Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 400451 |
|---|---|
| ensemblid | ENSG00000185442.13 |
| hgncid | 34339 |
| symbol | FAM174B |
| name | family with sequence similarity 174 member B |
| refseq_nuc | NM_207446.3 |
| refseq_prot | NP_997329.2 |
| ensembl_nuc | ENST00000327355.6 |
| ensembl_prot | ENSP00000329040.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 92617448 |
| end | 92655775 |
| strand | - |
| ver | v1.2 |
| region | chr15:92617448-92655775 |
| region5000 | chr15:92612448-92660775 |
| regionname0 | FAM174B_chr15_92617448_92655775 |
| regionname5000 | FAM174B_chr15_92612448_92660775 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 157 | 371 | 78 | 70 | 169 | 11 | 42 | 133 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0002 | 1/0 | 159 | 13 | 11 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0003 | 0/0 | 157 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0004 | 0/0 | 157 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0005 | 0/0 | 157 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0006 | 0/0 | 157 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0007 | 0/0 | 157 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0008 | 0/0 | 157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0009 | 0/0 | 157 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 474 | 363 | 71 | 70 | 169 | 11 | 41 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0002 | 1/0 | 480 | 13 | 11 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0003 | 0/0 | 474 | 5 | 5 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0004 | 0/0 | 474 | 3 | 2 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0005 | 0/0 | 474 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0006 | 0/0 | 474 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0007 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0008 | 0/0 | 474 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0009 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0010 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0011 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| c0012 | 0/0 | 474 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2125 | 61 | 6 | 12 | 38 | 0 | 5 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0002 | 0/0 | 2126 | 48 | 9 | 4 | 34 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0003 | 0/1 | 2124 | 34 | 4 | 10 | 9 | 5 | 5 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0004 | 1/0 | 2125 | 29 | 8 | 7 | 4 | 3 | 6 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0005 | 0/0 | 2124 | 28 | 0 | 4 | 19 | 1 | 4 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0006 | 0/0 | 2124 | 23 | 0 | 8 | 14 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0007 | 0/0 | 2124 | 19 | 2 | 5 | 7 | 0 | 5 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0008 | 0/0 | 2125 | 11 | 4 | 0 | 7 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0009 | 0/0 | 2125 | 11 | 10 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0010 | 0/0 | 2110 | 9 | 5 | 3 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0011 | 0/0 | 2126 | 8 | 7 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0012 | 0/0 | 2124 | 7 | 1 | 2 | 3 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0013 | 0/0 | 2123 | 7 | 0 | 0 | 6 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0014 | 0/0 | 2123 | 6 | 0 | 5 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0015 | 0/0 | 2125 | 6 | 6 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0016 | 0/0 | 2126 | 5 | 2 | 0 | 0 | 1 | 2 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0017 | 0/0 | 2125 | 5 | 0 | 0 | 5 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0018 | 0/0 | 2125 | 4 | 0 | 3 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0019 | 0/0 | 2124 | 3 | 0 | 0 | 2 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0020 | 0/0 | 2123 | 3 | 1 | 1 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0021 | 0/0 | 2126 | 3 | 0 | 0 | 1 | 0 | 2 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0022 | 0/0 | 2123 | 3 | 0 | 2 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0023 | 0/0 | 2123 | 3 | 0 | 0 | 3 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0024 | 0/0 | 2124 | 3 | 2 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0025 | 0/0 | 2125 | 3 | 0 | 0 | 3 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0026 | 0/0 | 2125 | 2 | 0 | 0 | 0 | 1 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0027 | 0/0 | 2123 | 2 | 1 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0028 | 0/0 | 2125 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0029 | 0/0 | 2125 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0030 | 0/0 | 2127 | 2 | 1 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0031 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0032 | 0/0 | 2109 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0033 | 0/0 | 2127 | 2 | 1 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0034 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0035 | 0/0 | 2126 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0036 | 0/0 | 2110 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0037 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0038 | 0/0 | 2125 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0039 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0040 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0041 | 0/0 | 2114 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0042 | 0/0 | 2125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0043 | 0/0 | 2125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0044 | 0/0 | 2122 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0045 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0046 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0047 | 0/0 | 2126 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0048 | 0/0 | 2126 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0049 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0050 | 0/0 | 2125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0051 | 0/0 | 2125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0052 | 0/0 | 2108 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0053 | 0/0 | 2125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0054 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0055 | 0/0 | 2123 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0056 | 0/0 | 2125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0057 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0058 | 0/0 | 2126 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0059 | 0/0 | 2126 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0060 | 0/0 | 2126 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0061 | 0/0 | 2125 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0062 | 0/0 | 2125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0063 | 0/0 | 2126 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0064 | 0/0 | 2125 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0065 | 0/0 | 2126 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| t0066 | 0/0 | 2125 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0006 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 474 | 363 | 71 | 70 | 169 | 11 | 41 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0003 | 0/0 | 474 | 5 | 5 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0006 | 0/0 | 474 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0008 | 0/0 | 474 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0002c0002 | 1/0 | 480 | 13 | 11 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0003c0004 | 0/0 | 474 | 3 | 2 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0004c0005 | 0/0 | 474 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0005c0012 | 0/0 | 474 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0006c0010 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0007c0009 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0008c0011 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0009c0007 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2598 | 58 | 5 | 12 | 37 | 0 | 4 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0002 | 0/0 | 2599 | 42 | 3 | 4 | 34 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0003 | 0/1 | 2597 | 33 | 4 | 10 | 9 | 4 | 5 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0004 | 0/0 | 2598 | 22 | 3 | 6 | 4 | 3 | 6 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0005 | 0/0 | 2597 | 27 | 0 | 4 | 18 | 1 | 4 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0006 | 0/0 | 2597 | 23 | 0 | 8 | 14 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0007 | 0/0 | 2597 | 19 | 2 | 5 | 7 | 0 | 5 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0008 | 0/0 | 2598 | 11 | 4 | 0 | 7 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0009 | 0/0 | 2598 | 9 | 8 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0010 | 0/0 | 2583 | 8 | 5 | 2 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0011 | 0/0 | 2599 | 8 | 7 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0012 | 0/0 | 2597 | 6 | 1 | 2 | 2 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0013 | 0/0 | 2596 | 7 | 0 | 0 | 6 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0014 | 0/0 | 2596 | 6 | 0 | 5 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0015 | 0/0 | 2598 | 4 | 4 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0016 | 0/0 | 2599 | 4 | 1 | 0 | 0 | 1 | 2 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0017 | 0/0 | 2598 | 5 | 0 | 0 | 5 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0018 | 0/0 | 2598 | 4 | 0 | 3 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0019 | 0/0 | 2597 | 3 | 0 | 0 | 2 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0020 | 0/0 | 2596 | 3 | 1 | 1 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0021 | 0/0 | 2599 | 3 | 0 | 0 | 1 | 0 | 2 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0022 | 0/0 | 2596 | 3 | 0 | 2 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0023 | 0/0 | 2596 | 3 | 0 | 0 | 3 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0024 | 0/0 | 2597 | 2 | 1 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0025 | 0/0 | 2598 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0026 | 0/0 | 2598 | 2 | 0 | 0 | 0 | 1 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0027 | 0/0 | 2596 | 2 | 1 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0028 | 0/0 | 2598 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0029 | 0/0 | 2598 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0030 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0031 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0032 | 0/0 | 2582 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0033 | 0/0 | 2600 | 2 | 1 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0034 | 0/0 | 2597 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0035 | 0/0 | 2599 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0036 | 0/0 | 2583 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0038 | 0/0 | 2598 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0039 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0040 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0041 | 0/0 | 2587 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0043 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0044 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0045 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0046 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0047 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0048 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0049 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0050 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0051 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0052 | 0/0 | 2581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0053 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0054 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0055 | 0/0 | 2596 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0056 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0057 | 0/0 | 2600 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0058 | 0/0 | 2599 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0059 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0060 | 0/0 | 2599 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0061 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0062 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0063 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0064 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0065 | 0/0 | 2599 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0001t0066 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0003t0002 | 0/0 | 2599 | 5 | 5 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0006t0002 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0006t0024 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0001c0008t0001 | 0/0 | 2598 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0002c0002t0004 | 1/0 | 2604 | 6 | 5 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0002c0002t0009 | 0/0 | 2604 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0002c0002t0010 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0002c0002t0015 | 0/0 | 2604 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0002c0002t0030 | 0/0 | 2606 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0002c0002t0031 | 0/0 | 2603 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0003c0004t0004 | 0/0 | 2598 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0003c0004t0016 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0003c0004t0037 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0004c0005t0001 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0004c0005t0042 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0005c0012t0003 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0006c0010t0012 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0007c0009t0005 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0008c0011t0025 | 0/0 | 2598 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| a0009c0007t0001 | 0/0 | 2598 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | copy fasta | chr15 | 92612448 | 92660775 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0007g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0010g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0012g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0013g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0014g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0015g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0016g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0016g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0016g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0016g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0017g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0017g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0017g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0017g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0018g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0018g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0018g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0018g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0019g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0019g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0019g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0020g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0020g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0020g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0021g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0021g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0021g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0022g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0022g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0022g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0023g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0023g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0023g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0024g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0024g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0025g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0025g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0026g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0026g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0027g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0027g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0028g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0028g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0029g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0029g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0030g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0031g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0032g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0032g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0033g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0033g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0034g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0034g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0035g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0035g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0036g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0036g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0038g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0039g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0040g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0041g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0043g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0044g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0045g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0046g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0047g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0048g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0049g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0050g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0051g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0052g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0053g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0054g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0055g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0056g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0057g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0058g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0059g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0060g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0061g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0062g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0063g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0064g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0065g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0001t0066g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0003t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0006t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0006t0024g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0001c0008t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0006 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0004g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0009g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0009g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0010g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0015g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0015g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0030g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0002c0002t0031g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0003c0004t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0003c0004t0016g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0003c0004t0037g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0004c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0004c0005t0042g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0005c0012t0003g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0006c0010t0012g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0007c0009t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0008c0011t0025g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| a0009c0007t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0016 | g0341 | EUR | GBR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0197 | EUR | GBR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00140 | hp1 | a0001 | c0001 | t0026 | g0127 | EUR | GBR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00140 | hp2 | a0001 | c0001 | t0010 | g0339 | EUR | GBR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0163 | EUR | FIN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0251 | EUR | FIN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0211 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00438 | hp1 | a0001 | c0001 | t0043 | g0184 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00544 | hp2 | a0001 | c0001 | t0020 | g0345 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00558 | hp1 | a0006 | c0010 | t0012 | g0094 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00597 | hp1 | a0001 | c0001 | t0028 | g0223 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00597 | hp2 | a0001 | c0001 | t0024 | g0208 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0138 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00642 | hp1 | a0003 | c0004 | t0004 | g0368 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0316 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0207 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00733 | hp1 | a0001 | c0001 | t0010 | g0349 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0102 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0247 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0135 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0348 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01074 | hp1 | a0001 | c0001 | t0018 | g0084 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0234 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0033 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0123 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01167 | hp1 | a0001 | c0001 | t0055 | g0162 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01167 | hp2 | a0001 | c0001 | t0032 | g0336 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01168 | hp1 | a0001 | c0001 | t0022 | g0260 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01168 | hp2 | a0001 | c0001 | t0022 | g0315 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01192 | hp1 | a0001 | c0001 | t0038 | g0274 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0347 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01243 | hp1 | a0001 | c0001 | t0020 | g0121 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01243 | hp2 | a0002 | c0002 | t0010 | g0378 | AMR | PUR | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01255 | hp2 | a0001 | c0001 | t0014 | g0233 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0258 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0152 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0203 