Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 26049 |
|---|---|
| ensemblid | ENSG00000198780.13 |
| hgncid | 29138 |
| symbol | FAM169A |
| name | family with sequence similarity 169 member A |
| refseq_nuc | NM_001376049.1 |
| refseq_prot | NP_001362978.1 |
| ensembl_nuc | ENST00000687041.1 |
| ensembl_prot | ENSP00000508577.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 74777574 |
| end | 74866387 |
| strand | - |
| ver | v1.2 |
| region | chr5:74777574-74866387 |
| region5000 | chr5:74772574-74871387 |
| regionname0 | FAM169A_chr5_74777574_74866387 |
| regionname5000 | FAM169A_chr5_74772574_74871387 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 670 | 307 | 88 | 64 | 101 | 14 | 38 | 65 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0002 | 0/0 | 670 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2013 | 261 | 55 | 55 | 98 | 13 | 38 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| c0002 | 0/0 | 2013 | 27 | 24 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| c0003 | 0/0 | 2013 | 14 | 9 | 2 | 3 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| c0004 | 0/0 | 2013 | 3 | 0 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| c0005 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| c0006 | 0/0 | 2013 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| c0007 | 0/0 | 2013 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4113 | 74 | 14 | 18 | 20 | 6 | 16 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0002 | 0/0 | 4112 | 45 | 2 | 12 | 25 | 1 | 5 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0003 | 1/0 | 4113 | 44 | 1 | 6 | 28 | 2 | 6 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0004 | 0/0 | 4111 | 34 | 14 | 11 | 2 | 2 | 5 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0005 | 0/0 | 4113 | 26 | 6 | 6 | 10 | 1 | 3 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0006 | 0/0 | 4112 | 20 | 15 | 2 | 3 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0007 | 0/0 | 4112 | 11 | 11 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0008 | 0/0 | 4111 | 11 | 11 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0009 | 0/0 | 4112 | 7 | 0 | 0 | 7 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0010 | 0/0 | 4112 | 6 | 3 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0011 | 0/1 | 4107 | 5 | 0 | 2 | 0 | 2 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0012 | 0/0 | 4107 | 2 | 2 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0013 | 0/0 | 4113 | 2 | 0 | 0 | 0 | 0 | 2 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0014 | 0/0 | 4111 | 2 | 2 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0015 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0016 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0017 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0018 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0019 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0020 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0021 | 0/0 | 4113 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0022 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0023 | 0/0 | 4113 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0024 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0025 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0026 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0027 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0028 | 0/0 | 4112 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0029 | 0/0 | 4111 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0030 | 0/0 | 4111 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0031 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0032 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| t0033 | 0/0 | 4113 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2013 | 261 | 55 | 55 | 98 | 13 | 38 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0002 | 0/0 | 2013 | 27 | 24 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0003 | 0/0 | 2013 | 14 | 9 | 2 | 3 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0004 | 0/0 | 2013 | 3 | 0 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0006 | 0/0 | 2013 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0007 | 0/0 | 2013 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0002c0005 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6125 | 74 | 14 | 18 | 20 | 6 | 16 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0002 | 0/0 | 6124 | 41 | 2 | 9 | 24 | 1 | 5 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0003 | 1/0 | 6125 | 43 | 1 | 5 | 28 | 2 | 6 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0004 | 0/0 | 6123 | 34 | 14 | 11 | 2 | 2 | 5 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0005 | 0/0 | 6125 | 26 | 6 | 6 | 10 | 1 | 3 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0006 | 0/0 | 6124 | 2 | 2 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0007 | 0/0 | 6124 | 11 | 11 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0009 | 0/0 | 6124 | 7 | 0 | 0 | 7 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0011 | 0/1 | 6119 | 4 | 0 | 2 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0013 | 0/0 | 6125 | 2 | 0 | 0 | 0 | 0 | 2 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0014 | 0/0 | 6123 | 2 | 2 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0017 | 0/0 | 6125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0019 | 0/0 | 6125 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0020 | 0/0 | 6125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0021 | 0/0 | 6125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0022 | 0/0 | 6125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0023 | 0/0 | 6125 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0024 | 0/0 | 6125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0025 | 0/0 | 6125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0026 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0027 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0028 | 0/0 | 6124 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0029 | 0/0 | 6123 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0031 | 0/0 | 6124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0032 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0001t0033 | 0/0 | 6125 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0002t0006 | 0/0 | 6124 | 5 | 5 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0002t0008 | 0/0 | 6123 | 11 | 11 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0002t0010 | 0/0 | 6124 | 6 | 3 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0002t0012 | 0/0 | 6119 | 2 | 2 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0002t0016 | 0/0 | 6124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0002t0018 | 0/0 | 6119 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0002t0030 | 0/0 | 6123 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0003t0006 | 0/0 | 6124 | 13 | 8 | 2 | 3 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0003t0015 | 0/0 | 6124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0004t0002 | 0/0 | 6124 | 3 | 0 | 3 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0006t0011 | 0/0 | 6119 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0001c0007t0003 | 0/0 | 6125 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| a0002c0005t0002 | 0/0 | 6124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | copy fasta | chr5 | 74772574 | 74871387 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0009g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0009g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0009g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0009g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0009g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0011g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0011g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0011g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0011g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0013g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0014g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0014g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0017g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0019g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0020g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0021g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0022g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0023g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0024g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0025g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0026g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0027g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0028g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0029g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0031g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0032g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0001t0033g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0010g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0010g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0010g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0010g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0016g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0018g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0002t0030g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0003t0015g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0004t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0004t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0004t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0006t0011g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0001c0007t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| a0002c0005t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0266 | EUR | GBR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | GBR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0037 | EUR | GBR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0107 | EUR | FIN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0031 | EUR | FIN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | FIN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00408 | hp1 | a0001 | c0001 | t0024 | g0191 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00438 | hp1 | a0001 | c0003 | t0006 | g0228 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00642 | hp2 | a0001 | c0001 | t0023 | g0186 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0153 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | CHS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0052 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00735 | hp2 | a0001 | c0003 | t0006 | g0227 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00738 | hp2 | a0001 | c0001 | t0011 | g0044 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0158 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG00741 | hp2 | a0001 | c0002 | t0010 | g0247 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01106 | hp2 | a0001 | c0002 | t0010 | g0248 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01109 | hp1 | a0001 | c0004 | t0002 | g0268 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01167 | hp1 | a0001 | c0002 | t0010 | g0243 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0215 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01175 | hp2 | a0001 | c0004 | t0002 | g0294 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0159 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01243 | hp1 | a0001 | c0001 | t0029 | g0022 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01257 | hp1 | a0001 | c0001 | t0019 | g0073 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01346 | hp2 | a0001 | c0004 | t0002 | g0267 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0042 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01361 | hp2 | a0001 | c0007 | t0003 | g0164 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01433 | hp2 | a0001 | c0001 | t0028 | g0272 | AMR | CLM | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0104 | EUR | IBS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0035 | EUR | IBS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01516 | hp1 | a0001 | c0006 | t0011 | g0040 | EUR | IBS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01884 | hp2 | a0001 | c0002 | t0006 | g0018 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01891 | hp2 | a0001 | c0001 | t0021 | g0094 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0182 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02071 | hp1 | a0001 | c0001 | t0009 | g0284 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02129 | hp1 | a0001 | c0001 | t0026 | g0089 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02135 | hp2 | a0001 | c0001 | t0009 | g0259 | EAS | KHV | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02145 | hp2 | a0001 | c0002 | t0008 | g0069 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | CDX | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | CDX | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02258 | hp1 | a0001 | c0002 | t0010 | g0242 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0154 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02293 | hp2 | a0001 | c0003 | t0006 | g0223 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0156 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02451 | hp1 | a0001 | c0003 | t0006 | g0249 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02451 | hp2 | a0001 | c0002 | t0008 | g0070 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02630 | hp1 | a0001 | c0002 | t0008 | g0071 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02647 | hp2 | a0001 | c0002 | t0006 | g0020 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0160 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02717 | hp1 | a0001 | c0003 | t0006 | g0251 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02723 | hp1 | a0001 | c0002 | t0008 | g0063 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0027 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0019 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02818 | hp1 | a0001 | c0003 | t0015 | g0241 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0068 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02895 | hp1 | a0001 | c0002 | t0010 | g0246 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02896 | hp1 | a0001 | c0001 | t0014 | g0306 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02896 | hp2 | a0001 | c0003 | t0006 | g0240 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0307 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02965 | hp1 | a0001 | c0002 | t0010 | g0244 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02976 | hp1 | a0001 | c0001 | t0020 | g0137 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03041 | hp2 | a0001 | c0002 | t0012 | g0233 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03098 | hp1 | a0001 | c0003 | t0006 | g0250 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03098 | hp2 | a0001 | c0002 | t0012 | g0232 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0016 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03139 | hp2 | a0001 | c0002 | t0008 | g0072 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03195 | hp2 | a0001 | c0002 | t0008 | g0064 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03209 | hp2 | a0001 | c0002 | t0006 | g0017 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03516 | hp1 | a0001 | c0002 | t0008 | g0067 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03540 | hp2 | a0001 | c0002 | t0030 | g0245 | AFR | GWD | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03579 | hp2 | a0001 | c0002 | t0008 | g0062 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0082 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03654 | hp2 | a0001 | c0001 | t0033 | g0091 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0229 | SAS | PJL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0152 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04184 | hp2 | a0001 | c0001 | t0013 | g0230 | SAS | BEB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18522 | hp2 | a0001 | c0003 | t0006 | g0222 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18906 | hp2 | a0001 | c0002 | t0016 | g0212 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18945 | hp1 | a0001 | c0001 | t0027 | g0303 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18948 | hp2 | a0002 | c0005 | t0002 | g0277 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0257 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18953 | hp1 | a0001 | c0001 | t0017 | g0130 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0157 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18964 | hp1 | a0001 | c0001 | t0032 | g0254 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18964 | hp2 | a0001 | c0001 | t0022 | g0181 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18970 | hp1 | a0001 | c0001 | t0009 | g0293 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18981 | hp1 | a0001 | c0001 | t0009 | g0261 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18982 | hp1 | a0001 | c0003 | t0006 | g0226 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18995 | hp2 | a0001 | c0001 | t0009 | g0288 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19001 | hp2 | a0001 | c0003 | t0006 | g0221 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0258 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19030 | hp2 | a0001 | c0001 | t0031 | g0004 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0224 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19090 | hp2 | a0001 | c0001 | t0025 | g0161 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA19240 | hp2 | a0001 | c0002 | t0008 | g0065 | AFR | YRI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0225 | AFR | ASW | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0127 | EUR | TSI | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | GIH | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | GIH | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02486 | hp1 | a0001 | c0003 | t0006 | g0103 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG02559 | hp2 | a0001 | c0002 | t0008 | g0066 | AFR | ACB | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | MSL | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | USA | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | USA | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA21309 | hp1 | a0001 | c0002 | t0018 | g0231 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0011 | g0041 | REF | REF | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0143 | REF | REF | FAM169A_chr5_74772574_74871387 | FAM169A | chr5 | 74772574 | 74871387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74805254
|
C | G | 1 | a0002 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.701G>C | p.Gly234Ala | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 7/13 | 927/6125 | 701/2013 | 234/670 | chr5 | 74805254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74781649
|
C | T | 2 | a0001c0002a0001c0003 | 41 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
synonymous_variant | LOW | c.1824G>A | p.Lys608Lys | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2050/6125 | 1824/2013 | 608/670 | chr5 | 74781649 | ||
| chr5:74801609
|
G | A | 1 | a0001c0006 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.933C>T | p.Ala311Ala | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 9/13 | 1159/6125 | 933/2013 | 311/670 | chr5 | 74801609 | ||
| chr5:74813861
|
G | A | 1 | a0001c0007 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.649C>T | p.Leu217Leu | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/13 | 875/6125 | 649/2013 | 217/670 | chr5 | 74813861 | ||
| chr5:74813868
|
C | A | 1 | a0001c0004 | 3 | HG01109.hp1 HG01175.hp2 HG01346.hp2 |
synonymous_variant | LOW | c.642G>T | p.Arg214Arg | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/13 | 868/6125 | 642/2013 | 214/670 | chr5 | 74813868 | ||
| chr5:74814015
|
G | A | 1 | a0001c0003 | 14 | HG00438.hp1 HG00735.hp2 HG02293.hp2 others(11): Show |
synonymous_variant | LOW | c.495C>T | p.Ser165Ser | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/13 | 721/6125 | 495/2013 | 165/670 | chr5 | 74814015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74777590
|
AT | A | 5 | a0001c0001t0004a0001c0001t0011a0001c0001t0014others(2): Show | 42 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3869delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3869 | chr5 | 74777590 | |||||
| chr5:74777717
|
G | A | 23 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(20): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*3743C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3743 | chr5 | 74777717 | |||||
| chr5:74777759
|
G | C | 2 | a0001c0001t0007a0001c0001t0031 | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3701C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3701 | chr5 | 74777759 | |||||
| chr5:74778223
|
C | T | 1 | a0001c0001t0023 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3237G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3237 | chr5 | 74778223 | |||||
| chr5:74778387
|
A | G | 1 | a0001c0001t0022 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3073T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 3073 | chr5 | 74778387 | |||||
| chr5:74778597
|
TA | T | 23 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(20): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*2862delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2862 | chr5 | 74778597 | |||||
| chr5:74778625
|
T | C | 1 | a0001c0001t0024 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2835A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2835 | chr5 | 74778625 | |||||
| chr5:74778627
|
T | C | 1 | a0001c0001t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2833A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2833 | chr5 | 74778627 | |||||
| chr5:74779087
|
G | A | 1 | a0001c0001t0020 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2373C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2373 | chr5 | 74779087 | |||||
| chr5:74779088
|
A | G | 1 | a0001c0001t0020 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2372T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2372 | chr5 | 74779088 | |||||
| chr5:74779401
|
G | A | 2 | a0001c0001t0025a0001c0002t0030 | 2 | HG03540.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2059C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2059 | chr5 | 74779401 | |||||
| chr5:74779442
|
C | G | 1 | a0001c0001t0031 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 2018 | chr5 | 74779442 | |||||
| chr5:74779528
|
ACAGAG | A | 2 | a0001c0002t0012a0001c0002t0018 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1927_*1931delCTCT others(1): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1927 | chr5 | 74779528 | |||||
