Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 153643 |
|---|---|
| ensemblid | ENSG00000153347.10 |
| hgncid | 26335 |
| symbol | FAM81B |
| name | family with sequence similarity 81 member B |
| refseq_nuc | NM_152548.3 |
| refseq_prot | NP_689761.2 |
| ensembl_nuc | ENST00000283357.10 |
| ensembl_prot | ENSP00000283357.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 95391366 |
| end | 95450441 |
| strand | + |
| ver | v1.2 |
| region | chr5:95391366-95450441 |
| region5000 | chr5:95386366-95455441 |
| regionname0 | FAM81B_chr5_95391366_95450441 |
| regionname5000 | FAM81B_chr5_95386366_95455441 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 452 | 330 | 88 | 66 | 123 | 11 | 40 | 97 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0002 | 0/0 | 452 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0003 | 0/0 | 143 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0004 | 0/0 | 452 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0005 | 0/0 | 452 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0006 | 0/0 | 452 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0007 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0008 | 0/0 | 452 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0009 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0010 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1359 | 255 | 63 | 48 | 101 | 8 | 33 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0002 | 0/0 | 1359 | 75 | 25 | 18 | 22 | 3 | 7 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0003 | 0/0 | 1359 | 6 | 0 | 3 | 0 | 1 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0004 | 0/0 | 1359 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0005 | 0/0 | 1359 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0006 | 0/0 | 1359 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0007 | 0/0 | 1359 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0008 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0009 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0010 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| c0011 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1359 | 255 | 63 | 48 | 101 | 8 | 33 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0001c0002 | 0/0 | 1359 | 75 | 25 | 18 | 22 | 3 | 7 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0002c0003 | 0/0 | 1359 | 6 | 0 | 3 | 0 | 1 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0003c0004 | 0/0 | 1359 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0004c0005 | 0/0 | 1359 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0005c0007 | 0/0 | 1359 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0006c0006 | 0/0 | 1359 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0007c0011 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0008c0008 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0009c0009 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0010c0010 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1542 | 190 | 31 | 43 | 83 | 7 | 25 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0001c0001t0002 | 0/1 | 1542 | 65 | 32 | 5 | 18 | 1 | 8 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0001c0002t0001 | 0/0 | 1542 | 57 | 14 | 14 | 20 | 3 | 6 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0001c0002t0002 | 0/0 | 1542 | 18 | 11 | 4 | 2 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0002c0003t0001 | 0/0 | 1542 | 5 | 0 | 2 | 0 | 1 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0002c0003t0002 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0003c0004t0001 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0003c0004t0002 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0004c0005t0002 | 0/0 | 1542 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0005c0007t0001 | 0/0 | 1542 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0006c0006t0001 | 0/0 | 1542 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0007c0011t0001 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0008c0008t0002 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0009c0009t0001 | 0/0 | 1542 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| a0010c0010t0001 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | copy fasta | chr5 | 95386366 | 95455441 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0002c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0003c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0003c0004t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0004c0005t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0004c0005t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0005c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0005c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0006c0006t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0006c0006t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0007c0011t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0008c0008t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0009c0009t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| a0010c0010t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | GBR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0053 | EUR | FIN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0014 | EUR | FIN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0045 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0063 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG00741 | hp2 | a0006 | c0006 | t0001 | g0262 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01167 | hp2 | a0004 | c0005 | t0002 | g0218 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0089 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01169 | hp1 | a0004 | c0005 | t0002 | g0219 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01255 | hp1 | a0003 | c0004 | t0002 | g0064 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0049 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0324 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01358 | hp2 | a0006 | c0006 | t0001 | g0314 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01361 | hp2 | a0008 | c0008 | t0002 | g0286 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01516 | hp1 | a0002 | c0003 | t0001 | g0050 | EUR | IBS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0280 | EUR | IBS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CDX | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CDX | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0186 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0312 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0327 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0325 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0326 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0307 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0331 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0335 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | STU | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18951 | hp1 | a0009 | c0009 | t0001 | g0166 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18981 | hp2 | a0005 | c0007 | t0001 | g0212 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18985 | hp1 | a0005 | c0007 | t0001 | g0149 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19043 | hp2 | a0010 | c0010 | t0001 | g0183 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | YRI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ASW | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | ASW | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0330 | EUR | TSI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | TSI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0139 | EUR | TSI | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | GIH | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | GIH | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | ACB | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0309 | AFR | USA | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | USA | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | USA | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | USA | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| NA21309 | hp2 | a0007 | c0011 | t0001 | g0097 | AFR | LWK | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0240 | REF | REF | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0161 | REF | REF | FAM81B_chr5_95386366_95455441 | FAM81B | chr5 | 95386366 | 95455441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95413979
|
C | G | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.326C>G | p.Thr109Ser | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/10 | 350/1542 | 326/1359 | 109/452 | chr5 | 95413979 | ||
| chr5:95414083
|
C | T | 1 | a0003 | 2 | HG00735.hp2 HG01255.hp1 |
stop_gained | HIGH | c.430C>T | p.Gln144* | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/10 | 454/1542 | 430/1359 | 144/452 | chr5 | 95414083 | ||
| chr5:95420306
|
C | T | 1 | a0002 | 6 | HG00733.hp2 HG01168.hp2 HG01257.hp1 others(3): Show |
missense_variant | MODERATE | c.560C>T | p.Ala187Val | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/10 | 584/1542 | 560/1359 | 187/452 | chr5 | 95420306 | ||
| chr5:95428662
|
G | A | 1 | a0004 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.716G>A | p.Arg239Gln | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/10 | 740/1542 | 716/1359 | 239/452 | chr5 | 95428662 | ||
| chr5:95436872
|
G | A | 1 | a0006 | 2 | HG00741.hp2 HG01358.hp2 |
missense_variant | MODERATE | c.859G>A | p.Asp287Asn | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/10 | 883/1542 | 859/1359 | 287/452 | chr5 | 95436872 | ||
| chr5:95448345
|
A | C | 1 | a0010 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1106A>C | p.Lys369Thr | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/10 | 1130/1542 | 1106/1359 | 369/452 | chr5 | 95448345 | ||
| chr5:95448422
|
A | G | 1 | a0009 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1183A>G | p.Ile395Val | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/10 | 1207/1542 | 1183/1359 | 395/452 | chr5 | 95448422 | ||
| chr5:95450254
|
G | A | 1 | a0005 | 2 | NA18981.hp2 NA18985.hp1 |
missense_variant | MODERATE | c.1331G>A | p.Arg444His | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 10/10 | 1355/1542 | 1331/1359 | 444/452 | chr5 | 95450254 | ||
| chr5:95450254
|
G | T | 1 | a0008 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1331G>T | p.Arg444Leu | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 10/10 | 1355/1542 | 1331/1359 | 444/452 | chr5 | 95450254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95414019
|
G | A | 4 | a0001c0002a0002c0003a0003c0004others(1): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
synonymous_variant | LOW | c.366G>A | p.Ala122Ala | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/10 | 390/1542 | 366/1359 | 122/452 | chr5 | 95414019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95450438
|
C | T | 6 | a0001c0001t0002a0001c0002t0002a0002c0003t0002others(3): Show | 88 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*156C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 10/10 | 156 | chr5 | 95450438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:95391648
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+135T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95391648 | ||||||
| chr5:95391663
|
G | GA | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 121 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.124+159dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 95391663 | |||||
| chr5:95391673
|
C | A | 3 | a0001c0001t0001g0001a0001c0001t0002g0015a0001c0002t0001g0014 | 4 | HG00280.hp2 HG02698.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+160C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95391673 | ||||||
| chr5:95391745
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0002g0015 | 3 | HG02698.hp2 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.124+232C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95391745 | ||||||
| chr5:95391947
|
TTCCTCAA others(5): Show |
T | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.124+436_124+447del others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 95391947 | |||||
| chr5:95391974
|
C | T | 1 | a0001c0001t0001g0336 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.124+461C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95391974 | ||||||
| chr5:95392053
|
G | C | 9 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0132others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+540G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392053 | ||||||
| chr5:95392082
|
G | A | 1 | a0001c0002t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.124+569G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392082 | ||||||
| chr5:95392141
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0002g0015a0001c0002t0001g0014 | 4 | HG00280.hp2 HG02698.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+628G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392141 | ||||||
| chr5:95392304
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.125-490G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392304 | ||||||
| chr5:95392374
|
A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 284 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.125-420A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392374 | ||||||
| chr5:95392465
|
A | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(98): Show | 105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.125-329A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392465 | ||||||
| chr5:95392590
|
C | T | 1 | a0001c0002t0002g0335 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.125-204C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392590 | ||||||
| chr5:95392624
|
G | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028 | 3 | HG02280.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.125-170G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392624 | ||||||
| chr5:95392625
|
G | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028 | 3 | HG02280.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.125-169G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 1/9 | chr5 | 95392625 | ||||||
| chr5:95392927
|
G | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 300 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.228+30G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95392927 | ||||||
| chr5:95393308
|
C | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0030 | 2 | HG00733.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.228+411C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393308 | ||||||
| chr5:95393473
|
C | CCT | 274 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 284 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.228+579_228+580dup others(2): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 95393473 | |||||
| chr5:95393478
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.228+581G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393478 | ||||||
| chr5:95393758
|
A | G | 1 | a0001c0001t0002g0334 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.228+861A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393758 | ||||||
| chr5:95393829
|
A | T | 1 | a0001c0002t0002g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.228+932A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393829 | ||||||
| chr5:95393935
|
T | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034others(60): Show | 66 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.228+1038T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95393935 | ||||||
| chr5:95394022
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.228+1125C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394022 | ||||||
| chr5:95394062
|
T | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0026others(100): Show | 107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.228+1165T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394062 | ||||||
| chr5:95394065
|
G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(270): Show | 283 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.228+1168G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394065 | ||||||
| chr5:95394097
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.228+1200C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394097 | ||||||
| chr5:95394215
|
C | T | 2 | a0001c0002t0002g0023a0001c0002t0002g0024 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.228+1318C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394215 | ||||||
| chr5:95394467
|
G | C | 1 | a0001c0001t0001g0090 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.228+1570G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394467 | ||||||
| chr5:95394473
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.228+1576A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394473 | ||||||
| chr5:95394636
|
G | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.229-1475G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394636 | ||||||
| chr5:95394780
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.229-1331C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394780 | ||||||
| chr5:95394844
|
T | C | 2 | a0001c0002t0002g0023a0001c0002t0002g0024 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.229-1267T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394844 | ||||||
| chr5:95394875
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(100): Show | 107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.229-1236A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95394875 | ||||||
| chr5:95395240
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.229-871C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395240 | ||||||
| chr5:95395253
|
C | A | 1 | a0001c0001t0001g0194 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.229-858C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395253 | ||||||
| chr5:95395315
|
C | T | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(98): Show | 105 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.229-796C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395315 | ||||||
| chr5:95395318
|
C | G | 1 | a0001c0002t0002g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.229-793C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395318 | ||||||
| chr5:95395400
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(100): Show | 107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.229-711G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395400 | ||||||
| chr5:95395442
|
C | CA | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(223): Show | 234 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.229-650dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 95395442 | |||||
| chr5:95395442
|
C | CAA | 28 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(25): Show | 29 | HG00621.hp1 HG00621.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.229-651_229-650dup others(2): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 95395442 | |||||
| chr5:95395643
|
A | G | 158 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0125others(155): Show | 163 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.229-468A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395643 | ||||||
| chr5:95395682
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0028others(4): Show | 7 | HG00741.hp1 HG01255.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.229-429C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395682 | ||||||
| chr5:95395716
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.229-395G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395716 | ||||||