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01358 | hp2 | a0001 | c0001 | t0018 | g0147 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0243 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0334 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0244 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01496 | hp1 | a0001 | c0001 | t0012 | g0097 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0248 | AMR | CLM | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01515 | hp1 | a0005 | c0012 | t0003 | g0380 | EUR | IBS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0267 | EUR | IBS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0085 | EUR | IBS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0269 | EUR | IBS | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0043 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0191 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01891 | hp2 | a0001 | c0006 | t0024 | g0113 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01928 | hp2 | a0001 | c0001 | t0014 | g0156 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0298 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01943 | hp1 | a0001 | c0001 | t0014 | g0236 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01943 | hp2 | a0001 | c0001 | t0014 | g0103 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0238 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0235 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0239 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01975 | hp2 | a0001 | c0001 | t0012 | g0350 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0266 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0242 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG01993 | hp2 | a0001 | c0001 | t0058 | g0249 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02027 | hp1 | a0001 | c0001 | t0013 | g0142 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0333 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0020 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0360 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02080 | hp2 | a0001 | c0001 | t0013 | g0290 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0328 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0154 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02155 | hp1 | a0001 | c0001 | t0007 | g0255 | EAS | CDX | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | CDX | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CDX | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0329 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02257 | hp2 | a0001 | c0006 | t0002 | g0013 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02258 | hp1 | a0002 | c0002 | t0030 | g0373 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02258 | hp2 | a0001 | c0001 | t0051 | g0026 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02280 | hp1 | a0001 | c0001 | t0040 | g0335 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0250 | AMR | PEL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02451 | hp1 | a0002 | c0002 | t0031 | g0370 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02451 | hp2 | a0001 | c0001 | t0033 | g0342 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02523 | hp1 | a0001 | c0001 | t0025 | g0289 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02523 | hp2 | a0001 | c0001 | t0025 | g0227 | EAS | KHV | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0375 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02602 | hp1 | a0001 | c0001 | t0013 | g0213 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0268 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02615 | hp1 | a0001 | c0001 | t0024 | g0057 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02622 | hp1 | a0001 | c0001 | t0047 | g0364 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02622 | hp2 | a0001 | c0001 | t0048 | g0122 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0132 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0190 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0324 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02683 | hp2 | a0001 | c0001 | t0016 | g0352 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02698 | hp1 | a0001 | c0001 | t0019 | g0061 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02698 | hp2 | a0001 | c0001 | t0018 | g0072 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02717 | hp1 | a0002 | c0002 | t0009 | g0371 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0112 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0014 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02723 | hp2 | a0003 | c0004 | t0016 | g0366 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0185 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02735 | hp2 | a0001 | c0008 | t0001 | g0011 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02809 | hp1 | a0002 | c0002 | t0004 | g0376 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0021 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0343 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0374 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0029 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02896 | hp1 | a0001 | c0001 | t0036 | g0382 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02897 | hp1 | a0001 | c0001 | t0031 | g0028 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02897 | hp2 | a0001 | c0001 | t0036 | g0381 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02965 | hp1 | a0001 | c0003 | t0002 | g0002 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02965 | hp2 | a0001 | c0001 | t0063 | g0051 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0189 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0035 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02976 | hp1 | a0001 | c0001 | t0050 | g0363 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02976 | hp2 | a0001 | c0001 | t0044 | g0120 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0111 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0362 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03041 | hp2 | a0001 | c0001 | t0062 | g0047 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0050 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03098 | hp2 | a0001 | c0001 | t0064 | g0030 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0117 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03130 | hp2 | a0003 | c0004 | t0037 | g0367 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03209 | hp1 | a0002 | c0002 | t0015 | g0379 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03209 | hp2 | a0001 | c0001 | t0034 | g0031 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03225 | hp2 | a0002 | c0002 | t0009 | g0369 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0024 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0118 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03491 | hp1 | a0001 | c0001 | t0012 | g0160 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03491 | hp2 | a0001 | c0001 | t0030 | g0045 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0196 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03492 | hp2 | a0001 | c0001 | t0021 | g0042 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03516 | hp2 | a0001 | c0001 | t0034 | g0034 | AFR | ESN | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03540 | hp1 | a0001 | c0001 | t0015 | g0119 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0039 | AFR | GWD | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03579 | hp1 | a0002 | c0002 | t0015 | g0377 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0037 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03654 | hp1 | a0001 | c0001 | t0045 | g0295 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0245 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0326 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0353 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0170 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0325 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03704 | hp2 | a0001 | c0001 | t0041 | g0321 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0340 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0044 | SAS | PJL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0181 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0183 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03834 | hp1 | a0001 | c0001 | t0033 | g0327 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0046 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03927 | hp1 | a0001 | c0001 | t0066 | g0387 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03927 | hp2 | a0001 | c0001 | t0026 | g0218 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03942 | hp1 | a0001 | c0001 | t0016 | g0351 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0063 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0048 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0264 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0323 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0204 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0225 | SAS | STU | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | YRI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18522 | hp2 | a0001 | c0001 | t0046 | g0041 | AFR | YRI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | CHB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | CHB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18747 | hp2 | a0007 | c0009 | t0005 | g0358 | EAS | CHB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0356 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18943 | hp2 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0331 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0357 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0280 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0306 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0194 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18948 | hp2 | a0001 | c0001 | t0035 | g0286 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18950 | hp1 | a0001 | c0001 | t0023 | g0237 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18953 | hp1 | a0001 | c0001 | t0017 | g0384 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0270 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18954 | hp1 | a0001 | c0001 | t0021 | g0361 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18956 | hp2 | a0001 | c0001 | t0049 | g0062 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18957 | hp2 | a0001 | c0001 | t0027 | g0359 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18961 | hp1 | a0001 | c0001 | t0065 | g0385 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18961 | hp2 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18962 | hp1 | a0001 | c0001 | t0008 | g0228 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18968 | hp1 | a0001 | c0001 | t0039 | g0172 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18970 | hp2 | a0001 | c0001 | t0007 | g0126 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18980 | hp2 | a0001 | c0001 | t0029 | g0158 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18982 | hp2 | a0001 | c0001 | t0029 | g0166 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18983 | hp2 | a0001 | c0001 | t0013 | g0110 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0066 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18990 | hp1 | a0001 | c0001 | t0013 | g0074 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18990 | hp2 | a0001 | c0001 | t0028 | g0215 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18992 | hp1 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18994 | hp2 | a0004 | c0005 | t0001 | g0010 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0256 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA18997 | hp2 | a0001 | c0001 | t0006 | g0240 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19001 | hp2 | a0001 | c0001 | t0022 | g0077 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0262 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0179 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19003 | hp2 | a0001 | c0001 | t0061 | g0134 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19006 | hp2 | a0001 | c0001 | t0057 | g0200 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19009 | hp2 | a0001 | c0001 | t0017 | g0386 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19030 | hp1 | a0002 | c0002 | t0004 | g0006 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19030 | hp2 | a0001 | c0001 | t0059 | g0055 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19043 | hp2 | a0001 | c0001 | t0027 | g0337 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19054 | hp1 | a0001 | c0001 | t0013 | g0257 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19054 | hp2 | a0001 | c0001 | t0012 | g0282 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19055 | hp1 | a0008 | c0011 | t0025 | g0365 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0332 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19058 | hp1 | a0001 | c0001 | t0019 | g0221 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19060 | hp1 | a0001 | c0001 | t0013 | g0259 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19065 | hp1 | a0001 | c0001 | t0053 | g0075 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0115 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19068 | hp2 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19083 | hp1 | a0001 | c0001 | t0008 | g0177 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19083 | hp2 | a0004 | c0005 | t0042 | g0009 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19084 | hp2 | a0001 | c0001 | t0023 | g0144 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0261 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19090 | hp1 | a0001 | c0001 | t0023 | g0193 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19090 | hp2 | a0001 | c0001 | t0017 | g0383 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19091 | hp1 | a0001 | c0001 | t0035 | g0285 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19091 | hp2 | a0001 | c0001 | t0019 | g0300 | EAS | JPT | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0186 | AFR | YRI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20129 | hp1 | a0001 | c0001 | t0032 | g0032 | AFR | ASW | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | ASW | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0131 | EUR | TSI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0253 | EUR | TSI | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20905 | hp1 | a0001 | c0001 | t0060 | g0322 | SAS | GIH | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0195 | SAS | GIH | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02109 | hp1 | a0002 | c0002 | t0004 | g0372 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02486 | hp2 | a0001 | c0001 | t0052 | g0317 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG02559 | hp2 | a0009 | c0007 | t0001 | g0008 | AFR | ACB | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG03471 | hp2 | a0001 | c0001 | t0054 | g0053 | AFR | MSL | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG06807 | hp1 | a0001 | c0001 | t0020 | g0136 | AFR | USA | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0338 | AFR | USA | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | USA | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0002 | AFR | USA | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA21309 | hp1 | a0001 | c0001 | t0056 | g0133 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0187 | AFR | LWK | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0164 | REF | REF | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0004 | g0006 | REF | REF | FAM174B_chr15_92612448_92660775 | FAM174B | chr15 | 92612448 | 92660775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92630254
|
C | A | 1 | a0007 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.436G>T | p.Asp146Tyr | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/3 | 552/2604 | 436/480 | 146/159 | chr15 | 92630254 | ||
| chr15:92630320
|
G | A | 1 | a0006 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.370C>T | p.Arg124Cys | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/3 | 486/2604 | 370/480 | 124/159 | chr15 | 92630320 | ||
| chr15:92655448
|
TTGGAGC | T | 8 | a0001a0003a0004others(5): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
disruptive_inframe_deletion | MODERATE | c.206_211delGCTCCA | p.Ser69_Ser70del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 327/2604 | 206/480 | 69/159 | chr15 | 92655448 | ||
| chr15:92655521
|
G | A | 1 | a0008 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.139C>T | p.Pro47Ser | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 255/2604 | 139/480 | 47/159 | chr15 | 92655521 | ||
| chr15:92655554
|
A | G | 7 | a0001a0004a0005others(4): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
missense_variant | MODERATE | c.106T>C | p.Trp36Arg | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 222/2604 | 106/480 | 36/159 | chr15 | 92655554 | ||
| chr15:92655559
|
G | T | 1 | a0004 | 2 | NA18994.hp2 NA19083.hp2 |
missense_variant | MODERATE | c.101C>A | p.Ala34Glu | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 217/2604 | 101/480 | 34/159 | chr15 | 92655559 | ||
| chr15:92655620
|
G | T | 1 | a0009 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.40C>A | p.Leu14Met | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 156/2604 | 40/480 | 14/159 | chr15 | 92655620 | ||
| chr15:92655635
|
G | C | 1 | a0005 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.25C>G | p.Pro9Ala | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 141/2604 | 25/480 | 9/159 | chr15 | 92655635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92630237
|
G | C | 1 | a0001c0006 | 2 | HG01891.hp2 HG02257.hp2 |
synonymous_variant | LOW | c.453C>G | p.Ser151Ser | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/3 | 569/2604 | 453/480 | 151/159 | chr15 | 92630237 | ||
| chr15:92630273
|
C | T | 1 | a0001c0003 | 5 | HG02630.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.417G>A | p.Ala139Ala | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/3 | 533/2604 | 417/480 | 139/159 | chr15 | 92630273 | ||
| chr15:92655441
|
A | G | 10 | a0001c0001a0001c0003a0001c0006others(7): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
synonymous_variant | LOW | c.219T>C | p.Ser73Ser | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 335/2604 | 219/480 | 73/159 | chr15 | 92655441 | ||
| chr15:92655492
|
C | T | 1 | a0001c0008 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.168G>A | p.Arg56Arg | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 284/2604 | 168/480 | 56/159 | chr15 | 92655492 | ||
| chr15:92655540
|
C | T | 1 | a0001c0008 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.120G>A | p.Glu40Glu | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 236/2604 | 120/480 | 40/159 | chr15 | 92655540 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92617590
|
G | A | 3 | a0001c0001t0047a0001c0001t0048a0001c0001t0050 | 3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1866C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1866 | chr15 | 92617590 | |||||
| chr15:92617707
|
C | T | 3 | a0001c0001t0060a0001c0001t0061a0004c0005t0042 | 3 | NA19003.hp2 NA19083.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1749 | chr15 | 92617707 | |||||
| chr15:92617719
|
C | G | 3 | a0001c0001t0060a0001c0001t0061a0004c0005t0042 | 3 | NA19003.hp2 NA19083.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1737G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1737 | chr15 | 92617719 | |||||
| chr15:92617868
|
GC | G | 3 | a0001c0001t0013a0001c0001t0023a0001c0001t0053 | 11 | HG02027.hp1 HG02080.hp2 HG02602.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1587delG | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1587 | chr15 | 92617868 | |||||
| chr15:92617904
|
G | A | 2 | a0001c0001t0028a0001c0001t0039 | 3 | HG00597.hp1 NA18968.hp1 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1552C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1552 | chr15 | 92617904 | |||||
| chr15:92617966
|
G | A | 1 | a0001c0001t0023 | 3 | NA18950.hp1 NA19084.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1490C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1490 | chr15 | 92617966 | |||||
| chr15:92617990
|
C | T | 1 | a0001c0001t0056 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1466G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1466 | chr15 | 92617990 | |||||
| chr15:92618105
|
C | A | 1 | a0001c0001t0043 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1351G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1351 | chr15 | 92618105 | |||||
| chr15:92618150
|
A | G | 3 | a0001c0001t0060a0001c0001t0061a0004c0005t0042 | 3 | NA19003.hp2 NA19083.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1306T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1306 | chr15 | 92618150 | |||||
| chr15:92618160
|
T | C | 1 | a0001c0001t0029 | 2 | NA18980.hp2 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1296A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1296 | chr15 | 92618160 | |||||
| chr15:92618216
|
G | A | 1 | a0001c0001t0048 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1240C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1240 | chr15 | 92618216 | |||||
| chr15:92618261
|
A | G | 2 | a0001c0001t0006a0001c0001t0014 | 29 | HG01099.hp1 HG01255.hp2 HG01346.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1195T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1195 | chr15 | 92618261 | |||||
| chr15:92618271
|
G | T | 9 | a0001c0001t0003a0001c0001t0022a0001c0001t0024others(6): Show | 44 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1185C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1185 | chr15 | 92618271 | |||||
| chr15:92618414
|
C | T | 1 | a0001c0001t0051 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1042G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 1042 | chr15 | 92618414 | |||||
| chr15:92618487
|
A | G | 3 | a0001c0001t0047a0001c0001t0048a0001c0001t0050 | 3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*969T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 969 | chr15 | 92618487 | |||||
| chr15:92618493
|
G | A | 3 | a0001c0001t0020a0001c0001t0044a0001c0001t0046 | 5 | HG00544.hp2 HG01243.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*963C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 963 | chr15 | 92618493 | |||||
| chr15:92618531
|
A | AT | 17 | a0001c0001t0001a0001c0001t0012a0001c0001t0017others(14): Show | 88 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*924dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 924 | chr15 | 92618531 | |||||
| chr15:92618608
|
G | C | 19 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(16): Show | 90 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*848C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 848 | chr15 | 92618608 | |||||
| chr15:92618695
|
A | G | 5 | a0001c0001t0009a0001c0001t0031a0001c0001t0056others(2): Show | 14 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 761 | chr15 | 92618695 | |||||
| chr15:92618718
|
TCACACAC others(9): Show |
T | 4 | a0001c0001t0010a0001c0001t0032a0001c0001t0036others(1): Show | 13 | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*722_*737delCGTGTG others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 722 | chr15 | 92618718 | |||||
