr11:126241300
|
C | A | 2 | a0001c0004t0002g0105a0001c0004t0002g0110 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.339+256C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241300 | ||||||
| chr11:126241398
|
T | TA | 49 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(46): Show | 49 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.339+356dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126241398 | |||||
| chr11:126241482
|
G | C | 1 | a0001c0001t0001g0066 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.339+438G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241482 | ||||||
| chr11:126241558
|
A | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0091others(2): Show | 6 | HG02280.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+514A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241558 | ||||||
| chr11:126241562
|
A | T | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(301): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.339+518A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241562 | ||||||
| chr11:126241579
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+535T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241579 | ||||||
| chr11:126241625
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.339+581T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241625 | ||||||
| chr11:126241827
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+783G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241827 | ||||||
| chr11:126241871
|
A | G | 1 | a0001c0001t0008g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.339+827A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241871 | ||||||
| chr11:126241985
|
A | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.339+941A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126241985 | ||||||
| chr11:126242019
|
C | T | 8 | a0001c0001t0002g0111a0001c0001t0002g0127a0001c0001t0002g0156others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.339+975C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242019 | ||||||
| chr11:126242024
|
CA | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.339+999delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126242024 | |||||
| chr11:126242024
|
CAA | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0251a0001c0001t0004g0010others(6): Show | 9 | HG01074.hp1 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.339+998_339+999del others(2): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126242024 | |||||
| chr11:126242035
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.339+991A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242035 | ||||||
| chr11:126242090
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+1046A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242090 | ||||||
| chr11:126242111
|
A | G | 2 | a0001c0002t0001g0309a0001c0002t0001g0310 | 2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.339+1067A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242111 | ||||||
| chr11:126242125
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+1081A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242125 | ||||||
| chr11:126242165
|
T | C | 39 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(36): Show | 39 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.339+1121T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242165 | ||||||
| chr11:126242305
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.339+1261G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242305 | ||||||
| chr11:126242452
|
C | T | 3 | a0001c0001t0001g0303a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG02647.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.339+1408C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242452 | ||||||
| chr11:126242499
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.339+1455G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242499 | ||||||
| chr11:126242680
|
A | G | 49 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(46): Show | 49 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.339+1636A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242680 | ||||||
| chr11:126242879
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.339+1835C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126242879 | ||||||
| chr11:126243183
|
T | G | 9 | a0001c0001t0001g0334a0001c0001t0004g0010a0001c0001t0004g0011others(6): Show | 9 | HG02145.hp2 HG02615.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.339+2139T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126243183 | ||||||
| chr11:126243352
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+2308G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126243352 | ||||||
| chr11:126243711
|
C | T | 1 | a0001c0005t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.339+2667C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126243711 | ||||||
| chr11:126243843
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.339+2799G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126243843 | ||||||
| chr11:126243883
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.339+2839G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126243883 | ||||||
| chr11:126243899
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.339+2855G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126243899 | ||||||
| chr11:126243903
|
C | CA | 51 | a0001c0001t0001g0009a0001c0001t0001g0057a0001c0001t0001g0098others(48): Show | 52 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.339+2875dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126243903 | |||||
| chr11:126243903
|
CA | C | 10 | a0001c0001t0001g0034a0001c0001t0001g0102a0001c0001t0001g0137others(7): Show | 10 | HG02145.hp1 HG02486.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.339+2875delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126243903 | |||||
| chr11:126243903
|
CAA | C | 37 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(34): Show | 37 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.339+2874_339+2875d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126243903 | |||||
| chr11:126244130
|
A | G | 47 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0169others(44): Show | 47 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.339+3086A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244130 | ||||||
| chr11:126244182
|
C | T | 3 | a0002c0003t0001g0261a0002c0003t0001g0262a0002c0003t0001g0264 | 3 | HG02572.hp2 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.339+3138C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244182 | ||||||
| chr11:126244394
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.339+3350A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244394 | ||||||
| chr11:126244497
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+3453T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244497 | ||||||
| chr11:126244620
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.339+3576A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244620 | ||||||
| chr11:126244645
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.339+3601A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244645 | ||||||
| chr11:126244723
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.339+3679G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244723 | ||||||
| chr11:126244735
|
A | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.339+3691A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244735 | ||||||
| chr11:126244833
|