| chr5:95395763
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.229-348C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395763 | ||||||
| chr5:95395921
|
T | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0002g0018others(3): Show | 6 | HG00741.hp1 HG01255.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-190T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395921 | ||||||
| chr5:95395934
|
T | A | 3 | a0001c0001t0002g0018a0001c0002t0002g0019a0001c0002t0002g0020 | 3 | HG02615.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.229-177T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95395934 | ||||||
| chr5:95396057
|
A | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0028others(4): Show | 7 | HG00741.hp1 HG01255.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.229-54A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 2/9 | chr5 | 95396057 | ||||||
| chr5:95396585
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.293+410T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95396585 | ||||||
| chr5:95396845
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293+670C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95396845 | ||||||
| chr5:95396850
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.293+675C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95396850 | ||||||
| chr5:95397052
|
T | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(159): Show | 168 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.293+877T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397052 | ||||||
| chr5:95397446
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 118 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.293+1271C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397446 | ||||||
| chr5:95397497
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(100): Show | 107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.293+1322G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397497 | ||||||
| chr5:95397551
|
C | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 9 | NA18974.hp1 NA18984.hp2 NA19004.hp2 others(6): Show |
intron_variant | MODIFIER | c.293+1376C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397551 | ||||||
| chr5:95397688
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0176 | 3 | NA18943.hp2 NA18954.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.293+1513G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95397688 | ||||||
| chr5:95398000
|
T | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(100): Show | 107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.293+1825T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398000 | ||||||
| chr5:95398030
|
C | T | 3 | a0001c0001t0002g0190a0001c0002t0001g0191a0001c0002t0001g0192 | 3 | HG02559.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.293+1855C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398030 | ||||||
| chr5:95398066
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.293+1891A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398066 | ||||||
| chr5:95398142
|
G | T | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.293+1967G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398142 | ||||||
| chr5:95398343
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293+2168C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398343 | ||||||
| chr5:95398346
|
G | A | 1 | a0005c0007t0001g0212 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.293+2171G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398346 | ||||||
| chr5:95398418
|
C | CTAAA | 171 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(168): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.293+2276_293+2279d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398418 | |||||
| chr5:95398418
|
C | CTAAATAA others(1): Show |
6 | a0001c0001t0001g0133a0001c0001t0001g0194a0001c0001t0001g0210others(3): Show | 6 | HG01358.hp2 HG02630.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+2272_293+2279d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398418 | |||||
| chr5:95398418
|
CTAAATAA others(1): Show |
C | 7 | a0001c0001t0001g0181a0001c0001t0002g0190a0001c0002t0001g0179others(4): Show | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.293+2272_293+2279d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398418 | |||||
| chr5:95398447
|
T | TA | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(96): Show | 103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.293+2275dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398447 | |||||
| chr5:95398451
|
T | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(96): Show | 103 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.293+2276T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398451 | ||||||
| chr5:95398451
|
T | TAAAAC | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0002g0121others(1): Show | 4 | HG02109.hp2 HG02257.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.293+2280_293+2281i others(7): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95398451 | |||||
| chr5:95398455
|
A | T | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0002g0316others(3): Show | 6 | HG01243.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+2280A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398455 | ||||||
| chr5:95398460
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293+2285T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398460 | ||||||
| chr5:95398511
|
C | G | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293+2336C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398511 | ||||||
| chr5:95398561
|
G | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(101): Show | 108 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.293+2386G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398561 | ||||||
| chr5:95398624
|
A | G | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0028others(4): Show | 7 | HG00741.hp1 HG01255.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.293+2449A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398624 | ||||||
| chr5:95398807
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(100): Show | 107 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.293+2632A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398807 | ||||||
| chr5:95398855
|
C | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0031others(54): Show | 59 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.293+2680C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398855 | ||||||
| chr5:95398965
|
A | T | 2 | a0001c0001t0002g0320a0001c0001t0002g0321 | 2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.293+2790A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95398965 | ||||||
| chr5:95399005
|
C | G | 5 | a0001c0001t0001g0181a0001c0001t0001g0313a0001c0002t0001g0179others(2): Show | 5 | HG01496.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+2830C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399005 | ||||||
| chr5:95399040
|
A | T | 106 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0031others(103): Show | 110 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.293+2865A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399040 | ||||||
| chr5:95399339
|
G | C | 125 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0022others(122): Show | 128 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(125): Show |
intron_variant | MODIFIER | c.293+3164G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399339 | ||||||
| chr5:95399480
|
G | GC | 16 | a0001c0001t0001g0065a0001c0001t0001g0080a0001c0001t0001g0303others(13): Show | 17 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.293+3314dupC | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95399480 | |||||
| chr5:95399485
|
C | A | 3 | a0001c0001t0002g0308a0001c0002t0001g0041a0001c0002t0001g0042 | 3 | NA18962.hp2 NA18969.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.293+3310C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399485 | ||||||
| chr5:95399498
|
G | C | 8 | a0001c0001t0002g0018a0001c0002t0001g0014a0001c0002t0001g0184others(5): Show | 8 | HG00280.hp2 HG01255.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.293+3323G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399498 | ||||||
| chr5:95399557
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293+3382G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399557 | ||||||
| chr5:95399610
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0031others(11): Show | 15 | HG00280.hp2 HG01109.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.293+3435T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399610 | ||||||
| chr5:95399657
|
C | G | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+3482C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399657 | ||||||
| chr5:95399829
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+3654C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399829 | ||||||
| chr5:95399963
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.293+3788C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95399963 | ||||||
| chr5:95400156
|
C | A | 10 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0001t0002g0129others(7): Show | 10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+3981C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400156 | ||||||
| chr5:95400156
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.293+3981C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400156 | ||||||
| chr5:95400157
|
G | T | 1 | a0010c0010t0001g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.293+3982G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400157 | ||||||
| chr5:95400246
|
G | T | 1 | a0001c0002t0001g0312 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.293+4071G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400246 | ||||||
| chr5:95400329
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.293+4154T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400329 | ||||||
| chr5:95400336
|
G | C | 10 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0001t0002g0129others(7): Show | 10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+4161G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400336 | ||||||
| chr5:95400382
|
G | A | 10 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0001t0002g0129others(7): Show | 10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+4207G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400382 | ||||||
| chr5:95400401
|
C | CACAT | 4 | a0001c0001t0001g0112a0001c0001t0001g0134a0001c0001t0002g0111others(1): Show | 4 | HG01069.hp2 HG01433.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.293+4258_293+4261d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400401 | |||||
| chr5:95400401
|
CACAT | C | 5 | a0001c0002t0001g0008a0001c0002t0001g0309a0001c0002t0001g0310others(2): Show | 6 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.293+4258_293+4261d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400401 | |||||
| chr5:95400433
|
T | C | 1 | a0001c0001t0002g0308 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.293+4258T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400433 | ||||||
| chr5:95400433
|
T | TACATACA others(3): Show |
1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293+4261_293+4262i others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | |||||
| chr5:95400433
|
T | TACATACA others(7): Show |
1 | a0001c0002t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.293+4261_293+4262i others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | |||||
| chr5:95400433
|
T | TACATACA others(15): Show |
7 | a0001c0002t0001g0128a0001c0002t0001g0179a0001c0002t0001g0184others(4): Show | 7 | HG02451.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | |||||
| chr5:95400433
|
T | TACATACA others(17): Show |
1 | a0001c0002t0002g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293+4261_293+4262i others(26): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | |||||
| chr5:95400433
|
T | TACATACA others(11): Show |
2 | a0001c0002t0001g0093a0001c0002t0001g0192 | 2 | HG01109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.293+4261_293+4262i others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | |||||
| chr5:95400433
|
T | TACATACA others(15): Show |
5 | a0001c0001t0002g0119a0001c0002t0001g0180a0001c0002t0001g0191others(2): Show | 5 | HG02559.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | |||||
| chr5:95400433
|
T | TACATACA others(15): Show |
1 | a0001c0002t0001g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.293+4261_293+4262i others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | |||||
| chr5:95400433
|
TAC | T | 9 | a0001c0001t0001g0085a0001c0001t0001g0140a0001c0001t0001g0141others(6): Show | 9 | HG01255.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.293+4274_293+4275d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400433 | |||||
| chr5:95400435
|
C | CAT | 5 | a0001c0001t0001g0006a0001c0001t0001g0123a0001c0001t0001g0194others(2): Show | 6 | HG01934.hp1 HG04115.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400435 | |||||
| chr5:95400435
|
C | CATACAT | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(154): Show | 162 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400435 | |||||
| chr5:95400435
|
C | CATACATA others(3): Show |
10 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0145others(7): Show | 11 | HG01192.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.293+4261_293+4262i others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400435 | |||||
| chr5:95400435
|
C | CATACATA others(11): Show |
1 | a0001c0002t0001g0307 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.293+4261_293+4262i others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95400435 | |||||
| chr5:95400437
|
C | T | 5 | a0001c0001t0001g0028a0001c0002t0001g0014a0001c0002t0001g0188others(2): Show | 5 | HG00280.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+4262C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400437 | ||||||
| chr5:95400438
|
A | G | 5 | a0001c0001t0002g0018a0001c0001t0002g0129a0001c0002t0002g0019others(2): Show | 5 | HG01255.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.293+4263A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400438 | ||||||
| chr5:95400439
|
C | CGT | 5 | a0001c0001t0001g0028a0001c0002t0001g0014a0001c0002t0001g0188others(2): Show | 5 | HG00280.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+4264_293+4265i others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400439 | ||||||
| chr5:95400439
|
C | T | 5 | a0001c0001t0002g0018a0001c0001t0002g0129a0001c0002t0002g0019others(2): Show | 5 | HG01255.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.293+4264C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400439 | ||||||
| chr5:95400447
|
C | T | 18 | a0001c0001t0002g0119a0001c0002t0001g0017a0001c0002t0001g0093others(15): Show | 18 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.293+4272C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400447 | ||||||
| chr5:95400658
|
T | A | 10 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0001t0002g0129others(7): Show | 10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+4483T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400658 | ||||||
| chr5:95400698
|
T | G | 10 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0001t0002g0129others(7): Show | 10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+4523T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400698 | ||||||
| chr5:95400764
|
G | A | 1 | a0001c0002t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.293+4589G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400764 | ||||||
| chr5:95400927
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.293+4752C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400927 | ||||||
| chr5:95400930
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.293+4755C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95400930 | ||||||
| chr5:95401014
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG01978.hp2 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.293+4839T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401014 | ||||||
| chr5:95401184
|
T | C | 10 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0001t0002g0129others(7): Show | 10 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.293+5009T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401184 | ||||||
| chr5:95401274
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.293+5099C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401274 | ||||||
| chr5:95401403
|
C | T | 13 | a0001c0002t0001g0017a0001c0002t0001g0093a0001c0002t0001g0177others(10): Show | 13 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.293+5228C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401403 | ||||||
| chr5:95401792
|
C | T | 1 | a0001c0001t0002g0297 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.293+5617C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401792 | ||||||
| chr5:95401815
|
G | T | 8 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0002t0001g0014others(5): Show | 8 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.293+5640G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401815 | ||||||
| chr5:95401913
|
A | G | 8 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0002t0001g0014others(5): Show | 8 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.293+5738A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401913 | ||||||
| chr5:95401920
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.293+5745G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95401920 | ||||||
| chr5:95402189
|
T | C | 8 | a0001c0001t0001g0028a0001c0001t0002g0018a0001c0002t0001g0014others(5): Show | 8 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.293+6014T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402189 | ||||||
| chr5:95402196
|
G | A | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.293+6021G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402196 | ||||||
| chr5:95402212
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.293+6037A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402212 | ||||||
| chr5:95402696
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.293+6521G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402696 | ||||||
| chr5:95402707
|
G | T | 6 | a0001c0002t0001g0014a0001c0002t0001g0188a0001c0002t0002g0019others(3): Show | 6 | HG00280.hp2 HG01255.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.293+6532G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402707 | ||||||
| chr5:95402744
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 181 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.293+6569A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402744 | ||||||
| chr5:95402824
|
C | G | 4 | a0001c0001t0001g0133a0001c0001t0002g0018a0001c0001t0002g0129others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.293+6649C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402824 | ||||||
| chr5:95402852
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.293+6677G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402852 | ||||||
| chr5:95402867
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.293+6692A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402867 | ||||||
| chr5:95402914
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.293+6739A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95402914 | ||||||
| chr5:95403000
|
G | A | 67 | a0001c0001t0002g0308a0001c0002t0001g0002a0001c0002t0001g0003others(64): Show | 71 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.293+6825G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403000 | ||||||