| chr5:74779529
|
C | T | 1 | a0001c0001t0019 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1931G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1931 | chr5 | 74779529 | |||||
| chr5:74779533
|
G | A | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(22): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1927C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1927 | chr5 | 74779533 | |||||
| chr5:74779604
|
C | G | 7 | a0001c0001t0001a0001c0001t0013a0001c0001t0019others(4): Show | 81 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1856G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1856 | chr5 | 74779604 | |||||
| chr5:74779621
|
CT | C | 4 | a0001c0001t0026a0001c0002t0008a0001c0002t0016others(1): Show | 14 | HG02129.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1838delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1838 | chr5 | 74779621 | |||||
| chr5:74780080
|
T | G | 1 | a0001c0001t0027 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1380 | chr5 | 74780080 | |||||
| chr5:74780232
|
A | G | 1 | a0001c0002t0018 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1228T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1228 | chr5 | 74780232 | |||||
| chr5:74780385
|
T | C | 12 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(9): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1075A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1075 | chr5 | 74780385 | |||||
| chr5:74780406
|
C | G | 1 | a0001c0001t0017 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1054G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1054 | chr5 | 74780406 | |||||
| chr5:74780454
|
G | C | 1 | a0001c0001t0028 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1006C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 1006 | chr5 | 74780454 | |||||
| chr5:74780472
|
G | A | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*988C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 988 | chr5 | 74780472 | |||||
| chr5:74780520
|
G | A | 1 | a0001c0001t0013 | 2 | HG03710.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*940C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 940 | chr5 | 74780520 | |||||
| chr5:74780531
|
C | T | 2 | a0001c0002t0016a0001c0003t0015 | 2 | HG02818.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*929G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 929 | chr5 | 74780531 | |||||
| chr5:74780555
|
G | C | 2 | a0001c0002t0010a0001c0002t0030 | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*905C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 905 | chr5 | 74780555 | |||||
| chr5:74780948
|
T | C | 1 | a0001c0001t0031 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 512 | chr5 | 74780948 | |||||
| chr5:74780951
|
C | T | 1 | a0001c0001t0032 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 509 | chr5 | 74780951 | |||||
| chr5:74781107
|
T | C | 2 | a0001c0001t0009a0001c0001t0032 | 8 | HG02071.hp1 HG02135.hp2 NA18952.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*353A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 353 | chr5 | 74781107 | |||||
| chr5:74781330
|
TAGTA | T | 2 | a0001c0001t0011a0001c0006t0011 | 5 | HG00140.hp2 HG00738.hp2 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*126_*129delTACT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 126 | chr5 | 74781330 | |||||
| chr5:74781355
|
T | C | 1 | a0001c0001t0033 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 13/13 | 105 | chr5 | 74781355 | |||||
| chr5:74866334
|
T | C | 1 | a0001c0001t0014 | 2 | HG02896.hp1 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-173A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/13 | 24658 | chr5 | 74866334 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:74782129
|
C | A | 2 | a0001c0003t0006g0249a0001c0003t0006g0250 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1465-121G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 12/12 | chr5 | 74782129 | ||||||
| chr5:74782294
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1465-286T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 12/12 | chr5 | 74782294 | ||||||
| chr5:74782380
|
C | T | 6 | a0001c0001t0002g0262a0001c0001t0002g0273a0001c0001t0002g0278others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-372G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 12/12 | chr5 | 74782380 | ||||||
| chr5:74782394
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1465-386C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 12/12 | chr5 | 74782394 | ||||||
| chr5:74783155
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1261-21C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783155 | ||||||
| chr5:74783196
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1261-62C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783196 | ||||||
| chr5:74783310
|
A | G | 1 | a0001c0001t0005g0210 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1261-176T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783310 | ||||||
| chr5:74783469
|
G | T | 149 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(146): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1261-335C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783469 | ||||||
| chr5:74783556
|
G | C | 2 | a0001c0001t0005g0113a0001c0001t0005g0155 | 2 | NA18963.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1261-422C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783556 | ||||||
| chr5:74783667
|
A | T | 1 | a0001c0001t0004g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1261-533T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783667 | ||||||
| chr5:74783793
|
T | C | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1261-659A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783793 | ||||||
| chr5:74783858
|
A | T | 1 | a0001c0001t0017g0130 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1261-724T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783858 | ||||||
| chr5:74783904
|
G | A | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-770C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783904 | ||||||
| chr5:74783923
|
A | T | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-789T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74783923 | ||||||
| chr5:74784096
|
C | G | 1 | a0001c0001t0011g0041 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1261-962G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784096 | ||||||
| chr5:74784171
|
G | A | 6 | a0001c0003t0006g0103a0001c0003t0006g0224a0001c0003t0006g0225others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1037C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784171 | ||||||
| chr5:74784210
|
A | G | 1 | a0001c0001t0002g0295 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1261-1076T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784210 | ||||||
| chr5:74784510
|
C | CA | 9 | a0001c0001t0001g0100a0001c0001t0001g0187a0001c0001t0001g0211others(6): Show | 9 | HG02976.hp1 HG04115.hp2 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-1377dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAA | 9 | a0001c0001t0004g0050a0001c0002t0008g0063a0001c0002t0008g0064others(6): Show | 9 | HG00642.hp1 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-1379_1261-137 others(7): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAA | 56 | a0001c0001t0002g0252a0001c0001t0002g0255a0001c0001t0002g0256others(53): Show | 56 | HG00408.hp2 HG00558.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1261-1380_1261-137 others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAA | 35 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(32): Show | 36 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1261-1381_1261-137 others(9): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAA | 7 | a0001c0001t0002g0264a0001c0001t0004g0028a0001c0001t0004g0029others(4): Show | 7 | HG00140.hp2 HG01069.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-1382_1261-137 others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA | 6 | a0001c0002t0010g0242a0001c0002t0010g0244a0001c0002t0010g0246others(3): Show | 6 | HG00741.hp2 HG01106.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1383_1261-137 others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0006g0061a0001c0002t0006g0017 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1261-1386_1261-137 others(14): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0006g0060a0001c0002t0006g0016a0001c0002t0006g0018others(3): Show | 6 | HG00735.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1387_1261-137 others(15): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(5): Show |
1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1261-1388_1261-137 others(16): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0007g0012a0001c0003t0006g0228 | 2 | HG00438.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1261-1389_1261-137 others(17): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0007g0007a0001c0001t0007g0009a0001c0001t0007g0010others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-1390_1261-137 others(18): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(8): Show |
6 | a0001c0001t0007g0005a0001c0001t0007g0008a0001c0001t0007g0013others(3): Show | 6 | HG02293.hp2 HG02723.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1391_1261-137 others(19): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0007g0011a0001c0003t0006g0221a0001c0003t0006g0240 | 3 | HG02896.hp2 HG03486.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1261-1392_1261-137 others(20): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0031g0004a0001c0003t0006g0224 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1261-1393_1261-137 others(21): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(11): Show |
1 | a0001c0003t0006g0225 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1261-1394_1261-137 others(22): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(12): Show |
1 | a0001c0003t0006g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1261-1395_1261-137 others(23): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(13): Show |
1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1261-1377_1261-137 others(24): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(26): Show |
1 | a0001c0003t0006g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1261-1377_1261-137 others(37): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784510
|
C | CAAAAAAA others(41): Show |
1 | a0001c0003t0006g0249 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1261-1377_1261-137 others(52): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784510 | ||||||
| chr5:74784607
|
T | TA | 16 | a0001c0001t0001g0101a0001c0001t0003g0118a0001c0001t0005g0125others(13): Show | 16 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-1474dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784607 | ||||||
| chr5:74784607
|
TA | T | 143 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1261-1474delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784607 | ||||||
| chr5:74784607
|
TAA | T | 55 | a0001c0001t0001g0149a0001c0001t0003g0204a0001c0001t0004g0003others(52): Show | 55 | HG00280.hp2 HG00438.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1261-1475_1261-147 others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784607 | ||||||
| chr5:74784607
|
TAAA | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(62): Show | 66 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1261-1476_1261-147 others(7): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784607 | ||||||
| chr5:74784780
|
G | A | 9 | a0001c0001t0005g0125a0001c0001t0005g0126a0001c0001t0005g0141others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-1646C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784780 | ||||||
| chr5:74784792
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1261-1658C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784792 | ||||||
| chr5:74784844
|
G | A | 1 | a0001c0002t0012g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1261-1710C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784844 | ||||||
| chr5:74784918
|
C | CA | 19 | a0001c0001t0002g0002a0001c0001t0003g0185a0001c0001t0003g0203others(16): Show | 19 | HG01243.hp1 HG01433.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1261-1785dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784918 | ||||||
| chr5:74784918
|
C | CAA | 7 | a0001c0002t0008g0071a0001c0002t0010g0242a0001c0002t0010g0243others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-1786_1261-178 others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784918 | ||||||
| chr5:74784918
|
CAA | C | 12 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1261-1786_1261-178 others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784918 | ||||||
| chr5:74784938
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1261-1804A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784938 | ||||||
| chr5:74784998
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1261-1864T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74784998 | ||||||
| chr5:74785027
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1261-1893T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785027 | ||||||
| chr5:74785137
|
G | A | 6 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1261-2003C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785137 | ||||||
| chr5:74785231
|
T | G | 1 | a0001c0001t0007g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1261-2097A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785231 | ||||||
| chr5:74785305
|
C | T | 108 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1261-2171G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785305 | ||||||
| chr5:74785490
|
C | T | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-2356G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785490 | ||||||
| chr5:74785491
|
G | A | 2 | a0001c0001t0004g0023a0001c0001t0004g0036 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1261-2357C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785491 | ||||||
| chr5:74785535
|
G | A | 1 | a0001c0003t0006g0221 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1261-2401C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785535 | ||||||
| chr5:74785737
|
G | T | 11 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0033others(8): Show | 11 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-2603C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785737 | ||||||
| chr5:74785815
|
C | T | 7 | a0001c0001t0004g0052a0001c0001t0004g0053a0001c0001t0004g0054others(4): Show | 7 | HG00733.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1261-2681G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785815 | ||||||
| chr5:74785914
|
T | C | 2 | a0001c0003t0006g0249a0001c0003t0006g0250 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1261-2780A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74785914 | ||||||
| chr5:74786118
|
T | C | 44 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0078others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1261-2984A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786118 | ||||||
| chr5:74786537
|
G | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0098others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-3403C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786537 | ||||||
| chr5:74786617
|
CTAAGTTC others(18): Show |
C | 1 | a0001c0001t0009g0259 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1261-3508_1261-348 others(29): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786617 | ||||||
| chr5:74786686
|
C | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1261-3552G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786686 | ||||||
| chr5:74786695
|
G | A | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1261-3561C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786695 | ||||||
| chr5:74786752
|
G | A | 1 | a0001c0001t0005g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1261-3618C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786752 | ||||||
| chr5:74786969
|
G | A | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-3835C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786969 | ||||||
| chr5:74786979
|
G | A | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-3845C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74786979 | ||||||
| chr5:74787109
|
T | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1261-3975A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787109 | ||||||
| chr5:74787157
|
G | A | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1261-4023C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787157 | ||||||
| chr5:74787240
|
G | A | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1261-4106C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787240 | ||||||
| chr5:74787286
|
A | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1261-4152T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787286 | ||||||
| chr5:74787496
|
C | T | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-4362G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787496 | ||||||
| chr5:74787621
|
C | T | 1 | a0001c0003t0006g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1261-4487G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787621 | ||||||
| chr5:74787883
|
T | TA | 51 | a0001c0001t0003g0114a0001c0001t0006g0060a0001c0001t0006g0061others(48): Show | 51 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1261-4750dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787883 | ||||||
| chr5:74787892
|
G | A | 151 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1261-4758C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74787892 | ||||||
| chr5:74788232
|
G | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1261-5098C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788232 | ||||||
| chr5:74788242
|
G | A | 2 | a0001c0001t0007g0007a0001c0001t0007g0010 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1261-5108C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788242 | ||||||
| chr5:74788425
|
G | A | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1261-5291C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788425 | ||||||
| chr5:74788474
|
G | A | 12 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1261-5340C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788474 | ||||||
| chr5:74788477
|
G | A | 2 | a0001c0001t0002g0252a0001c0001t0002g0263 | 2 | HG02056.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1261-5343C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788477 | ||||||
| chr5:74788504
|
G | A | 1 | a0001c0002t0012g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1261-5370C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788504 | ||||||
| chr5:74788524
|
G | A | 2 | a0001c0001t0002g0275a0001c0001t0002g0286 | 2 | NA18953.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1261-5390C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788524 | ||||||
| chr5:74788562
|
G | A | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1261-5428C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788562 | ||||||
| chr5:74788620
|
G | A | 2 | a0001c0001t0014g0306a0001c0001t0014g0307 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1261-5486C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74788620 | ||||||
| chr5:74789054
|
C | T | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1261-5920G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789054 | ||||||
| chr5:74789085
|
A | G | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1261-5951T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789085 | ||||||
| chr5:74789141
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0188 | 2 | HG00735.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1261-6007T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789141 | ||||||
| chr5:74789164
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1261-6030G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789164 | ||||||
| chr5:74789209
|
T | C | 5 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0281others(2): Show | 5 | HG00558.hp2 HG02015.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-6075A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789209 | ||||||
| chr5:74789320
|
T | C | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1261-6186A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789320 | ||||||
| chr5:74789321
|
A | G | 2 | a0001c0001t0004g0021a0001c0001t0004g0038 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1261-6187T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789321 | ||||||
| chr5:74789332
|
G | A | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1261-6198C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789332 | ||||||
| chr5:74789382
|
AG | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0136a0001c0001t0001g0139others(2): Show | 5 | NA18945.hp2 NA18975.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-6249delC | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789382 | ||||||
| chr5:74789390
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1261-6256C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789390 | ||||||
| chr5:74789404
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0234 | 2 | HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1261-6270G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789404 | ||||||
| chr5:74789620
|
G | A | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1260+6410C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789620 | ||||||
| chr5:74789758
|
G | C | 2 | a0001c0001t0004g0021a0001c0001t0004g0038 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1260+6272C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789758 | ||||||
| chr5:74789888
|
C | T | 1 | a0001c0001t0003g0178 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1260+6142G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789888 | ||||||
| chr5:74789898
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1260+6132C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74789898 | ||||||
| chr5:74790116
|
T | C | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+5914A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790116 | ||||||
| chr5:74790307
|
G | C | 1 | a0001c0003t0006g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1260+5723C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790307 | ||||||
| chr5:74790364
|
G | T | 292 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(289): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1260+5666C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790364 | ||||||
| chr5:74790545
|
C | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1260+5485G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790545 | ||||||