| chr15:92618728
|
GCACACGC others(11): Show |
G | 1 | a0001c0001t0052 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710_*727delTGCACG others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 710 | chr15 | 92618728 | |||||
| chr15:92618733
|
CGCACACA others(3): Show |
C | 1 | a0001c0001t0041 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*713_*722delACGTGT others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 713 | chr15 | 92618733 | |||||
| chr15:92618744
|
G | GCA | 3 | a0001c0001t0021a0001c0001t0030a0002c0002t0030 | 5 | HG02258.hp1 HG02735.hp1 HG03491.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*710_*711dupTG | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 711 | chr15 | 92618744 | |||||
| chr15:92618744
|
GCA | G | 40 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(37): Show | 191 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*710_*711delTG | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 710 | chr15 | 92618744 | |||||
| chr15:92618746
|
A | G | 17 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(14): Show | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*710T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 710 | chr15 | 92618746 | |||||
| chr15:92618748
|
A | G | 1 | a0001c0001t0034 | 2 | HG03209.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*708T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 708 | chr15 | 92618748 | |||||
| chr15:92618782
|
A | C | 1 | a0001c0001t0058 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*674T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 674 | chr15 | 92618782 | |||||
| chr15:92618786
|
T | A | 1 | a0001c0001t0054 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 670 | chr15 | 92618786 | |||||
| chr15:92618828
|
C | CT | 17 | a0001c0001t0001a0001c0001t0017a0001c0001t0026others(14): Show | 81 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*627dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 627 | chr15 | 92618828 | |||||
| chr15:92618839
|
T | A | 2 | a0001c0001t0025a0008c0011t0025 | 3 | HG02523.hp1 HG02523.hp2 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*617A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 617 | chr15 | 92618839 | |||||
| chr15:92618839
|
T | TA | 14 | a0001c0001t0002a0001c0001t0010a0001c0001t0024others(11): Show | 70 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*616_*617insT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 616 | chr15 | 92618839 | |||||
| chr15:92618840
|
T | A | 22 | a0001c0001t0002a0001c0001t0008a0001c0001t0010others(19): Show | 93 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*616A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 616 | chr15 | 92618840 | |||||
| chr15:92618840
|
T | TA | 14 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(11): Show | 75 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*615dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 615 | chr15 | 92618840 | |||||
| chr15:92618840
|
T | TAA | 6 | a0001c0001t0009a0001c0001t0011a0001c0001t0033others(3): Show | 23 | HG01109.hp1 HG01109.hp2 HG02055.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*614_*615dupTT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 615 | chr15 | 92618840 | |||||
| chr15:92618840
|
TA | T | 7 | a0001c0001t0005a0001c0001t0006a0001c0001t0021others(4): Show | 57 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*615delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 615 | chr15 | 92618840 | |||||
| chr15:92618840
|
TAA | T | 2 | a0001c0001t0014a0001c0001t0027 | 8 | HG01099.hp1 HG01255.hp2 HG01928.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*614_*615delTT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 614 | chr15 | 92618840 | |||||
| chr15:92618841
|
A | T | 19 | a0001c0001t0001a0001c0001t0012a0001c0001t0015others(16): Show | 96 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*615T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 615 | chr15 | 92618841 | |||||
| chr15:92618842
|
A | T | 6 | a0001c0001t0012a0001c0001t0026a0001c0001t0039others(3): Show | 12 | HG00140.hp1 HG00558.hp1 HG01496.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*614T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 614 | chr15 | 92618842 | |||||
| chr15:92618844
|
A | G | 1 | a0001c0001t0038 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 612 | chr15 | 92618844 | |||||
| chr15:92618881
|
G | A | 2 | a0001c0001t0060a0001c0001t0061 | 2 | NA19003.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*575C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 575 | chr15 | 92618881 | |||||
| chr15:92618976
|
C | CA | 2 | a0001c0001t0011a0001c0001t0062 | 9 | HG01109.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*479dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 479 | chr15 | 92618976 | |||||
| chr15:92619155
|
T | A | 1 | a0001c0001t0035 | 2 | NA18948.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*301A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 301 | chr15 | 92619155 | |||||
| chr15:92619301
|
T | C | 1 | a0001c0001t0063 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*155A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 155 | chr15 | 92619301 | |||||
| chr15:92619310
|
C | A | 1 | a0001c0001t0064 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 146 | chr15 | 92619310 | |||||
| chr15:92619419
|
A | G | 1 | a0003c0004t0037 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*37T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 37 | chr15 | 92619419 | |||||
| chr15:92655666
|
G | A | 1 | a0001c0001t0036 | 2 | HG02896.hp1 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-7C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 7 | chr15 | 92655666 | |||||
| chr15:92655705
|
G | C | 2 | a0001c0001t0017a0001c0001t0065 | 6 | NA18953.hp1 NA18961.hp1 NA18961.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-46C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 46 | chr15 | 92655705 | |||||
| chr15:92655717
|
G | A | 1 | a0001c0001t0066 | 1 | HG03927.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/3 | 58 | chr15 | 92655717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92619476
|
G | T | 8 | a0001c0001t0011g0024a0001c0001t0011g0033a0001c0001t0011g0035others(5): Show | 8 | HG01109.hp1 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.477-17C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92619476 | ||||||
| chr15:92619672
|
C | T | 79 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(76): Show | 80 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.477-213G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92619672 | ||||||
| chr15:92619795
|
G | A | 63 | a0001c0001t0001g0302a0001c0001t0004g0064a0001c0001t0004g0232others(60): Show | 65 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.477-336C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92619795 | ||||||
| chr15:92619833
|
G | A | 1 | a0001c0001t0002g0125 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.477-374C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92619833 | ||||||
| chr15:92620240
|
G | A | 1 | a0001c0001t0003g0164 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.477-781C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620240 | ||||||
| chr15:92620269
|
C | T | 13 | a0001c0001t0009g0019a0001c0001t0009g0020a0001c0001t0009g0029others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.477-810G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620269 | ||||||
| chr15:92620291
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.477-832C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620291 | ||||||
| chr15:92620477
|
A | AAG | 12 | a0001c0001t0005g0231a0001c0001t0013g0074a0001c0001t0013g0110others(9): Show | 12 | HG02027.hp1 HG02027.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.477-1019_477-1018i others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620477 | ||||||
| chr15:92620492
|
C | T | 11 | a0001c0001t0013g0074a0001c0001t0013g0110a0001c0001t0013g0142others(8): Show | 11 | HG02027.hp1 HG02080.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.477-1033G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620492 | ||||||
| chr15:92620613
|
G | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.477-1154C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620613 | ||||||
| chr15:92620771
|
C | T | 11 | a0001c0001t0013g0074a0001c0001t0013g0110a0001c0001t0013g0142others(8): Show | 11 | HG02027.hp1 HG02080.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.477-1312G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620771 | ||||||
| chr15:92620814
|
C | CA | 102 | a0001c0001t0001g0040a0001c0001t0001g0302a0001c0001t0002g0005others(99): Show | 104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.477-1356dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620814 | ||||||
| chr15:92620814
|
C | CAA | 84 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0001g0082others(81): Show | 85 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.477-1357_477-1356d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620814 | ||||||
| chr15:92620814
|
C | CAAA | 32 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0095others(29): Show | 32 | HG01074.hp2 HG01106.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.477-1358_477-1356d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620814 | ||||||
| chr15:92620814
|
CA | C | 58 | a0001c0001t0004g0046a0001c0001t0004g0085a0001c0001t0004g0093others(55): Show | 58 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.477-1356delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620814 | ||||||
| chr15:92620854
|
A | C | 1 | a0001c0001t0063g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.477-1395T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620854 | ||||||
| chr15:92620857
|
T | C | 2 | a0001c0001t0035g0285a0001c0001t0035g0286 | 2 | NA18948.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.477-1398A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620857 | ||||||
| chr15:92620883
|
G | T | 1 | a0001c0001t0008g0280 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.477-1424C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620883 | ||||||
| chr15:92620984
|
T | G | 88 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(85): Show | 89 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.477-1525A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620984 | ||||||
| chr15:92620986
|
C | T | 59 | a0001c0001t0003g0060a0001c0001t0003g0067a0001c0001t0003g0080others(56): Show | 59 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.477-1527G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92620986 | ||||||
| chr15:92621169
|
C | T | 1 | a0001c0001t0026g0127 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.477-1710G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621169 | ||||||
| chr15:92621257
|
C | T | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.477-1798G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621257 | ||||||
| chr15:92621261
|
C | T | 1 | a0001c0001t0022g0315 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.477-1802G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621261 | ||||||
| chr15:92621347
|
C | T | 4 | a0001c0001t0020g0121a0001c0001t0020g0136a0001c0001t0020g0345others(1): Show | 4 | HG00544.hp2 HG01243.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-1888G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621347 | ||||||
| chr15:92621393
|
C | T | 1 | a0001c0001t0021g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.477-1934G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621393 | ||||||
| chr15:92621553
|
T | C | 2 | a0001c0001t0003g0254a0001c0001t0007g0268 | 2 | HG02004.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.477-2094A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621553 | ||||||
| chr15:92621594
|
G | C | 19 | a0001c0001t0011g0024a0001c0001t0011g0033a0001c0001t0011g0035others(16): Show | 19 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.477-2135C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621594 | ||||||
| chr15:92621608
|
C | CA | 82 | a0001c0001t0001g0058a0001c0001t0001g0151a0001c0001t0001g0209others(79): Show | 84 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.477-2150dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621608 | ||||||
| chr15:92621608
|
CA | C | 95 | a0001c0001t0001g0100a0001c0001t0002g0159a0001c0001t0002g0173others(92): Show | 95 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.477-2150delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621608 | ||||||
| chr15:92621735
|
C | A | 289 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.477-2276G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621735 | ||||||
| chr15:92621736
|
A | C | 289 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.477-2277T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621736 | ||||||
| chr15:92621763
|
T | C | 87 | a0001c0001t0001g0157a0001c0001t0004g0064a0001c0001t0004g0232others(84): Show | 89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.477-2304A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621763 | ||||||
| chr15:92621928
|
C | T | 1 | a0001c0001t0027g0337 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.477-2469G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92621928 | ||||||
| chr15:92622114
|
G | A | 1 | a0001c0001t0052g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.477-2655C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622114 | ||||||
| chr15:92622269
|
G | A | 7 | a0001c0001t0011g0024a0001c0001t0011g0033a0001c0001t0011g0035others(4): Show | 7 | HG01109.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-2810C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622269 | ||||||
| chr15:92622304
|
G | A | 1 | a0001c0001t0015g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.477-2845C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622304 | ||||||
| chr15:92622366
|
A | G | 193 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(190): Show | 197 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.477-2907T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622366 | ||||||
| chr15:92622389
|
G | A | 1 | a0001c0001t0054g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.477-2930C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622389 | ||||||
| chr15:92622418
|
A | G | 177 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(174): Show | 181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.477-2959T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622418 | ||||||
| chr15:92622526
|
T | C | 1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.477-3067A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622526 | ||||||
| chr15:92622556
|
TC | T | 41 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(38): Show | 42 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.477-3098delG | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622556 | ||||||
| chr15:92622572
|
T | C | 1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.477-3113A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622572 | ||||||
| chr15:92622683
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.477-3224C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622683 | ||||||
| chr15:92622733
|
C | T | 160 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.477-3274G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622733 | ||||||
| chr15:92622766
|
T | C | 2 | a0001c0001t0001g0104a0009c0007t0001g0008 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.477-3307A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622766 | ||||||
| chr15:92622808
|
G | A | 7 | a0001c0001t0011g0024a0001c0001t0011g0033a0001c0001t0011g0035others(4): Show | 7 | HG01109.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-3349C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622808 | ||||||
| chr15:92622867
|
T | G | 1 | a0001c0001t0051g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.477-3408A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92622867 | ||||||
| chr15:92623223
|
G | A | 69 | a0001c0001t0003g0088a0001c0001t0004g0064a0001c0001t0004g0232others(66): Show | 71 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.477-3764C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623223 | ||||||
| chr15:92623471
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.477-4012G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623471 | ||||||
| chr15:92623547
|
T | A | 2 | a0001c0001t0020g0121a0001c0001t0044g0120 | 2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.477-4088A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623547 | ||||||
| chr15:92623560
|
T | G | 187 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(184): Show | 191 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.477-4101A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623560 | ||||||
| chr15:92623644
|
G | C | 4 | a0002c0002t0004g0372a0002c0002t0004g0375a0002c0002t0004g0376others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.477-4185C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623644 | ||||||
| chr15:92623668
|
G | A | 3 | a0001c0001t0005g0323a0001c0001t0005g0325a0001c0001t0010g0102 | 3 | HG00735.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.477-4209C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623668 | ||||||
| chr15:92623670
|
C | T | 41 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(38): Show | 42 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.477-4211G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623670 | ||||||
| chr15:92623682
|
G | A | 3 | a0001c0001t0047g0364a0001c0001t0048g0122a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.477-4223C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623682 | ||||||
| chr15:92623688
|
G | C | 1 | a0001c0001t0002g0188 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.477-4229C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623688 | ||||||
| chr15:92623788
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.477-4329G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623788 | ||||||
| chr15:92623792
|
T | G | 183 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(180): Show | 187 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.477-4333A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623792 | ||||||
| chr15:92623804
|
C | G | 1 | a0001c0001t0002g0263 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.477-4345G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623804 | ||||||
| chr15:92623820
|
C | A | 40 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(37): Show | 41 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.477-4361G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623820 | ||||||
| chr15:92623829
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.477-4370C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623829 | ||||||
| chr15:92623968
|
T | C | 2 | a0001c0001t0001g0104a0009c0007t0001g0008 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.477-4509A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92623968 | ||||||
| chr15:92624004
|
T | C | 1 | a0001c0001t0003g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.477-4545A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624004 | ||||||
| chr15:92624107
|
T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | NA18963.hp1 NA18968.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.477-4648A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624107 | ||||||
| chr15:92624261
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0104a0001c0001t0064g0030others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-4802G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624261 | ||||||
| chr15:92624299
|
T | C | 2 | a0001c0001t0020g0136a0001c0001t0020g0345 | 2 | HG00544.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.477-4840A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624299 | ||||||
| chr15:92624324
|
C | T | 11 | a0001c0001t0006g0261a0001c0001t0006g0262a0001c0001t0006g0265others(8): Show | 11 | HG02027.hp1 HG02602.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.477-4865G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624324 | ||||||
| chr15:92624402
|
CCATT | C | 64 | a0001c0001t0003g0088a0001c0001t0004g0064a0001c0001t0004g0232others(61): Show | 66 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.477-4947_477-4944d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624402 | ||||||
| chr15:92624570
|
T | G | 33 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0199others(30): Show | 33 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.477-5111A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624570 | ||||||
| chr15:92624627
|
C | T | 72 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(69): Show | 73 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.477-5168G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624627 | ||||||
| chr15:92624739
|
C | T | 199 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(196): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.477-5280G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624739 | ||||||
| chr15:92624758
|
C | G | 187 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(184): Show | 191 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.477-5299G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624758 | ||||||
| chr15:92624822
|
G | C | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.477-5363C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624822 | ||||||
| chr15:92624847
|
C | T | 1 | a0008c0011t0025g0365 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.476+5367G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624847 | ||||||
| chr15:92624859
|
C | T | 148 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(145): Show | 149 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.476+5355G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624859 | ||||||
| chr15:92624897
|
C | G | 1 | a0001c0001t0002g0125 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.476+5317G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624897 | ||||||
| chr15:92624899
|
C | T | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.476+5315G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624899 | ||||||
| chr15:92624920
|
G | A | 21 | a0001c0001t0004g0046a0001c0001t0004g0048a0001c0001t0004g0085others(18): Show | 21 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.476+5294C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624920 | ||||||
| chr15:92624954
|
G | A | 70 | a0001c0001t0001g0302a0001c0001t0003g0088a0001c0001t0004g0064others(67): Show | 72 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.476+5260C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624954 | ||||||
| chr15:92624965
|
C | G | 2 | a0002c0002t0004g0372a0002c0002t0030g0373 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.476+5249G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92624965 | ||||||
| chr15:92625061
|
G | C | 1 | a0001c0001t0049g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.476+5153C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625061 | ||||||
| chr15:92625663
|
T | C | 1 | a0001c0001t0054g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.476+4551A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625663 | ||||||