| chr5:95403029
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.293+6854T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403029 | ||||||
| chr5:95403077
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0002g0015others(2): Show | 6 | HG02698.hp2 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.293+6902G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403077 | ||||||
| chr5:95403148
|
C | T | 70 | a0001c0001t0002g0109a0001c0001t0002g0119a0001c0001t0002g0308others(67): Show | 74 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.293+6973C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403148 | ||||||
| chr5:95403243
|
G | A | 78 | a0001c0001t0002g0109a0001c0001t0002g0119a0001c0001t0002g0308others(75): Show | 82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.293+7068G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403243 | ||||||
| chr5:95403244
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.293+7069C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403244 | ||||||
| chr5:95403303
|
T | C | 78 | a0001c0001t0002g0109a0001c0001t0002g0119a0001c0001t0002g0308others(75): Show | 82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.293+7128T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403303 | ||||||
| chr5:95403329
|
T | G | 3 | a0001c0002t0002g0019a0001c0002t0002g0020a0001c0002t0002g0025 | 3 | HG01255.hp2 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.293+7154T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403329 | ||||||
| chr5:95403391
|
A | G | 14 | a0001c0002t0001g0093a0001c0002t0001g0120a0001c0002t0001g0128others(11): Show | 14 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.293+7216A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403391 | ||||||
| chr5:95403420
|
T | C | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.293+7245T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403420 | ||||||
| chr5:95403625
|
T | G | 79 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(76): Show | 83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.293+7450T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403625 | ||||||
| chr5:95403710
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.293+7535G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403710 | ||||||
| chr5:95403737
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+7562G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403737 | ||||||
| chr5:95403916
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.293+7741G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403916 | ||||||
| chr5:95403986
|
C | T | 78 | a0001c0001t0002g0109a0001c0001t0002g0119a0001c0001t0002g0308others(75): Show | 82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.293+7811C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95403986 | ||||||
| chr5:95404071
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.293+7896A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404071 | ||||||
| chr5:95404074
|
G | A | 79 | a0001c0001t0002g0068a0001c0001t0002g0109a0001c0001t0002g0119others(76): Show | 83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.293+7899G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404074 | ||||||
| chr5:95404104
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.293+7929G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404104 | ||||||
| chr5:95404110
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.293+7935T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404110 | ||||||
| chr5:95404148
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293+7973G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404148 | ||||||
| chr5:95404303
|
G | T | 1 | a0001c0002t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293+8128G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404303 | ||||||
| chr5:95404311
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.293+8136C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404311 | ||||||
| chr5:95404410
|
T | C | 1 | a0001c0002t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.293+8235T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404410 | ||||||
| chr5:95404604
|
T | C | 2 | a0001c0002t0002g0019a0001c0002t0002g0025 | 2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.293+8429T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404604 | ||||||
| chr5:95404612
|
C | CT | 14 | a0001c0002t0001g0093a0001c0002t0001g0120a0001c0002t0001g0128others(11): Show | 14 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.293+8445dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95404612 | |||||
| chr5:95404621
|
G | T | 78 | a0001c0001t0002g0109a0001c0001t0002g0119a0001c0001t0002g0308others(75): Show | 82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.293+8446G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95404621 | ||||||
| chr5:95405051
|
G | A | 2 | a0001c0002t0001g0177a0001c0002t0001g0192 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.293+8876G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405051 | ||||||
| chr5:95405102
|
G | A | 1 | a0007c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.294-8845G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405102 | ||||||
| chr5:95405138
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.294-8809C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405138 | ||||||
| chr5:95405377
|
A | T | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294-8570A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405377 | ||||||
| chr5:95405405
|
A | G | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.294-8542A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405405 | ||||||
| chr5:95405600
|
C | T | 78 | a0001c0001t0002g0109a0001c0001t0002g0119a0001c0001t0002g0308others(75): Show | 82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.294-8347C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405600 | ||||||
| chr5:95405746
|
G | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0101others(11): Show | 14 | HG00738.hp1 HG00741.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.294-8201G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405746 | ||||||
| chr5:95405840
|
G | A | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-8107G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405840 | ||||||
| chr5:95405964
|
T | C | 79 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(76): Show | 83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-7983T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95405964 | ||||||
| chr5:95406012
|
A | G | 6 | a0001c0002t0001g0177a0001c0002t0001g0188a0001c0002t0001g0192others(3): Show | 6 | HG02055.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.294-7935A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406012 | ||||||
| chr5:95406037
|
C | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 183 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.294-7910C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406037 | ||||||
| chr5:95406133
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(257): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.294-7814A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406133 | ||||||
| chr5:95406269
|
T | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.294-7678T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406269 | ||||||
| chr5:95406410
|
A | C | 79 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(76): Show | 83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-7537A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406410 | ||||||
| chr5:95406423
|
G | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0030 | 2 | HG00733.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.294-7524G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95406423 | ||||||
| chr5:95407012
|
C | T | 2 | a0001c0001t0002g0109a0001c0001t0002g0119 | 2 | HG01167.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.294-6935C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407012 | ||||||
| chr5:95407161
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.294-6786T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407161 | ||||||
| chr5:95407261
|
T | TAC | 10 | a0001c0001t0001g0125a0001c0001t0001g0133a0001c0001t0001g0136others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-6655_294-6654d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | |||||
| chr5:95407261
|
TAC | T | 10 | a0001c0001t0001g0163a0001c0001t0001g0234a0001c0001t0002g0029others(7): Show | 10 | HG00733.hp1 HG01255.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-6655_294-6654d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | |||||
| chr5:95407261
|
TACAC | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 180 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.294-6657_294-6654d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | |||||
| chr5:95407261
|
TACACAC | T | 60 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(57): Show | 64 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.294-6659_294-6654d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | |||||
| chr5:95407261
|
TACACACA others(1): Show |
T | 17 | a0001c0001t0001g0296a0001c0001t0002g0109a0001c0001t0002g0119others(14): Show | 17 | HG00280.hp2 HG01167.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.294-6661_294-6654d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407261 | |||||
| chr5:95407362
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294-6585G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407362 | ||||||
| chr5:95407391
|
T | TAC | 8 | a0001c0001t0001g0133a0001c0001t0001g0298a0001c0001t0002g0018others(5): Show | 8 | HG02486.hp1 HG02630.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.294-6539_294-6538d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407391 | |||||
| chr5:95407391
|
T | TACAC | 66 | a0001c0001t0001g0216a0001c0001t0002g0308a0001c0002t0001g0002others(63): Show | 70 | HG00280.hp1 HG00438.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.294-6541_294-6538d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407391 | |||||
| chr5:95407391
|
T | TACACAC | 4 | a0001c0001t0002g0119a0001c0002t0002g0019a0001c0002t0002g0025others(1): Show | 4 | HG01255.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-6543_294-6538d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407391 | |||||
| chr5:95407391
|
T | TACACACA others(3): Show |
1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-6547_294-6538d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95407391 | |||||
| chr5:95407410
|
G | A | 1 | a0001c0002t0002g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.294-6537G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407410 | ||||||
| chr5:95407412
|
A | G | 4 | a0001c0001t0001g0216a0001c0002t0001g0191a0001c0002t0002g0023others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-6535A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407412 | ||||||
| chr5:95407420
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.294-6527A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407420 | ||||||
| chr5:95407425
|
T | C | 78 | a0001c0001t0002g0109a0001c0001t0002g0119a0001c0001t0002g0308others(75): Show | 82 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.294-6522T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407425 | ||||||
| chr5:95407427
|
C | T | 66 | a0001c0001t0002g0308a0001c0002t0001g0002a0001c0002t0001g0003others(63): Show | 70 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.294-6520C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407427 | ||||||
| chr5:95407428
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0148 | 2 | NA18959.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.294-6519G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407428 | ||||||
| chr5:95407429
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 183 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.294-6518C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407429 | ||||||
| chr5:95407430
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.294-6517G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407430 | ||||||
| chr5:95407437
|
A | C | 79 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(76): Show | 83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-6510A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407437 | ||||||
| chr5:95407494
|
A | G | 62 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0058others(59): Show | 64 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.294-6453A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407494 | ||||||
| chr5:95407640
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.294-6307T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407640 | ||||||
| chr5:95407765
|
C | T | 79 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(76): Show | 83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-6182C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407765 | ||||||
| chr5:95407864
|
C | T | 7 | a0001c0002t0001g0177a0001c0002t0001g0188a0001c0002t0001g0192others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.294-6083C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95407864 | ||||||
| chr5:95408075
|
T | TGA | 13 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0101others(10): Show | 13 | HG00621.hp1 HG00738.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.294-5836_294-5835d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
T | TGAGA | 67 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0033others(64): Show | 70 | HG00544.hp1 HG00642.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.294-5838_294-5835d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
T | TGAGAGA | 10 | a0001c0001t0002g0308a0001c0002t0001g0053a0001c0002t0001g0059others(7): Show | 10 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.294-5840_294-5835d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
T | TGAGAGAG others(1): Show |
6 | a0001c0001t0001g0133a0001c0001t0001g0303a0001c0001t0002g0018others(3): Show | 6 | HG00597.hp1 HG01070.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.294-5842_294-5835d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
T | TGAGAGAG others(3): Show |
2 | a0001c0001t0002g0189a0007c0011t0001g0097 | 2 | HG02965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.294-5844_294-5835d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
T | TGAGAGAG others(5): Show |
1 | a0001c0002t0001g0139 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.294-5846_294-5835d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
T | TGAGAGAG others(7): Show |
1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-5848_294-5835d others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
T | TGAGAGAG others(9): Show |
2 | a0001c0001t0002g0129a0001c0002t0001g0093 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.294-5850_294-5835d others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
TGA | T | 22 | a0001c0001t0001g0022a0001c0001t0001g0061a0001c0001t0001g0130others(19): Show | 22 | HG00438.hp1 HG00741.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.294-5836_294-5835d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
TGAGA | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(164): Show | 173 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.294-5838_294-5835d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
TGAGAGA | T | 6 | a0001c0001t0001g0058a0001c0001t0001g0103a0001c0001t0001g0209others(3): Show | 6 | HG02572.hp2 HG03139.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.294-5840_294-5835d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408075
|
TGAGAGAG others(1): Show |
T | 10 | a0001c0001t0001g0010a0001c0001t0001g0175a0001c0001t0001g0263others(7): Show | 13 | HG00140.hp2 HG00438.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.294-5842_294-5835d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95408075 | |||||
| chr5:95408291
|
T | A | 2 | a0002c0003t0001g0325a0002c0003t0001g0326 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.294-5656T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408291 | ||||||
| chr5:95408338
|
T | C | 79 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(76): Show | 83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-5609T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408338 | ||||||
| chr5:95408537
|
T | A | 79 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(76): Show | 83 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.294-5410T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408537 | ||||||
| chr5:95408646
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.294-5301C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408646 | ||||||
| chr5:95408784
|
T | C | 2 | a0001c0002t0002g0019a0001c0002t0002g0025 | 2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.294-5163T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408784 | ||||||
| chr5:95408908
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.294-5039C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408908 | ||||||
| chr5:95408989
|
A | G | 82 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(79): Show | 87 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.294-4958A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95408989 | ||||||
| chr5:95409007
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.294-4940A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409007 | ||||||
| chr5:95409105
|
T | A | 83 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(80): Show | 88 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.294-4842T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409105 | ||||||
| chr5:95409128
|
T | C | 1 | a0001c0002t0002g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.294-4819T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409128 | ||||||
| chr5:95409213
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(258): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.294-4734T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409213 | ||||||
| chr5:95409254
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.294-4693G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409254 | ||||||
| chr5:95409289
|
T | G | 83 | a0001c0001t0001g0216a0001c0001t0002g0109a0001c0001t0002g0119others(80): Show | 88 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.294-4658T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409289 | ||||||
| chr5:95409439
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.294-4508G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409439 | ||||||
| chr5:95409472
|
T | TAAAGAAT others(146): Show |
1 | a0007c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.294-4461_294-4460i others(155): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | |||||
| chr5:95409472
|
T | TAAAGAAT others(145): Show |
2 | a0001c0001t0002g0109a0001c0002t0002g0178 | 2 | HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.294-4461_294-4460i others(154): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | |||||
| chr5:95409472
|
T | TAAAGAAT others(146): Show |
24 | a0001c0001t0002g0119a0001c0002t0001g0017a0001c0002t0001g0044others(21): Show | 24 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.294-4461_294-4460i others(155): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | |||||
| chr5:95409472
|
T | TAAAGAAT others(146): Show |
4 | a0001c0002t0001g0177a0001c0002t0001g0192a0001c0002t0002g0016others(1): Show | 4 | HG02922.hp1 HG02922.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.294-4461_294-4460i others(155): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | |||||
| chr5:95409472
|
T | TAAAGAAT others(147): Show |