| chr5:74790674
|
C | G | 1 | a0001c0001t0006g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1260+5356G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790674 | ||||||
| chr5:74790763
|
G | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1260+5267C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790763 | ||||||
| chr5:74790997
|
G | A | 3 | a0001c0002t0012g0232a0001c0002t0012g0233a0001c0002t0018g0231 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1260+5033C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74790997 | ||||||
| chr5:74791035
|
T | C | 6 | a0001c0001t0003g0114a0001c0003t0006g0221a0001c0003t0006g0223others(3): Show | 6 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+4995A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791035 | ||||||
| chr5:74791057
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1260+4973G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791057 | ||||||
| chr5:74791077
|
G | A | 30 | a0001c0001t0003g0114a0001c0002t0006g0016a0001c0002t0006g0017others(27): Show | 30 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+4953C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791077 | ||||||
| chr5:74791121
|
C | T | 3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0029 | 3 | HG03239.hp2 HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1260+4909G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791121 | ||||||
| chr5:74791206
|
C | T | 5 | a0001c0001t0003g0114a0001c0003t0006g0221a0001c0003t0006g0223others(2): Show | 5 | HG00438.hp1 HG00673.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+4824G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791206 | ||||||
| chr5:74791441
|
G | A | 1 | a0001c0004t0002g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1260+4589C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791441 | ||||||
| chr5:74791540
|
G | A | 30 | a0001c0001t0003g0114a0001c0002t0006g0016a0001c0002t0006g0017others(27): Show | 30 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+4490C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791540 | ||||||
| chr5:74791779
|
G | GA | 7 | a0001c0001t0003g0114a0001c0001t0005g0152a0001c0003t0006g0221others(4): Show | 7 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+4250dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791779 | ||||||
| chr5:74791885
|
T | C | 23 | a0001c0001t0002g0253a0001c0001t0002g0255a0001c0001t0002g0260others(20): Show | 23 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1260+4145A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74791885 | ||||||
| chr5:74792516
|
T | G | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3514A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792516 | ||||||
| chr5:74792517
|
C | A | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3513G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792517 | ||||||
| chr5:74792520
|
T | G | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3510A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792520 | ||||||
| chr5:74792524
|
TCCTTGCT others(1): Show |
T | 139 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1260+3498_1260+350 others(12): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792524 | ||||||
| chr5:74792532
|
C | T | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3498G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792532 | ||||||
| chr5:74792534
|
C | T | 1 | a0001c0001t0005g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1260+3496G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792534 | ||||||
| chr5:74792660
|
CCTGA | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+3366_1260+336 others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792660 | ||||||
| chr5:74792920
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1260+3110T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792920 | ||||||
| chr5:74792949
|
A | G | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1260+3081T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74792949 | ||||||
| chr5:74793123
|
G | A | 6 | a0001c0003t0006g0103a0001c0003t0006g0224a0001c0003t0006g0225others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+2907C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793123 | ||||||
| chr5:74793323
|
C | CA | 22 | a0001c0001t0001g0112a0001c0001t0001g0217a0001c0001t0003g0118others(19): Show | 22 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1260+2706dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793323 | ||||||
| chr5:74793323
|
CA | C | 11 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0002g0286others(8): Show | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1260+2706delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793323 | ||||||
| chr5:74793519
|
G | A | 2 | a0001c0003t0006g0249a0001c0003t0006g0250 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1260+2511C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793519 | ||||||
| chr5:74793620
|
A | G | 151 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1260+2410T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793620 | ||||||
| chr5:74793779
|
G | A | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1260+2251C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793779 | ||||||
| chr5:74793858
|
C | G | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1260+2172G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793858 | ||||||
| chr5:74793902
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0097others(3): Show | 6 | HG01074.hp1 HG01346.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+2128G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793902 | ||||||
| chr5:74793952
|
G | A | 3 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0008 | 3 | HG02559.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1260+2078C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74793952 | ||||||
| chr5:74794002
|
C | CA | 19 | a0001c0001t0001g0184a0001c0001t0002g0299a0001c0001t0003g0145others(16): Show | 19 | HG02071.hp2 HG02145.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.1260+2027dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794002 | ||||||
| chr5:74794167
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1260+1863C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794167 | ||||||
| chr5:74794237
|
T | A | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1260+1793A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794237 | ||||||
| chr5:74794337
|
T | A | 1 | a0001c0002t0010g0243 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1260+1693A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794337 | ||||||
| chr5:74794377
|
G | C | 1 | a0001c0003t0006g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1260+1653C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794377 | ||||||
| chr5:74794393
|
C | CA | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+1636dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794393 | ||||||
| chr5:74794511
|
G | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1260+1519C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794511 | ||||||
| chr5:74794546
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1260+1484C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794546 | ||||||
| chr5:74794595
|
G | A | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1260+1435C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794595 | ||||||
| chr5:74794631
|
T | C | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1260+1399A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794631 | ||||||
| chr5:74794768
|
A | G | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(134): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1260+1262T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794768 | ||||||
| chr5:74794778
|
C | CA | 30 | a0001c0001t0001g0101a0001c0001t0001g0163a0001c0001t0001g0170others(27): Show | 30 | HG00642.hp1 HG01978.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+1251dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794778 | ||||||
| chr5:74794812
|
C | G | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+1218G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74794812 | ||||||
| chr5:74795029
|
G | A | 1 | a0001c0001t0004g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1260+1001C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795029 | ||||||
| chr5:74795060
|
C | G | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1260+970G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795060 | ||||||
| chr5:74795127
|
G | A | 1 | a0001c0002t0010g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1260+903C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795127 | ||||||
| chr5:74795224
|
C | T | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1260+806G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795224 | ||||||
| chr5:74795226
|
C | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1260+804G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795226 | ||||||
| chr5:74795379
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1260+651C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795379 | ||||||
| chr5:74795399
|
A | G | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+631T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795399 | ||||||
| chr5:74795432
|
T | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1260+598A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795432 | ||||||
| chr5:74795525
|
AT | A | 29 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(26): Show | 29 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1260+504delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795525 | ||||||
| chr5:74795649
|
C | A | 150 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(147): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1260+381G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795649 | ||||||
| chr5:74795709
|
A | T | 40 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(37): Show | 40 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.1260+321T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795709 | ||||||
| chr5:74795784
|
C | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1260+246G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795784 | ||||||
| chr5:74795792
|
T | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1260+238A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795792 | ||||||
| chr5:74795946
|
G | A | 2 | a0001c0003t0006g0240a0001c0003t0015g0241 | 2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1260+84C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | 74795946 | ||||||
| chr5:74796420
|
TTC | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1104-236_1104-235d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796420 | ||||||
| chr5:74796422
|
C | T | 162 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1104-236G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796422 | ||||||
| chr5:74796466
|
C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1104-280G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796466 | ||||||
| chr5:74796475
|
G | A | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1104-289C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796475 | ||||||
| chr5:74796632
|
G | A | 1 | a0001c0003t0006g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1104-446C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796632 | ||||||
| chr5:74796747
|
A | G | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1104-561T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796747 | ||||||
| chr5:74796975
|
G | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1104-789C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74796975 | ||||||
| chr5:74797184
|
T | C | 5 | a0001c0001t0004g0039a0001c0001t0004g0045a0001c0001t0004g0046others(2): Show | 5 | HG01081.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1104-998A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797184 | ||||||
| chr5:74797208
|
CCT | C | 5 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0033others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1104-1024_1104-102 others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797208 | ||||||
| chr5:74797229
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0234 | 2 | HG00323.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1104-1043A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797229 | ||||||
| chr5:74797344
|
T | C | 5 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0206others(2): Show | 5 | HG01884.hp1 HG02698.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1104-1158A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797344 | ||||||
| chr5:74797388
|
G | A | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1104-1202C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797388 | ||||||
| chr5:74797434
|
C | T | 15 | a0001c0001t0001g0133a0001c0001t0001g0149a0001c0001t0001g0150others(12): Show | 15 | HG00323.hp2 HG00733.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1104-1248G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797434 | ||||||
| chr5:74797520
|
A | C | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1104-1334T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797520 | ||||||
| chr5:74797522
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1104-1336G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797522 | ||||||
| chr5:74797750
|
A | T | 1 | a0001c0001t0003g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1104-1564T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797750 | ||||||
| chr5:74797808
|
C | G | 12 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1104-1622G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797808 | ||||||
| chr5:74797945
|
A | T | 24 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(21): Show | 24 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1104-1759T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797945 | ||||||
| chr5:74797960
|
A | T | 138 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1104-1774T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74797960 | ||||||
| chr5:74798320
|
C | T | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1104-2134G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74798320 | ||||||
| chr5:74799035
|
T | C | 5 | a0001c0001t0003g0114a0001c0003t0006g0221a0001c0003t0006g0223others(2): Show | 5 | HG00438.hp1 HG00673.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1103+1845A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799035 | ||||||
| chr5:74799594
|
G | A | 151 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1103+1286C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799594 | ||||||
| chr5:74799626
|
C | T | 22 | a0001c0001t0005g0082a0001c0001t0005g0113a0001c0001t0005g0125others(19): Show | 22 | HG00673.hp1 HG00741.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1103+1254G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799626 | ||||||
| chr5:74799707
|
T | C | 6 | a0001c0001t0003g0114a0001c0003t0006g0221a0001c0003t0006g0223others(3): Show | 6 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1103+1173A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799707 | ||||||
| chr5:74799717
|
T | C | 24 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0133others(21): Show | 24 | HG00323.hp2 HG00733.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1103+1163A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799717 | ||||||
| chr5:74799754
|
T | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1103+1126A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799754 | ||||||
| chr5:74799800
|
A | G | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1103+1080T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799800 | ||||||
| chr5:74799814
|
C | T | 23 | a0001c0001t0005g0082a0001c0001t0005g0113a0001c0001t0005g0125others(20): Show | 23 | HG00673.hp1 HG00741.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1103+1066G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799814 | ||||||
| chr5:74799821
|
C | T | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1103+1059G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799821 | ||||||
| chr5:74799880
|
CAT | C | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1103+998_1103+999d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799880 | ||||||
| chr5:74799893
|
G | T | 7 | a0001c0001t0004g0052a0001c0001t0004g0053a0001c0001t0004g0054others(4): Show | 7 | HG00733.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1103+987C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74799893 | ||||||
| chr5:74800009
|
T | C | 1 | a0001c0002t0008g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1103+871A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800009 | ||||||
| chr5:74800183
|
A | G | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1103+697T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800183 | ||||||
| chr5:74800264
|
GT | G | 149 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(146): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1103+615delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800264 | ||||||
| chr5:74800411
|
A | T | 1 | a0001c0001t0004g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1103+469T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800411 | ||||||
| chr5:74800458
|
T | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1103+422A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800458 | ||||||
| chr5:74800463
|
C | T | 2 | a0001c0001t0005g0157a0001c0001t0005g0214 | 2 | NA18956.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1103+417G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800463 | ||||||
| chr5:74800553
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1103+327A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800553 | ||||||
| chr5:74800575
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1103+305A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800575 | ||||||
| chr5:74800584
|
C | T | 138 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1103+296G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800584 | ||||||
| chr5:74800608
|
T | G | 20 | a0001c0001t0003g0114a0001c0002t0006g0016a0001c0002t0006g0017others(17): Show | 20 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1103+272A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800608 | ||||||
| chr5:74800619
|
T | C | 1 | a0001c0001t0005g0141 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1103+261A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800619 | ||||||
| chr5:74800719
|
AAAAAGTA others(4): Show |
A | 1 | a0001c0001t0002g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1103+150_1103+160d others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 10/12 | chr5 | 74800719 | ||||||
| chr5:74801316
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.952+274G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 9/12 | chr5 | 74801316 | ||||||
| chr5:74801467
|
G | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG01081.hp1 HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.952+123C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 9/12 | chr5 | 74801467 | ||||||
| chr5:74801556
|
A | C | 49 | a0001c0001t0001g0095a0001c0001t0001g0131a0001c0001t0001g0132others(46): Show | 49 | HG00438.hp1 HG00639.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.952+34T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 9/12 | chr5 | 74801556 | ||||||
| chr5:74801650
|
A | C | 1 | a0001c0001t0003g0114 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.913-21T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74801650 | ||||||
| chr5:74801721
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.913-92T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74801721 | ||||||
| chr5:74801727
|
T | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.913-98A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74801727 | ||||||
| chr5:74802014
|
AGTG | A | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.913-388_913-386del others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802014 | ||||||
| chr5:74802357
|
C | T | 1 | a0001c0001t0021g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.913-728G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802357 | ||||||
| chr5:74802396
|
A | G | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.913-767T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802396 | ||||||
| chr5:74802407
|
C | A | 1 | a0001c0001t0004g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.913-778G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802407 | ||||||
| chr5:74802696
|
A | G | 12 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.913-1067T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74802696 | ||||||
| chr5:74803225
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.912+1268C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803225 | ||||||
| chr5:74803366
|
A | G | 1 | a0001c0001t0029g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.912+1127T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803366 | ||||||
| chr5:74803381
|
G | A | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.912+1112C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803381 | ||||||
| chr5:74803476
|
G | A | 1 | a0001c0001t0004g0025 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.912+1017C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803476 | ||||||
| chr5:74803564
|
A | C | 29 | a0001c0001t0003g0114a0001c0001t0013g0229a0001c0001t0013g0230others(26): Show | 29 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.912+929T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803564 | ||||||
| chr5:74803733
|
G | A | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.912+760C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803733 | ||||||
| chr5:74803809
|
C | T | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.912+684G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803809 | ||||||
| chr5:74803932
|
T | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.912+561A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803932 | ||||||
| chr5:74803988
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.912+505C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74803988 | ||||||
| chr5:74804018
|
T | C | 3 | a0001c0002t0012g0232a0001c0002t0012g0233a0001c0002t0018g0231 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.912+475A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74804018 | ||||||
| chr5:74804044
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.912+449A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74804044 | ||||||
| chr5:74804165
|