| chr15:92625692
|
A | G | 198 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(195): Show | 203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.476+4522T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625692 | ||||||
| chr15:92625710
|
G | A | 1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.476+4504C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625710 | ||||||
| chr15:92625717
|
G | A | 13 | a0001c0001t0002g0022a0001c0001t0008g0012a0001c0001t0008g0015others(10): Show | 14 | HG00099.hp1 HG02257.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.476+4497C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625717 | ||||||
| chr15:92625751
|
C | T | 1 | a0001c0001t0017g0386 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.476+4463G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625751 | ||||||
| chr15:92625786
|
T | C | 2 | a0001c0001t0010g0014a0001c0001t0010g0036 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.476+4428A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625786 | ||||||
| chr15:92625857
|
T | A | 1 | a0001c0001t0005g0323 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.476+4357A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625857 | ||||||
| chr15:92625978
|
GA | G | 42 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0288others(39): Show | 42 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.476+4235delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92625978 | ||||||
| chr15:92626028
|
A | G | 1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.476+4186T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626028 | ||||||
| chr15:92626114
|
A | AT | 53 | a0001c0001t0001g0302a0001c0001t0002g0005a0001c0001t0002g0069others(50): Show | 54 | HG00639.hp1 HG00673.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.476+4099dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626114 | ||||||
| chr15:92626114
|
A | ATT | 6 | a0001c0001t0006g0265a0001c0001t0007g0154a0001c0001t0007g0256others(3): Show | 6 | HG01071.hp2 HG02027.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.476+4098_476+4099d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626114 | ||||||
| chr15:92626114
|
AT | A | 168 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(165): Show | 171 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.476+4099delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626114 | ||||||
| chr15:92626134
|
T | G | 2 | a0001c0001t0003g0143a0001c0001t0039g0172 | 2 | HG02080.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.476+4080A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626134 | ||||||
| chr15:92626135
|
T | A | 2 | a0001c0001t0003g0143a0001c0001t0039g0172 | 2 | HG02080.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.476+4079A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626135 | ||||||
| chr15:92626139
|
A | ACGGAGTC others(12): Show |
352 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(349): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.476+4074_476+4075i others(21): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626139 | ||||||
| chr15:92626139
|
A | AGTCTCGC others(8): Show |
2 | a0001c0001t0003g0143a0001c0001t0039g0172 | 2 | HG02080.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.476+4074_476+4075i others(17): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626139 | ||||||
| chr15:92626159
|
C | A | 3 | a0001c0001t0006g0091a0001c0001t0006g0242a0001c0001t0014g0236 | 3 | HG01943.hp1 HG01981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.476+4055G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626159 | ||||||
| chr15:92626167
|
T | C | 2 | a0001c0001t0003g0001a0001c0001t0003g0018 | 3 | HG01891.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.476+4047A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626167 | ||||||
| chr15:92626199
|
C | T | 71 | a0001c0001t0003g0088a0001c0001t0004g0064a0001c0001t0004g0232others(68): Show | 73 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.476+4015G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626199 | ||||||
| chr15:92626212
|
C | T | 5 | a0001c0001t0020g0121a0001c0001t0044g0120a0001c0001t0047g0364others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+4002G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626212 | ||||||
| chr15:92626230
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.476+3984G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626230 | ||||||
| chr15:92626369
|
T | A | 68 | a0001c0001t0003g0088a0001c0001t0004g0064a0001c0001t0004g0232others(65): Show | 70 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.476+3845A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626369 | ||||||
| chr15:92626379
|
G | A | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.476+3835C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626379 | ||||||
| chr15:92626414
|
T | A | 69 | a0001c0001t0003g0088a0001c0001t0004g0048a0001c0001t0004g0064others(66): Show | 71 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.476+3800A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626414 | ||||||
| chr15:92626415
|
A | T | 42 | a0001c0001t0001g0302a0001c0001t0002g0005a0001c0001t0002g0069others(39): Show | 43 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.476+3799T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626415 | ||||||
| chr15:92626462
|
A | T | 3 | a0001c0001t0047g0364a0001c0001t0048g0122a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.476+3752T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626462 | ||||||
| chr15:92626548
|
A | C | 69 | a0001c0001t0003g0088a0001c0001t0004g0064a0001c0001t0004g0232others(66): Show | 71 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.476+3666T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626548 | ||||||
| chr15:92626635
|
G | A | 4 | a0001c0001t0003g0271a0001c0001t0047g0364a0001c0001t0048g0122others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+3579C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626635 | ||||||
| chr15:92626827
|
T | G | 7 | a0001c0001t0015g0118a0001c0001t0015g0119a0001c0001t0015g0189others(4): Show | 7 | HG02280.hp1 HG02970.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.476+3387A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626827 | ||||||
| chr15:92626870
|
G | A | 2 | a0001c0001t0003g0001a0001c0001t0003g0018 | 3 | HG01891.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.476+3344C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626870 | ||||||
| chr15:92626929
|
G | A | 1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.476+3285C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92626929 | ||||||
| chr15:92627027
|
G | A | 1 | a0001c0001t0015g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.476+3187C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627027 | ||||||
| chr15:92627068
|
C | A | 1 | a0001c0001t0049g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.476+3146G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627068 | ||||||
| chr15:92627082
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.476+3132G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627082 | ||||||
| chr15:92627101
|
G | A | 41 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(38): Show | 42 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.476+3113C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627101 | ||||||
| chr15:92627113
|
T | C | 1 | a0001c0001t0014g0156 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.476+3101A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627113 | ||||||
| chr15:92627176
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0104a0001c0001t0064g0030others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+3038C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627176 | ||||||
| chr15:92627179
|
G | A | 8 | a0001c0001t0001g0109a0001c0001t0001g0153a0001c0001t0001g0157others(5): Show | 8 | HG00140.hp1 HG01175.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.476+3035C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627179 | ||||||
| chr15:92627232
|
C | G | 43 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(40): Show | 44 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.476+2982G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627232 | ||||||
| chr15:92627306
|
T | C | 1 | a0001c0006t0024g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.476+2908A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627306 | ||||||
| chr15:92627355
|
C | T | 1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.476+2859G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627355 | ||||||
| chr15:92627389
|
C | G | 3 | a0001c0001t0004g0340a0001c0001t0004g0347a0001c0001t0051g0026 | 3 | HG01192.hp2 HG02258.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.476+2825G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627389 | ||||||
| chr15:92627426
|
G | A | 2 | a0001c0001t0023g0144a0001c0001t0023g0237 | 2 | NA18950.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.476+2788C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627426 | ||||||
| chr15:92627574
|
T | C | 68 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0069others(65): Show | 70 | HG00099.hp1 HG00639.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.476+2640A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627574 | ||||||
| chr15:92627630
|
C | G | 4 | a0001c0001t0010g0333a0001c0001t0010g0362a0001c0001t0032g0032others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.476+2584G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627630 | ||||||
| chr15:92627697
|
G | A | 1 | a0001c0001t0054g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.476+2517C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627697 | ||||||
| chr15:92627713
|
G | C | 1 | a0001c0001t0013g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.476+2501C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627713 | ||||||
| chr15:92627792
|
C | T | 2 | a0001c0001t0011g0050a0001c0001t0063g0051 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.476+2422G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627792 | ||||||
| chr15:92627793
|
G | A | 3 | a0002c0002t0009g0369a0002c0002t0009g0371a0002c0002t0031g0370 | 3 | HG02451.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.476+2421C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627793 | ||||||
| chr15:92627800
|
T | C | 1 | a0003c0004t0037g0367 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.476+2414A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627800 | ||||||
| chr15:92627809
|
G | C | 44 | a0001c0001t0001g0302a0001c0001t0002g0005a0001c0001t0002g0069others(41): Show | 45 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.476+2405C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627809 | ||||||
| chr15:92627864
|
A | T | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2350T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627864 | ||||||
| chr15:92627866
|
G | C | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2348C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627866 | ||||||
| chr15:92627868
|
G | A | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2346C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627868 | ||||||
| chr15:92627871
|
A | C | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2343T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627871 | ||||||
| chr15:92627874
|
G | T | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2340C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627874 | ||||||
| chr15:92627875
|
A | T | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2339T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627875 | ||||||
| chr15:92627877
|
A | T | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2337T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627877 | ||||||
| chr15:92627879
|
A | T | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2335T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627879 | ||||||
| chr15:92627880
|
A | C | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2334T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627880 | ||||||
| chr15:92627883
|
G | T | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2331C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627883 | ||||||
| chr15:92627892
|
T | C | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2322A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627892 | ||||||
| chr15:92627894
|
A | C | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2320T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627894 | ||||||
| chr15:92627896
|
A | T | 1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.476+2318T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627896 | ||||||
| chr15:92627914
|
T | G | 44 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(41): Show | 45 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.476+2300A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627914 | ||||||
| chr15:92627928
|
G | A | 2 | a0001c0001t0005g0169a0001c0001t0005g0176 | 2 | NA18979.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.476+2286C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627928 | ||||||
| chr15:92627930
|
A | T | 189 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(186): Show | 193 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.476+2284T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92627930 | ||||||
| chr15:92628052
|
A | C | 4 | a0001c0001t0016g0351a0001c0001t0016g0352a0001c0001t0033g0327others(1): Show | 4 | HG02451.hp2 HG02683.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.476+2162T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628052 | ||||||
| chr15:92628171
|
AT | A | 72 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(69): Show | 73 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.476+2042delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628171 | ||||||
| chr15:92628338
|
CT | C | 179 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(176): Show | 181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.476+1875delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628338 | ||||||
| chr15:92628338
|
CTT | C | 113 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0083others(110): Show | 115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.476+1874_476+1875d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628338 | ||||||
| chr15:92628338
|
CTTT | C | 38 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(35): Show | 39 | HG00639.hp1 HG01071.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.476+1873_476+1875d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628338 | ||||||
| chr15:92628338
|
CTTTTTTT others(5): Show |
C | 1 | a0003c0004t0037g0367 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.476+1864_476+1875d others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628338 | ||||||
| chr15:92628443
|
A | G | 43 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(40): Show | 44 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.476+1771T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628443 | ||||||
| chr15:92628537
|
G | T | 4 | a0001c0001t0017g0007a0001c0001t0017g0383a0001c0001t0017g0384others(1): Show | 5 | NA18953.hp1 NA18961.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.476+1677C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628537 | ||||||
| chr15:92628538
|
A | C | 3 | a0001c0001t0047g0364a0001c0001t0048g0122a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.476+1676T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628538 | ||||||
| chr15:92628745
|
C | T | 2 | a0001c0001t0004g0181a0001c0001t0004g0204 | 2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.476+1469G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628745 | ||||||
| chr15:92628800
|
T | A | 1 | a0001c0001t0003g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.476+1414A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628800 | ||||||
| chr15:92628964
|
C | G | 43 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(40): Show | 44 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.476+1250G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92628964 | ||||||
| chr15:92629084
|
ACCG | A | 8 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0008g0191others(5): Show | 8 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.476+1127_476+1129d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629084 | ||||||
| chr15:92629250
|
A | G | 44 | a0001c0001t0002g0005a0001c0001t0002g0069a0001c0001t0002g0205others(41): Show | 45 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.476+964T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629250 | ||||||
| chr15:92629340
|
C | T | 4 | a0001c0001t0004g0329a0001c0001t0047g0364a0001c0001t0048g0122others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+874G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629340 | ||||||
| chr15:92629346
|
A | G | 3 | a0001c0001t0009g0020a0001c0001t0015g0043a0003c0004t0037g0367 | 3 | HG01884.hp1 HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.476+868T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629346 | ||||||
| chr15:92629361
|
A | G | 2 | a0001c0001t0016g0341a0001c0001t0020g0345 | 2 | HG00099.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.476+853T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629361 | ||||||
| chr15:92629375
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.476+839A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629375 | ||||||
| chr15:92629445
|
C | A | 1 | a0001c0001t0005g0323 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.476+769G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629445 | ||||||
| chr15:92629445
|
CGCCACCC others(5): Show |
C | 1 | a0001c0001t0005g0196 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.476+757_476+768del others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629445 | ||||||
| chr15:92629446
|
G | A | 10 | a0001c0001t0001g0283a0001c0001t0002g0069a0001c0001t0002g0205others(7): Show | 10 | HG02165.hp1 NA18946.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.476+768C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629446 | ||||||
| chr15:92629537
|
C | T | 1 | a0001c0001t0022g0260 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.476+677G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629537 | ||||||
| chr15:92629652
|
A | G | 2 | a0001c0001t0023g0144a0001c0001t0023g0237 | 2 | NA18950.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.476+562T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629652 | ||||||
| chr15:92629783
|
C | T | 1 | a0001c0001t0015g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.476+431G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629783 | ||||||
| chr15:92629806
|
C | A | 1 | a0001c0001t0011g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.476+408G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629806 | ||||||
| chr15:92629842
|
A | G | 271 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.476+372T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629842 | ||||||
| chr15:92629906
|
C | T | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.476+308G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92629906 | ||||||
| chr15:92630155
|
G | A | 1 | a0001c0001t0022g0315 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.476+59C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 2/2 | chr15 | 92630155 | ||||||
| chr15:92630357
|
G | A | 1 | a0001c0001t0004g0131 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.345-12C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630357 | ||||||
| chr15:92630423
|
G | A | 49 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(46): Show | 50 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.345-78C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630423 | ||||||
| chr15:92630539
|
C | T | 2 | a0001c0001t0036g0381a0001c0001t0036g0382 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-194G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630539 | ||||||
| chr15:92630601
|
G | A | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-256C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630601 | ||||||
| chr15:92630667
|
TAATACAC others(1): Show |
T | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-330_345-323del others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630667 | ||||||
| chr15:92630678
|
T | C | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-333A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630678 | ||||||
| chr15:92630716
|
AT | A | 16 | a0001c0001t0002g0146a0001c0001t0003g0001a0001c0001t0003g0018others(13): Show | 18 | HG01109.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-372delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630716 | ||||||
| chr15:92630717
|
T | TA | 80 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(77): Show | 82 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.345-373_345-372ins others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630717 | ||||||
| chr15:92630729
|
T | C | 4 | a0001c0001t0003g0334a0001c0001t0010g0339a0001c0001t0027g0337others(1): Show | 4 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-384A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630729 | ||||||
| chr15:92630731
|
T | C | 1 | a0001c0001t0006g0078 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.345-386A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630731 | ||||||
| chr15:92630740
|
AT | A | 9 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0009g0123others(6): Show | 9 | HG01109.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-396delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630740 | ||||||
| chr15:92630753
|
TATA | T | 6 | a0001c0001t0002g0005a0001c0001t0003g0334a0001c0001t0009g0338others(3): Show | 7 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-411_345-409del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630753 | ||||||
| chr15:92630759
|
A | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0099 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.345-414T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630759 | ||||||
| chr15:92630763
|
TATA | T | 83 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(80): Show | 85 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-421_345-419del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630763 | ||||||
| chr15:92630765
|
T | TTTTTTAT others(16): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0099 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.345-421_345-420ins others(23): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630765 | ||||||
| chr15:92630765
|
TA | T | 287 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(284): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.345-421delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630765 | ||||||
| chr15:92630766
|
A | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0099 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.345-421T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630766 | ||||||
| chr15:92630786
|
ATTACATA others(62): Show |
A | 3 | a0001c0001t0007g0044a0001c0001t0021g0042a0001c0001t0030g0045 | 3 | HG03491.hp2 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.345-510_345-442del others(69): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630786 | ||||||
| chr15:92630797
|