49 | a0001c0001t0001g0216a0001c0001t0002g0308a0001c0002t0001g0002others(46): Show | 54 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.294-4461_294-4460i others(156): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | |||||
| chr5:95409472
|
T | TAAAGAAT others(148): Show |
3 | a0001c0002t0001g0055a0001c0002t0001g0099a0001c0002t0002g0335 | 3 | HG01433.hp2 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.294-4461_294-4460i others(157): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95409472 | |||||
| chr5:95409632
|
C | T | 2 | a0001c0002t0001g0043a0001c0002t0001g0076 | 2 | HG01070.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.294-4315C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409632 | ||||||
| chr5:95409654
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.294-4293A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409654 | ||||||
| chr5:95409656
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.294-4291C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409656 | ||||||
| chr5:95409891
|
T | C | 69 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(66): Show | 74 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.294-4056T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409891 | ||||||
| chr5:95409901
|
G | A | 2 | a0001c0002t0002g0019a0001c0002t0002g0025 | 2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.294-4046G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409901 | ||||||
| chr5:95409943
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.294-4004G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409943 | ||||||
| chr5:95409991
|
A | T | 3 | a0001c0002t0001g0191a0001c0002t0002g0023a0001c0002t0002g0024 | 3 | HG02559.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.294-3956A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95409991 | ||||||
| chr5:95410129
|
T | C | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-3818T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410129 | ||||||
| chr5:95410190
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.294-3757C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410190 | ||||||
| chr5:95410255
|
T | C | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-3692T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410255 | ||||||
| chr5:95410312
|
A | G | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-3635A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410312 | ||||||
| chr5:95410476
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294-3471C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410476 | ||||||
| chr5:95410561
|
G | T | 2 | a0001c0002t0002g0019a0001c0002t0002g0025 | 2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.294-3386G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410561 | ||||||
| chr5:95410699
|
G | A | 1 | a0001c0002t0001g0100 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.294-3248G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410699 | ||||||
| chr5:95410809
|
G | A | 70 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(67): Show | 75 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.294-3138G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410809 | ||||||
| chr5:95410815
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.294-3132A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95410815 | ||||||
| chr5:95411192
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.294-2755A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411192 | ||||||
| chr5:95411234
|
C | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-2713C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411234 | ||||||
| chr5:95411283
|
A | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-2664A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411283 | ||||||
| chr5:95411386
|
CAT | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(65): Show | 73 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.294-2557_294-2556d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95411386 | |||||
| chr5:95411462
|
C | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-2485C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411462 | ||||||
| chr5:95411570
|
A | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-2377A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411570 | ||||||
| chr5:95411616
|
T | C | 4 | a0001c0002t0001g0128a0001c0002t0001g0179a0001c0002t0002g0127others(1): Show | 4 | HG02451.hp2 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-2331T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411616 | ||||||
| chr5:95411685
|
G | A | 1 | a0001c0002t0001g0312 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.294-2262G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411685 | ||||||
| chr5:95411732
|
T | C | 1 | a0001c0001t0002g0268 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.294-2215T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411732 | ||||||
| chr5:95411948
|
C | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1999C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95411948 | ||||||
| chr5:95412029
|
G | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1918G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412029 | ||||||
| chr5:95412085
|
T | G | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-1862T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412085 | ||||||
| chr5:95412144
|
C | CT | 76 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(73): Show | 81 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.294-1793dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 95412144 | |||||
| chr5:95412162
|
G | A | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1785G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412162 | ||||||
| chr5:95412214
|
C | T | 1 | a0001c0002t0002g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.294-1733C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412214 | ||||||
| chr5:95412260
|
A | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1687A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412260 | ||||||
| chr5:95412352
|
A | C | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1595A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412352 | ||||||
| chr5:95412476
|
T | C | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1471T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412476 | ||||||
| chr5:95412648
|
A | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1299A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412648 | ||||||
| chr5:95412656
|
A | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1291A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412656 | ||||||
| chr5:95412850
|
C | T | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294-1097C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412850 | ||||||
| chr5:95412903
|
A | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-1044A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412903 | ||||||
| chr5:95412958
|
A | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-989A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95412958 | ||||||
| chr5:95413174
|
C | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-773C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413174 | ||||||
| chr5:95413185
|
A | G | 7 | a0001c0002t0001g0092a0001c0002t0001g0177a0001c0002t0001g0188others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.294-762A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413185 | ||||||
| chr5:95413207
|
C | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-740C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413207 | ||||||
| chr5:95413240
|
T | A | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-707T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413240 | ||||||
| chr5:95413264
|
A | C | 3 | a0001c0001t0001g0261a0006c0006t0001g0262a0006c0006t0001g0314 | 3 | HG00741.hp2 HG01123.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.294-683A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413264 | ||||||
| chr5:95413300
|
A | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.294-647A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413300 | ||||||
| chr5:95413307
|
G | A | 1 | a0002c0003t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.294-640G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413307 | ||||||
| chr5:95413459
|
G | A | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0299others(1): Show | 4 | NA18953.hp2 NA18964.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.294-488G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413459 | ||||||
| chr5:95413464
|
A | T | 2 | a0001c0002t0002g0019a0001c0002t0002g0025 | 2 | HG01255.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.294-483A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413464 | ||||||
| chr5:95413513
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.294-434T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413513 | ||||||
| chr5:95413584
|
T | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(38): Show | 44 | HG00140.hp2 HG00738.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.294-363T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413584 | ||||||
| chr5:95413607
|
T | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 194 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.294-340T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413607 | ||||||
| chr5:95413718
|
G | C | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.294-229G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413718 | ||||||
| chr5:95413910
|
T | C | 10 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0329others(7): Show | 10 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.294-37T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 3/9 | chr5 | 95413910 | ||||||
| chr5:95414199
|
C | CT | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+14dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 95414199 | |||||
| chr5:95414265
|
C | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+75C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414265 | ||||||
| chr5:95414405
|
A | G | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0002g0316others(3): Show | 6 | HG01243.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+215A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414405 | ||||||
| chr5:95414528
|
T | A | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+338T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414528 | ||||||
| chr5:95414589
|
A | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+399A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414589 | ||||||
| chr5:95414595
|
G | A | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+405G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414595 | ||||||
| chr5:95414634
|
C | T | 1 | a0007c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.537+444C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414634 | ||||||
| chr5:95414739
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.537+549G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414739 | ||||||
| chr5:95414741
|
G | T | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+551G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95414741 | ||||||
| chr5:95415054
|
T | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.537+864T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415054 | ||||||
| chr5:95415063
|
T | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.537+873T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415063 | ||||||
| chr5:95415065
|
A | T | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.537+875A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415065 | ||||||
| chr5:95415068
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.537+878G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415068 | ||||||
| chr5:95415069
|
C | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.537+879C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415069 | ||||||
| chr5:95415190
|
G | C | 1 | a0007c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.537+1000G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415190 | ||||||
| chr5:95415429
|
A | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+1239A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415429 | ||||||
| chr5:95415463
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.537+1273A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415463 | ||||||
| chr5:95415658
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.537+1468C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415658 | ||||||
| chr5:95415689
|
G | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(178): Show | 187 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.537+1499G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415689 | ||||||
| chr5:95415784
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.537+1594A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415784 | ||||||
| chr5:95415785
|
T | C | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(76): Show | 84 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.537+1595T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415785 | ||||||
| chr5:95415843
|
C | T | 2 | a0001c0002t0001g0188a0001c0002t0002g0187 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.537+1653C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415843 | ||||||
| chr5:95415922
|
G | A | 1 | a0007c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.537+1732G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95415922 | ||||||
| chr5:95416237
|
C | A | 1 | a0001c0002t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.537+2047C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95416237 | ||||||
| chr5:95416255
|
C | A | 2 | a0001c0002t0001g0188a0001c0002t0002g0187 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.537+2065C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95416255 | ||||||
| chr5:95416525
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.537+2335T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95416525 | ||||||
| chr5:95416805
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.537+2615G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95416805 | ||||||
| chr5:95417092
|
C | T | 71 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(68): Show | 71 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.537+2902C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417092 | ||||||
| chr5:95417189
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0336 | 2 | NA18942.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.537+2999G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417189 | ||||||
| chr5:95417312
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.538-2972T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417312 | ||||||
| chr5:95417599
|
C | T | 71 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(68): Show | 71 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.538-2685C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417599 | ||||||
| chr5:95417600
|
G | A | 1 | a0007c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.538-2684G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417600 | ||||||
| chr5:95417711
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 190 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.538-2573T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417711 | ||||||
| chr5:95417834
|
T | C | 1 | a0001c0002t0001g0014 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.538-2450T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95417834 | ||||||
| chr5:95418087
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0129a0001c0001t0002g0189 | 3 | HG02486.hp1 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.538-2197G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418087 | ||||||
| chr5:95418140
|
C | T | 1 | a0001c0002t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.538-2144C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418140 | ||||||
| chr5:95418475
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.538-1809A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418475 | ||||||
| chr5:95418501
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.538-1783C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418501 | ||||||
| chr5:95418676
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.538-1608C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418676 | ||||||
| chr5:95418989
|
A | G | 53 | a0001c0001t0001g0134a0001c0001t0001g0213a0001c0002t0001g0002others(50): Show | 58 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.538-1295A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95418989 | ||||||
| chr5:95419026
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.538-1258T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419026 | ||||||
| chr5:95419467
|
A | G | 4 | a0001c0001t0001g0133a0001c0001t0002g0018a0001c0001t0002g0129others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.538-817A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419467 | ||||||
| chr5:95419525
|
A | T | 81 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(78): Show | 81 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.538-759A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419525 | ||||||
| chr5:95419557
|
C | T | 82 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-727C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419557 | ||||||
| chr5:95419603
|
C | A | 5 | a0001c0002t0001g0180a0001c0002t0001g0184a0001c0002t0001g0185others(2): Show | 5 | HG02818.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-681C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419603 | ||||||
| chr5:95419648
|
T | A | 82 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-636T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419648 | ||||||
| chr5:95419675
|
T | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0330a0001c0001t0002g0331 | 3 | HG03654.hp2 HG03710.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.538-609T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419675 | ||||||
| chr5:95419690
|
G | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0313 | 2 | HG01496.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.538-594G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419690 | ||||||
| chr5:95419699
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.538-585C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419699 | ||||||
| chr5:95419773
|
C | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.538-511C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419773 | ||||||
| chr5:95419804
|
A | G | 82 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-480A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419804 | ||||||
| chr5:95419834
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.538-450T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419834 | ||||||
| chr5:95419857
|
T | G | 2 | a0001c0001t0001g0133a0001c0002t0001g0017 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.538-427T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419857 | ||||||
| chr5:95419882
|
T | G | 1 | a0001c0002t0001g0098 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.538-402T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419882 | ||||||
| chr5:95419932
|
T | C | 82 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-352T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95419932 | ||||||
| chr5:95420005
|
T | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.538-279T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95420005 | ||||||