C | T | 1 | a0001c0006t0011g0040 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.912+328G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74804165 | ||||||
| chr5:74804254
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.912+239C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 8/12 | chr5 | 74804254 | ||||||
| chr5:74804771
|
C | T | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.800-166G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 7/12 | chr5 | 74804771 | ||||||
| chr5:74804816
|
T | C | 1 | a0001c0001t0005g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.800-211A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 7/12 | chr5 | 74804816 | ||||||
| chr5:74805325
|
C | G | 2 | a0001c0001t0004g0050a0001c0001t0004g0051 | 2 | HG00642.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.671-41G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805325 | ||||||
| chr5:74805442
|
ATAAATAA others(6): Show |
A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.671-171_671-159del others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805442 | ||||||
| chr5:74805522
|
C | G | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-238G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805522 | ||||||
| chr5:74805524
|
C | CT | 32 | a0001c0001t0001g0074a0001c0001t0001g0111a0001c0001t0001g0139others(29): Show | 32 | HG00621.hp1 HG00621.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.671-241dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
C | CTT | 16 | a0001c0001t0001g0136a0001c0002t0008g0063a0001c0002t0008g0064others(13): Show | 16 | HG01167.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.671-242_671-241dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
C | CTTTTTT | 45 | a0001c0001t0002g0001a0001c0001t0002g0252a0001c0001t0002g0253others(42): Show | 46 | HG00099.hp1 HG00558.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.671-246_671-241dup others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
C | CTTTTTTT | 21 | a0001c0001t0002g0002a0001c0001t0002g0271a0001c0001t0002g0279others(18): Show | 21 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.671-247_671-241dup others(7): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
C | CTTTTTTT others(9): Show |
1 | a0001c0003t0006g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.671-256_671-241dup others(16): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0004g0050a0001c0002t0006g0016a0001c0002t0006g0019 | 3 | HG00642.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.671-257_671-241dup others(17): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
C | CTTTTTTT others(11): Show |
3 | a0001c0002t0006g0017a0001c0002t0006g0018a0001c0002t0006g0020 | 3 | HG01884.hp2 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.671-258_671-241dup others(18): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
CTT | C | 30 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.671-242_671-241del others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
CTTT | C | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.671-243_671-241del others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.671-250_671-241del others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805524
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.671-251_671-241del others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805524 | ||||||
| chr5:74805619
|
C | T | 29 | a0001c0001t0003g0114a0001c0001t0013g0229a0001c0001t0013g0230others(26): Show | 29 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.671-335G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805619 | ||||||
| chr5:74805633
|
C | T | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.671-349G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805633 | ||||||
| chr5:74805707
|
A | G | 1 | a0001c0002t0012g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.671-423T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805707 | ||||||
| chr5:74805752
|
A | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.671-468T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805752 | ||||||
| chr5:74805793
|
T | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0188a0001c0001t0001g0217 | 3 | HG00735.hp1 HG02148.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.671-509A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805793 | ||||||
| chr5:74805976
|
C | CA | 15 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0133others(12): Show | 15 | HG00642.hp1 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.671-693dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805976 | ||||||
| chr5:74805976
|
C | CAA | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.671-694_671-693dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805976 | ||||||
| chr5:74805976
|
C | CAAA | 11 | a0001c0001t0004g0029a0001c0001t0004g0052a0001c0001t0004g0053others(8): Show | 11 | HG00733.hp1 HG01175.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.671-695_671-693dup others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805976 | ||||||
| chr5:74805976
|
CA | C | 14 | a0001c0001t0003g0114a0001c0001t0003g0128a0001c0001t0003g0180others(11): Show | 14 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.671-693delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74805976 | ||||||
| chr5:74806256
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.671-972C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806256 | ||||||
| chr5:74806440
|
A | C | 1 | a0001c0003t0006g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.671-1156T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806440 | ||||||
| chr5:74806493
|
C | CA | 153 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.671-1210dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806493 | ||||||
| chr5:74806591
|
T | C | 2 | a0001c0003t0006g0224a0001c0003t0006g0225 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.671-1307A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806591 | ||||||
| chr5:74806625
|
G | A | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671-1341C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806625 | ||||||
| chr5:74806960
|
A | AG | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.671-1677dupC | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806960 | ||||||
| chr5:74806984
|
A | G | 2 | a0001c0001t0004g0026a0001c0001t0029g0022 | 2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.671-1700T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74806984 | ||||||
| chr5:74807086
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.671-1802G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807086 | ||||||
| chr5:74807263
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.671-1979G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807263 | ||||||
| chr5:74807370
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.671-2086A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807370 | ||||||
| chr5:74807372
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.671-2088C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807372 | ||||||
| chr5:74807453
|
A | G | 29 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(26): Show | 29 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.671-2169T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807453 | ||||||
| chr5:74807850
|
G | A | 1 | a0001c0001t0032g0254 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.671-2566C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74807850 | ||||||
| chr5:74808255
|
T | C | 1 | a0001c0001t0003g0185 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.671-2971A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808255 | ||||||
| chr5:74808421
|
AT | A | 41 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(38): Show | 41 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.671-3138delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808421 | ||||||
| chr5:74808426
|
C | G | 41 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(38): Show | 41 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.671-3142G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808426 | ||||||
| chr5:74808544
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.671-3260A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808544 | ||||||
| chr5:74808577
|
CTG | C | 3 | a0001c0001t0002g0001a0001c0001t0002g0264a0001c0001t0002g0266 | 4 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-3295_671-3294d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808577 | ||||||
| chr5:74808664
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.671-3380T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808664 | ||||||
| chr5:74808686
|
T | C | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.671-3402A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808686 | ||||||
| chr5:74808709
|
A | C | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.671-3425T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808709 | ||||||
| chr5:74808742
|
G | C | 8 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(5): Show | 8 | HG02559.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-3458C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808742 | ||||||
| chr5:74808757
|
C | A | 1 | a0001c0001t0029g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.671-3473G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808757 | ||||||
| chr5:74808984
|
T | A | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.671-3700A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74808984 | ||||||
| chr5:74809364
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.671-4080C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809364 | ||||||
| chr5:74809469
|
G | A | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.671-4185C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809469 | ||||||
| chr5:74809501
|
CAGG | C | 12 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.671-4220_671-4218d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809501 | ||||||
| chr5:74809512
|
C | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.671-4228G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809512 | ||||||
| chr5:74809513
|
G | A | 3 | a0001c0001t0001g0193a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01884.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.671-4229C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809513 | ||||||
| chr5:74809679
|
T | C | 1 | a0001c0001t0009g0261 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.670+4161A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809679 | ||||||
| chr5:74809908
|
A | G | 1 | a0001c0003t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670+3932T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74809908 | ||||||
| chr5:74810233
|
C | A | 1 | a0001c0001t0003g0180 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.670+3607G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810233 | ||||||
| chr5:74810414
|
C | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG01884.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.670+3426G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810414 | ||||||
| chr5:74810415
|
A | G | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.670+3425T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810415 | ||||||
| chr5:74810441
|
GTGTACGG others(4): Show |
G | 1 | a0001c0003t0006g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.670+3388_670+3398d others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810441 | ||||||
| chr5:74810675
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.670+3165C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810675 | ||||||
| chr5:74810751
|
C | CA | 9 | a0001c0001t0001g0239a0001c0001t0003g0104a0001c0001t0003g0106others(6): Show | 9 | HG00738.hp1 HG01515.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+3088dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810751 | ||||||
| chr5:74810751
|
CA | C | 86 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0092others(83): Show | 86 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.670+3088delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810751 | ||||||
| chr5:74810751
|
CAA | C | 149 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.670+3087_670+3088d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810751 | ||||||
| chr5:74810751
|
CAAA | C | 17 | a0001c0001t0004g0030a0001c0002t0008g0062a0001c0002t0008g0063others(14): Show | 17 | HG00438.hp1 HG00735.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+3086_670+3088d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810751 | ||||||
| chr5:74810819
|
C | CT | 17 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0001g0100others(14): Show | 17 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+3020dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | ||||||
| chr5:74810819
|
CT | C | 15 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0003g0119others(12): Show | 15 | HG00323.hp1 HG00741.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+3020delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | ||||||
| chr5:74810819
|
CTT | C | 20 | a0001c0001t0007g0012a0001c0001t0007g0014a0001c0002t0008g0062others(17): Show | 20 | HG01167.hp1 HG02145.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.670+3019_670+3020d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | ||||||
| chr5:74810819
|
CTTT | C | 19 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(16): Show | 19 | HG00438.hp1 HG00735.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.670+3018_670+3020d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | ||||||
| chr5:74810819
|
CTTTTTTT | C | 94 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(91): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.670+3014_670+3020d others(9): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810819 | ||||||
| chr5:74810974
|
A | AT | 95 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0100others(92): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.670+2865dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810974 | ||||||
| chr5:74810974
|
A | ATT | 26 | a0001c0001t0002g0252a0001c0001t0002g0255a0001c0001t0002g0273others(23): Show | 26 | HG00642.hp1 HG01109.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.670+2864_670+2865d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810974 | ||||||
| chr5:74810974
|
AT | A | 36 | a0001c0001t0001g0238a0001c0001t0006g0060a0001c0001t0007g0006others(33): Show | 36 | HG00438.hp1 HG00735.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.670+2865delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74810974 | ||||||
| chr5:74811166
|
T | A | 2 | a0001c0001t0005g0157a0001c0001t0005g0214 | 2 | NA18956.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.670+2674A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811166 | ||||||
| chr5:74811505
|
C | G | 41 | a0001c0001t0031g0004a0001c0002t0006g0016a0001c0002t0006g0017others(38): Show | 41 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.670+2335G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811505 | ||||||
| chr5:74811694
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.670+2146T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811694 | ||||||
| chr5:74811789
|
G | A | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(117): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.670+2051C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811789 | ||||||
| chr5:74811832
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0021g0094 | 3 | HG01891.hp2 HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.670+2008A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811832 | ||||||
| chr5:74811912
|
C | G | 1 | a0001c0003t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670+1928G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74811912 | ||||||
| chr5:74812021
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.670+1819A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812021 | ||||||
| chr5:74812185
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0021g0094 | 3 | HG01891.hp2 HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.670+1655C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812185 | ||||||
| chr5:74812255
|
C | T | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+1585G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812255 | ||||||
| chr5:74812466
|
G | A | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.670+1374C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812466 | ||||||
| chr5:74812565
|
C | A | 13 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0001t0007g0005others(10): Show | 13 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.670+1275G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812565 | ||||||
| chr5:74812653
|
C | A | 1 | a0001c0001t0017g0130 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.670+1187G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812653 | ||||||
| chr5:74812819
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.670+1021C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812819 | ||||||
| chr5:74812958
|
C | T | 1 | a0001c0002t0012g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.670+882G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74812958 | ||||||
| chr5:74813247
|
A | T | 6 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+593T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813247 | ||||||
| chr5:74813249
|
A | T | 6 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+591T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813249 | ||||||
| chr5:74813289
|
A | C | 4 | a0001c0001t0005g0122a0001c0001t0005g0124a0001c0001t0005g0147others(1): Show | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+551T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813289 | ||||||
| chr5:74813507
|
G | A | 19 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(16): Show | 19 | HG00438.hp1 HG00735.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.670+333C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813507 | ||||||
| chr5:74813677
|
G | A | 8 | a0001c0001t0003g0079a0001c0001t0003g0108a0001c0001t0003g0146others(5): Show | 8 | HG00438.hp2 HG02015.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+163C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813677 | ||||||
| chr5:74813691
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.670+149T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813691 | ||||||
| chr5:74813701
|
A | T | 1 | a0001c0002t0008g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.670+139T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813701 | ||||||
| chr5:74813807
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.670+33G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | 74813807 | ||||||
| chr5:74814076
|
T | C | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-57A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74814076 | ||||||
| chr5:74814584
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.491-565A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74814584 | ||||||
| chr5:74814616
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.491-597A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74814616 | ||||||
| chr5:74815026
|
C | A | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-1007G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815026 | ||||||
| chr5:74815161
|
AATATACT others(5): Show |
A | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.491-1154_491-1143d others(14): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815161 | ||||||
| chr5:74815196
|
CT | C | 152 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.491-1178delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815196 | ||||||
| chr5:74815228
|
T | G | 33 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.491-1209A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815228 | ||||||
| chr5:74815247
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.491-1228A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815247 | ||||||
| chr5:74815249
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.491-1230C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815249 | ||||||
| chr5:74815338
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.491-1319G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815338 | ||||||
| chr5:74815339
|
G | A | 3 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0003t0006g0228 | 3 | HG00438.hp1 HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-1320C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815339 | ||||||
| chr5:74815380
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.491-1361C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815380 | ||||||
| chr5:74815425
|
A | G | 1 | a0001c0001t0004g0025 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.491-1406T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815425 | ||||||
| chr5:74815510
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.491-1491A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815510 | ||||||
| chr5:74815576
|
C | T | 21 | a0001c0001t0013g0229a0001c0001t0013g0230a0001c0002t0006g0016others(18): Show | 21 | HG00438.hp1 HG00735.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.491-1557G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815576 | ||||||
| chr5:74815878
|
T | C | 1 | a0001c0001t0007g0009 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.491-1859A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815878 | ||||||
| chr5:74815912
|
C | G | 152 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.491-1893G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74815912 | ||||||
| chr5:74816147
|
T | C | 7 | a0001c0001t0013g0229a0001c0001t0013g0230a0001c0003t0006g0221others(4): Show | 7 | HG00438.hp1 HG00735.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-2128A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816147 | ||||||
| chr5:74816159
|
C | T | 1 | a0001c0003t0006g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.491-2140G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816159 | ||||||
| chr5:74816165
|
A | G | 1 | a0001c0001t0007g0011 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.491-2146T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816165 | ||||||
| chr5:74816271
|
T | A | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.491-2252A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816271 | ||||||
| chr5:74816409
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.491-2390A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816409 | ||||||
| chr5:74816445
|
A | T | 1 | a0001c0001t0004g0038 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.491-2426T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816445 | ||||||
| chr5:74816465
|
C | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.491-2446G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74816465 | ||||||