C | T | 1 | a0001c0001t0005g0325 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.345-452G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630797 | ||||||
| chr15:92630801
|
TTATATAT others(27): Show |
T | 29 | a0001c0001t0001g0153a0001c0001t0001g0199a0001c0001t0001g0209others(26): Show | 29 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.345-490_345-457del others(34): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630801 | ||||||
| chr15:92630804
|
T | C | 3 | a0001c0001t0007g0248a0001c0001t0007g0250a0001c0001t0058g0249 | 3 | HG01496.hp2 HG01993.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.345-459A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630804 | ||||||
| chr15:92630805
|
A | ATAT | 90 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0157others(87): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.345-463_345-461dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630805 | ||||||
| chr15:92630809
|
A | T | 4 | a0001c0001t0002g0146a0001c0001t0003g0067a0001c0001t0003g0139others(1): Show | 4 | HG01258.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-464T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630809 | ||||||
| chr15:92630809
|
ATT | A | 5 | a0001c0001t0001g0040a0001c0001t0008g0012a0001c0001t0011g0035others(2): Show | 5 | HG02970.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-466_345-465del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630809 | ||||||
| chr15:92630811
|
T | A | 90 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0157others(87): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.345-466A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630811 | ||||||
| chr15:92630811
|
T | TACGTATT others(5): Show |
7 | a0001c0001t0002g0022a0001c0001t0008g0015a0001c0001t0008g0052others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-467_345-466ins others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630811 | ||||||
| chr15:92630811
|
TTTATATA others(58): Show |
T | 1 | a0001c0001t0016g0352 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.345-531_345-467del others(65): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630811 | ||||||
| chr15:92630811
|
TTTATATA others(93): Show |
T | 1 | a0001c0001t0016g0351 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345-566_345-467del others(100): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630811 | ||||||
| chr15:92630813
|
T | C | 3 | a0001c0001t0010g0362a0001c0001t0047g0364a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.345-468A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630813 | ||||||
| chr15:92630815
|
T | C | 104 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(101): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.345-470A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630815 | ||||||
| chr15:92630815
|
TATATTAC others(23): Show |
T | 4 | a0001c0001t0004g0347a0001c0001t0012g0350a0001c0001t0020g0345others(1): Show | 4 | HG00544.hp2 HG01192.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-500_345-471del others(30): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630815 | ||||||
| chr15:92630816
|
A | G | 95 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(92): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.345-471T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630816 | ||||||
| chr15:92630816
|
ATATTACA others(170): Show |
A | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-648_345-472del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630816 | ||||||
| chr15:92630818
|
A | G | 90 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0157others(87): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.345-473T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630818 | ||||||
| chr15:92630818
|
ATTACATA others(30): Show |
A | 1 | a0001c0001t0010g0349 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.345-510_345-474del others(37): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630818 | ||||||
| chr15:92630822
|
C | T | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-477G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630822 | ||||||
| chr15:92630822
|
CATATTAT others(121): Show |
C | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.345-605_345-478del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630822 | ||||||
| chr15:92630823
|
A | G | 5 | a0001c0001t0001g0040a0001c0001t0008g0012a0001c0001t0011g0035others(2): Show | 5 | HG02970.hp2 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-478T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630823 | ||||||
| chr15:92630825
|
A | G | 14 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0002g0005others(11): Show | 15 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.345-480T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630825 | ||||||
| chr15:92630829
|
T | C | 108 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.345-484A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630829 | ||||||
| chr15:92630830
|
A | G | 1 | a0001c0001t0001g0346 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.345-485T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630830 | ||||||
| chr15:92630832
|
A | T | 1 | a0001c0001t0004g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.345-487T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630832 | ||||||
| chr15:92630833
|
T | A | 1 | a0001c0001t0004g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.345-488A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630833 | ||||||
| chr15:92630833
|
T | TTA | 91 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(88): Show | 95 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.345-490_345-489dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630833 | ||||||
| chr15:92630833
|
TTA | T | 95 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(92): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.345-490_345-489del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630833 | ||||||
| chr15:92630835
|
A | ACATATTA others(271): Show |
1 | a0001c0001t0002g0005 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.345-491_345-490ins others(278): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | ||||||
| chr15:92630835
|
A | ACATATTA others(341): Show |
1 | a0001c0001t0001g0344 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.345-491_345-490ins others(348): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | ||||||
| chr15:92630835
|
A | ACATATTA others(341): Show |
1 | a0001c0001t0003g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.345-491_345-490ins others(348): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | ||||||
| chr15:92630835
|
A | ACATATTA others(306): Show |
2 | a0001c0001t0009g0338a0001c0001t0010g0339 | 2 | HG00140.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.345-491_345-490ins others(313): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | ||||||
| chr15:92630835
|
A | ACATATTA others(271): Show |
1 | a0001c0001t0027g0337 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.345-491_345-490ins others(278): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | ||||||
| chr15:92630835
|
A | ACGTATTA others(12): Show |
7 | a0001c0001t0002g0022a0001c0001t0008g0015a0001c0001t0008g0052others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-491_345-490ins others(19): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | ||||||
| chr15:92630835
|
A | ATATATTA others(19): Show |
1 | a0001c0001t0018g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345-491_345-490ins others(26): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | ||||||
| chr15:92630835
|
ATATATAT others(35): Show |
A | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-532_345-491del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630835 | ||||||
| chr15:92630836
|
T | TATATATT others(16): Show |
1 | a0001c0001t0008g0306 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.345-514_345-492dup others(23): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630836 | ||||||
| chr15:92630838
|
T | C | 17 | a0001c0001t0001g0040a0001c0001t0001g0153a0001c0001t0001g0346others(14): Show | 17 | HG01109.hp1 HG01175.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-493A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630838 | ||||||
| chr15:92630839
|
A | G | 1 | a0001c0001t0001g0346 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.345-494T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630839 | ||||||
| chr15:92630845
|
C | T | 140 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(137): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.345-500G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630845 | ||||||
| chr15:92630846
|
A | G | 2 | a0001c0001t0001g0346a0001c0001t0016g0341 | 2 | HG00099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.345-501T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630846 | ||||||
| chr15:92630853
|
A | ATGTTACA others(28): Show |
1 | a0001c0001t0009g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.345-543_345-509dup others(35): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630853 | ||||||
| chr15:92630853
|
A | G | 146 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.345-508T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630853 | ||||||
| chr15:92630855
|
G | A | 23 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(20): Show | 24 | HG00099.hp1 HG00140.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.345-510C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
G | GTTACATA others(100): Show |
2 | a0001c0001t0005g0325a0001c0001t0010g0102 | 2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.345-511_345-510ins others(107): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
G | GTTACATA others(135): Show |
3 | a0001c0001t0003g0324a0001c0001t0005g0323a0001c0001t0033g0327 | 3 | HG02683.hp1 HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.345-511_345-510ins others(142): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
G | GTTACATA others(135): Show |
1 | a0001c0001t0003g0326 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.345-511_345-510ins others(142): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
G | GTTACATA others(98): Show |
4 | a0001c0001t0004g0085a0001c0001t0004g0114a0001c0001t0018g0072others(1): Show | 4 | HG00735.hp1 HG01074.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-511_345-510ins others(105): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
G | GTTACATA others(21): Show |
3 | a0001c0001t0002g0146a0001c0001t0003g0139a0001c0001t0007g0145 | 3 | NA18973.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.345-511_345-510ins others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
G | GTTACATA others(98): Show |
1 | a0001c0001t0013g0110 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.345-511_345-510ins others(105): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
G | GTTACATA others(28): Show |
2 | a0001c0001t0006g0298a0001c0001t0007g0111 | 2 | HG01934.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.345-545_345-511dup others(35): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
G | GTTACATA others(63): Show |
1 | a0001c0001t0053g0075 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.345-511_345-510ins others(70): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
GTTACATA others(28): Show |
G | 95 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(92): Show | 99 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.345-545_345-511del others(35): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630855
|
GTTACATA others(63): Show |
G | 4 | a0001c0001t0004g0347a0001c0001t0010g0362a0001c0001t0047g0364others(1): Show | 4 | HG01192.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-580_345-511del others(70): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630855 | ||||||
| chr15:92630860
|
A | G | 20 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(17): Show | 21 | HG00099.hp1 HG00140.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.345-515T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630860 | ||||||
| chr15:92630862
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0010g0349a0001c0001t0011g0035 | 3 | HG00733.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.345-517T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630862 | ||||||
| chr15:92630866
|
CATATTAT others(35): Show |
C | 1 | a0001c0001t0003g0067 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.345-563_345-522del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630866 | ||||||
| chr15:92630867
|
A | G | 3 | a0001c0001t0001g0346a0001c0001t0004g0340a0001c0001t0016g0341 | 3 | HG00099.hp1 HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.345-522T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630867 | ||||||
| chr15:92630873
|
T | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0346a0001c0001t0004g0340others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-528A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630873 | ||||||
| chr15:92630873
|
T | TATATTAC others(266): Show |
1 | a0001c0001t0032g0336 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.345-529_345-528ins others(273): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630873 | ||||||
| chr15:92630874
|
A | G | 2 | a0001c0001t0001g0346a0001c0001t0016g0341 | 2 | HG00099.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.345-529T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630874 | ||||||
| chr15:92630880
|
T | C | 10 | a0001c0001t0001g0346a0001c0001t0004g0093a0001c0001t0004g0340others(7): Show | 10 | HG00099.hp1 HG00544.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-535A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630880 | ||||||
| chr15:92630881
|
A | G | 4 | a0001c0001t0001g0346a0001c0001t0012g0343a0001c0001t0012g0350others(1): Show | 4 | HG00099.hp1 HG01175.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-536T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630881 | ||||||
| chr15:92630888
|
G | A | 2 | a0001c0001t0004g0093a0005c0012t0003g0380 | 2 | HG01361.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.345-543C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630888 | ||||||
| chr15:92630890
|
A | G | 91 | a0001c0001t0001g0058a0001c0001t0001g0153a0001c0001t0001g0157others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.345-545T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630890 | ||||||
| chr15:92630891
|
T | C | 1 | a0001c0001t0005g0325 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.345-546A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630891 | ||||||
| chr15:92630895
|
A | G | 25 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.345-550T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630895 | ||||||
| chr15:92630897
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-552T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630897 | ||||||
| chr15:92630901
|
CATATTAT others(7): Show |
C | 2 | a0001c0001t0012g0350a0001c0001t0033g0342 | 2 | HG01975.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.345-570_345-557del others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630901 | ||||||
| chr15:92630902
|
A | G | 3 | a0001c0001t0001g0346a0001c0001t0010g0349a0001c0001t0016g0341 | 3 | HG00099.hp1 HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.345-557T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630902 | ||||||
| chr15:92630908
|
T | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0346a0001c0001t0010g0349others(1): Show | 4 | HG00099.hp1 HG00733.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-563A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630908 | ||||||
| chr15:92630908
|
T | TATATTAC others(329): Show |
1 | a0001c0001t0012g0343 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.345-564_345-563ins others(336): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630908 | ||||||
| chr15:92630909
|
A | G | 5 | a0001c0001t0001g0346a0001c0001t0004g0340a0001c0001t0010g0349others(2): Show | 5 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-564T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630909 | ||||||
| chr15:92630915
|
T | C | 12 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0004g0093others(9): Show | 12 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-570A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630915 | ||||||
| chr15:92630916
|
A | G | 6 | a0001c0001t0004g0340a0001c0001t0010g0349a0001c0001t0012g0350others(3): Show | 6 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-571T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630916 | ||||||
| chr15:92630922
|
C | T | 1 | a0001c0001t0018g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.345-577G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630922 | ||||||
| chr15:92630923
|
G | A | 1 | a0001c0001t0002g0297 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.345-578C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630923 | ||||||
| chr15:92630925
|
A | G | 38 | a0001c0001t0001g0206a0001c0001t0001g0209a0001c0001t0002g0065others(35): Show | 38 | HG00323.hp2 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.345-580T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630925 | ||||||
| chr15:92630927
|
T | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-582A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630927 | ||||||
| chr15:92630929
|
C | T | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-584G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630929 | ||||||
| chr15:92630930
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.345-585T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630930 | ||||||
| chr15:92630931
|
T | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-586A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630931 | ||||||
| chr15:92630932
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-587T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630932 | ||||||
| chr15:92630932
|
A | T | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-587T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630932 | ||||||
| chr15:92630936
|
C | T | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-591G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630936 | ||||||
| chr15:92630936
|
CATATTAT others(7): Show |
C | 1 | a0001c0001t0016g0352 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.345-605_345-592del others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630936 | ||||||
| chr15:92630937
|
A | G | 8 | a0001c0001t0001g0346a0001c0001t0004g0340a0001c0001t0010g0349others(5): Show | 8 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-592T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630937 | ||||||
| chr15:92630943
|
T | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0346a0001c0001t0004g0340others(5): Show | 8 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-598A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630943 | ||||||
| chr15:92630944
|
A | G | 7 | a0001c0001t0001g0346a0001c0001t0004g0340a0001c0001t0010g0349others(4): Show | 7 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-599T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630944 | ||||||
| chr15:92630950
|
T | C | 18 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0099others(15): Show | 18 | HG00544.hp2 HG00558.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.345-605A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630950 | ||||||
| chr15:92630951
|
A | G | 8 | a0001c0001t0001g0095a0001c0001t0004g0340a0001c0001t0010g0349others(5): Show | 8 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-606T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630951 | ||||||
| chr15:92630953
|
A | G | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.345-608T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630953 | ||||||
| chr15:92630958
|
G | A | 4 | a0001c0001t0007g0348a0001c0001t0010g0362a0001c0001t0047g0364others(1): Show | 4 | HG01071.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-613C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630958 | ||||||
| chr15:92630960
|
A | G | 18 | a0001c0001t0002g0217a0001c0001t0002g0314a0001c0001t0003g0182others(15): Show | 18 | HG00733.hp2 HG00741.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-615T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630960 | ||||||
| chr15:92630964
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0308 | 2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-619G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630964 | ||||||
| chr15:92630965
|
A | ATATTACA others(56): Show |
1 | a0001c0001t0003g0080 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.345-621_345-620ins others(63): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630965 | ||||||
| chr15:92630965
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.345-620T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630965 | ||||||
| chr15:92630967
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0007g0348 | 2 | HG01071.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.345-622T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630967 | ||||||
| chr15:92630971
|
CATATTAT others(7): Show |
C | 1 | a0001c0001t0016g0351 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345-640_345-627del others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630971 | ||||||
| chr15:92630971
|
CATATTAT others(35): Show |
C | 1 | a0001c0001t0005g0225 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.345-668_345-627del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630971 | ||||||
| chr15:92630972
|
A | G | 11 | a0001c0001t0001g0346a0001c0001t0004g0340a0001c0001t0004g0347others(8): Show | 11 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-627T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630972 | ||||||
| chr15:92630977
|
ATAT | A | 3 | a0001c0001t0001g0220a0001c0001t0002g0159a0001c0001t0024g0208 | 3 | HG00597.hp2 HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.345-635_345-633del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630977 | ||||||
| chr15:92630978
|
T | C | 9 | a0001c0001t0001g0346a0001c0001t0004g0347a0001c0001t0007g0348others(6): Show | 9 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-633A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630978 | ||||||
| chr15:92630978
|
T | TATATTAC others(21): Show |
1 | a0001c0001t0012g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.345-634_345-633ins others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630978 | ||||||
| chr15:92630979
|
A | G | 8 | a0001c0001t0001g0346a0001c0001t0004g0347a0001c0001t0007g0348others(5): Show | 8 | HG00099.hp1 HG00733.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-634T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630979 | ||||||
| chr15:92630983
|
TATATATT others(44): Show |
T | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-689_345-639del others(51): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630983 | ||||||
| chr15:92630985
|
T | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0001g0096others(10): Show | 13 | HG00558.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.345-640A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630985 | ||||||
| chr15:92630986
|
A | G | 6 | a0001c0001t0001g0095a0001c0001t0004g0347a0001c0001t0007g0348others(3): Show | 6 | HG01071.hp2 HG01192.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-641T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630986 | ||||||