| chr5:95420097
|
TCAAA | T | 82 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 82 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.538-185_538-182del others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 95420097 | |||||
| chr5:95420103
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.538-181C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 4/9 | chr5 | 95420103 | ||||||
| chr5:95420512
|
C | A | 10 | a0001c0002t0001g0179a0001c0002t0001g0184a0001c0002t0001g0185others(7): Show | 10 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.656+110C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420512 | ||||||
| chr5:95420557
|
C | G | 77 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(74): Show | 77 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.656+155C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420557 | ||||||
| chr5:95420567
|
C | T | 1 | a0005c0007t0001g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.656+165C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420567 | ||||||
| chr5:95420574
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656+172G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420574 | ||||||
| chr5:95420574
|
G | C | 88 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+172G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420574 | ||||||
| chr5:95420593
|
G | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0322 | 3 | HG02698.hp1 HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.656+191G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420593 | ||||||
| chr5:95420647
|
T | C | 87 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 87 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.656+245T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420647 | ||||||
| chr5:95420648
|
G | A | 87 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 87 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.656+246G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420648 | ||||||
| chr5:95420660
|
G | A | 139 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(136): Show | 144 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.656+258G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420660 | ||||||
| chr5:95420678
|
A | G | 87 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 87 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.656+276A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420678 | ||||||
| chr5:95420700
|
C | A | 88 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+298C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420700 | ||||||
| chr5:95420716
|
CAT | C | 88 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+317_656+318del others(2): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95420716 | |||||
| chr5:95420732
|
G | T | 88 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+330G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420732 | ||||||
| chr5:95420792
|
A | G | 88 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.656+390A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420792 | ||||||
| chr5:95420846
|
T | C | 3 | a0001c0002t0001g0093a0001c0002t0001g0120a0001c0002t0002g0019 | 3 | HG01109.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.656+444T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420846 | ||||||
| chr5:95420906
|
A | G | 91 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.656+504A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420906 | ||||||
| chr5:95420976
|
C | A | 55 | a0001c0001t0001g0213a0001c0001t0002g0131a0001c0002t0001g0002others(52): Show | 60 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.656+574C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95420976 | ||||||
| chr5:95421039
|
T | C | 110 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(107): Show | 110 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.656+637T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421039 | ||||||
| chr5:95421074
|
C | G | 1 | a0001c0002t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.656+672C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421074 | ||||||
| chr5:95421232
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.656+830C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421232 | ||||||
| chr5:95421486
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656+1084G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421486 | ||||||
| chr5:95421495
|
T | C | 2 | a0001c0002t0001g0188a0001c0002t0002g0187 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.656+1093T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421495 | ||||||
| chr5:95421554
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.656+1152T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421554 | ||||||
| chr5:95421606
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(111): Show | 117 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.656+1204T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421606 | ||||||
| chr5:95421625
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0272 | 3 | HG00673.hp2 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.656+1223G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421625 | ||||||
| chr5:95421678
|
C | CA | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 240 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.656+1283dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95421678 | |||||
| chr5:95421785
|
A | T | 3 | a0001c0002t0001g0003a0001c0002t0001g0083a0001c0002t0001g0084 | 4 | NA18984.hp2 NA19004.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+1383A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421785 | ||||||
| chr5:95421796
|
A | T | 3 | a0001c0001t0001g0118a0001c0001t0002g0078a0001c0001t0002g0122 | 3 | HG02258.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.656+1394A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421796 | ||||||
| chr5:95421980
|
A | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(72): Show | 76 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.656+1578A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95421980 | ||||||
| chr5:95422062
|
A | G | 67 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(64): Show | 68 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.656+1660A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422062 | ||||||
| chr5:95422093
|
C | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(60): Show | 64 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.656+1691C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422093 | ||||||
| chr5:95422122
|
T | C | 4 | a0001c0001t0001g0133a0001c0001t0002g0018a0001c0001t0002g0129others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+1720T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422122 | ||||||
| chr5:95422138
|
GGAAAGAC others(2): Show |
G | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(58): Show | 62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+1746_656+1754d others(11): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95422138 | |||||
| chr5:95422174
|
A | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(58): Show | 62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+1772A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422174 | ||||||
| chr5:95422204
|
G | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(76): Show | 87 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.656+1802G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422204 | ||||||
| chr5:95422224
|
G | T | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.656+1822G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422224 | ||||||
| chr5:95422235
|
A | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(58): Show | 62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+1833A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422235 | ||||||
| chr5:95422456
|
A | G | 14 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0075others(11): Show | 14 | HG00741.hp2 HG01074.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.656+2054A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422456 | ||||||
| chr5:95422500
|
C | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(58): Show | 62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+2098C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422500 | ||||||
| chr5:95422514
|
G | A | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(58): Show | 62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.656+2112G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422514 | ||||||
| chr5:95422557
|
ACTGCAGC others(2): Show |
A | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(78): Show | 89 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.656+2160_656+2168d others(11): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95422557 | |||||
| chr5:95422656
|
A | G | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+2254A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422656 | ||||||
| chr5:95422680
|
T | A | 3 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0002g0316 | 3 | HG02818.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.656+2278T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422680 | ||||||
| chr5:95422761
|
T | G | 44 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(41): Show | 44 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.656+2359T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422761 | ||||||
| chr5:95422864
|
C | T | 1 | a0001c0001t0002g0253 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.656+2462C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422864 | ||||||
| chr5:95422881
|
T | A | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+2479T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422881 | ||||||
| chr5:95422948
|
A | G | 5 | a0001c0001t0001g0133a0001c0001t0002g0018a0001c0001t0002g0129others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+2546A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422948 | ||||||
| chr5:95422998
|
C | G | 100 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(97): Show | 101 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.656+2596C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95422998 | ||||||
| chr5:95423070
|
T | G | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+2668T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95423070 | ||||||
| chr5:95423148
|
A | ATTAAG | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+2748_656+2749i others(7): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423148 | |||||
| chr5:95423371
|
C | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0013others(58): Show | 63 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.656+2969C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95423371 | ||||||
| chr5:95423547
|
T | TA | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 8 | HG02258.hp1 HG06807.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.656+3166dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | |||||
| chr5:95423547
|
T | TAA | 37 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(34): Show | 37 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.656+3165_656+3166d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | |||||
| chr5:95423547
|
TA | T | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(80): Show | 91 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.656+3166delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | |||||
| chr5:95423547
|
TAAAAA | T | 54 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(51): Show | 55 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.656+3162_656+3166d others(7): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | |||||
| chr5:95423547
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0002t0001g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.656+3155_656+3166d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95423547 | |||||
| chr5:95423862
|
T | C | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.656+3460T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95423862 | ||||||
| chr5:95423933
|
G | A | 1 | a0001c0002t0002g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.656+3531G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95423933 | ||||||
| chr5:95424013
|
G | A | 24 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0028others(21): Show | 24 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.656+3611G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424013 | ||||||
| chr5:95424098
|
G | A | 60 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(57): Show | 61 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.656+3696G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424098 | ||||||
| chr5:95424155
|
T | C | 2 | a0001c0002t0001g0128a0001c0002t0002g0127 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.656+3753T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424155 | ||||||
| chr5:95424206
|
A | G | 1 | a0001c0002t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.656+3804A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424206 | ||||||
| chr5:95424331
|
A | T | 1 | a0001c0002t0001g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.656+3929A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424331 | ||||||
| chr5:95424448
|
T | TA | 74 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0026others(71): Show | 76 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.656+4063dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95424448 | |||||
| chr5:95424448
|
TA | T | 63 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(60): Show | 64 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.656+4063delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95424448 | |||||
| chr5:95424472
|
C | G | 2 | a0004c0005t0002g0218a0004c0005t0002g0219 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.656+4070C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424472 | ||||||
| chr5:95424509
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.657-4094G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424509 | ||||||
| chr5:95424745
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.657-3858C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424745 | ||||||
| chr5:95424787
|
C | CTTATTAG others(3): Show |
62 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(59): Show | 63 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.657-3810_657-3809i others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95424787 | |||||
| chr5:95424952
|
A | G | 2 | a0001c0002t0001g0092a0001c0002t0002g0019 | 2 | HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.657-3651A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95424952 | ||||||
| chr5:95425100
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(305): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.657-3503G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425100 | ||||||
| chr5:95425105
|
A | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(58): Show | 62 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.657-3498A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425105 | ||||||
| chr5:95425146
|
C | T | 55 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(52): Show | 56 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.657-3457C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425146 | ||||||
| chr5:95425174
|
C | CA | 43 | a0001c0001t0001g0027a0001c0001t0001g0116a0001c0001t0001g0117others(40): Show | 43 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.657-3416dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95425174 | |||||
| chr5:95425631
|
G | A | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.657-2972G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425631 | ||||||
| chr5:95425631
|
G | C | 1 | a0001c0001t0001g0265 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.657-2972G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425631 | ||||||
| chr5:95425632
|
A | G | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.657-2971A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425632 | ||||||
| chr5:95425839
|
ATATC | A | 5 | a0001c0001t0001g0132a0001c0001t0001g0209a0001c0001t0001g0317others(2): Show | 5 | HG02630.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-2761_657-2758d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95425839 | |||||
| chr5:95425997
|
T | A | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0021others(56): Show | 60 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.657-2606T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95425997 | ||||||
| chr5:95426088
|
CTG | C | 9 | a0001c0001t0001g0296a0001c0002t0001g0008a0001c0002t0001g0012others(6): Show | 11 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-2509_657-2508d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426088 | |||||
| chr5:95426092
|
G | GTA | 10 | a0001c0001t0001g0195a0001c0001t0001g0264a0001c0002t0001g0003others(7): Show | 11 | HG00280.hp2 HG00735.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-2510_657-2509i others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | |||||
| chr5:95426092
|
G | GTATA | 5 | a0001c0001t0001g0151a0001c0001t0001g0206a0001c0002t0001g0128others(2): Show | 5 | HG00733.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-2510_657-2509i others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | |||||
| chr5:95426092
|
G | GTATATAT others(3): Show |
1 | a0001c0002t0002g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.657-2510_657-2509i others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | |||||
| chr5:95426092
|
GTGTA | G | 3 | a0001c0001t0001g0273a0001c0002t0001g0076a0001c0002t0001g0138 | 3 | HG01070.hp2 HG02293.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.657-2509_657-2506d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | |||||
| chr5:95426092
|
GTGTATA | G | 4 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0002g0243others(1): Show | 4 | NA18948.hp2 NA18973.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-2509_657-2504d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426092 | |||||
| chr5:95426094
|
G | A | 52 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0060others(49): Show | 55 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.657-2509G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426094 | ||||||
| chr5:95426094
|
G | GTA | 37 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0038others(34): Show | 38 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.657-2481_657-2480d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATA | 38 | a0001c0001t0001g0007a0001c0001t0001g0086a0001c0001t0001g0088others(35): Show | 39 | HG00621.hp2 HG01099.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.657-2483_657-2480d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATA | 26 | a0001c0001t0001g0075a0001c0001t0001g0087a0001c0001t0001g0103others(23): Show | 26 | HG01069.hp1 HG01071.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.657-2485_657-2480d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATAT others(1): Show |
10 | a0001c0001t0001g0118a0001c0001t0001g0205a0001c0001t0001g0330others(7): Show | 10 | HG01243.hp2 HG01358.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.657-2487_657-2480d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATAT others(3): Show |
6 | a0001c0001t0001g0027a0001c0001t0001g0261a0001c0001t0002g0091others(3): Show | 6 | HG00741.hp2 HG01123.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-2489_657-2480d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.657-2491_657-2480d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0147a0001c0002t0002g0178 | 2 | HG02622.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.657-2493_657-2480d others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATAT others(9): Show |