| chr5:74817010
|
G | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.491-2991C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817010 | ||||||
| chr5:74817395
|
C | T | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(117): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.491-3376G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817395 | ||||||
| chr5:74817797
|
C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.491-3778G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817797 | ||||||
| chr5:74817869
|
T | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.491-3850A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817869 | ||||||
| chr5:74817927
|
T | C | 1 | a0001c0001t0011g0041 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.491-3908A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74817927 | ||||||
| chr5:74818570
|
G | GC | 39 | a0001c0001t0001g0086a0001c0001t0001g0097a0001c0001t0001g0171others(36): Show | 39 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.491-4552dupG | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818570 | ||||||
| chr5:74818572
|
C | G | 2 | a0001c0001t0004g0057a0001c0001t0004g0058 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.491-4553G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818572 | ||||||
| chr5:74818577
|
C | G | 2 | a0001c0001t0002g0275a0001c0001t0002g0286 | 2 | NA18953.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.491-4558G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818577 | ||||||
| chr5:74818704
|
A | G | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-4685T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818704 | ||||||
| chr5:74818736
|
C | T | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-4717G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818736 | ||||||
| chr5:74818737
|
G | A | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-4718C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818737 | ||||||
| chr5:74818753
|
G | A | 1 | a0001c0001t0020g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.491-4734C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818753 | ||||||
| chr5:74818770
|
G | GCT | 15 | a0001c0001t0001g0085a0001c0001t0001g0163a0001c0001t0001g0192others(12): Show | 15 | HG00673.hp1 HG01192.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.491-4753_491-4752d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | ||||||
| chr5:74818770
|
GCT | G | 10 | a0001c0001t0001g0235a0001c0001t0004g0051a0001c0001t0007g0011others(7): Show | 10 | HG01884.hp2 HG02647.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-4753_491-4752d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | ||||||
| chr5:74818770
|
GCTCT | G | 14 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(11): Show | 14 | HG01167.hp1 HG02258.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.491-4755_491-4752d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | ||||||
| chr5:74818770
|
GCTCTCT | G | 3 | a0001c0001t0001g0097a0001c0001t0002g0300a0001c0001t0004g0052 | 3 | HG00733.hp1 HG02027.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.491-4757_491-4752d others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | ||||||
| chr5:74818770
|
GCTCTCTC others(1): Show |
G | 59 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0255others(56): Show | 59 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.491-4759_491-4752d others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | ||||||
| chr5:74818770
|
GCTCTCTC others(3): Show |
G | 3 | a0001c0002t0008g0066a0001c0002t0008g0070a0001c0002t0008g0071 | 3 | HG02451.hp2 HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.491-4761_491-4752d others(12): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818770 | ||||||
| chr5:74818789
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-4786_491-4771d others(18): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818789 | ||||||
| chr5:74818795
|
CTCTCTCT others(3): Show |
C | 8 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(5): Show | 8 | HG02145.hp2 HG02723.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-4786_491-4777d others(12): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818795 | ||||||
| chr5:74818797
|
C | A | 1 | a0001c0001t0004g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.491-4778G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818797 | ||||||
| chr5:74818797
|
C | CTA | 4 | a0001c0001t0004g0034a0001c0001t0004g0035a0001c0001t0004g0047others(1): Show | 4 | HG01069.hp2 HG01515.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-4779_491-4778i others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818797 | ||||||
| chr5:74818797
|
CTCTCTCT others(1): Show |
C | 12 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0264others(9): Show | 13 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.491-4786_491-4779d others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818797 | ||||||
| chr5:74818797
|
CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.491-4790_491-4779d others(14): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818797 | ||||||
| chr5:74818799
|
C | A | 9 | a0001c0001t0001g0084a0001c0001t0004g0030a0001c0001t0004g0034others(6): Show | 9 | HG01069.hp2 HG01081.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-4780G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818799 | ||||||
| chr5:74818799
|
C | CTA | 11 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0033others(8): Show | 11 | HG00140.hp2 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-4781_491-4780i others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818799 | ||||||
| chr5:74818799
|
C | CTATA | 3 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0039 | 3 | HG00280.hp2 HG01255.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.491-4781_491-4780i others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818799 | ||||||
| chr5:74818799
|
CTCTCTA | C | 3 | a0001c0002t0010g0247a0001c0002t0010g0248a0001c0002t0018g0231 | 3 | HG00741.hp2 HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.491-4786_491-4781d others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818799 | ||||||
| chr5:74818801
|
C | A | 25 | a0001c0001t0001g0084a0001c0001t0004g0003a0001c0001t0004g0021others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.491-4782G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818801 | ||||||
| chr5:74818801
|
C | CTA | 4 | a0001c0001t0004g0026a0001c0001t0004g0029a0001c0001t0011g0044others(1): Show | 4 | HG00738.hp2 HG01243.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-4783_491-4782i others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818801 | ||||||
| chr5:74818801
|
CTCTA | C | 3 | a0001c0003t0006g0223a0001c0003t0006g0227a0001c0003t0006g0228 | 3 | HG00438.hp1 HG00735.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.491-4786_491-4783d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818801 | ||||||
| chr5:74818803
|
C | A | 60 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0084others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.491-4784G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | ||||||
| chr5:74818803
|
C | CTA | 8 | a0001c0001t0001g0102a0001c0001t0001g0302a0001c0001t0003g0114others(5): Show | 8 | HG00673.hp2 HG01074.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-4786_491-4785d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | ||||||
| chr5:74818803
|
C | CTATATA | 4 | a0001c0001t0004g0023a0001c0001t0004g0036a0001c0001t0006g0060others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-4790_491-4785d others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | ||||||
| chr5:74818803
|
CTA | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0002t0006g0017 | 3 | HG02083.hp2 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.491-4786_491-4785d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | ||||||
| chr5:74818803
|
CTATA | C | 3 | a0001c0002t0012g0232a0001c0003t0006g0221a0001c0003t0006g0226 | 3 | HG03098.hp2 NA18982.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.491-4788_491-4785d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818803 | ||||||
| chr5:74818805
|
A | C | 82 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0085others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.491-4786T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818805 | ||||||
| chr5:74818807
|
A | C | 56 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0081others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.491-4788T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818807 | ||||||
| chr5:74818809
|
A | C | 14 | a0001c0001t0001g0090a0001c0001t0001g0135a0001c0001t0001g0305others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.491-4790T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818809 | ||||||
| chr5:74818811
|
A | C | 3 | a0001c0001t0005g0158a0001c0001t0005g0182a0001c0001t0005g0210 | 3 | HG00741.hp1 HG01978.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.491-4792T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818811 | ||||||
| chr5:74818841
|
C | A | 150 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(147): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.491-4822G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818841 | ||||||
| chr5:74818947
|
C | T | 13 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0001t0007g0005others(10): Show | 13 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-4928G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74818947 | ||||||
| chr5:74819024
|
G | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.491-5005C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819024 | ||||||
| chr5:74819162
|
C | T | 110 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.491-5143G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819162 | ||||||
| chr5:74819257
|
C | A | 1 | a0001c0001t0002g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.491-5238G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819257 | ||||||
| chr5:74819362
|
C | G | 1 | a0001c0001t0005g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.491-5343G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819362 | ||||||
| chr5:74819501
|
A | C | 1 | a0001c0001t0011g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.491-5482T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819501 | ||||||
| chr5:74819513
|
G | A | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(176): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.491-5494C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819513 | ||||||
| chr5:74819665
|
A | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.491-5646T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819665 | ||||||
| chr5:74819804
|
A | G | 1 | a0001c0001t0003g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.491-5785T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819804 | ||||||
| chr5:74819911
|
G | T | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-5892C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819911 | ||||||
| chr5:74819924
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.491-5905A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819924 | ||||||
| chr5:74819993
|
C | CT | 68 | a0001c0001t0001g0093a0001c0001t0001g0100a0001c0001t0001g0172others(65): Show | 68 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.491-5975dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819993 | ||||||
| chr5:74819993
|
C | CTT | 15 | a0001c0001t0002g0001a0001c0001t0002g0264a0001c0001t0002g0266others(12): Show | 16 | HG00099.hp1 HG00408.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.491-5976_491-5975d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819993 | ||||||
| chr5:74819993
|
C | CTTT | 39 | a0001c0001t0004g0003a0001c0001t0004g0023a0001c0001t0004g0024others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.491-5977_491-5975d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819993 | ||||||
| chr5:74819993
|
CTTTT | C | 6 | a0001c0003t0006g0103a0001c0003t0006g0224a0001c0003t0006g0225others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-5978_491-5975d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74819993 | ||||||
| chr5:74820059
|
G | A | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-6040C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74820059 | ||||||
| chr5:74820610
|
C | T | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-6591G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74820610 | ||||||
| chr5:74820951
|
G | C | 8 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(5): Show | 8 | HG02559.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-6932C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74820951 | ||||||
| chr5:74821195
|
T | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.491-7176A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821195 | ||||||
| chr5:74821328
|
T | C | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.491-7309A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821328 | ||||||
| chr5:74821671
|
A | G | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-7652T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821671 | ||||||
| chr5:74821697
|
C | T | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-7678G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821697 | ||||||
| chr5:74821814
|
T | G | 1 | a0001c0001t0009g0288 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.491-7795A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821814 | ||||||
| chr5:74821949
|
G | A | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.491-7930C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74821949 | ||||||
| chr5:74822117
|
T | G | 1 | a0001c0004t0002g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.491-8098A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822117 | ||||||
| chr5:74822132
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.491-8113C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822132 | ||||||
| chr5:74822483
|
A | G | 1 | a0001c0003t0006g0226 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.491-8464T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822483 | ||||||
| chr5:74822660
|
C | T | 1 | a0001c0001t0007g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.491-8641G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822660 | ||||||
| chr5:74822812
|
ACTC | A | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-8796_491-8794d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822812 | ||||||
| chr5:74822893
|
T | C | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-8874A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822893 | ||||||
| chr5:74822970
|
T | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.491-8951A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74822970 | ||||||
| chr5:74823006
|
G | A | 40 | a0001c0001t0031g0004a0001c0002t0006g0016a0001c0002t0006g0017others(37): Show | 40 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.491-8987C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823006 | ||||||
| chr5:74823121
|
C | T | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-9102G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823121 | ||||||
| chr5:74823289
|
C | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0211 | 3 | HG01516.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.491-9270G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823289 | ||||||
| chr5:74823355
|
C | T | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.491-9336G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823355 | ||||||
| chr5:74823477
|
G | A | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(117): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.491-9458C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823477 | ||||||
| chr5:74823636
|
G | A | 1 | a0001c0001t0022g0181 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.491-9617C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823636 | ||||||
| chr5:74823661
|
G | A | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.491-9642C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823661 | ||||||
| chr5:74823713
|
G | A | 2 | a0001c0001t0009g0257a0001c0001t0009g0258 | 2 | NA18952.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.491-9694C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823713 | ||||||
| chr5:74823850
|
T | G | 1 | a0001c0001t0003g0197 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.491-9831A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823850 | ||||||
| chr5:74823901
|
C | G | 13 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0080others(10): Show | 13 | HG01074.hp1 HG01346.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-9882G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74823901 | ||||||
| chr5:74824141
|
C | T | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(133): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.491-10122G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824141 | ||||||
| chr5:74824157
|
T | C | 1 | a0001c0003t0006g0249 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.491-10138A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824157 | ||||||
| chr5:74824301
|
T | C | 1 | a0001c0002t0008g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+10125A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824301 | ||||||
| chr5:74824334
|
G | A | 1 | a0001c0001t0004g0049 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.490+10092C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824334 | ||||||
| chr5:74824402
|
C | T | 7 | a0001c0001t0004g0003a0001c0001t0004g0024a0001c0001t0004g0025others(4): Show | 7 | HG02735.hp1 HG03239.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.490+10024G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824402 | ||||||
| chr5:74824677
|
GCT | G | 13 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0001t0007g0005others(10): Show | 13 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.490+9747_490+9748d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824677 | ||||||
| chr5:74824708
|
TAC | T | 49 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0006g0060others(46): Show | 49 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.490+9716_490+9717d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824708 | ||||||
| chr5:74824708
|
TACAC | T | 97 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.490+9714_490+9717d others(6): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824708 | ||||||
| chr5:74824972
|
C | T | 1 | a0001c0001t0004g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.490+9454G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74824972 | ||||||
| chr5:74825577
|
C | T | 44 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0078others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.490+8849G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825577 | ||||||
| chr5:74825773
|
C | T | 8 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(5): Show | 8 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.490+8653G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825773 | ||||||
| chr5:74825797
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.490+8629A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825797 | ||||||
| chr5:74825815
|
T | C | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+8611A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825815 | ||||||
| chr5:74825821
|
G | A | 44 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0078others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.490+8605C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74825821 | ||||||
| chr5:74826250
|
A | G | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+8176T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826250 | ||||||
| chr5:74826503
|
G | A | 109 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.490+7923C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826503 | ||||||
| chr5:74826574
|
T | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.490+7852A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826574 | ||||||
| chr5:74826602
|
C | T | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.490+7824G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826602 | ||||||
| chr5:74826658
|
T | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.490+7768A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74826658 | ||||||
| chr5:74827144
|
T | C | 1 | a0001c0001t0002g0256 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.490+7282A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827144 | ||||||
| chr5:74827302
|
G | A | 151 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.490+7124C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827302 | ||||||
| chr5:74827669
|
C | CT | 11 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0003g0114others(8): Show | 11 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+6756dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827669 | ||||||
| chr5:74827694
|
T | G | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.490+6732A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827694 | ||||||
| chr5:74827706
|
A | T | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+6720T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827706 | ||||||
| chr5:74827837
|
A | AT | 59 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(56): Show | 60 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.490+6588dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827837 | ||||||
| chr5:74827930
|
T | A | 1 | a0001c0001t0005g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490+6496A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827930 | ||||||
| chr5:74827937
|
A | G | 1 | a0001c0001t0002g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+6489T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827937 | ||||||
| chr5:74827979
|
T | C | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+6447A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74827979 | ||||||
| chr5:74828021
|
A | G | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+6405T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828021 | ||||||
| chr5:74828054
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490+6372A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828054 | ||||||
| chr5:74828092
|
T | C | 1 | a0001c0002t0012g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490+6334A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828092 | ||||||
| chr5:74828119
|
T | C | 3 | a0001c0001t0004g0033a0001c0001t0004g0034a0001c0001t0004g0035 | 3 | HG01069.hp2 HG01071.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.490+6307A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828119 | ||||||
| chr5:74828209
|