| chr15:92630993
|
GTATTACA others(35): Show |
G | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-690_345-649del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630993 | ||||||
| chr15:92630995
|
A | G | 7 | a0001c0001t0002g0173a0001c0001t0002g0205a0001c0001t0003g0130others(4): Show | 7 | HG00733.hp2 HG01099.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-650T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630995 | ||||||
| chr15:92630999
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0308 | 2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-654G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92630999 | ||||||
| chr15:92631000
|
A | G | 34 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.345-655T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631000 | ||||||
| chr15:92631002
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-657T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631002 | ||||||
| chr15:92631004
|
T | A | 2 | a0001c0001t0001g0301a0001c0001t0001g0308 | 2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-659A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631004 | ||||||
| chr15:92631006
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0308 | 2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-661G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631006 | ||||||
| chr15:92631007
|
A | G | 11 | a0001c0001t0001g0346a0001c0001t0004g0347a0001c0001t0007g0348others(8): Show | 11 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-662T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631007 | ||||||
| chr15:92631012
|
A | ATATATTA others(464): Show |
1 | a0001c0001t0001g0099 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.345-668_345-667ins others(471): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631012 | ||||||
| chr15:92631013
|
T | C | 15 | a0001c0001t0004g0131a0001c0001t0004g0347a0001c0001t0007g0348others(12): Show | 15 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.345-668A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631013 | ||||||
| chr15:92631013
|
T | TATATTAC others(126): Show |
1 | a0001c0001t0001g0098 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.345-669_345-668ins others(133): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631013 | ||||||
| chr15:92631014
|
A | G | 5 | a0001c0001t0001g0346a0001c0001t0004g0347a0001c0001t0007g0348others(2): Show | 5 | HG01071.hp2 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-669T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631014 | ||||||
| chr15:92631019
|
ATATATTA others(146): Show |
A | 2 | a0001c0001t0001g0301a0001c0001t0001g0308 | 2 | HG00673.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.345-827_345-675del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631019 | ||||||
| chr15:92631020
|
T | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0001g0096others(10): Show | 13 | HG00558.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.345-675A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631020 | ||||||
| chr15:92631021
|
A | G | 5 | a0001c0001t0001g0095a0001c0001t0004g0347a0001c0001t0007g0348others(2): Show | 5 | HG01071.hp2 HG01192.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-676T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631021 | ||||||
| chr15:92631030
|
A | G | 4 | a0001c0001t0002g0205a0001c0001t0003g0182a0001c0001t0007g0248others(1): Show | 4 | HG00733.hp2 HG01496.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-685T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631030 | ||||||
| chr15:92631035
|
A | G | 36 | a0001c0001t0001g0040a0001c0001t0001g0098a0001c0001t0001g0099others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.345-690T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631035 | ||||||
| chr15:92631037
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-692T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631037 | ||||||
| chr15:92631041
|
C | T | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-696G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631041 | ||||||
| chr15:92631042
|
A | G | 11 | a0001c0001t0001g0346a0001c0001t0004g0347a0001c0001t0007g0348others(8): Show | 11 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-697T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631042 | ||||||
| chr15:92631045
|
TTA | T | 8 | a0001c0001t0001g0209a0001c0001t0001g0299a0001c0001t0004g0046others(5): Show | 8 | HG03710.hp1 HG03834.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-702_345-701del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631045 | ||||||
| chr15:92631046
|
T | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-701A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631046 | ||||||
| chr15:92631047
|
A | ATATATTA others(289): Show |
1 | a0001c0001t0001g0096 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.345-703_345-702ins others(296): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631047 | ||||||
| chr15:92631047
|
A | ATATATTA others(157): Show |
1 | a0006c0010t0012g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.345-703_345-702ins others(164): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631047 | ||||||
| chr15:92631047
|
A | ATGTATTA others(328): Show |
1 | a0001c0001t0001g0095 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.345-703_345-702ins others(335): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631047 | ||||||
| chr15:92631047
|
ATATATTA others(61): Show |
A | 6 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0009g0123others(3): Show | 6 | HG01109.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-770_345-703del others(68): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631047 | ||||||
| chr15:92631048
|
T | C | 5 | a0001c0001t0001g0098a0001c0001t0004g0085a0001c0001t0004g0114others(2): Show | 5 | HG00735.hp1 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-703A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631048 | ||||||
| chr15:92631049
|
A | G | 2 | a0001c0001t0001g0346a0001c0001t0007g0348 | 2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.345-704T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631049 | ||||||
| chr15:92631055
|
T | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0137a0001c0001t0001g0219others(10): Show | 13 | HG01106.hp1 HG01943.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.345-710A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631055 | ||||||
| chr15:92631056
|
A | G | 5 | a0001c0001t0001g0059a0001c0001t0001g0219a0001c0001t0007g0348others(2): Show | 5 | HG01071.hp2 HG01106.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-711T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631056 | ||||||
| chr15:92631061
|
ACG | A | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340 | 3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-718_345-717del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631061 | ||||||
| chr15:92631063
|
G | A | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-718C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631063 | ||||||
| chr15:92631065
|
A | G | 1 | a0001c0001t0007g0248 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.345-720T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631065 | ||||||
| chr15:92631067
|
T | A | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-722A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631067 | ||||||
| chr15:92631069
|
C | T | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340 | 3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-724G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631069 | ||||||
| chr15:92631070
|
A | G | 37 | a0001c0001t0001g0040a0001c0001t0001g0095a0001c0001t0001g0096others(34): Show | 38 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.345-725T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631070 | ||||||
| chr15:92631071
|
T | A | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-726A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631071 | ||||||
| chr15:92631072
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-727T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631072 | ||||||
| chr15:92631072
|
A | T | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-727T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631072 | ||||||
| chr15:92631076
|
C | T | 2 | a0001c0001t0004g0340a0001c0001t0022g0077 | 2 | HG03710.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.345-731G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631076 | ||||||
| chr15:92631077
|
A | G | 10 | a0001c0001t0001g0346a0001c0001t0004g0347a0001c0001t0007g0348others(7): Show | 10 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-732T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631077 | ||||||
| chr15:92631080
|
TTA | T | 91 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0100others(88): Show | 92 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.345-737_345-736del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631080 | ||||||
| chr15:92631082
|
A | ACATATTA others(129): Show |
1 | a0001c0001t0004g0093 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.345-738_345-737ins others(136): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | ||||||
| chr15:92631082
|
A | ATATATTA others(124): Show |
1 | a0001c0001t0002g0076 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.345-738_345-737ins others(131): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | ||||||
| chr15:92631082
|
A | ATATATTA others(89): Show |
1 | a0001c0001t0001g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345-738_345-737ins others(96): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | ||||||
| chr15:92631082
|
A | ATATATTA others(54): Show |
1 | a0001c0001t0022g0077 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.345-738_345-737ins others(61): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | ||||||
| chr15:92631082
|
A | ATATATTA others(89): Show |
7 | a0001c0001t0001g0137a0001c0001t0002g0079a0001c0001t0002g0090others(4): Show | 7 | NA18948.hp1 NA18966.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-738_345-737ins others(96): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | ||||||
| chr15:92631082
|
A | ATATATTA others(68): Show |
1 | a0001c0001t0001g0296 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-738_345-737ins others(75): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | ||||||
| chr15:92631082
|
A | ATATATTA others(95): Show |
1 | a0001c0001t0002g0313 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.345-738_345-737ins others(102): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | ||||||
| chr15:92631082
|
ATATATTA others(26): Show |
A | 2 | a0001c0001t0010g0349a0001c0001t0012g0350 | 2 | HG00733.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.345-770_345-738del others(33): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631082 | ||||||
| chr15:92631083
|
T | C | 2 | a0001c0001t0012g0097a0005c0012t0003g0380 | 2 | HG01496.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.345-738A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631083 | ||||||
| chr15:92631084
|
A | G | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.345-739T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631084 | ||||||
| chr15:92631088
|
T | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-743A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631088 | ||||||
| chr15:92631090
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0014g0103 | 2 | HG01106.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.345-745A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631090 | ||||||
| chr15:92631091
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0014g0103 | 2 | HG01106.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.345-746T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631091 | ||||||
| chr15:92631097
|
C | T | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340 | 3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-752G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631097 | ||||||
| chr15:92631098
|
G | A | 5 | a0001c0001t0001g0241a0001c0001t0004g0328a0001c0001t0004g0329others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-753C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631098 | ||||||
| chr15:92631100
|
A | T | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-755T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631100 | ||||||
| chr15:92631101
|
T | A | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-756A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631101 | ||||||
| chr15:92631104
|
C | T | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.345-759G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631104 | ||||||
| chr15:92631105
|
A | G | 34 | a0001c0001t0001g0040a0001c0001t0001g0095a0001c0001t0001g0098others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.345-760T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631105 | ||||||
| chr15:92631107
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-762T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631107 | ||||||
| chr15:92631111
|
C | T | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340 | 3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-766G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631111 | ||||||
| chr15:92631111
|
CATATTAT others(57): Show |
C | 3 | a0001c0001t0001g0209a0001c0001t0007g0063a0001c0001t0035g0285 | 3 | HG04184.hp1 NA19087.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.345-830_345-767del others(64): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631111 | ||||||
| chr15:92631112
|
A | G | 2 | a0001c0001t0007g0348a0001c0001t0016g0341 | 2 | HG00099.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.345-767T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631112 | ||||||
| chr15:92631115
|
T | TTA | 166 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(163): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.345-772_345-771dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631115 | ||||||
| chr15:92631115
|
T | TTATATAT others(258): Show |
1 | a0001c0001t0001g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.345-771_345-770ins others(265): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631115 | ||||||
| chr15:92631123
|
T | C | 1 | a0001c0001t0014g0103 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.345-778A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631123 | ||||||
| chr15:92631124
|
A | G | 1 | a0001c0001t0014g0103 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.345-779T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631124 | ||||||
| chr15:92631128
|
T | A | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340 | 3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-783A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631128 | ||||||
| chr15:92631130
|
C | T | 5 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-785G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631130 | ||||||
| chr15:92631131
|
G | A | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340 | 3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-786C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631131 | ||||||
| chr15:92631137
|
C | T | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340 | 3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-792G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631137 | ||||||
| chr15:92631138
|
A | G | 36 | a0001c0001t0001g0040a0001c0001t0001g0095a0001c0001t0001g0098others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.345-793T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631138 | ||||||
| chr15:92631140
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-795T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631140 | ||||||
| chr15:92631144
|
C | T | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0004g0340 | 3 | HG02145.hp2 HG02257.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-799G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631144 | ||||||
| chr15:92631144
|
CATATTAT others(24): Show |
C | 83 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0153others(80): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.345-830_345-800del others(31): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631144 | ||||||
| chr15:92631145
|
A | G | 1 | a0001c0001t0016g0341 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.345-800T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631145 | ||||||
| chr15:92631145
|
ATATTATA others(27): Show |
A | 1 | a0001c0001t0024g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.345-834_345-801del others(34): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631145 | ||||||
| chr15:92631147
|
A | T | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-802T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631147 | ||||||
| chr15:92631148
|
T | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-803A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | ||||||
| chr15:92631148
|
T | TTA | 67 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0137others(64): Show | 68 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.345-805_345-804dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | ||||||
| chr15:92631148
|
T | TTACATAT others(316): Show |
1 | a0001c0001t0012g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.345-804_345-803ins others(323): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | ||||||
| chr15:92631148
|
T | TTATATAT others(274): Show |
1 | a0001c0001t0014g0103 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.345-804_345-803ins others(281): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | ||||||
| chr15:92631148
|
T | TTATATAT others(215): Show |
1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.345-804_345-803ins others(222): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | ||||||
| chr15:92631148
|
T | TTATATAT others(180): Show |
1 | a0001c0001t0002g0101 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.345-804_345-803ins others(187): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631148 | ||||||
| chr15:92631149
|
T | TATATATT others(16): Show |
1 | a0001c0001t0001g0281 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.345-805_345-804ins others(23): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631149
|
T | TATATATT others(23): Show |
2 | a0001c0001t0015g0118a0001c0001t0015g0119 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.345-805_345-804ins others(30): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631149
|
T | TATATATT others(227): Show |
2 | a0001c0001t0001g0104a0009c0007t0001g0008 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.345-805_345-804ins others(234): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631149
|
T | TATATATT others(91): Show |
1 | a0001c0001t0019g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.345-805_345-804ins others(98): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631149
|
T | TATATATT others(157): Show |
1 | a0001c0001t0007g0081 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.345-805_345-804ins others(164): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631149
|
T | TATATATT others(56): Show |
1 | a0001c0001t0003g0060 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.345-805_345-804ins others(63): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631149
|
T | TATATATT others(84): Show |
1 | a0001c0001t0001g0279 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.345-805_345-804ins others(91): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631149
|
T | TATATATT others(89): Show |
8 | a0001c0001t0001g0302a0001c0001t0002g0069a0001c0001t0002g0070others(5): Show | 8 | HG00423.hp1 HG02071.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-805_345-804ins others(96): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631149
|
T | TATATATT others(122): Show |
1 | a0001c0001t0005g0307 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.345-805_345-804ins others(129): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631149 | ||||||
| chr15:92631159
|
A | T | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-814T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631159 | ||||||
| chr15:92631160
|
T | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-815A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | ||||||
| chr15:92631160
|
T | TTA | 4 | a0001c0001t0001g0083a0001c0001t0002g0101a0001c0001t0012g0097others(1): Show | 4 | HG01496.hp1 HG01943.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-817_345-816dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | ||||||
| chr15:92631160
|
T | TTACGTAT others(114): Show |
2 | a0001c0001t0007g0111a0001c0001t0013g0110 | 2 | HG03017.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.345-816_345-815ins others(121): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | ||||||
| chr15:92631160
|
T | TTACGTAT others(163): Show |
1 | a0001c0001t0013g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.345-816_345-815ins others(170): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | ||||||
| chr15:92631160
|
T | TTACGTAT others(147): Show |
1 | a0001c0001t0002g0092 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.345-816_345-815ins others(154): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | ||||||
| chr15:92631160
|
T | TTACGTAT others(182): Show |
1 | a0001c0001t0001g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.345-816_345-815ins others(189): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | ||||||
| chr15:92631160
|
T | TTACGTAT others(250): Show |
1 | a0001c0001t0001g0098 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.345-816_345-815ins others(257): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | ||||||
| chr15:92631160
|
TTATATAA others(26): Show |
T | 2 | a0001c0001t0001g0319a0001c0001t0002g0284 | 2 | HG02056.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.345-848_345-816del others(33): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631160 | ||||||
| chr15:92631161
|
T | TACGTATT others(9): Show |
1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-817_345-816ins others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631161 | ||||||
| chr15:92631162
|
A | ACG | 63 | a0001c0001t0001g0059a0001c0001t0001g0137a0001c0001t0001g0171others(60): Show | 64 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.345-818_345-817ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | ||||||
| chr15:92631162
|
A | ACGTATTA others(58): Show |
3 | a0001c0001t0001g0283a0001c0001t0001g0287a0001c0001t0012g0282 | 3 | NA18952.hp2 NA18970.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.345-818_345-817ins others(65): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | ||||||
| chr15:92631162
|
A | ACGTATTA others(30): Show |
11 | a0001c0001t0001g0310a0001c0001t0002g0105a0001c0001t0004g0085others(8): Show | 11 | HG00735.hp1 HG00735.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-818_345-817ins others(37): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | ||||||
| chr15:92631162
|
A | ACGTATTA others(63): Show |
21 | a0001c0001t0001g0082a0001c0001t0001g0106a0001c0001t0001g0108others(18): Show | 21 | HG00558.hp2 HG02683.hp1 HG03669.hp2 others(18): Show |
intron_variant | MODIFIER | c.345-818_345-817ins others(70): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | ||||||
| chr15:92631162
|
A | ACGTATTA others(98): Show |