T | A | 1 | a0001c0001t0004g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.339+3789T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244833 | ||||||
| chr11:126244834
|
G | T | 1 | a0001c0001t0004g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.339+3790G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126244834 | ||||||
| chr11:126245028
|
A | G | 2 | a0001c0001t0001g0168a0003c0006t0001g0167 | 2 | HG02523.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.339+3984A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245028 | ||||||
| chr11:126245055
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.339+4011C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245055 | ||||||
| chr11:126245360
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.339+4316A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245360 | ||||||
| chr11:126245386
|
C | G | 1 | a0001c0001t0001g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.339+4342C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245386 | ||||||
| chr11:126245576
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.339+4532C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245576 | ||||||
| chr11:126245689
|
C | T | 1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.339+4645C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245689 | ||||||
| chr11:126245732
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.339+4688A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245732 | ||||||
| chr11:126245823
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340-4683C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245823 | ||||||
| chr11:126245865
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.340-4641G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245865 | ||||||
| chr11:126245882
|
G | A | 2 | a0001c0001t0004g0010a0001c0001t0004g0011 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.340-4624G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245882 | ||||||
| chr11:126245928
|
G | A | 2 | a0001c0001t0001g0168a0003c0006t0001g0167 | 2 | HG02523.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.340-4578G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245928 | ||||||
| chr11:126245992
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.340-4514G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245992 | ||||||
| chr11:126245995
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-4511C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126245995 | ||||||
| chr11:126246064
|
A | G | 39 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(36): Show | 39 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.340-4442A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246064 | ||||||
| chr11:126246111
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.340-4395A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246111 | ||||||
| chr11:126246138
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.340-4368G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246138 | ||||||
| chr11:126246140
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.340-4366G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246140 | ||||||
| chr11:126246197
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.340-4309C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246197 | ||||||
| chr11:126246202
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.340-4304A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246202 | ||||||
| chr11:126246324
|
T | C | 29 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0132others(26): Show | 30 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.340-4182T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246324 | ||||||
| chr11:126246446
|
G | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0205 | 2 | NA18955.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.340-4060G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246446 | ||||||
| chr11:126246496
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-4010C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246496 | ||||||
| chr11:126246579
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.340-3927C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246579 | ||||||
| chr11:126246620
|
T | A | 1 | a0001c0001t0001g0317 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.340-3886T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246620 | ||||||
| chr11:126246638
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0324a0001c0001t0001g0330 | 3 | NA18970.hp2 NA19055.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.340-3868C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246638 | ||||||
| chr11:126246741
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.340-3765T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246741 | ||||||
| chr11:126246757
|
A | C | 49 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(46): Show | 49 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.340-3749A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246757 | ||||||
| chr11:126246957
|
T | G | 3 | a0001c0001t0001g0303a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG02647.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.340-3549T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246957 | ||||||
| chr11:126246968
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.340-3538G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246968 | ||||||
| chr11:126246977
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.340-3529C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126246977 | ||||||
| chr11:126247048
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.340-3458C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247048 | ||||||
| chr11:126247109
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.340-3397A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247109 | ||||||
| chr11:126247379
|
T | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0220 | 2 | NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.340-3127T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247379 | ||||||
| chr11:126247667
|
A | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0040a0004c0007t0001g0044 | 3 | HG01496.hp1 HG01517.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.340-2839A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247667 | ||||||
| chr11:126247750
|
C | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-2756C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247750 | ||||||
| chr11:126247857
|
C | CA | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 112 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.340-2639dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126247857 | |||||
| chr11:126247866
|
A | AT | 3 | a0001c0001t0001g0160a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG01167.hp1 HG01175.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.340-2640_340-2639i others(3): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247866 | ||||||
| chr11:126247866
|
A | T | 5 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0277others(2): Show | 5 | HG01978.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-2640A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247866 | ||||||
| chr11:126247868
|
T | A | 86 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0036others(83): Show | 88 | HG00408.hp2 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.340-2638T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247868 | ||||||
| chr11:126247870
|