T | C | 1 | a0001c0001t0002g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+6217A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828209 | ||||||
| chr5:74828307
|
C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490+6119G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828307 | ||||||
| chr5:74828456
|
T | A | 1 | a0001c0001t0002g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+5970A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828456 | ||||||
| chr5:74828460
|
T | A | 1 | a0001c0001t0002g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+5966A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828460 | ||||||
| chr5:74828461
|
T | A | 1 | a0001c0001t0002g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+5965A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828461 | ||||||
| chr5:74828501
|
C | T | 139 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.490+5925G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828501 | ||||||
| chr5:74828715
|
C | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.490+5711G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828715 | ||||||
| chr5:74828780
|
G | A | 1 | a0001c0002t0008g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+5646C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828780 | ||||||
| chr5:74828964
|
C | T | 109 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.490+5462G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828964 | ||||||
| chr5:74828973
|
G | A | 1 | a0001c0001t0017g0130 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.490+5453C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74828973 | ||||||
| chr5:74829056
|
G | A | 54 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.490+5370C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829056 | ||||||
| chr5:74829056
|
G | T | 1 | a0001c0001t0005g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.490+5370C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829056 | ||||||
| chr5:74829065
|
A | G | 16 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(13): Show | 16 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.490+5361T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829065 | ||||||
| chr5:74829437
|
A | T | 22 | a0001c0001t0001g0074a0001c0001t0001g0095a0001c0001t0001g0109others(19): Show | 22 | HG00639.hp1 HG01074.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.490+4989T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829437 | ||||||
| chr5:74829463
|
C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490+4963G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829463 | ||||||
| chr5:74829475
|
A | T | 8 | a0001c0001t0003g0114a0001c0001t0013g0229a0001c0001t0013g0230others(5): Show | 8 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+4951T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829475 | ||||||
| chr5:74829611
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490+4815A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829611 | ||||||
| chr5:74829615
|
G | A | 2 | a0001c0002t0008g0070a0001c0002t0008g0072 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.490+4811C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829615 | ||||||
| chr5:74829636
|
C | A | 1 | a0001c0001t0002g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490+4790G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829636 | ||||||
| chr5:74829668
|
T | C | 1 | a0001c0001t0005g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490+4758A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829668 | ||||||
| chr5:74829680
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.490+4746A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829680 | ||||||
| chr5:74829684
|
A | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+4742T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829684 | ||||||
| chr5:74829771
|
C | T | 1 | a0001c0002t0008g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490+4655G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829771 | ||||||
| chr5:74829825
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.490+4601A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74829825 | ||||||
| chr5:74830517
|
A | G | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+3909T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74830517 | ||||||
| chr5:74830532
|
T | C | 1 | a0001c0001t0004g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490+3894A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74830532 | ||||||
| chr5:74830539
|
A | C | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+3887T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74830539 | ||||||
| chr5:74830785
|
G | A | 1 | a0001c0002t0016g0212 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.490+3641C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74830785 | ||||||
| chr5:74831057
|
C | A | 1 | a0001c0001t0004g0024 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.490+3369G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831057 | ||||||
| chr5:74831138
|
GA | G | 3 | a0001c0001t0002g0001a0001c0001t0002g0264a0001c0001t0002g0266 | 4 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+3287delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831138 | ||||||
| chr5:74831157
|
C | T | 110 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.490+3269G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831157 | ||||||
| chr5:74831286
|
C | T | 152 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.490+3140G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831286 | ||||||
| chr5:74831360
|
T | G | 1 | a0001c0001t0003g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490+3066A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831360 | ||||||
| chr5:74831879
|
T | C | 1 | a0001c0001t0004g0035 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.490+2547A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831879 | ||||||
| chr5:74831985
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0021g0094 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.490+2441G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74831985 | ||||||
| chr5:74832377
|
A | C | 2 | a0001c0003t0006g0240a0001c0003t0015g0241 | 2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.490+2049T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832377 | ||||||
| chr5:74832576
|
C | T | 150 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(147): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.490+1850G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832576 | ||||||
| chr5:74832587
|
A | T | 1 | a0001c0001t0028g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.490+1839T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832587 | ||||||
| chr5:74832672
|
T | C | 1 | a0001c0003t0006g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.490+1754A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832672 | ||||||
| chr5:74832675
|
A | G | 5 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0033others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+1751T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74832675 | ||||||
| chr5:74833008
|
A | C | 2 | a0001c0001t0004g0050a0001c0001t0004g0051 | 2 | HG00642.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.490+1418T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833008 | ||||||
| chr5:74833123
|
A | G | 1 | a0001c0003t0006g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.490+1303T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833123 | ||||||
| chr5:74833139
|
A | G | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.490+1287T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833139 | ||||||
| chr5:74833181
|
G | A | 2 | a0001c0001t0002g0270a0001c0001t0002g0281 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.490+1245C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833181 | ||||||
| chr5:74833285
|
AAAC | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.490+1138_490+1140d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833285 | ||||||
| chr5:74833292
|
A | G | 8 | a0001c0001t0031g0004a0001c0002t0010g0242a0001c0002t0010g0243others(5): Show | 8 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.490+1134T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833292 | ||||||
| chr5:74833679
|
A | C | 1 | a0001c0001t0003g0114 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.490+747T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833679 | ||||||
| chr5:74833738
|
T | C | 1 | a0001c0001t0003g0185 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.490+688A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833738 | ||||||
| chr5:74833935
|
T | C | 1 | a0001c0002t0012g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.490+491A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74833935 | ||||||
| chr5:74834029
|
A | C | 8 | a0001c0001t0001g0078a0001c0002t0010g0242a0001c0002t0010g0243others(5): Show | 8 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.490+397T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834029 | ||||||
| chr5:74834217
|
G | A | 1 | a0001c0003t0006g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.490+209C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834217 | ||||||
| chr5:74834295
|
C | T | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.490+131G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834295 | ||||||
| chr5:74834329
|
T | A | 1 | a0001c0001t0005g0158 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.490+97A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834329 | ||||||
| chr5:74834353
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.490+73A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 5/12 | chr5 | 74834353 | ||||||
| chr5:74834779
|
C | T | 3 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0219 | 3 | HG02056.hp2 NA18949.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.319-182G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834779 | ||||||
| chr5:74834839
|
T | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.319-242A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834839 | ||||||
| chr5:74834840
|
C | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.319-243G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834840 | ||||||
| chr5:74834848
|
A | G | 1 | a0001c0002t0010g0244 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.319-251T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834848 | ||||||
| chr5:74834999
|
T | TA | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(99): Show | 103 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.319-403dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834999 | ||||||
| chr5:74834999
|
T | TAA | 45 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0024others(42): Show | 45 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.319-404_319-403dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74834999 | ||||||
| chr5:74835041
|
C | T | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-444G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835041 | ||||||
| chr5:74835185
|
T | C | 1 | a0001c0001t0004g0043 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.319-588A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835185 | ||||||
| chr5:74835250
|
A | G | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-653T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835250 | ||||||
| chr5:74835276
|
C | T | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-679G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835276 | ||||||
| chr5:74835405
|
C | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.319-808G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835405 | ||||||
| chr5:74835601
|
C | CA | 69 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0097others(66): Show | 69 | HG00140.hp2 HG00673.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.319-1005dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835601 | ||||||
| chr5:74835601
|
CA | C | 71 | a0001c0001t0001g0195a0001c0001t0002g0001a0001c0001t0002g0002others(68): Show | 72 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.319-1005delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74835601 | ||||||
| chr5:74836067
|
A | G | 1 | a0001c0001t0011g0041 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.319-1470T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836067 | ||||||
| chr5:74836326
|
GTTT | G | 40 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(37): Show | 40 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.319-1732_319-1730d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836326 | ||||||
| chr5:74836458
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.319-1861C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836458 | ||||||
| chr5:74836514
|
A | C | 1 | a0001c0003t0006g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.319-1917T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836514 | ||||||
| chr5:74836662
|
C | T | 1 | a0001c0001t0005g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.319-2065G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836662 | ||||||
| chr5:74836663
|
G | A | 2 | a0001c0001t0007g0007a0001c0001t0007g0010 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.319-2066C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836663 | ||||||
| chr5:74836872
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0151a0001c0001t0001g0183others(1): Show | 4 | HG01928.hp2 HG01975.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+2093G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836872 | ||||||
| chr5:74836892
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0134 | 3 | HG01346.hp1 HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.318+2073C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836892 | ||||||
| chr5:74836935
|
G | C | 1 | a0001c0003t0015g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.318+2030C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836935 | ||||||
| chr5:74836943
|
CA | C | 172 | a0001c0001t0001g0086a0001c0001t0001g0097a0001c0001t0001g0101others(169): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.318+2021delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74836943 | ||||||
| chr5:74837184
|
T | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.318+1781A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837184 | ||||||
| chr5:74837461
|
G | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.318+1504C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837461 | ||||||
| chr5:74837692
|
G | A | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.318+1273C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837692 | ||||||
| chr5:74837737
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0021g0094 | 3 | HG01891.hp2 HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.318+1228C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837737 | ||||||
| chr5:74837939
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.318+1026C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74837939 | ||||||
| chr5:74838114
|
C | CA | 35 | a0001c0001t0001g0188a0001c0001t0002g0002a0001c0001t0002g0260others(32): Show | 35 | HG00438.hp1 HG00738.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.318+850dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838114 | ||||||
| chr5:74838208
|
T | C | 1 | a0001c0001t0003g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.318+757A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838208 | ||||||
| chr5:74838418
|
A | G | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.318+547T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838418 | ||||||
| chr5:74838434
|
A | G | 1 | a0001c0001t0002g0265 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.318+531T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838434 | ||||||
| chr5:74838489
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.318+476G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838489 | ||||||
| chr5:74838515
|
A | G | 1 | a0001c0003t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318+450T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838515 | ||||||
| chr5:74838802
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0131a0001c0001t0001g0194others(1): Show | 4 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+163C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838802 | ||||||
| chr5:74838829
|
C | T | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.318+136G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838829 | ||||||
| chr5:74838917
|
T | C | 39 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.318+48A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838917 | ||||||
| chr5:74838951
|
G | GAGGATCT others(4): Show |
1 | a0001c0001t0001g0187 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.318+3_318+13dupAAC others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 4/12 | chr5 | 74838951 | ||||||
| chr5:74839131
|
G | C | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-81C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839131 | ||||||
| chr5:74839265
|
G | A | 1 | a0001c0001t0011g0041 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.233-215C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839265 | ||||||
| chr5:74839386
|
T | C | 1 | a0001c0004t0002g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.233-336A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839386 | ||||||
| chr5:74839463
|
C | T | 1 | a0001c0003t0006g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.233-413G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839463 | ||||||
| chr5:74839465
|
T | C | 2 | a0001c0003t0006g0249a0001c0003t0006g0250 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.233-415A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839465 | ||||||
| chr5:74839522
|
A | ATT | 13 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(10): Show | 13 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.233-474_233-473dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839522 | ||||||
| chr5:74839522
|
AT | A | 92 | a0001c0001t0001g0081a0001c0001t0001g0195a0001c0001t0002g0001others(89): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.233-473delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839522 | ||||||
| chr5:74839617
|
T | C | 1 | a0001c0004t0002g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.232+457A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839617 | ||||||
| chr5:74839627
|
C | T | 3 | a0001c0002t0012g0232a0001c0002t0012g0233a0001c0002t0018g0231 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.232+447G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839627 | ||||||
| chr5:74839989
|
T | C | 1 | a0001c0001t0009g0259 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.232+85A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74839989 | ||||||
| chr5:74840006
|
C | A | 6 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+68G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74840006 | ||||||
| chr5:74840057
|
A | C | 1 | a0001c0001t0001g0216 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.232+17T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3/12 | chr5 | 74840057 | ||||||
| chr5:74840290
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.133-117C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840290 | ||||||
| chr5:74840374
|
T | C | 47 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.133-201A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840374 | ||||||
| chr5:74840396
|
T | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.133-223A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840396 | ||||||
| chr5:74840526
|
TA | T | 15 | a0001c0001t0004g0027a0001c0001t0006g0060a0001c0001t0006g0061others(12): Show | 15 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.133-354delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840526 | ||||||
| chr5:74840567
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.133-394T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840567 | ||||||
| chr5:74840646
|
A | G | 4 | a0001c0001t0001g0080a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG01516.hp2 HG02735.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-473T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840646 | ||||||
| chr5:74840657
|
A | G | 1 | a0001c0001t0004g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.133-484T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840657 | ||||||
| chr5:74840791
|
T | A | 1 | a0001c0001t0033g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133-618A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840791 | ||||||
| chr5:74840974
|
T | C | 2 | a0001c0001t0013g0229a0001c0001t0013g0230 | 2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.132+571A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 2/12 | chr5 | 74840974 | ||||||
| chr5:74841716
|
T | C | 24 | a0001c0001t0002g0253a0001c0001t0002g0255a0001c0001t0002g0260others(21): Show | 24 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3-37A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74841716 | ||||||
| chr5:74841809
|
G | A | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-3-130C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74841809 | ||||||
| chr5:74841914
|
T | C | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3-235A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74841914 | ||||||
| chr5:74842010
|
A | T | 1 | a0001c0001t0005g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-3-331T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842010 | ||||||
| chr5:74842011
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-3-332G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842011 | ||||||
| chr5:74842041
|
G | A | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-362C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842041 | ||||||
| chr5:74842043
|
G | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-364C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842043 | ||||||
| chr5:74842057
|
A | T | 1 | a0001c0001t0002g0287 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-3-378T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842057 | ||||||
| chr5:74842058
|
A | C | 1 | a0001c0001t0002g0287 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-3-379T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842058 | ||||||
| chr5:74842125
|
AT | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-447delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842125 | ||||||
| chr5:74842144
|
G | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-3-465C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842144 | ||||||
| chr5:74842193
|
AG | A | 153 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(150): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-3-515delC | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842193 | ||||||