1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-818_345-817ins others(105): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | ||||||
| chr15:92631162
|
A | ACGTATTA others(96): Show |
6 | a0001c0001t0001g0068a0001c0001t0001g0107a0001c0001t0001g0109others(3): Show | 6 | HG00408.hp1 HG01515.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-818_345-817ins others(103): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | ||||||
| chr15:92631162
|
ATATAATA others(22): Show |
A | 1 | a0001c0001t0009g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.345-846_345-818del others(29): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | ||||||
| chr15:92631162
|
ATATAATA others(92): Show |
A | 1 | a0001c0001t0021g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.345-916_345-818del others(99): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631162 | ||||||
| chr15:92631163
|
T | C | 10 | a0001c0001t0002g0022a0001c0001t0002g0125a0001c0001t0006g0265others(7): Show | 10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-818A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631163 | ||||||
| chr15:92631163
|
TATAATAA others(59): Show |
T | 2 | a0001c0001t0036g0381a0001c0001t0036g0382 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-884_345-819del others(66): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631163 | ||||||
| chr15:92631163
|
TATAATAA others(85): Show |
T | 3 | a0001c0001t0002g0148a0001c0001t0057g0200a0008c0011t0025g0365 | 3 | NA18947.hp1 NA19006.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.345-910_345-819del others(92): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631163 | ||||||
| chr15:92631164
|
A | G | 10 | a0001c0001t0002g0022a0001c0001t0002g0125a0001c0001t0006g0265others(7): Show | 10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-819T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631164 | ||||||
| chr15:92631164
|
ATAATAAT others(50): Show |
A | 1 | a0001c0001t0020g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.345-876_345-820del others(57): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631164 | ||||||
| chr15:92631166
|
A | ATATTAC | 4 | a0001c0001t0001g0100a0001c0001t0001g0299a0001c0001t0002g0056others(1): Show | 4 | HG02280.hp2 NA19055.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-822_345-821ins others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | ||||||
| chr15:92631166
|
A | ATATTACA others(43): Show |
2 | a0001c0001t0001g0096a0006c0010t0012g0094 | 2 | HG00558.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.345-822_345-821ins others(50): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | ||||||
| chr15:92631166
|
A | ATATTACA others(81): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0099 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.345-822_345-821ins others(88): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | ||||||
| chr15:92631166
|
A | T | 106 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0068others(103): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.345-821T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | ||||||
| chr15:92631166
|
AATAAT | A | 12 | a0001c0001t0002g0022a0001c0001t0002g0125a0001c0001t0006g0261others(9): Show | 12 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-826_345-822del others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631166 | ||||||
| chr15:92631167
|
A | ACG | 3 | a0001c0001t0008g0012a0001c0001t0008g0015a0001c0001t0032g0032 | 3 | HG02895.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-823_345-822ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631167 | ||||||
| chr15:92631167
|
A | T | 18 | a0001c0001t0001g0104a0001c0001t0001g0279a0001c0001t0001g0281others(15): Show | 18 | HG00423.hp1 HG00741.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.345-822T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631167 | ||||||
| chr15:92631168
|
T | C | 101 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(98): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.345-823A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631168 | ||||||
| chr15:92631169
|
A | ACGTATTA others(1): Show |
18 | a0001c0001t0001g0104a0001c0001t0001g0279a0001c0001t0001g0281others(15): Show | 18 | HG00423.hp1 HG00741.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.345-825_345-824ins others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631169 | ||||||
| chr15:92631169
|
A | G | 8 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0003g0334others(5): Show | 9 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-824T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631169 | ||||||
| chr15:92631170
|
A | T | 124 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0068others(121): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.345-825T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631170 | ||||||
| chr15:92631171
|
T | A | 119 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0068others(116): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.345-826A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631171 | ||||||
| chr15:92631171
|
T | TA | 18 | a0001c0001t0001g0104a0001c0001t0001g0279a0001c0001t0001g0281others(15): Show | 18 | HG00423.hp1 HG00741.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.345-827_345-826ins others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631171 | ||||||
| chr15:92631172
|
T | A | 7 | a0001c0001t0001g0095a0001c0001t0001g0099a0001c0001t0004g0340others(4): Show | 7 | HG01928.hp1 HG01978.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-827A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631172 | ||||||
| chr15:92631173
|
T | C | 3 | a0001c0001t0008g0012a0001c0001t0008g0015a0001c0001t0032g0032 | 3 | HG02895.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-828A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631173 | ||||||
| chr15:92631175
|
T | C | 131 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(128): Show | 132 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.345-830A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631175 | ||||||
| chr15:92631176
|
A | G | 10 | a0001c0001t0002g0022a0001c0001t0006g0261a0001c0001t0006g0262others(7): Show | 10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-831T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631176 | ||||||
| chr15:92631178
|
A | T | 3 | a0001c0001t0008g0012a0001c0001t0008g0015a0001c0001t0032g0032 | 3 | HG02895.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-833T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631178 | ||||||
| chr15:92631179
|
T | A | 9 | a0001c0001t0001g0095a0001c0001t0001g0099a0001c0001t0001g0301others(6): Show | 9 | HG00673.hp2 HG01928.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-834A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631179 | ||||||
| chr15:92631179
|
T | TTA | 3 | a0001c0001t0004g0046a0001c0001t0004g0048a0001c0001t0018g0247 | 3 | HG00741.hp1 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345-836_345-835dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631179 | ||||||
| chr15:92631179
|
TTATATTA | T | 4 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0048g0122others(1): Show | 4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-841_345-835del others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631179 | ||||||
| chr15:92631179
|
TTATATTA others(70): Show |
T | 1 | a0001c0001t0009g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.345-911_345-835del others(77): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631179 | ||||||
| chr15:92631180
|
T | TAC | 12 | a0001c0001t0002g0022a0001c0001t0002g0125a0001c0001t0006g0261others(9): Show | 12 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-836_345-835ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631180 | ||||||
| chr15:92631180
|
T | TACGTATT others(9): Show |
1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-836_345-835ins others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631180 | ||||||
| chr15:92631187
|
T | C | 2 | a0001c0001t0006g0261a0001c0001t0006g0262 | 2 | NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-842A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631187 | ||||||
| chr15:92631191
|
TTATA | T | 7 | a0001c0001t0001g0301a0001c0001t0001g0308a0001c0001t0001g0346others(4): Show | 7 | HG00673.hp2 HG00733.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-850_345-847del others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631191 | ||||||
| chr15:92631191
|
TTATATAT others(91): Show |
T | 1 | a0001c0001t0024g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.345-944_345-847del others(98): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631191 | ||||||
| chr15:92631192
|
T | A | 16 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0098others(13): Show | 16 | HG00544.hp1 HG00558.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-847A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631192 | ||||||
| chr15:92631193
|
A | ACGTAT | 14 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0003g0334others(11): Show | 15 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-849_345-848ins others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631193 | ||||||
| chr15:92631193
|
A | ATATAT | 5 | a0001c0001t0001g0100a0001c0001t0001g0299a0001c0001t0002g0056others(2): Show | 5 | HG02280.hp2 NA19003.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-853_345-849dup others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631193 | ||||||
| chr15:92631194
|
T | TATATA | 10 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0098others(7): Show | 10 | HG00544.hp1 HG00558.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-854_345-850dup others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631194 | ||||||
| chr15:92631195
|
A | AT | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0013g0142 | 3 | HG02027.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-851dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631195 | ||||||
| chr15:92631196
|
T | C | 16 | a0001c0001t0001g0319a0001c0001t0001g0344a0001c0001t0002g0005others(13): Show | 17 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-851A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631196 | ||||||
| chr15:92631196
|
TATATTAC others(48): Show |
T | 5 | a0001c0001t0007g0348a0001c0001t0016g0341a0001c0001t0016g0351others(2): Show | 5 | HG00099.hp1 HG00544.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-906_345-852del others(55): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631196 | ||||||
| chr15:92631197
|
A | ATTACG | 10 | a0001c0001t0001g0040a0001c0001t0002g0022a0001c0001t0006g0265others(7): Show | 10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-853_345-852ins others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631197 | ||||||
| chr15:92631197
|
A | G | 13 | a0001c0001t0001g0319a0001c0001t0001g0344a0001c0001t0002g0005others(10): Show | 14 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.345-852T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631197 | ||||||
| chr15:92631197
|
ATATTACA others(65): Show |
A | 1 | a0001c0001t0006g0243 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-924_345-853del others(72): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631197 | ||||||
| chr15:92631199
|
ATTAC | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0099a0001c0001t0004g0340 | 3 | HG01928.hp1 HG01978.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.345-858_345-855del others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631199 | ||||||
| chr15:92631200
|
T | A | 1 | a0001c0001t0014g0086 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.345-855A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631200 | ||||||
| chr15:92631201
|
T | A | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0013g0142 | 3 | HG02027.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-856A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631201 | ||||||
| chr15:92631201
|
TAC | T | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-858_345-857del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631201 | ||||||
| chr15:92631202
|
A | ATATAT | 4 | a0001c0001t0001g0100a0001c0001t0002g0056a0001c0001t0010g0036others(1): Show | 4 | HG02280.hp2 NA19003.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-858_345-857ins others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631202 | ||||||
| chr15:92631202
|
A | T | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0013g0142 | 3 | HG02027.hp1 HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-857T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631202 | ||||||
| chr15:92631203
|
C | A | 7 | a0001c0001t0001g0100a0001c0001t0002g0056a0001c0001t0004g0328others(4): Show | 7 | HG02027.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-858G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | ||||||
| chr15:92631203
|
C | CATATATT others(19): Show |
1 | a0002c0002t0004g0374 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.345-884_345-859dup others(26): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | ||||||
| chr15:92631203
|
C | CGTGTTAC others(5): Show |
1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-859_345-858ins others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | ||||||
| chr15:92631203
|
C | T | 23 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0098others(20): Show | 23 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.345-858G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | ||||||
| chr15:92631203
|
CAT | C | 12 | a0001c0001t0001g0319a0001c0001t0002g0022a0001c0001t0002g0125others(9): Show | 12 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-860_345-859del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | ||||||
| chr15:92631203
|
CATATATT others(19): Show |
C | 8 | a0001c0001t0046g0041a0001c0001t0056g0133a0002c0002t0004g0372others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-884_345-859del others(26): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631203 | ||||||
| chr15:92631204
|
A | ATAT | 12 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0003g0334others(9): Show | 13 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-862_345-860dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631204 | ||||||
| chr15:92631206
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0125a0001c0001t0008g0052others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-861T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631206 | ||||||
| chr15:92631206
|
A | T | 92 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(89): Show | 96 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.345-861T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631206 | ||||||
| chr15:92631208
|
A | T | 2 | a0001c0001t0008g0012a0001c0001t0032g0032 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-863T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631208 | ||||||
| chr15:92631209
|
T | A | 16 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0098others(13): Show | 16 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-864A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631209 | ||||||
| chr15:92631212
|
T | C | 14 | a0001c0001t0001g0319a0001c0001t0002g0022a0001c0001t0002g0125others(11): Show | 14 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-867A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631212 | ||||||
| chr15:92631213
|
A | G | 2 | a0001c0001t0006g0261a0001c0001t0006g0262 | 2 | NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-868T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631213 | ||||||
| chr15:92631215
|
A | T | 15 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0098others(12): Show | 15 | HG00544.hp1 HG00558.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-870T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631215 | ||||||
| chr15:92631216
|
T | A | 17 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0098others(14): Show | 17 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-871A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | ||||||
| chr15:92631216
|
T | TTATATTA others(82): Show |
1 | a0001c0001t0002g0297 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.345-872_345-871ins others(89): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | ||||||
| chr15:92631216
|
T | TTATATTA others(129): Show |
1 | a0001c0001t0006g0091 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.345-872_345-871ins others(136): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | ||||||
| chr15:92631216
|
TTATATTA others(66): Show |
T | 2 | a0001c0001t0002g0168a0001c0001t0005g0210 | 2 | NA19001.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.345-944_345-872del others(73): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | ||||||
| chr15:92631216
|
TTATATTA others(113): Show |
T | 1 | a0001c0001t0003g0067 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.345-991_345-872del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631216 | ||||||
| chr15:92631217
|
T | TACGTATT others(2): Show |
3 | a0001c0001t0004g0046a0001c0001t0004g0048a0001c0001t0018g0247 | 3 | HG00741.hp1 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345-873_345-872ins others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631217 | ||||||
| chr15:92631217
|
TATATTAT others(92): Show |
T | 1 | a0001c0001t0064g0030 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.345-971_345-873del others(99): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631217 | ||||||
| chr15:92631219
|
T | C | 2 | a0001c0001t0006g0261a0001c0001t0006g0262 | 2 | NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-874A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631219 | ||||||
| chr15:92631221
|
TTATATAT others(181): Show |
T | 1 | a0001c0001t0009g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.345-1064_345-877de others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631221 | ||||||
| chr15:92631222
|
T | A | 11 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0003g0334others(8): Show | 12 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-877A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631222 | ||||||
| chr15:92631223
|
A | T | 2 | a0001c0001t0006g0261a0001c0001t0006g0262 | 2 | NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-878T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631223 | ||||||
| chr15:92631223
|
ATATATAA others(104): Show |
A | 69 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(66): Show | 70 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.345-989_345-879del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631223 | ||||||
| chr15:92631224
|
T | C | 5 | a0001c0001t0004g0046a0001c0001t0004g0048a0001c0001t0008g0012others(2): Show | 5 | HG00741.hp1 HG03225.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-879A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631224 | ||||||
| chr15:92631224
|
TATATAAT others(97): Show |
T | 8 | a0001c0001t0002g0355a0001c0001t0009g0187a0001c0001t0015g0189others(5): Show | 9 | HG02970.hp1 NA18953.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-983_345-880del | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631224 | ||||||
| chr15:92631225
|
A | G | 2 | a0001c0001t0008g0012a0001c0001t0032g0032 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-880T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631225 | ||||||
| chr15:92631225
|
ATATAATA others(174): Show |
A | 7 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(4): Show | 9 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-1061_345-881de others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631225 | ||||||
| chr15:92631226
|
T | A | 8 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0003g0334others(5): Show | 9 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-881A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631226 | ||||||
| chr15:92631226
|
T | C | 5 | a0001c0001t0001g0040a0001c0001t0002g0125a0001c0001t0006g0261others(2): Show | 5 | HG02895.hp2 NA19002.hp1 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-881A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631226 | ||||||
| chr15:92631226
|
TATAATAT others(83): Show |
T | 1 | a0001c0001t0007g0256 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.345-971_345-882del others(90): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631226 | ||||||
| chr15:92631227
|
A | T | 10 | a0001c0001t0001g0299a0001c0001t0001g0344a0001c0001t0002g0005others(7): Show | 11 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-882T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631227 | ||||||
| chr15:92631228
|
T | A | 2 | a0001c0001t0001g0299a0001c0001t0020g0136 | 2 | HG06807.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.345-883A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631228 | ||||||
| chr15:92631229
|
A | ATT | 3 | a0001c0001t0003g0161a0001c0001t0003g0267a0001c0001t0021g0361 | 3 | HG01346.hp1 HG01515.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.345-885_345-884ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631229 | ||||||
| chr15:92631229
|
A | C | 1 | a0001c0001t0020g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.345-884T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631229 | ||||||
| chr15:92631229
|
A | T | 25 | a0001c0001t0001g0299a0001c0001t0001g0319a0001c0001t0001g0344others(22): Show | 26 | HG00140.hp2 HG00741.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.345-884T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631229 | ||||||
| chr15:92631230
|
A | T | 6 | a0001c0001t0001g0040a0001c0001t0002g0125a0001c0001t0006g0261others(3): Show | 6 | HG00673.hp1 HG02895.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-885T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631230 | ||||||
| chr15:92631231
|
T | C | 12 | a0001c0001t0001g0319a0001c0001t0002g0022a0001c0001t0002g0284others(9): Show | 12 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-886A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631231 | ||||||
| chr15:92631232
|
A | G | 12 | a0001c0001t0001g0319a0001c0001t0002g0022a0001c0001t0002g0284others(9): Show | 12 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-887T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631232 | ||||||
| chr15:92631232
|
ATATTATA others(3): Show |
A | 1 | a0001c0001t0007g0207 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.345-897_345-888del others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631232 | ||||||
| chr15:92631235
|
T | A | 1 | a0001c0001t0001g0299 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.345-890A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631235 | ||||||
| chr15:92631236
|
T | A | 4 | a0001c0001t0001g0100a0001c0001t0002g0056a0001c0001t0006g0265others(1): Show | 4 | NA18940.hp2 NA19003.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-891A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631236 | ||||||
| chr15:92631236
|
T | TATATATT others(54): Show |
1 | a0001c0001t0008g0280 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.345-892_345-891ins others(61): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631236 | ||||||
| chr15:92631236
|
TATATATT others(12): Show |
T | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.345-910_345-892del others(19): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631236 | ||||||
| chr15:92631237
|
A | T | 1 | a0001c0001t0006g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-892T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631237 | ||||||