6 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0002g0121others(3): Show | 6 | HG01074.hp1 HG02523.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.657-2495_657-2480d others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0002g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.657-2497_657-2480d others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.657-2499_657-2480d others(22): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTATATAT others(15): Show |
2 | a0001c0001t0001g0011a0001c0001t0002g0110 | 3 | HG00673.hp2 HG02071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.657-2501_657-2480d others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0002g0109 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.657-2508_657-2507i others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
G | GTGTATAT others(17): Show |
1 | a0001c0001t0002g0119 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.657-2508_657-2507i others(26): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
GTA | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0062others(28): Show | 32 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.657-2481_657-2480d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
GTATA | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0322a0001c0001t0002g0189 | 3 | HG02630.hp2 HG02698.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.657-2483_657-2480d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426094
|
GTATATA | G | 7 | a0001c0001t0001g0117a0001c0001t0001g0124a0001c0001t0001g0207others(4): Show | 7 | HG01496.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-2485_657-2480d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426094 | |||||
| chr5:95426096
|
A | G | 7 | a0001c0001t0001g0181a0001c0001t0001g0213a0001c0001t0002g0201others(4): Show | 9 | HG00438.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.657-2507A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426096 | ||||||
| chr5:95426098
|
A | G | 1 | a0001c0001t0002g0284 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.657-2505A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426098 | ||||||
| chr5:95426100
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.657-2503A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426100 | ||||||
| chr5:95426116
|
ATATATAT others(1): Show |
A | 36 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0031others(33): Show | 37 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.657-2484_657-2477d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426116 | |||||
| chr5:95426118
|
ATATATG | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0036others(13): Show | 16 | HG00738.hp1 HG00741.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.657-2482_657-2477d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426118 | |||||
| chr5:95426122
|
ATG | A | 3 | a0001c0001t0001g0028a0001c0001t0002g0131a0001c0001t0002g0201 | 3 | HG02165.hp1 HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.657-2479_657-2478d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95426122 | |||||
| chr5:95426124
|
G | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0026others(99): Show | 109 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.657-2479G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426124 | ||||||
| chr5:95426125
|
T | C | 9 | a0001c0002t0001g0008a0001c0002t0001g0012a0001c0002t0001g0305others(6): Show | 11 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-2478T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426125 | ||||||
| chr5:95426483
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.657-2120T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426483 | ||||||
| chr5:95426524
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0002t0001g0053others(5): Show | 9 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.657-2079G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426524 | ||||||
| chr5:95426602
|
C | A | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(194): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.657-2001C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426602 | ||||||
| chr5:95426747
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.657-1856G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426747 | ||||||
| chr5:95426819
|
C | T | 1 | a0001c0001t0002g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.657-1784C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426819 | ||||||
| chr5:95426831
|
G | A | 28 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0124others(25): Show | 28 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.657-1772G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426831 | ||||||
| chr5:95426862
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.657-1741G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426862 | ||||||
| chr5:95426890
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.657-1713T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426890 | ||||||
| chr5:95426914
|
T | C | 3 | a0001c0002t0001g0012a0001c0002t0001g0305a0001c0002t0001g0307 | 4 | HG01192.hp1 HG02683.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1689T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426914 | ||||||
| chr5:95426919
|
C | G | 6 | a0001c0001t0001g0135a0001c0001t0001g0148a0001c0001t0002g0283others(3): Show | 7 | HG01192.hp1 HG02040.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1684C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426919 | ||||||
| chr5:95426920
|
A | G | 6 | a0001c0001t0001g0135a0001c0001t0001g0148a0001c0001t0002g0283others(3): Show | 7 | HG01192.hp1 HG02040.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1683A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426920 | ||||||
| chr5:95426921
|
T | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0148a0001c0001t0002g0283others(3): Show | 7 | HG01192.hp1 HG02040.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1682T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426921 | ||||||
| chr5:95426933
|
T | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(70): Show | 75 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.657-1670T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426933 | ||||||
| chr5:95426938
|
A | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0021others(67): Show | 72 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.657-1665A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426938 | ||||||
| chr5:95426948
|
G | C | 1 | a0001c0002t0001g0008 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.657-1655G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426948 | ||||||
| chr5:95426954
|
C | T | 4 | a0001c0002t0001g0043a0001c0002t0001g0059a0001c0002t0001g0076others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1649C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426954 | ||||||
| chr5:95426970
|
A | G | 2 | a0001c0002t0001g0177a0001c0002t0001g0192 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.657-1633A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426970 | ||||||
| chr5:95426973
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0315a0001c0001t0002g0072others(3): Show | 6 | NA18957.hp1 NA18960.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.657-1630T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95426973 | ||||||
| chr5:95427003
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0002g0300a0001c0002t0001g0309 | 3 | HG03579.hp2 HG04184.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.657-1600T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427003 | ||||||
| chr5:95427003
|
T | G | 1 | a0001c0001t0001g0315 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.657-1600T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427003 | ||||||
| chr5:95427005
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.657-1598T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427005 | ||||||
| chr5:95427015
|
C | G | 1 | a0001c0002t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.657-1588C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427015 | ||||||
| chr5:95427030
|
T | C | 2 | a0001c0001t0002g0040a0001c0002t0002g0173 | 2 | HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.657-1573T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427030 | ||||||
| chr5:95427055
|
AAG | A | 39 | a0001c0001t0001g0028a0001c0001t0001g0101a0001c0001t0001g0103others(36): Show | 39 | HG01106.hp2 HG01109.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.657-1546_657-1545d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 95427055 | |||||
| chr5:95427057
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.657-1546G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427057 | ||||||
| chr5:95427062
|
G | A | 40 | a0001c0001t0001g0028a0001c0001t0001g0101a0001c0001t0001g0103others(37): Show | 40 | HG01106.hp2 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.657-1541G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427062 | ||||||
| chr5:95427112
|
C | T | 3 | a0001c0001t0001g0202a0001c0001t0001g0258a0001c0001t0001g0287 | 3 | HG01496.hp1 HG02273.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.657-1491C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427112 | ||||||
| chr5:95427223
|
A | G | 1 | a0001c0002t0001g0046 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.657-1380A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427223 | ||||||
| chr5:95427278
|
A | G | 2 | a0001c0002t0001g0177a0001c0002t0001g0192 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.657-1325A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427278 | ||||||
| chr5:95427290
|
A | G | 4 | a0001c0001t0001g0133a0001c0001t0002g0091a0001c0001t0002g0232others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1313A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427290 | ||||||
| chr5:95427411
|
A | C | 1 | a0001c0001t0001g0301 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.657-1192A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427411 | ||||||
| chr5:95427440
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.657-1163C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427440 | ||||||
| chr5:95427476
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.657-1127A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427476 | ||||||
| chr5:95427563
|
A | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0317a0001c0002t0001g0092 | 3 | HG01884.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.657-1040A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427563 | ||||||
| chr5:95427988
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0329a0001c0002t0001g0177others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-615C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95427988 | ||||||
| chr5:95428198
|
A | C | 4 | a0001c0001t0001g0236a0001c0001t0001g0329a0001c0002t0001g0177others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-405A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428198 | ||||||
| chr5:95428302
|
A | G | 30 | a0001c0001t0001g0071a0001c0001t0001g0125a0001c0001t0001g0143others(27): Show | 30 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.657-301A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428302 | ||||||
| chr5:95428305
|
A | G | 2 | a0001c0001t0002g0068a0001c0002t0002g0173 | 2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.657-298A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428305 | ||||||
| chr5:95428463
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.657-140T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428463 | ||||||
| chr5:95428488
|
T | C | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-115T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428488 | ||||||
| chr5:95428516
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.657-87G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428516 | ||||||
| chr5:95428584
|
A | G | 15 | a0001c0001t0001g0152a0001c0001t0002g0030a0001c0001t0002g0091others(12): Show | 15 | HG00733.hp1 HG01167.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.657-19A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 5/9 | chr5 | 95428584 | ||||||
| chr5:95429134
|
C | T | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+402C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429134 | ||||||
| chr5:95429151
|
C | T | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.786+419C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429151 | ||||||
| chr5:95429371
|
T | A | 1 | a0001c0001t0001g0317 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+639T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429371 | ||||||
| chr5:95429650
|
C | T | 7 | a0001c0001t0001g0125a0001c0001t0001g0181a0001c0001t0001g0236others(4): Show | 7 | HG01884.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+918C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429650 | ||||||
| chr5:95429657
|
A | G | 8 | a0001c0001t0001g0118a0001c0001t0002g0280a0001c0002t0002g0054others(5): Show | 8 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+925A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429657 | ||||||
| chr5:95429675
|
T | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0181a0001c0001t0001g0236others(4): Show | 7 | HG01884.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+943T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429675 | ||||||
| chr5:95429898
|
G | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0034others(72): Show | 79 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.786+1166G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429898 | ||||||
| chr5:95429910
|
T | C | 5 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0248others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+1178T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95429910 | ||||||
| chr5:95430034
|
A | G | 44 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0152others(41): Show | 44 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.786+1302A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430034 | ||||||
| chr5:95430220
|
G | A | 1 | a0001c0002t0002g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.786+1488G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430220 | ||||||
| chr5:95430277
|
T | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0181a0001c0001t0001g0236others(4): Show | 7 | HG01884.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+1545T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430277 | ||||||
| chr5:95430292
|
G | A | 1 | a0001c0002t0001g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.786+1560G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430292 | ||||||
| chr5:95430328
|
A | G | 2 | a0001c0001t0001g0155a0003c0004t0001g0063 | 2 | HG00735.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.786+1596A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430328 | ||||||
| chr5:95430383
|
G | GTA | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 230 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(227): Show |
intron_variant | MODIFIER | c.786+1662_786+1663d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95430383 | |||||
| chr5:95430383
|
G | GTATA | 16 | a0001c0001t0001g0125a0001c0001t0001g0181a0001c0001t0001g0236others(13): Show | 16 | HG01884.hp2 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+1660_786+1663d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95430383 | |||||
| chr5:95430422
|
T | G | 1 | a0001c0002t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.786+1690T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430422 | ||||||
| chr5:95430436
|
TA | T | 40 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0036others(37): Show | 40 | HG00544.hp1 HG00597.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.786+1716delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95430436 | |||||
| chr5:95430436
|
TAA | T | 39 | a0001c0001t0001g0130a0001c0001t0001g0152a0001c0001t0002g0030others(36): Show | 39 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.786+1715_786+1716d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95430436 | |||||
| chr5:95430544
|
G | C | 16 | a0001c0001t0001g0133a0001c0001t0002g0018a0001c0001t0002g0108others(13): Show | 16 | HG02040.hp1 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+1812G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430544 | ||||||
| chr5:95430572
|
A | G | 2 | a0001c0001t0002g0068a0001c0002t0002g0173 | 2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.786+1840A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430572 | ||||||
| chr5:95430618
|
A | G | 28 | a0001c0001t0002g0015a0001c0001t0002g0029a0001c0001t0002g0037others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.786+1886A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430618 | ||||||
| chr5:95430640
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786+1908C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430640 | ||||||
| chr5:95430649
|
T | C | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.786+1917T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430649 | ||||||
| chr5:95430664
|
C | A | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.786+1932C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430664 | ||||||
| chr5:95430858
|
C | T | 32 | a0001c0001t0002g0015a0001c0001t0002g0029a0001c0001t0002g0037others(29): Show | 32 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.786+2126C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430858 | ||||||
| chr5:95430947
|
G | C | 5 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0002t0001g0128others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2215G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95430947 | ||||||
| chr5:95431072
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.786+2340T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431072 | ||||||
| chr5:95431135
|
T | C | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2403T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431135 | ||||||
| chr5:95431580
|
T | C | 32 | a0001c0001t0002g0015a0001c0001t0002g0029a0001c0001t0002g0037others(29): Show | 32 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.786+2848T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431580 | ||||||
| chr5:95431587
|
T | A | 2 | a0005c0007t0001g0149a0005c0007t0001g0212 | 2 | NA18981.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.786+2855T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431587 | ||||||
| chr5:95431641
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0254 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.786+2909G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431641 | ||||||
| chr5:95431653
|
A | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0299a0001c0002t0001g0009others(1): Show | 5 | NA18953.hp2 NA18983.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+2921A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431653 | ||||||
| chr5:95431752
|
C | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.786+3020C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431752 | ||||||
| chr5:95431769
|
A | G | 8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0112others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+3037A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431769 | ||||||
| chr5:95431830
|
T | G | 1 | a0001c0001t0002g0321 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.786+3098T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431830 | ||||||
| chr5:95431900