T | A | 37 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(34): Show | 37 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.340-2636T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247870 | ||||||
| chr11:126247872
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.340-2634T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247872 | ||||||
| chr11:126247913
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.340-2593A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247913 | ||||||
| chr11:126247923
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.340-2583A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126247923 | ||||||
| chr11:126248025
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.340-2481A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248025 | ||||||
| chr11:126248358
|
C | CT | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.340-2119dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126248358 | |||||
| chr11:126248358
|
C | CTT | 47 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(44): Show | 48 | HG00408.hp1 HG00544.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.340-2120_340-2119d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126248358 | |||||
| chr11:126248358
|
C | CTTT | 39 | a0001c0001t0001g0009a0001c0001t0001g0121a0001c0001t0001g0123others(36): Show | 40 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.340-2121_340-2119d others(5): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126248358 | |||||
| chr11:126248358
|
C | CTTTT | 34 | a0001c0001t0001g0165a0001c0001t0001g0194a0001c0001t0001g0226others(31): Show | 34 | HG00099.hp2 HG01192.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.340-2122_340-2119d others(6): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126248358 | |||||
| chr11:126248358
|
C | CTTTTT | 26 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0137others(23): Show | 27 | HG01106.hp1 HG01109.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.340-2123_340-2119d others(7): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126248358 | |||||
| chr11:126248358
|
C | CTTTTTT | 23 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(20): Show | 23 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-2124_340-2119d others(8): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126248358 | |||||
| chr11:126248358
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0001g0008a0001c0001t0001g0315a0001c0001t0001g0316others(1): Show | 5 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-2130_340-2119d others(14): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126248358 | |||||
| chr11:126248358
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0192 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.340-2133_340-2119d others(17): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126248358 | |||||
| chr11:126248401
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0128 | 3 | HG00140.hp2 HG00280.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.340-2105G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248401 | ||||||
| chr11:126248425
|
C | T | 4 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0162others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-2081C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248425 | ||||||
| chr11:126248523
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.340-1983C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248523 | ||||||
| chr11:126248606
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.340-1900G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248606 | ||||||
| chr11:126248616
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.340-1890C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248616 | ||||||
| chr11:126248677
|
G | A | 1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.340-1829G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248677 | ||||||
| chr11:126248771
|
G | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0303others(2): Show | 5 | HG01099.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-1735G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248771 | ||||||
| chr11:126248804
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.340-1702G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248804 | ||||||
| chr11:126248896
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-1610C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248896 | ||||||
| chr11:126248945
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-1561A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126248945 | ||||||
| chr11:126249137
|
C | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0072 | 3 | NA18999.hp2 NA19063.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.340-1369C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249137 | ||||||
| chr11:126249392
|
T | G | 1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.340-1114T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249392 | ||||||
| chr11:126249479
|
TCC | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(38): Show | 42 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.340-1025_340-1024d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126249479 | |||||
| chr11:126249485
|
CA | C | 39 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(36): Show | 39 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.340-1020delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249485 | ||||||
| chr11:126249560
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-946G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249560 | ||||||
| chr11:126249726
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0045others(18): Show | 22 | HG02129.hp2 NA18747.hp2 NA18941.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-780C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249726 | ||||||
| chr11:126249731
|
C | CA | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.340-752dupA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126249731 | |||||
| chr11:126249731
|
C | CAA | 17 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(14): Show | 18 | HG01175.hp1 HG01175.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.340-753_340-752dup others(2): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126249731 | |||||
| chr11:126249731
|
CA | C | 14 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(11): Show | 14 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.340-752delA | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126249731 | |||||
| chr11:126249731
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0243 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.340-763_340-752del others(12): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126249731 | |||||
| chr11:126249741
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-765A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249741 | ||||||
| chr11:126249743
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.340-758_340-741del others(18): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126249743 | |||||
| chr11:126249748
|
A | G | 3 | a0002c0003t0001g0261a0002c0003t0001g0262a0002c0003t0001g0264 | 3 | HG02572.hp2 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.340-758A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249748 | ||||||
| chr11:126249749
|
A | AG | 44 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(41): Show | 44 | HG00544.hp1 HG00741.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.340-757_340-756ins others(1): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249749 | ||||||