| chr5:74842231
|
G | A | 1 | a0001c0004t0002g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-3-552C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842231 | ||||||
| chr5:74842420
|
C | CA | 28 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0088others(25): Show | 28 | HG00408.hp1 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.-3-742dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
C | CAA | 20 | a0001c0001t0001g0187a0001c0001t0001g0208a0001c0001t0002g0265others(17): Show | 20 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.-3-743_-3-742dupTT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
C | CAAA | 25 | a0001c0001t0002g0252a0001c0001t0002g0256a0001c0001t0002g0262others(22): Show | 25 | HG01109.hp1 HG01175.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3-744_-3-742dupTT others(1): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
C | CAAAA | 8 | a0001c0001t0001g0140a0001c0001t0002g0255a0001c0001t0002g0260others(5): Show | 8 | HG00408.hp2 HG00558.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3-745_-3-742dupTT others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
CA | C | 61 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(58): Show | 61 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-3-742delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
CAA | C | 19 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0001g0120others(16): Show | 19 | HG00733.hp1 HG01074.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3-743_-3-742delTT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
CAAA | C | 23 | a0001c0001t0001g0084a0001c0001t0001g0133a0001c0001t0001g0149others(20): Show | 23 | HG00642.hp1 HG00733.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.-3-744_-3-742delTT others(1): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
CAAAA | C | 19 | a0001c0001t0004g0003a0001c0001t0004g0025a0001c0001t0004g0027others(16): Show | 19 | HG01109.hp2 HG01243.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.-3-745_-3-742delTT others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
CAAAAA | C | 16 | a0001c0001t0004g0021a0001c0001t0004g0023a0001c0001t0004g0024others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3-746_-3-742delTT others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0006g0017 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-754_-3-742delTT others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842420
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-3-756_-3-742delTT others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842420 | ||||||
| chr5:74842456
|
A | G | 1 | a0001c0003t0006g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3-777T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842456 | ||||||
| chr5:74842535
|
CT | C | 17 | a0001c0001t0004g0030a0001c0001t0007g0005a0001c0001t0007g0006others(14): Show | 17 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3-857delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842535 | ||||||
| chr5:74842830
|
T | TCAATC | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-3-1152_-3-1151ins others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842830 | ||||||
| chr5:74842891
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-3-1212C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74842891 | ||||||
| chr5:74843014
|
C | T | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-1335G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843014 | ||||||
| chr5:74843111
|
G | C | 1 | a0001c0001t0005g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-3-1432C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843111 | ||||||
| chr5:74843529
|
T | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-1850A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843529 | ||||||
| chr5:74843671
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-3-1992A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843671 | ||||||
| chr5:74843776
|
A | G | 151 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-3-2097T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74843776 | ||||||
| chr5:74844142
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-3-2463C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844142 | ||||||
| chr5:74844336
|
C | A | 1 | a0001c0001t0005g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-3-2657G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844336 | ||||||
| chr5:74844384
|
C | T | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-3-2705G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844384 | ||||||
| chr5:74844401
|
G | A | 8 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(5): Show | 8 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3-2722C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844401 | ||||||
| chr5:74844570
|
G | A | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-3-2891C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844570 | ||||||
| chr5:74844631
|
A | G | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-3-2952T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844631 | ||||||
| chr5:74844710
|
G | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-3031C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844710 | ||||||
| chr5:74844758
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-3-3079C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844758 | ||||||
| chr5:74844792
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-3-3113C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74844792 | ||||||
| chr5:74845027
|
C | T | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-3348G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845027 | ||||||
| chr5:74845130
|
T | C | 24 | a0001c0001t0002g0253a0001c0001t0002g0255a0001c0001t0002g0260others(21): Show | 24 | HG01257.hp2 HG01258.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3-3451A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845130 | ||||||
| chr5:74845198
|
T | G | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-3-3519A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845198 | ||||||
| chr5:74845257
|
G | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-3578C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845257 | ||||||
| chr5:74845406
|
T | C | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-3-3727A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845406 | ||||||
| chr5:74845505
|
G | A | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-3-3826C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845505 | ||||||
| chr5:74845738
|
T | C | 6 | a0001c0001t0001g0076a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 6 | HG00323.hp1 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3-4059A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845738 | ||||||
| chr5:74845795
|
G | A | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-4116C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74845795 | ||||||
| chr5:74846211
|
A | C | 2 | a0001c0001t0013g0229a0001c0001t0013g0230 | 2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-3-4532T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846211 | ||||||
| chr5:74846352
|
C | T | 151 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(148): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-3-4673G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846352 | ||||||
| chr5:74846380
|
A | G | 1 | a0001c0001t0007g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3-4701T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846380 | ||||||
| chr5:74846476
|
T | C | 1 | a0001c0001t0002g0255 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-3-4797A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846476 | ||||||
| chr5:74846811
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-3-5132A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846811 | ||||||
| chr5:74846904
|
T | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0305 | 2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.-3-5225A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846904 | ||||||
| chr5:74846910
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-3-5231C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74846910 | ||||||
| chr5:74847019
|
A | C | 1 | a0001c0003t0006g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-3-5340T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847019 | ||||||
| chr5:74847040
|
C | T | 76 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-3-5361G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847040 | ||||||
| chr5:74847133
|
T | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-5454A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847133 | ||||||
| chr5:74847262
|
G | C | 63 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(60): Show | 64 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-3-5583C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847262 | ||||||
| chr5:74847380
|
G | A | 1 | a0001c0001t0005g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-3-5701C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847380 | ||||||
| chr5:74847499
|
A | G | 1 | a0001c0001t0004g0024 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-3-5820T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847499 | ||||||
| chr5:74847555
|
T | G | 1 | a0001c0001t0011g0042 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-3-5876A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847555 | ||||||
| chr5:74847571
|
G | A | 123 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(120): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-3-5892C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847571 | ||||||
| chr5:74847700
|
T | C | 1 | a0001c0001t0005g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-3-6021A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847700 | ||||||
| chr5:74847733
|
T | C | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-6054A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847733 | ||||||
| chr5:74847741
|
C | T | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-6062G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847741 | ||||||
| chr5:74847850
|
T | C | 6 | a0001c0001t0005g0122a0001c0001t0005g0123a0001c0001t0005g0124others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3-6171A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847850 | ||||||
| chr5:74847909
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-3-6230A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847909 | ||||||
| chr5:74847935
|
G | A | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-6256C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847935 | ||||||
| chr5:74847939
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-3-6260T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847939 | ||||||
| chr5:74847963
|
T | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-6284A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74847963 | ||||||
| chr5:74848338
|
T | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-6659A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848338 | ||||||
| chr5:74848378
|
A | G | 97 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-3-6699T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848378 | ||||||
| chr5:74848497
|
A | C | 1 | a0001c0001t0023g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-3-6818T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848497 | ||||||
| chr5:74848616
|
T | C | 3 | a0001c0002t0012g0232a0001c0002t0012g0233a0001c0002t0018g0231 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-3-6937A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848616 | ||||||
| chr5:74848656
|
T | C | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-3-6977A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848656 | ||||||
| chr5:74848744
|
T | G | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-7065A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848744 | ||||||
| chr5:74848919
|
C | A | 1 | a0001c0001t0001g0199 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-3-7240G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74848919 | ||||||
| chr5:74849066
|
G | A | 1 | a0001c0003t0006g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-3-7387C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849066 | ||||||
| chr5:74849132
|
A | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0083 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-3-7453T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849132 | ||||||
| chr5:74849330
|
T | C | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-7651A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849330 | ||||||
| chr5:74849391
|
G | C | 3 | a0001c0002t0008g0070a0001c0002t0008g0071a0001c0002t0008g0072 | 3 | HG02451.hp2 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-3-7712C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849391 | ||||||
| chr5:74849479
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-3-7800A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849479 | ||||||
| chr5:74849573
|
T | G | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-3-7894A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849573 | ||||||
| chr5:74849753
|
A | G | 97 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-3-8074T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849753 | ||||||
| chr5:74849822
|
C | T | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-3-8143G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74849822 | ||||||
| chr5:74850035
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3-8356G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850035 | ||||||
| chr5:74850130
|
A | G | 2 | a0001c0002t0008g0070a0001c0002t0008g0072 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-3-8451T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850130 | ||||||
| chr5:74850181
|
A | G | 3 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0003g0219 | 3 | HG02056.hp2 NA18949.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-3-8502T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850181 | ||||||
| chr5:74850208
|
T | G | 1 | a0001c0002t0030g0245 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-3-8529A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850208 | ||||||
| chr5:74850253
|
G | A | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-8574C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850253 | ||||||
| chr5:74850260
|
G | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-3-8581C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850260 | ||||||
| chr5:74850327
|
A | C | 1 | a0001c0003t0006g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-3-8648T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850327 | ||||||
| chr5:74850424
|
T | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-8745A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850424 | ||||||
| chr5:74850648
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-3-8969A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850648 | ||||||
| chr5:74850897
|
C | T | 1 | a0001c0001t0019g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-3-9218G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850897 | ||||||
| chr5:74850980
|
G | A | 2 | a0001c0003t0006g0249a0001c0003t0006g0250 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-3-9301C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74850980 | ||||||
| chr5:74851048
|
TAAG | T | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-3-9372_-3-9370del others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851048 | ||||||
| chr5:74851237
|
T | TCCTC | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-9562_-3-9559dup others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851237 | ||||||
| chr5:74851253
|
T | TTCGTAGT others(6): Show |
1 | a0001c0001t0003g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-3-9587_-3-9575dup others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851253 | ||||||
| chr5:74851739
|
C | T | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-10060G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851739 | ||||||
| chr5:74851856
|
C | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0264 | 3 | HG01069.hp1 HG01071.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-3-10177G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851856 | ||||||
| chr5:74851860
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-3-10181C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851860 | ||||||
| chr5:74851898
|
G | T | 1 | a0001c0001t0002g0256 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-3-10219C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851898 | ||||||
| chr5:74851945
|
G | A | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-3-10266C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74851945 | ||||||
| chr5:74852014
|
G | T | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-3-10335C>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852014 | ||||||
| chr5:74852176
|
C | T | 11 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3-10497G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852176 | ||||||
| chr5:74852200
|
C | T | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-3-10521G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852200 | ||||||
| chr5:74852381
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-3-10702C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852381 | ||||||
| chr5:74852403
|
G | A | 28 | a0001c0001t0013g0229a0001c0001t0013g0230a0001c0002t0006g0016others(25): Show | 28 | HG00438.hp1 HG00735.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-3-10724C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852403 | ||||||
| chr5:74852426
|
T | C | 107 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-3-10747A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852426 | ||||||
| chr5:74852477
|
G | C | 1 | a0001c0001t0001g0149 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-3-10798C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852477 | ||||||
| chr5:74852665
|
T | A | 1 | a0001c0003t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-3-10986A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852665 | ||||||
| chr5:74852820
|
T | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0151a0001c0001t0001g0183others(1): Show | 4 | HG01928.hp2 HG01975.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3-11141A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852820 | ||||||
| chr5:74852876
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-3-11197G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74852876 | ||||||
| chr5:74853485
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0239 | 2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-3-11806G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853485 | ||||||
| chr5:74853547
|
G | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(58): Show | 62 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3-11868C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853547 | ||||||
| chr5:74853653
|
T | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-3-11974A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853653 | ||||||
| chr5:74853701
|
A | AT | 17 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0131others(14): Show | 17 | HG01106.hp2 HG01109.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3-12023dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853701 | ||||||
| chr5:74853701
|
A | T | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-3-12022T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853701 | ||||||
| chr5:74853701
|
AT | A | 91 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0002g0001others(88): Show | 92 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-3-12023delA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853701 | ||||||
| chr5:74853701
|
ATT | A | 14 | a0001c0001t0002g0296a0001c0001t0004g0057a0001c0001t0004g0058others(11): Show | 14 | HG01975.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3-12024_-3-12023d others(4): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853701 | ||||||
| chr5:74853733
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-3-12054T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853733 | ||||||
| chr5:74853905
|
A | G | 152 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-3-12226T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74853905 | ||||||
| chr5:74854264
|
G | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0184a0001c0001t0003g0185 | 3 | HG02572.hp2 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-4+11901C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854264 | ||||||
| chr5:74854357
|
T | C | 152 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(149): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-4+11808A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854357 | ||||||
| chr5:74854358
|
G | A | 3 | a0001c0002t0012g0232a0001c0002t0012g0233a0001c0002t0018g0231 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+11807C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854358 | ||||||
| chr5:74854397
|
AAAT | A | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(133): Show | 137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-4+11765_-4+11767d others(5): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854397 | ||||||
| chr5:74854871
|
C | A | 150 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(147): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-4+11294G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854871 | ||||||
| chr5:74854875
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-4+11290C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854875 | ||||||
| chr5:74854885
|
C | G | 1 | a0001c0003t0006g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-4+11280G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74854885 | ||||||
| chr5:74855115
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-4+11050C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855115 | ||||||
| chr5:74855126
|
T | C | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-4+11039A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855126 | ||||||
| chr5:74855215
|
C | G | 138 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-4+10950G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855215 | ||||||
| chr5:74855261
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-4+10904A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855261 | ||||||
| chr5:74855472
|
A | C | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+10693T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855472 | ||||||