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0074 | 2 | HG00544.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.786+3168C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431900 | ||||||
| chr5:95431936
|
C | G | 1 | a0001c0001t0002g0283 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.786+3204C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95431936 | ||||||
| chr5:95432027
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.786+3295T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432027 | ||||||
| chr5:95432045
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.786+3313T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432045 | ||||||
| chr5:95432127
|
C | T | 16 | a0001c0001t0001g0133a0001c0001t0002g0018a0001c0001t0002g0108others(13): Show | 16 | HG02040.hp1 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.786+3395C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432127 | ||||||
| chr5:95432219
|
T | C | 2 | a0001c0001t0001g0208a0001c0002t0001g0093 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.786+3487T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432219 | ||||||
| chr5:95432346
|
C | G | 101 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0130others(98): Show | 101 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.786+3614C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432346 | ||||||
| chr5:95432387
|
T | C | 102 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0130others(99): Show | 102 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.786+3655T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432387 | ||||||
| chr5:95432457
|
T | C | 1 | a0001c0001t0002g0275 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.786+3725T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432457 | ||||||
| chr5:95432645
|
GA | G | 5 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0248others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3921delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95432645 | |||||
| chr5:95432845
|
T | C | 2 | a0001c0001t0001g0133a0001c0002t0001g0017 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.787-3955T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95432845 | ||||||
| chr5:95433112
|
A | G | 5 | a0001c0001t0002g0018a0001c0001t0002g0122a0001c0001t0002g0283others(2): Show | 5 | HG02040.hp1 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-3688A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433112 | ||||||
| chr5:95433261
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0255 | 2 | NA18955.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.787-3539G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433261 | ||||||
| chr5:95433261
|
G | GA | 85 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0130others(82): Show | 85 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.787-3539_787-3538i others(3): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433261 | ||||||
| chr5:95433419
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0002t0001g0128others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-3381C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433419 | ||||||
| chr5:95433455
|
T | C | 34 | a0001c0001t0001g0125a0001c0001t0001g0317a0001c0001t0002g0015others(31): Show | 34 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.787-3345T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433455 | ||||||
| chr5:95433528
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0002t0001g0128others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-3272G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433528 | ||||||
| chr5:95433669
|
A | G | 1 | a0001c0001t0001g0330 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.787-3131A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433669 | ||||||
| chr5:95433899
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.787-2901C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95433899 | ||||||
| chr5:95434018
|
A | G | 49 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0181others(46): Show | 49 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.787-2782A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434018 | ||||||
| chr5:95434041
|
A | G | 36 | a0001c0001t0001g0125a0001c0001t0001g0317a0001c0001t0002g0015others(33): Show | 36 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.787-2759A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434041 | ||||||
| chr5:95434165
|
A | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0264 | 2 | HG02109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.787-2635A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434165 | ||||||
| chr5:95434447
|
C | T | 9 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0119others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-2353C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434447 | ||||||
| chr5:95434514
|
T | C | 2 | a0001c0001t0002g0068a0001c0002t0002g0173 | 2 | HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.787-2286T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434514 | ||||||
| chr5:95434616
|
CT | C | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-2180delT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 95434616 | |||||
| chr5:95434641
|
C | T | 4 | a0001c0001t0002g0131a0001c0001t0002g0232a0001c0001t0002g0321others(1): Show | 4 | HG01243.hp2 HG01891.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-2159C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434641 | ||||||
| chr5:95434805
|
C | T | 9 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0119others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-1995C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434805 | ||||||
| chr5:95434854
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.787-1946T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434854 | ||||||
| chr5:95434875
|
C | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0105a0001c0001t0002g0254others(1): Show | 4 | HG03654.hp1 HG03927.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-1925C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95434875 | ||||||
| chr5:95435094
|
C | T | 9 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0119others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-1706C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435094 | ||||||
| chr5:95435134
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.787-1666G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435134 | ||||||
| chr5:95435168
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.787-1632T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435168 | ||||||
| chr5:95435234
|
T | C | 4 | a0001c0001t0001g0236a0001c0001t0001g0329a0001c0002t0001g0177others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-1566T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435234 | ||||||
| chr5:95435297
|
G | T | 1 | a0001c0001t0002g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.787-1503G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435297 | ||||||
| chr5:95435406
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.787-1394T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95435406 | ||||||
| chr5:95436020
|
G | A | 1 | a0001c0002t0002g0335 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.787-780G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436020 | ||||||
| chr5:95436103
|
T | C | 2 | a0001c0001t0002g0318a0001c0001t0002g0320 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.787-697T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436103 | ||||||
| chr5:95436308
|
A | T | 32 | a0001c0001t0002g0015a0001c0001t0002g0029a0001c0001t0002g0037others(29): Show | 32 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.787-492A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436308 | ||||||
| chr5:95436427
|
C | T | 1 | a0001c0002t0001g0076 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.787-373C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436427 | ||||||
| chr5:95436718
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0091a0001c0001t0002g0105others(2): Show | 5 | HG03225.hp2 HG03654.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-82G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436718 | ||||||
| chr5:95436791
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0317 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.787-9T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 6/9 | chr5 | 95436791 | ||||||
| chr5:95436908
|
TA | T | 4 | a0001c0001t0002g0015a0001c0001t0002g0105a0001c0001t0002g0254others(1): Show | 4 | HG03654.hp1 HG03927.hp1 HG04204.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.893+4delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95436908 | |||||
| chr5:95436990
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.893+84C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95436990 | ||||||
| chr5:95437084
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.893+178A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437084 | ||||||
| chr5:95437346
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0143a0001c0001t0001g0235 | 3 | HG02602.hp2 HG02738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.893+440T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437346 | ||||||
| chr5:95437445
|
C | T | 43 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0233others(40): Show | 43 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.893+539C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437445 | ||||||
| chr5:95437499
|
G | A | 44 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0233others(41): Show | 44 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.893+593G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437499 | ||||||
| chr5:95437777
|
TC | T | 4 | a0001c0001t0001g0133a0001c0002t0001g0017a0001c0002t0002g0023others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.893+872delC | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437777 | ||||||
| chr5:95437778
|
C | T | 97 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0130others(94): Show | 97 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.893+872C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437778 | ||||||
| chr5:95437880
|
A | C | 60 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0130others(57): Show | 60 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.893+974A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95437880 | ||||||
| chr5:95438008
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0002g0256 | 3 | NA18948.hp2 NA18960.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.893+1102T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438008 | ||||||
| chr5:95438057
|
C | T | 1 | a0001c0002t0001g0311 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.893+1151C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438057 | ||||||
| chr5:95438058
|
G | A | 44 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0233others(41): Show | 44 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.893+1152G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438058 | ||||||
| chr5:95438109
|
C | A | 14 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(11): Show | 14 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.893+1203C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438109 | ||||||
| chr5:95438194
|
T | C | 101 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0130others(98): Show | 101 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.893+1288T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438194 | ||||||
| chr5:95438319
|
G | A | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+1413G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438319 | ||||||
| chr5:95438363
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.893+1457T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438363 | ||||||
| chr5:95438470
|
A | C | 1 | a0001c0001t0002g0283 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.893+1564A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438470 | ||||||
| chr5:95438498
|
G | A | 44 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0233others(41): Show | 44 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.893+1592G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438498 | ||||||
| chr5:95438629
|
G | A | 1 | a0001c0002t0002g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.893+1723G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438629 | ||||||
| chr5:95438752
|
C | T | 1 | a0002c0003t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.893+1846C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438752 | ||||||
| chr5:95438785
|
T | TA | 11 | a0001c0001t0001g0033a0001c0001t0001g0069a0001c0001t0001g0133others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.893+1895dupA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95438785 | |||||
| chr5:95438785
|
TA | T | 90 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0130others(87): Show | 90 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.893+1895delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95438785 | |||||
| chr5:95438797
|
A | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG00738.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.893+1891A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438797 | ||||||
| chr5:95438798
|
A | C | 1 | a0001c0001t0001g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.893+1892A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95438798 | ||||||
| chr5:95439215
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0323 | 2 | HG01106.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.893+2309G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439215 | ||||||
| chr5:95439232
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.893+2326A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439232 | ||||||
| chr5:95439236
|
G | GTA | 78 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0035others(75): Show | 82 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.893+2358_893+2359d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATA | 51 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0061others(48): Show | 54 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.893+2356_893+2359d others(6): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATA | 27 | a0001c0001t0001g0011a0001c0001t0001g0065a0001c0001t0001g0115others(24): Show | 28 | HG00140.hp2 HG00438.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.893+2354_893+2359d others(8): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(1): Show |
21 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0086others(18): Show | 22 | HG00280.hp1 HG00280.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.893+2352_893+2359d others(10): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(3): Show |
13 | a0001c0001t0001g0033a0001c0001t0001g0087a0001c0001t0001g0265others(10): Show | 13 | HG00733.hp2 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.893+2350_893+2359d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(5): Show |
11 | a0001c0001t0001g0067a0001c0001t0001g0096a0001c0001t0001g0157others(8): Show | 11 | HG01069.hp2 HG01070.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.893+2348_893+2359d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(7): Show |
11 | a0001c0001t0001g0289a0001c0001t0002g0111a0001c0001t0002g0240others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.893+2346_893+2359d others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(9): Show |
7 | a0001c0001t0001g0133a0001c0001t0001g0257a0001c0001t0001g0269others(4): Show | 7 | HG02071.hp2 HG02257.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.893+2344_893+2359d others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(11): Show |
8 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0001t0001g0260others(5): Show | 8 | HG01074.hp1 HG01081.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.893+2342_893+2359d others(20): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(13): Show |
7 | a0001c0001t0002g0029a0001c0001t0002g0119a0001c0001t0002g0211others(4): Show | 7 | HG01255.hp1 HG03041.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.893+2340_893+2359d others(22): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(15): Show |
6 | a0001c0001t0001g0075a0001c0001t0002g0091a0001c0001t0002g0114others(3): Show | 6 | HG01934.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.893+2338_893+2359d others(24): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(17): Show |
5 | a0001c0001t0002g0015a0001c0001t0002g0105a0001c0001t0002g0137others(2): Show | 5 | HG00544.hp1 HG01361.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.893+2336_893+2359d others(26): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(19): Show |
2 | a0001c0001t0002g0283a0001c0001t0002g0320 | 2 | HG02040.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.893+2334_893+2359d others(28): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0002g0275 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.893+2332_893+2359d others(30): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTATATAT others(41): Show |
1 | a0001c0001t0002g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.893+2359_893+2360i others(50): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.893+2331_893+2332i others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
G | GTGTATAT others(13): Show |
1 | a0001c0001t0002g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.893+2331_893+2332i others(22): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
GTA | G | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0028others(12): Show | 15 | HG00741.hp1 HG01109.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.893+2358_893+2359d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
GTATATAT others(3): Show |
G | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+2350_893+2359d others(12): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
GTATATAT others(5): Show |
G | 1 | a0001c0002t0002g0094 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.893+2348_893+2359d others(14): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
GTATATAT others(7): Show |
G | 12 | a0001c0001t0002g0037a0001c0001t0002g0072a0001c0001t0002g0197others(9): Show | 12 | HG00597.hp2 HG02165.hp1 NA18960.hp2 others(9): Show |
intron_variant | MODIFIER | c.893+2346_893+2359d others(16): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439236
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.893+2344_893+2359d others(18): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439236 | |||||
| chr5:95439321
|
G | A | 5 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0248others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.893+2415G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439321 | ||||||
| chr5:95439526
|
T | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0154a0001c0001t0001g0229others(1): Show | 4 | HG01943.hp2 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.893+2620T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439526 | ||||||
| chr5:95439594
|
GTAAGACA others(8): Show |
G | 84 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(81): Show | 87 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.893+2690_893+2704d others(17): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439594 | |||||
| chr5:95439595
|
T | G | 1 | a0001c0002t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.893+2689T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439595 | ||||||
| chr5:95439607
|
AT | A | 49 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0181others(46): Show | 49 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.893+2711delT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95439607 | |||||