| chr11:126249749
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.340-757A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249749 | ||||||
| chr11:126249750
|
A | G | 8 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(5): Show | 8 | HG02155.hp2 NA18954.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.340-756A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249750 | ||||||
| chr11:126249751
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.340-755A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249751 | ||||||
| chr11:126249761
|
G | T | 2 | a0001c0001t0003g0005a0001c0001t0003g0100 | 3 | HG00423.hp1 HG02083.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.340-745G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249761 | ||||||
| chr11:126249939
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.340-567G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126249939 | ||||||
| chr11:126250024
|
C | A | 54 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(51): Show | 56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.340-482C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126250024 | ||||||
| chr11:126250029
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.340-477G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126250029 | ||||||
| chr11:126250039
|
A | G | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.340-467A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126250039 | ||||||
| chr11:126250092
|
A | AT | 8 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0001g0132others(5): Show | 8 | HG01891.hp1 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-397dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126250092 | |||||
| chr11:126250092
|
AT | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(219): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.340-397delT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 126250092 | |||||
| chr11:126250126
|
C | T | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-380C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126250126 | ||||||
| chr11:126250132
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.340-374C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126250132 | ||||||
| chr11:126250313
|
G | A | 16 | a0001c0001t0001g0203a0001c0001t0001g0317a0001c0001t0001g0318others(13): Show | 16 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-193G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126250313 | ||||||
| chr11:126250333
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.340-173C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126250333 | ||||||
| chr11:126250382
|
C | T | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.340-124C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | chr11 | 126250382 | ||||||
| chr11:126250844
|
T | A | 1 | a0001c0001t0001g0286 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.567+111T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126250844 | ||||||
| chr11:126251147
|
C | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | NA18939.hp1 NA18959.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.567+414C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126251147 | ||||||
| chr11:126251369
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.567+636C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126251369 | ||||||
| chr11:126251377
|
G | A | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.567+644G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126251377 | ||||||
| chr11:126251715
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.567+982T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126251715 | ||||||
| chr11:126251731
|
C | CT | 7 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0074others(4): Show | 7 | HG01106.hp2 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+1015dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 126251731 | |||||
| chr11:126251743
|
T | C | 1 | a0001c0004t0002g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.567+1010T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126251743 | ||||||
| chr11:126251870
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0315a0001c0001t0001g0316 | 4 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+1137C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126251870 | ||||||
| chr11:126251973
|
C | CGTTTT | 9 | a0001c0001t0001g0122a0001c0001t0001g0297a0001c0001t0001g0298others(6): Show | 9 | HG00639.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.567+1267_567+1271d others(7): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 126251973 | |||||
| chr11:126251973
|
C | CGTTTTGT others(3): Show |
2 | a0002c0003t0001g0261a0002c0003t0001g0264 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.567+1262_567+1271d others(12): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 126251973 | |||||
| chr11:126252005
|
A | T | 1 | a0001c0001t0001g0297 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.567+1272A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126252005 | ||||||
| chr11:126252107
|
G | A | 1 | a0001c0005t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.567+1374G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126252107 | ||||||
| chr11:126252143
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.567+1410C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126252143 | ||||||
| chr11:126252470
|
G | C | 1 | a0003c0006t0001g0167 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.567+1737G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126252470 | ||||||
| chr11:126252599
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.568-1706C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126252599 | ||||||
| chr11:126252608
|
T | G | 1 | a0001c0001t0001g0296 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.568-1697T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126252608 | ||||||
| chr11:126252709
|
C | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0265a0001c0001t0001g0266others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.568-1596C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126252709 | ||||||
| chr11:126252899
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.568-1406G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126252899 | ||||||
| chr11:126253011
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.568-1294G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253011 | ||||||
| chr11:126253038
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0260 | 2 | HG04204.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.568-1267A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253038 | ||||||
| chr11:126253199
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0069 | 3 | NA18747.hp1 NA18943.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.568-1106C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253199 | ||||||
| chr11:126253306
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.568-999C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253306 | ||||||
| chr11:126253487
|
G | T | 1 | a0001c0001t0001g0059 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.568-818G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253487 | ||||||
| chr11:126253526
|
T | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.568-779T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253526 | ||||||
| chr11:126253549