| chr5:74855511
|
G | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-4+10654C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855511 | ||||||
| chr5:74855548
|
C | A | 1 | a0001c0001t0002g0282 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-4+10617G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855548 | ||||||
| chr5:74855573
|
G | C | 1 | a0001c0001t0026g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-4+10592C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855573 | ||||||
| chr5:74855619
|
T | C | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-4+10546A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855619 | ||||||
| chr5:74855995
|
C | T | 1 | a0001c0002t0018g0231 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-4+10170G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855995 | ||||||
| chr5:74855996
|
G | A | 94 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(91): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-4+10169C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74855996 | ||||||
| chr5:74856412
|
T | C | 22 | a0001c0001t0003g0128a0001c0001t0003g0129a0001c0001t0005g0082others(19): Show | 22 | HG00673.hp1 HG00741.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-4+9753A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856412 | ||||||
| chr5:74856583
|
T | C | 1 | a0001c0003t0006g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-4+9582A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856583 | ||||||
| chr5:74856589
|
A | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-4+9576T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856589 | ||||||
| chr5:74856612
|
T | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-4+9553A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856612 | ||||||
| chr5:74856813
|
GA | G | 10 | a0001c0001t0002g0286a0001c0001t0005g0122a0001c0002t0008g0062others(7): Show | 10 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-4+9351delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74856813 | ||||||
| chr5:74857044
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-4+9121C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857044 | ||||||
| chr5:74857108
|
C | CA | 100 | a0001c0001t0001g0078a0001c0001t0001g0097a0001c0001t0001g0098others(97): Show | 101 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-4+9056dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857108 | ||||||
| chr5:74857108
|
C | CAA | 13 | a0001c0001t0002g0002a0001c0001t0002g0283a0001c0001t0002g0285others(10): Show | 13 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-4+9055_-4+9056dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857108 | ||||||
| chr5:74857108
|
CA | C | 48 | a0001c0001t0001g0074a0001c0001t0001g0163a0001c0001t0003g0119others(45): Show | 48 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4+9056delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857108 | ||||||
| chr5:74857187
|
T | C | 139 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-4+8978A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857187 | ||||||
| chr5:74857368
|
C | T | 2 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | NA18948.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-4+8797G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857368 | ||||||
| chr5:74857369
|
G | A | 1 | a0001c0001t0005g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-4+8796C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857369 | ||||||
| chr5:74857380
|
G | A | 2 | a0001c0001t0004g0045a0001c0001t0004g0046 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-4+8785C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857380 | ||||||
| chr5:74857447
|
G | C | 2 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | NA18948.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-4+8718C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857447 | ||||||
| chr5:74857456
|
G | A | 1 | a0001c0003t0006g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-4+8709C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857456 | ||||||
| chr5:74857475
|
G | A | 2 | a0001c0003t0006g0224a0001c0003t0006g0225 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-4+8690C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857475 | ||||||
| chr5:74857567
|
C | T | 1 | a0001c0001t0017g0130 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-4+8598G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857567 | ||||||
| chr5:74857571
|
G | GA | 8 | a0001c0002t0006g0018a0001c0002t0006g0019a0001c0002t0006g0020others(5): Show | 8 | HG01884.hp2 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(1): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | ||||||
| chr5:74857571
|
G | GAA | 10 | a0001c0001t0013g0229a0001c0002t0008g0062a0001c0002t0008g0065others(7): Show | 10 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | ||||||
| chr5:74857571
|
G | GAAA | 6 | a0001c0001t0003g0114a0001c0001t0013g0230a0001c0002t0008g0072others(3): Show | 6 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | ||||||
| chr5:74857571
|
G | GAAAAAAA others(3): Show |
1 | a0001c0002t0010g0246 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(10): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | ||||||
| chr5:74857571
|
G | GAAAAAAA others(5): Show |
2 | a0001c0002t0010g0247a0001c0002t0010g0248 | 2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-4+8593_-4+8594ins others(12): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | ||||||
| chr5:74857571
|
GGAAAAAA | G | 16 | a0001c0001t0002g0002a0001c0001t0002g0260a0001c0001t0002g0286others(13): Show | 16 | HG00408.hp2 HG01175.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4+8587_-4+8593del others(7): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | ||||||
| chr5:74857571
|
GGAAAAAA others(1): Show |
G | 45 | a0001c0001t0002g0001a0001c0001t0002g0252a0001c0001t0002g0253others(42): Show | 46 | HG00099.hp1 HG00558.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-4+8586_-4+8593del others(8): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857571 | ||||||
| chr5:74857572
|
G | A | 41 | a0001c0001t0003g0114a0001c0001t0013g0229a0001c0001t0013g0230others(38): Show | 41 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-4+8593C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
G | GA | 48 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-4+8592dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
G | GAA | 23 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4+8591_-4+8592dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
G | GAAA | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4+8590_-4+8592dup others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
GA | G | 16 | a0001c0001t0003g0128a0001c0001t0003g0129a0001c0001t0005g0122others(13): Show | 16 | HG01978.hp2 HG02615.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4+8592delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
GAA | G | 7 | a0001c0001t0006g0060a0001c0001t0007g0006a0001c0001t0007g0007others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+8591_-4+8592del others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-4+8582_-4+8592del others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
GAAAAAAA others(6): Show |
G | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0211 | 3 | HG01516.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-4+8580_-4+8592del others(13): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
GAAAAAAA others(7): Show |
G | 2 | a0001c0001t0003g0079a0001c0001t0004g0049 | 2 | HG01109.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.-4+8579_-4+8592del others(14): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857572
|
GAAAAAAA others(8): Show |
G | 34 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-4+8578_-4+8592del others(15): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857572 | ||||||
| chr5:74857573
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-4+8592T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857573 | ||||||
| chr5:74857585
|
A | G | 1 | a0001c0001t0007g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-4+8580T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857585 | ||||||
| chr5:74857666
|
TCTGTATA others(19): Show |
T | 12 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+8473_-4+8498del others(26): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857666 | ||||||
| chr5:74857702
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-4+8463A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857702 | ||||||
| chr5:74857794
|
G | A | 43 | a0001c0001t0003g0114a0001c0001t0013g0229a0001c0001t0013g0230others(40): Show | 43 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-4+8371C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857794 | ||||||
| chr5:74857833
|
C | G | 7 | a0001c0001t0004g0003a0001c0001t0004g0024a0001c0001t0004g0025others(4): Show | 7 | HG02735.hp1 HG03239.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+8332G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857833 | ||||||
| chr5:74857861
|
C | T | 5 | a0001c0001t0003g0115a0001c0001t0003g0116a0001c0001t0003g0117others(2): Show | 5 | HG03491.hp1 HG03492.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4+8304G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857861 | ||||||
| chr5:74857949
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-4+8216T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74857949 | ||||||
| chr5:74858113
|
C | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(57): Show | 61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+8052G>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858113 | ||||||
| chr5:74858203
|
T | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-4+7962A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858203 | ||||||
| chr5:74858301
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-4+7864A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858301 | ||||||
| chr5:74858574
|
G | A | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-4+7591C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858574 | ||||||
| chr5:74858837
|
T | C | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+7328A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858837 | ||||||
| chr5:74858907
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-4+7258A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858907 | ||||||
| chr5:74858920
|
A | C | 60 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(57): Show | 61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+7245T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858920 | ||||||
| chr5:74858980
|
A | G | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+7185T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74858980 | ||||||
| chr5:74859287
|
C | CT | 18 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0100others(15): Show | 19 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-4+6877dupA | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859287 | ||||||
| chr5:74859345
|
C | T | 60 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(57): Show | 61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+6820G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859345 | ||||||
| chr5:74859450
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-4+6715A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859450 | ||||||
| chr5:74859523
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-4+6642G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859523 | ||||||
| chr5:74859690
|
A | G | 2 | a0001c0001t0004g0024a0001c0001t0004g0025 | 2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-4+6475T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859690 | ||||||
| chr5:74859720
|
C | T | 1 | a0001c0001t0031g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-4+6445G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859720 | ||||||
| chr5:74859746
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-4+6419C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859746 | ||||||
| chr5:74859821
|
C | T | 149 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(146): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-4+6344G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859821 | ||||||
| chr5:74859946
|
G | A | 1 | a0001c0002t0016g0212 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-4+6219C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859946 | ||||||
| chr5:74859993
|
G | A | 95 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(92): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-4+6172C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74859993 | ||||||
| chr5:74860166
|
T | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-4+5999A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860166 | ||||||
| chr5:74860231
|
A | G | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+5934T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860231 | ||||||
| chr5:74860453
|
A | C | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-4+5712T>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860453 | ||||||
| chr5:74860519
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-4+5646G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860519 | ||||||
| chr5:74860726
|
T | A | 3 | a0001c0002t0012g0232a0001c0002t0012g0233a0001c0002t0018g0231 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+5439A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860726 | ||||||
| chr5:74860733
|
C | T | 1 | a0001c0001t0002g0297 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-4+5432G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860733 | ||||||
| chr5:74860734
|
T | C | 1 | a0001c0001t0002g0297 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-4+5431A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860734 | ||||||
| chr5:74860827
|
T | TA | 17 | a0001c0001t0001g0101a0001c0001t0001g0216a0001c0001t0001g0217others(14): Show | 17 | HG01109.hp2 HG01175.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.-4+5337dupT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860827 | ||||||
| chr5:74860827
|
TA | T | 56 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(53): Show | 56 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.-4+5337delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860827 | ||||||
| chr5:74860895
|
T | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-4+5270A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860895 | ||||||
| chr5:74860980
|
T | C | 95 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(92): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-4+5185A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74860980 | ||||||
| chr5:74861037
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-4+5128A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861037 | ||||||
| chr5:74861056
|
G | A | 3 | a0001c0002t0012g0232a0001c0002t0012g0233a0001c0002t0018g0231 | 3 | HG03041.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-4+5109C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861056 | ||||||
| chr5:74861069
|
T | G | 150 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(147): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-4+5096A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861069 | ||||||
| chr5:74861087
|
A | G | 1 | a0001c0001t0002g0255 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-4+5078T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861087 | ||||||
| chr5:74861190
|
T | C | 1 | a0001c0002t0008g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-4+4975A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861190 | ||||||
| chr5:74861416
|
T | A | 2 | a0001c0002t0012g0232a0001c0002t0012g0233 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-4+4749A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861416 | ||||||
| chr5:74861489
|
C | G | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+4676G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861489 | ||||||
| chr5:74861532
|
T | C | 1 | a0001c0001t0004g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-4+4633A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861532 | ||||||
| chr5:74861622
|
G | A | 2 | a0001c0001t0006g0060a0001c0001t0006g0061 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-4+4543C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74861622 | ||||||
| chr5:74862003
|
CTG | C | 7 | a0001c0001t0004g0052a0001c0001t0004g0053a0001c0001t0004g0054others(4): Show | 7 | HG00733.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4+4160_-4+4161del others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862003 | ||||||
| chr5:74862127
|
C | T | 1 | a0001c0001t0004g0021 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-4+4038G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862127 | ||||||
| chr5:74862411
|
G | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(57): Show | 61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+3754C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862411 | ||||||
| chr5:74862411
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-4+3754C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862411 | ||||||
| chr5:74862415
|
T | A | 5 | a0001c0002t0006g0016a0001c0002t0006g0017a0001c0002t0006g0018others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+3750A>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862415 | ||||||
| chr5:74862515
|
C | G | 60 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(57): Show | 61 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-4+3650G>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862515 | ||||||
| chr5:74862541
|
G | A | 4 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG02809.hp1 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+3624C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862541 | ||||||
| chr5:74862764
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-4+3401C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862764 | ||||||
| chr5:74862790
|
A | T | 4 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0106others(1): Show | 4 | HG00280.hp1 HG00738.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4+3375T>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74862790 | ||||||
| chr5:74863023
|
T | TAA | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-4+3140_-4+3141dup others(2): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863023 | ||||||
| chr5:74863023
|
TA | T | 37 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.-4+3141delT | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863023 | ||||||
| chr5:74863043
|
A | G | 119 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(116): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-4+3122T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863043 | ||||||
| chr5:74863046
|
G | A | 11 | a0001c0002t0008g0062a0001c0002t0008g0063a0001c0002t0008g0064others(8): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4+3119C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863046 | ||||||
| chr5:74863143
|
A | G | 1 | a0001c0001t0019g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-4+3022T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863143 | ||||||
| chr5:74863312
|
C | T | 120 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(117): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-4+2853G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863312 | ||||||
| chr5:74863332
|
T | C | 35 | a0001c0001t0004g0003a0001c0001t0004g0021a0001c0001t0004g0023others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-4+2833A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863332 | ||||||
| chr5:74863504
|
C | T | 1 | a0001c0001t0002g0253 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-4+2661G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863504 | ||||||
| chr5:74863871
|
T | G | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+2294A>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863871 | ||||||
| chr5:74863960
|
T | C | 2 | a0001c0003t0006g0240a0001c0003t0015g0241 | 2 | HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-4+2205A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74863960 | ||||||
| chr5:74864126
|
T | C | 71 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0253others(68): Show | 72 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-4+2039A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864126 | ||||||
| chr5:74864225
|
A | G | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-4+1940T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864225 | ||||||
| chr5:74864294
|
G | A | 7 | a0001c0002t0010g0242a0001c0002t0010g0243a0001c0002t0010g0244others(4): Show | 7 | HG00741.hp2 HG01106.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+1871C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864294 | ||||||
| chr5:74864497
|
G | C | 3 | a0001c0003t0006g0249a0001c0003t0006g0250a0001c0003t0006g0251 | 3 | HG02451.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-4+1668C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864497 | ||||||
| chr5:74864532
|
T | C | 1 | a0001c0001t0004g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-4+1633A>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864532 | ||||||
| chr5:74864630
|
A | G | 101 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-4+1535T>C | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864630 | ||||||
| chr5:74864829
|
G | A | 54 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0252others(51): Show | 55 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-4+1336C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864829 | ||||||
| chr5:74864972
|
GATC | G | 12 | a0001c0001t0007g0005a0001c0001t0007g0006a0001c0001t0007g0007others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4+1190_-4+1192del others(3): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74864972 | ||||||
| chr5:74865251
|
C | T | 1 | a0001c0001t0004g0003 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-4+914G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74865251 | ||||||
| chr5:74865806
|
T | TGGGGAGA others(6): Show |
1 | a0001c0001t0001g0302 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-4+346_-4+358dupTC others(11): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74865806 | ||||||
| chr5:74865951
|
G | A | 2 | a0001c0001t0002g0304a0001c0001t0027g0303 | 2 | NA18945.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-4+214C>T | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74865951 | ||||||
| chr5:74865992
|
C | T | 1 | a0001c0001t0002g0002 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4+173G>A | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74865992 | ||||||
| chr5:74866069
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-4+96C>G | FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | 74866069 |