| chr5:95439610
|
T | A | 1 | a0001c0002t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.893+2704T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439610 | ||||||
| chr5:95439954
|
G | A | 2 | a0001c0001t0001g0005a0002c0003t0001g0050 | 3 | HG01256.hp1 HG01258.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.893+3048G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95439954 | ||||||
| chr5:95440110
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.893+3204A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440110 | ||||||
| chr5:95440170
|
CA | C | 49 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0181others(46): Show | 49 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.893+3266delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95440170 | |||||
| chr5:95440303
|
T | C | 2 | a0001c0001t0001g0205a0001c0002t0001g0032 | 2 | NA18966.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.893+3397T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440303 | ||||||
| chr5:95440452
|
T | C | 9 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0119others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.893+3546T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440452 | ||||||
| chr5:95440719
|
T | C | 7 | a0001c0001t0001g0133a0001c0001t0002g0018a0001c0001t0002g0122others(4): Show | 7 | HG02040.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.893+3813T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440719 | ||||||
| chr5:95440808
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.893+3902T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95440808 | ||||||
| chr5:95440962
|
GAA | G | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0117others(4): Show | 7 | HG00738.hp1 HG01496.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.893+4060_893+4061d others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95440962 | |||||
| chr5:95441212
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0002t0001g0128others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+4306C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441212 | ||||||
| chr5:95441291
|
C | T | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+4385C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441291 | ||||||
| chr5:95441297
|
G | A | 79 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(76): Show | 82 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.893+4391G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441297 | ||||||
| chr5:95441342
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0002t0001g0128others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+4436G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441342 | ||||||
| chr5:95441373
|
A | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0002t0001g0128others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+4467A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441373 | ||||||
| chr5:95441378
|
G | C | 1 | a0001c0002t0001g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.893+4472G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441378 | ||||||
| chr5:95441429
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.893+4523C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441429 | ||||||
| chr5:95441442
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.893+4536G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441442 | ||||||
| chr5:95441493
|
C | T | 27 | a0001c0001t0002g0029a0001c0001t0002g0037a0001c0001t0002g0040others(24): Show | 27 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.893+4587C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441493 | ||||||
| chr5:95441507
|
T | G | 2 | a0001c0001t0001g0153a0009c0009t0001g0166 | 2 | HG04184.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.893+4601T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441507 | ||||||
| chr5:95441541
|
C | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0040a0001c0002t0002g0052 | 3 | HG01081.hp1 HG02257.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.893+4635C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441541 | ||||||
| chr5:95441838
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.894-4724A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441838 | ||||||
| chr5:95441842
|
T | C | 9 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0119others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-4720T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441842 | ||||||
| chr5:95441914
|
T | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0116others(3): Show | 7 | HG00280.hp2 HG01074.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.894-4648T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441914 | ||||||
| chr5:95441975
|
AG | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.894-4586delG | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95441975 | ||||||
| chr5:95442100
|
A | T | 1 | a0001c0002t0002g0324 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.894-4462A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442100 | ||||||
| chr5:95442262
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.894-4300T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442262 | ||||||
| chr5:95442331
|
C | CAGAAATA others(2): Show |
3 | a0001c0002t0002g0025a0003c0004t0002g0064a0008c0008t0002g0286 | 3 | HG01255.hp1 HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.894-4229_894-4221d others(11): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95442331 | |||||
| chr5:95442392
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.894-4170T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442392 | ||||||
| chr5:95442433
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.894-4129C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442433 | ||||||
| chr5:95442452
|
C | A | 1 | a0001c0001t0001g0301 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.894-4110C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442452 | ||||||
| chr5:95442611
|
AC | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0002t0001g0128others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-3950delC | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442611 | ||||||
| chr5:95442999
|
T | C | 9 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0119others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-3563T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95442999 | ||||||
| chr5:95443071
|
C | T | 178 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 180 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.894-3491C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95443071 | ||||||
| chr5:95443114
|
T | C | 178 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 180 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.894-3448T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95443114 | ||||||
| chr5:95443236
|
C | T | 59 | a0001c0001t0001g0130a0001c0001t0002g0015a0001c0001t0002g0018others(56): Show | 59 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.894-3326C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95443236 | ||||||
| chr5:95443638
|
GA | G | 83 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(80): Show | 86 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.894-2919delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 95443638 | |||||
| chr5:95444091
|
A | T | 1 | a0001c0002t0001g0003 | 2 | NA18984.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.894-2471A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444091 | ||||||
| chr5:95444151
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.894-2411T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444151 | ||||||
| chr5:95444163
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0329a0001c0002t0001g0177others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.894-2399C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444163 | ||||||
| chr5:95444412
|
A | T | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.894-2150A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444412 | ||||||
| chr5:95444599
|
T | A | 1 | a0001c0001t0002g0030 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.894-1963T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444599 | ||||||
| chr5:95444633
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0329a0001c0002t0001g0177others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.894-1929C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444633 | ||||||
| chr5:95444645
|
C | T | 1 | a0006c0006t0001g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.894-1917C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444645 | ||||||
| chr5:95444685
|
T | C | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-1877T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444685 | ||||||
| chr5:95444711
|
G | A | 1 | a0007c0011t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.894-1851G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444711 | ||||||
| chr5:95444774
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.894-1788T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95444774 | ||||||
| chr5:95445167
|
T | C | 9 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0119others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-1395T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445167 | ||||||
| chr5:95445263
|
C | G | 9 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0119others(6): Show | 9 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-1299C>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445263 | ||||||
| chr5:95445569
|
T | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0145a0001c0002t0001g0043others(2): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-993T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445569 | ||||||
| chr5:95445590
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.894-972A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445590 | ||||||
| chr5:95445647
|
C | T | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-915C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445647 | ||||||
| chr5:95445657
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.894-905A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445657 | ||||||
| chr5:95445903
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.894-659G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 7/9 | chr5 | 95445903 | ||||||
| chr5:95446790
|
G | A | 2 | a0002c0003t0001g0045a0002c0003t0001g0089 | 2 | HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1029+93G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446790 | ||||||
| chr5:95446793
|
A | G | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1029+96A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446793 | ||||||
| chr5:95446812
|
C | CT | 62 | a0001c0001t0001g0133a0001c0001t0002g0015a0001c0001t0002g0018others(59): Show | 62 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.1029+127dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 95446812 | |||||
| chr5:95446948
|
T | TA | 5 | a0001c0001t0002g0109a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG01167.hp1 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029+251_1029+252i others(3): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446948 | ||||||
| chr5:95446949
|
T | A | 6 | a0001c0001t0002g0109a0001c0001t0002g0246a0001c0001t0002g0247others(3): Show | 6 | HG01167.hp1 HG02040.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1029+252T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446949 | ||||||
| chr5:95446949
|
T | TA | 34 | a0001c0001t0002g0018a0001c0001t0002g0030a0001c0001t0002g0057others(31): Show | 34 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1029+252_1029+253i others(3): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446949 | ||||||
| chr5:95446949
|
T | TAA | 5 | a0001c0001t0002g0111a0001c0001t0002g0113a0001c0001t0002g0126others(2): Show | 5 | HG01884.hp1 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029+252_1029+253i others(4): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446949 | ||||||
| chr5:95446950
|
T | A | 45 | a0001c0001t0002g0018a0001c0001t0002g0030a0001c0001t0002g0057others(42): Show | 45 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.1029+253T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446950 | ||||||
| chr5:95446950
|
T | TA | 14 | a0001c0001t0002g0015a0001c0001t0002g0091a0001c0001t0002g0105others(11): Show | 14 | HG02451.hp2 HG02486.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1029+253_1029+254i others(3): Show |
FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446950 | ||||||
| chr5:95446951
|
T | A | 77 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(74): Show | 77 | HG00642.hp1 HG00733.hp1 HG01074.hp1 others(74): Show |
intron_variant | MODIFIER | c.1029+254T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446951 | ||||||
| chr5:95446951
|
TA | T | 7 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0001g0154others(4): Show | 7 | HG01516.hp2 HG01943.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1029+267delA | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 95446951 | |||||
| chr5:95446952
|
A | T | 32 | a0001c0001t0001g0133a0001c0001t0001g0162a0001c0001t0001g0181others(29): Show | 32 | HG00544.hp1 HG00597.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1029+255A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446952 | ||||||
| chr5:95446953
|
A | T | 2 | a0001c0001t0001g0133a0001c0002t0001g0017 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1029+256A>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95446953 | ||||||
| chr5:95447095
|
T | A | 1 | a0001c0001t0001g0332 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1029+398T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447095 | ||||||
| chr5:95447171
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0233others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029+474G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447171 | ||||||
| chr5:95447471
|
A | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(104): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1029+774A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447471 | ||||||
| chr5:95447485
|
G | A | 4 | a0001c0001t0001g0194a0001c0001t0001g0291a0001c0001t0001g0304others(1): Show | 4 | NA18947.hp2 NA18949.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1030-784G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447485 | ||||||
| chr5:95447720
|
G | A | 1 | a0001c0001t0001g0336 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1030-549G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447720 | ||||||
| chr5:95447887
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1030-382C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447887 | ||||||
| chr5:95447916
|
C | T | 100 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0133others(97): Show | 100 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.1030-353C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447916 | ||||||
| chr5:95447917
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1030-352G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447917 | ||||||
| chr5:95447918
|
A | C | 1 | a0001c0001t0002g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1030-351A>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95447918 | ||||||
| chr5:95448172
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1030-97C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 8/9 | chr5 | 95448172 | ||||||
| chr5:95448635
|
C | A | 1 | a0001c0002t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1225+171C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95448635 | ||||||
| chr5:95448693
|
A | AT | 8 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0242others(5): Show | 8 | HG01358.hp1 HG02738.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1225+250dupT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 95448693 | |||||
| chr5:95448693
|
AT | A | 40 | a0001c0001t0001g0056a0001c0001t0001g0062a0001c0001t0001g0176others(37): Show | 40 | HG00642.hp1 HG00733.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1225+250delT | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 95448693 | |||||
| chr5:95448714
|
T | A | 5 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0248others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1225+250T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95448714 | ||||||
| chr5:95448858
|
C | T | 5 | a0001c0001t0001g0181a0001c0001t0001g0236a0001c0001t0001g0329others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+394C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95448858 | ||||||
| chr5:95448922
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0036others(2): Show | 5 | HG00741.hp1 HG01243.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+458G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95448922 | ||||||
| chr5:95449161
|
T | C | 1 | a0001c0001t0002g0215 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1225+697T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449161 | ||||||
| chr5:95449188
|
A | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0130a0001c0001t0001g0233others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+724A>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449188 | ||||||
| chr5:95449480
|
C | T | 88 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0002g0029others(85): Show | 88 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.1226-669C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449480 | ||||||
| chr5:95449655
|
G | T | 5 | a0001c0001t0002g0015a0001c0001t0002g0091a0001c0001t0002g0105others(2): Show | 5 | HG03225.hp2 HG03654.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1226-494G>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449655 | ||||||
| chr5:95449697
|
T | C | 95 | a0001c0001t0001g0133a0001c0001t0001g0181a0001c0001t0001g0236others(92): Show | 95 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1226-452T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449697 | ||||||
| chr5:95449807
|
C | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0221 | 3 | NA18961.hp1 NA19007.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1226-342C>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449807 | ||||||
| chr5:95449834
|
T | A | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1226-315T>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449834 | ||||||
| chr5:95449835
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1226-314C>T | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449835 | ||||||
| chr5:95449861
|
T | G | 1 | a0001c0001t0001g0278 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1226-288T>G | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449861 | ||||||
| chr5:95449943
|
T | C | 192 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0021others(189): Show | 196 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.1226-206T>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95449943 | ||||||
| chr5:95450039
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1226-110G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95450039 | ||||||
| chr5:95450070
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG00738.hp2 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-79G>A | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95450070 | ||||||
| chr5:95450071
|
G | C | 1 | a0001c0001t0002g0328 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1226-78G>C | FAM81B | ENSG00000153347.10 | transcript | ENST00000283357.10 | protein_coding | 9/9 | chr5 | 95450071 |