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 112 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.568-756C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253549 | ||||||
| chr11:126253611
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.568-694A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253611 | ||||||
| chr11:126253695
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0270 | 2 | NA18989.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.568-610C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253695 | ||||||
| chr11:126253963
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.568-342A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126253963 | ||||||
| chr11:126254184
|
A | T | 1 | a0001c0001t0001g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.568-121A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126254184 | ||||||
| chr11:126254195
|
A | G | 8 | a0001c0001t0004g0010a0001c0001t0004g0011a0001c0002t0001g0309others(5): Show | 8 | HG02145.hp2 HG02615.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-110A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126254195 | ||||||
| chr11:126254266
|
G | C | 1 | a0002c0003t0001g0261 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.568-39G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 5/8 | chr11 | 126254266 | ||||||
| chr11:126254743
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.696+310T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126254743 | ||||||
| chr11:126254940
|
C | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.696+507C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126254940 | ||||||
| chr11:126254940
|
CTTTG | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0128 | 3 | HG00140.hp2 HG00280.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.696+513_696+516del others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr11 | 126254940 | |||||
| chr11:126255062
|
A | C | 1 | a0001c0001t0001g0180 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.696+629A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255062 | ||||||
| chr11:126255180
|
T | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.696+747T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255180 | ||||||
| chr11:126255199
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.696+766G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255199 | ||||||
| chr11:126255259
|
C | T | 41 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0171others(38): Show | 41 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.696+826C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255259 | ||||||
| chr11:126255504
|
C | T | 18 | a0001c0001t0001g0013a0001c0001t0001g0045a0001c0001t0001g0050others(15): Show | 18 | HG01358.hp2 HG02129.hp2 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.697-1063C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255504 | ||||||
| chr11:126255505
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.697-1062A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255505 | ||||||
| chr11:126255559
|
T | G | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.697-1008T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255559 | ||||||
| chr11:126255646
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.697-921A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255646 | ||||||
| chr11:126255674
|
T | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0303a0001c0001t0001g0304others(14): Show | 18 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.697-893T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255674 | ||||||
| chr11:126255814
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.697-753G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255814 | ||||||
| chr11:126255858
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.697-709C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126255858 | ||||||
| chr11:126256214
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0295 | 2 | NA18959.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.697-353C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126256214 | ||||||
| chr11:126256310
|
C | G | 1 | a0001c0001t0001g0078 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.697-257C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 6/8 | chr11 | 126256310 | ||||||
| chr11:126256915
|
TTGTGA | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0332a0001c0001t0001g0333 | 3 | HG02109.hp2 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.982+71_982+75delTG others(3): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126256915 | |||||
| chr11:126256943
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.982+91A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126256943 | ||||||
| chr11:126257491
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.982+639A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126257491 | ||||||
| chr11:126257526
|
A | T | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.982+674A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126257526 | ||||||
| chr11:126257605
|
A | AT | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.982+769dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126257605 | |||||
| chr11:126257605
|
A | ATT | 8 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0060others(5): Show | 8 | HG02148.hp1 HG02293.hp1 NA18985.hp1 others(5): Show |
intron_variant | MODIFIER | c.982+768_982+769dup others(2): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126257605 | |||||
| chr11:126258097
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.982+1245G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258097 | ||||||
| chr11:126258542
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.982+1690C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258542 | ||||||
| chr11:126258642
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.982+1790C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258642 | ||||||
| chr11:126258744
|
A | G | 2 | a0001c0001t0001g0168a0003c0006t0001g0167 | 2 | HG02523.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.982+1892A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258744 | ||||||
| chr11:126258807
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.982+1955C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258807 | ||||||
| chr11:126258867
|
A | G | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.982+2015A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258867 | ||||||
| chr11:126258881
|
A | C | 2 | a0001c0001t0004g0010a0001c0001t0004g0011 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.982+2029A>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258881 | ||||||
| chr11:126258930
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.982+2078T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258930 | ||||||
| chr11:126258946
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.982+2094C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126258946 | ||||||
| chr11:126259176
|
A | G | 3 | a0002c0003t0001g0261a0002c0003t0001g0262a0002c0003t0001g0264 | 3 | HG02572.hp2 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.983-2249A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259176 | ||||||
| chr11:126259208
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.983-2217G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259208 | ||||||
| chr11:126259219
|
G | C | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.983-2206G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259219 | ||||||
| chr11:126259255
|
C | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.983-2170C>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259255 | ||||||
| chr11:126259370
|
G | A | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.983-2055G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259370 | ||||||
| chr11:126259425
|
C | CT | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(63): Show | 70 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.983-1981dupT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126259425 | |||||
| chr11:126259425
|
C | CTT | 46 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(43): Show | 48 | HG00408.hp1 HG01358.hp2 HG02071.hp2 others(45): Show |
intron_variant | MODIFIER | c.983-1982_983-1981d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126259425 | |||||
| chr11:126259425
|
C | CTTT | 6 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0087others(3): Show | 6 | HG00423.hp1 HG00423.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.983-1983_983-1981d others(5): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126259425 | |||||
| chr11:126259425
|
CT | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0187a0001c0001t0001g0315others(3): Show | 7 | HG01515.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.983-1981delT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126259425 | |||||
| chr11:126259487
|
A | G | 50 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0168others(47): Show | 50 | HG00544.hp1 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.983-1938A>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259487 | ||||||
| chr11:126259511
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.983-1914C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259511 | ||||||
| chr11:126259516
|
C | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0315a0001c0001t0001g0316 | 4 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.983-1909C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259516 | ||||||
| chr11:126259571
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.983-1854G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259571 | ||||||
| chr11:126259632
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0103a0001c0001t0001g0265others(40): Show | 44 | HG00408.hp2 HG00639.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.983-1793G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259632 | ||||||
| chr11:126259675
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.983-1750C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259675 | ||||||
| chr11:126259781
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.983-1644C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259781 | ||||||
| chr11:126259870
|
G | A | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-1555G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126259870 | ||||||
| chr11:126260157
|
C | T | 1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.983-1268C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126260157 | ||||||
| chr11:126260158
|
G | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG01884.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.983-1267G>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126260158 | ||||||
| chr11:126260336
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.983-1089G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126260336 | ||||||
| chr11:126260337
|
C | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.983-1088C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126260337 | ||||||
| chr11:126260369
|
T | A | 7 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(4): Show | 7 | HG00323.hp1 HG01099.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.983-1056T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126260369 | ||||||
| chr11:126260396
|
AT | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 242 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.983-1014delT | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126260396 | |||||
| chr11:126260396
|
ATT | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0170others(3): Show | 6 | HG02647.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-1015_983-1014d others(4): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126260396 | |||||
| chr11:126260396
|
ATTT | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0132others(26): Show | 30 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.983-1016_983-1014d others(5): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126260396 | |||||
| chr11:126260485
|
CTT | C | 39 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(36): Show | 39 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.983-937_983-936del others(2): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126260485 | |||||
| chr11:126260539
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.983-886C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126260539 | ||||||
| chr11:126260867
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.983-558G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126260867 | ||||||
| chr11:126260921
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.983-504C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126260921 | ||||||
| chr11:126261006
|
A | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 112 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.983-419A>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126261006 | ||||||
| chr11:126261155
|
G | A | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG00323.hp1 HG01099.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.983-270G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126261155 | ||||||
| chr11:126261155
|
G | GAAATGTA | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.983-249_983-243dup others(7): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126261155 | |||||
| chr11:126261155
|
G | GAAATGTA others(7): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0085others(2): Show | 5 | HG02698.hp2 HG03704.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.983-256_983-243dup others(14): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 126261155 | |||||
| chr11:126261347
|
T | C | 29 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0132others(26): Show | 30 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.983-78T>C | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126261347 | ||||||
| chr11:126261387
|
T | G | 1 | a0001c0001t0001g0334 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.983-38T>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 7/8 | chr11 | 126261387 | ||||||
| chr11:126261718
|
G | T | 1 | a0002c0003t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1042+234G>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 8/8 | chr11 | 126261718 | ||||||
| chr11:126261729
|
C | T | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1042+245C>T | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 8/8 | chr11 | 126261729 | ||||||
| chr11:126261982
|
T | A | 3 | a0002c0003t0001g0261a0002c0003t0001g0262a0002c0003t0001g0264 | 3 | HG02572.hp2 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1043-138T>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 8/8 | chr11 | 126261982 | ||||||
| chr11:126262030
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1043-90G>A | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 8/8 | chr11 | 126262030 | ||||||
| chr11:126262043
|
C | G | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1043-77C>G | FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 8/8 | chr11 | 126262043 |