| chr15:92631237
|
ATATAT | A | 27 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0109others(24): Show | 27 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.345-897_345-893del others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631237 | ||||||
| chr15:92631238
|
T | C | 14 | a0001c0001t0001g0319a0001c0001t0002g0022a0001c0001t0002g0284others(11): Show | 14 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-893A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631238 | ||||||
| chr15:92631238
|
TATATTAT others(71): Show |
T | 5 | a0001c0001t0002g0205a0001c0001t0002g0314a0001c0001t0015g0043others(2): Show | 5 | HG00140.hp1 HG01884.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-971_345-894del others(78): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631238 | ||||||
| chr15:92631239
|
A | G | 8 | a0001c0001t0002g0022a0001c0001t0008g0052a0001c0001t0010g0014others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-894T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631239 | ||||||
| chr15:92631240
|
T | C | 1 | a0001c0001t0006g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-895A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631240 | ||||||
| chr15:92631241
|
A | T | 8 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0003g0334others(5): Show | 9 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-896T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631241 | ||||||
| chr15:92631242
|
T | A | 10 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0344others(7): Show | 11 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-897A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTA | 7 | a0001c0001t0001g0330a0001c0001t0003g0116a0001c0001t0006g0240others(4): Show | 7 | HG02055.hp1 HG04184.hp1 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-899_345-898dup others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0100a0001c0001t0002g0056 | 2 | NA19056.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.345-898_345-897ins others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTATATAT others(21): Show |
3 | a0001c0001t0003g0060a0001c0001t0019g0061a0001c0008t0001g0011 | 3 | HG00741.hp2 HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.345-898_345-897ins others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTATATAT others(53): Show |
1 | a0001c0001t0002g0313 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.345-898_345-897ins others(60): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTATATAT others(56): Show |
19 | a0001c0001t0001g0082a0001c0001t0001g0106a0001c0001t0001g0107others(16): Show | 19 | HG00423.hp1 HG01934.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.345-898_345-897ins others(63): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTATATAT others(77): Show |
2 | a0001c0001t0001g0059a0001c0001t0006g0078 | 2 | HG01106.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.345-898_345-897ins others(84): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTATATAT others(54): Show |
1 | a0001c0001t0001g0288 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.345-898_345-897ins others(61): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTATATAT others(56): Show |
1 | a0001c0001t0001g0296 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-898_345-897ins others(63): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631242
|
T | TTATATAT others(4): Show |
1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.345-898_345-897ins others(11): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631242 | ||||||
| chr15:92631243
|
TATATTAT others(5): Show |
T | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-910_345-899del others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631243 | ||||||
| chr15:92631243
|
TATATTAT others(31): Show |
T | 3 | a0001c0001t0007g0044a0001c0001t0021g0042a0001c0001t0030g0045 | 3 | HG03491.hp2 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.345-936_345-899del others(38): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631243 | ||||||
| chr15:92631244
|
A | ACG | 4 | a0001c0001t0001g0040a0001c0001t0004g0046a0001c0001t0004g0048others(1): Show | 4 | HG00741.hp1 HG03834.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-900_345-899ins others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631244 | ||||||
| chr15:92631245
|
T | C | 8 | a0001c0001t0002g0022a0001c0001t0008g0052a0001c0001t0010g0014others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-900A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631245 | ||||||
| chr15:92631245
|
TATTATAT others(64): Show |
T | 84 | a0001c0001t0001g0058a0001c0001t0001g0153a0001c0001t0001g0157others(81): Show | 85 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.345-971_345-901del others(71): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631245 | ||||||
| chr15:92631246
|
AT | A | 3 | a0001c0001t0002g0125a0001c0001t0006g0261a0001c0001t0006g0262 | 3 | NA19002.hp1 NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.345-902delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631246 | ||||||
| chr15:92631247
|
T | TATAATA | 37 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0001g0276others(34): Show | 37 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.345-903_345-902ins others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631247 | ||||||
| chr15:92631248
|
T | A | 13 | a0001c0001t0002g0022a0001c0001t0003g0060a0001c0001t0003g0116others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-903A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631248 | ||||||
| chr15:92631249
|
A | AT | 37 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0001g0276others(34): Show | 37 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.345-905dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631249 | ||||||
| chr15:92631249
|
A | T | 10 | a0001c0001t0002g0022a0001c0001t0008g0015a0001c0001t0008g0052others(7): Show | 10 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-904T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631249 | ||||||
| chr15:92631250
|
T | C | 3 | a0001c0001t0004g0046a0001c0001t0004g0048a0001c0001t0018g0247 | 3 | HG00741.hp1 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345-905A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631250 | ||||||
| chr15:92631252
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.345-907A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631252 | ||||||
| chr15:92631253
|
A | T | 11 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0002g0125others(8): Show | 12 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-908T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631253 | ||||||
| chr15:92631254
|
T | A | 11 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0002g0125others(8): Show | 12 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-909A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631254 | ||||||
| chr15:92631254
|
TA | T | 5 | a0001c0001t0007g0348a0001c0001t0016g0341a0001c0001t0016g0351others(2): Show | 5 | HG00099.hp1 HG00544.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-910delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631254 | ||||||
| chr15:92631255
|
A | C | 3 | a0001c0001t0002g0125a0001c0001t0006g0261a0001c0001t0006g0262 | 3 | NA19002.hp1 NA19079.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.345-910T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631255 | ||||||
| chr15:92631255
|
A | T | 42 | a0001c0001t0001g0049a0001c0001t0001g0220a0001c0001t0001g0278others(39): Show | 43 | HG00140.hp2 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.345-910T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631255 | ||||||
| chr15:92631256
|
A | T | 39 | a0001c0001t0001g0040a0001c0001t0001g0068a0001c0001t0001g0137others(36): Show | 39 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.345-911T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631256 | ||||||
| chr15:92631257
|
T | C | 5 | a0001c0001t0004g0046a0001c0001t0004g0048a0001c0001t0008g0012others(2): Show | 5 | HG00741.hp1 HG03225.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-912A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631257 | ||||||
| chr15:92631258
|
A | G | 2 | a0001c0001t0008g0012a0001c0001t0032g0032 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-913T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631258 | ||||||
| chr15:92631260
|
A | T | 1 | a0001c0001t0006g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-915T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631260 | ||||||
| chr15:92631261
|
T | A | 2 | a0001c0001t0001g0199a0001c0001t0006g0265 | 2 | HG03942.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.345-916A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631261 | ||||||
| chr15:92631262
|
T | A | 3 | a0001c0001t0002g0087a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02135.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.345-917A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631262 | ||||||
| chr15:92631264
|
T | C | 7 | a0001c0001t0001g0319a0001c0001t0002g0148a0001c0001t0002g0284others(4): Show | 7 | HG02056.hp2 HG03225.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-919A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631264 | ||||||
| chr15:92631265
|
A | G | 4 | a0001c0001t0001g0319a0001c0001t0002g0284a0001c0001t0008g0012others(1): Show | 4 | HG02056.hp2 HG03225.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-920T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631265 | ||||||
| chr15:92631265
|
ATAT | A | 3 | a0001c0001t0002g0148a0001c0001t0057g0200a0008c0011t0025g0365 | 3 | NA18947.hp1 NA19006.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.345-923_345-921del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631265 | ||||||
| chr15:92631267
|
A | T | 6 | a0001c0001t0003g0116a0001c0001t0003g0161a0001c0001t0003g0267others(3): Show | 6 | HG00741.hp1 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-922T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631267 | ||||||
| chr15:92631268
|
T | A | 16 | a0001c0001t0001g0199a0001c0001t0002g0022a0001c0001t0003g0116others(13): Show | 16 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.345-923A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | ||||||
| chr15:92631268
|
T | TAATA | 6 | a0001c0001t0004g0085a0001c0001t0004g0093a0001c0001t0004g0114others(3): Show | 6 | HG00735.hp1 HG01074.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-924_345-923ins others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | ||||||
| chr15:92631268
|
T | TAATATAT others(2): Show |
31 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0001g0276others(28): Show | 31 | HG00408.hp1 HG00558.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-924_345-923ins others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | ||||||
| chr15:92631268
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0002g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.345-924_345-923ins others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | ||||||
| chr15:92631268
|
T | TTATATAT others(28): Show |
2 | a0001c0001t0001g0104a0009c0007t0001g0008 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.345-924_345-923ins others(35): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | ||||||
| chr15:92631268
|
T | TTATATAT others(35): Show |
5 | a0001c0001t0015g0118a0001c0001t0015g0119a0001c0001t0020g0121others(2): Show | 5 | HG01243.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-924_345-923ins others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | ||||||
| chr15:92631268
|
TTATATTA others(61): Show |
T | 9 | a0001c0001t0001g0027a0001c0001t0001g0330a0001c0001t0006g0240others(6): Show | 9 | HG02055.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-991_345-924del others(68): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631268 | ||||||
| chr15:92631269
|
T | A | 3 | a0001c0001t0010g0362a0001c0001t0047g0364a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.345-924A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631269 | ||||||
| chr15:92631271
|
T | A | 8 | a0001c0001t0002g0022a0001c0001t0008g0052a0001c0001t0010g0014others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-926A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631271 | ||||||
| chr15:92631271
|
T | C | 4 | a0001c0001t0001g0319a0001c0001t0002g0284a0001c0001t0008g0012others(1): Show | 4 | HG02056.hp2 HG03225.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-926A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631271 | ||||||
| chr15:92631271
|
TATTATAT others(38): Show |
T | 3 | a0001c0001t0007g0248a0001c0001t0007g0250a0001c0001t0058g0249 | 3 | HG01496.hp2 HG01993.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.345-971_345-927del others(45): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631271 | ||||||
| chr15:92631272
|
A | T | 8 | a0001c0001t0002g0022a0001c0001t0008g0052a0001c0001t0010g0014others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-927T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631272 | ||||||
| chr15:92631273
|
T | A | 1 | a0001c0001t0006g0243 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-928A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631273 | ||||||
| chr15:92631274
|
T | A | 13 | a0001c0001t0001g0319a0001c0001t0002g0092a0001c0001t0002g0146others(10): Show | 13 | HG00544.hp1 HG02056.hp2 HG03130.hp1 others(10): Show |
intron_variant | MODIFIER | c.345-929A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631274 | ||||||
| chr15:92631274
|
T | C | 1 | a0001c0001t0021g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.345-929A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631274 | ||||||
| chr15:92631274
|
TATATATA others(68): Show |
T | 1 | a0001c0001t0021g0361 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.345-1004_345-930de others(76): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631274 | ||||||
| chr15:92631275
|
A | T | 14 | a0001c0001t0001g0040a0001c0001t0001g0319a0001c0001t0002g0092others(11): Show | 14 | HG00544.hp1 HG01361.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-930T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631275 | ||||||
| chr15:92631275
|
ATATATAA others(113): Show |
A | 2 | a0001c0001t0003g0161a0001c0001t0003g0267 | 2 | HG01346.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.345-1050_345-931de others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631275 | ||||||
| chr15:92631276
|
T | A | 2 | a0001c0001t0002g0092a0001c0001t0009g0117 | 2 | HG00544.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.345-931A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631276 | ||||||
| chr15:92631276
|
TATATAAT others(53): Show |
T | 1 | a0001c0001t0009g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.345-991_345-932del others(60): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631276 | ||||||
| chr15:92631276
|
TATATAAT others(66): Show |
T | 1 | a0001c0001t0001g0049 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.345-1004_345-932de others(74): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631276 | ||||||
| chr15:92631277
|
A | ATAT | 8 | a0001c0001t0002g0022a0001c0001t0008g0052a0001c0001t0010g0014others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-935_345-933dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631277 | ||||||
| chr15:92631278
|
T | C | 2 | a0001c0001t0001g0319a0001c0001t0002g0284 | 2 | HG02056.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.345-933A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631278 | ||||||
| chr15:92631280
|
TAATATAT others(2): Show |
T | 3 | a0001c0001t0002g0146a0001c0001t0003g0139a0001c0001t0007g0145 | 3 | NA18973.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.345-944_345-936del others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631280 | ||||||
| chr15:92631281
|
A | ATTAC | 3 | a0001c0001t0004g0046a0001c0001t0004g0048a0001c0001t0018g0247 | 3 | HG00741.hp1 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.345-937_345-936ins others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631281 | ||||||
| chr15:92631281
|
A | T | 8 | a0001c0001t0001g0206a0001c0001t0003g0116a0001c0001t0006g0265others(5): Show | 8 | HG01261.hp1 HG02735.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-936T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631281 | ||||||
| chr15:92631282
|
A | T | 16 | a0001c0001t0001g0040a0001c0001t0001g0319a0001c0001t0002g0022others(13): Show | 16 | HG00544.hp1 HG01109.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-937T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631282 | ||||||
| chr15:92631286
|
ATTATATA others(2): Show |
A | 3 | a0001c0001t0002g0148a0001c0001t0057g0200a0008c0011t0025g0365 | 3 | NA18947.hp1 NA19006.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.345-950_345-942del others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631286 | ||||||
| chr15:92631286
|
ATTATATA others(113): Show |
A | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.345-1061_345-942de others(1): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631286 | ||||||
| chr15:92631288
|
T | A | 12 | a0001c0001t0002g0022a0001c0001t0002g0092a0001c0001t0008g0052others(9): Show | 12 | HG00544.hp1 HG01109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-943A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631288 | ||||||
| chr15:92631289
|
A | ATATAT | 54 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0082others(51): Show | 54 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.345-949_345-945dup others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631289 | ||||||
| chr15:92631289
|
A | T | 10 | a0001c0001t0002g0022a0001c0001t0002g0092a0001c0001t0008g0052others(7): Show | 10 | HG00544.hp1 HG01109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-944T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631289 | ||||||
| chr15:92631290
|
T | A | 2 | a0001c0001t0002g0168a0001c0001t0005g0210 | 2 | NA19001.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.345-945A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631290 | ||||||
| chr15:92631290
|
T | C | 2 | a0001c0001t0010g0339a0001c0001t0032g0336 | 2 | HG00140.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.345-945A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631290 | ||||||
| chr15:92631292
|
TATTATAT others(46): Show |
T | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-1000_345-948de others(54): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631292 | ||||||
| chr15:92631294
|
T | A | 2 | a0001c0001t0008g0012a0001c0001t0032g0032 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-949A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631294 | ||||||
| chr15:92631294
|
TTA | T | 3 | a0001c0001t0001g0083a0001c0001t0002g0101a0001c0001t0006g0091 | 3 | HG02074.hp2 NA18983.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.345-951_345-950del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631294 | ||||||
| chr15:92631294
|
TTATATAT others(35): Show |
T | 2 | a0001c0001t0007g0207a0001c0001t0024g0208 | 2 | HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.345-991_345-950del others(42): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631294 | ||||||
| chr15:92631295
|
T | A | 8 | a0001c0001t0002g0168a0001c0001t0003g0124a0001c0001t0005g0210others(5): Show | 8 | HG03579.hp1 NA18522.hp2 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-950A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631295 | ||||||
| chr15:92631296
|
A | ATAT | 4 | a0001c0001t0003g0060a0001c0001t0004g0328a0001c0001t0004g0329others(1): Show | 4 | HG00741.hp2 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-954_345-952dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631296 | ||||||
| chr15:92631299
|
TATAATAT others(65): Show |
T | 1 | a0001c0001t0001g0278 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.345-1026_345-955de others(73): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631299 | ||||||
| chr15:92631300
|
A | T | 1 | a0001c0001t0002g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.345-955T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631300 | ||||||
| chr15:92631300
|
ATAATATA others(14): Show |
A | 1 | a0001c0001t0009g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.345-976_345-956del others(21): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631300 | ||||||
| chr15:92631300
|
ATAATATA others(61): Show |
A | 1 | a0001c0001t0038g0274 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.345-1023_345-956de others(69): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631300 | ||||||
| chr15:92631301
|
T | A | 1 | a0001c0001t0002g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.345-956A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631301 | ||||||
| chr15:92631302
|
A | T | 17 | a0001c0001t0001g0083a0001c0001t0001g0206a0001c0001t0002g0101others(14): Show | 17 | HG01099.hp2 HG01261.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-957T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631302 | ||||||
| chr15:92631303
|
A | T | 3 | a0001c0001t0006g0243a0001c0001t0008g0012a0001c0001t0032g0032 | 3 | HG01361.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-958T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631303 | ||||||
| chr15:92631306
|
T | C | 1 | a0001c0001t0006g0243 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-961A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631306 | ||||||
| chr15:92631308
|
T | A | 1 | a0001c0001t0002g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.345-963A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631308 | ||||||
| chr15:92631309
|
T | A | 3 | a0001c0001t0001g0083a0001c0001t0002g0101a0001c0001t0006g0091 | 3 | HG02074.hp2 NA18983.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.345-964A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631309 | ||||||
| chr15:92631313
|
TATAA | T | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-972_345-969del others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631313 | ||||||
| chr15:92631314
|
A | T | 1 | a0001c0001t0006g0265 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.345-969T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631314 | ||||||
| chr15:92631315
|
T | A | 2 | a0001c0001t0002g0311a0001c0001t0006g0265 | 2 | NA18940.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.345-970A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631315 | ||||||
| chr15:92631315
|
TAATATTA others(14): Show |
T | 4 | a0001c0001t0002g0125a0001c0001t0003g0130a0001c0001t0006g0261others(1): Show | 4 | HG01099.hp2 NA19002.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-991_345-971del others(21): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631315 | ||||||
| chr15:92631315
|
TAATATTA others(21): Show |
T | 1 | a0001c0001t0059g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-998_345-971del others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631315 | ||||||
| chr15:92631316
|
A | T | 143 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0068others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.345-971T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631316 | ||||||
| chr15:92631316
|
AATATT | A | 3 | a0001c0001t0007g0044a0001c0001t0021g0042a0001c0001t0030g0045 | 3 | HG03491.hp2 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.345-976_345-972del others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631316 | ||||||
| chr15:92631316
|
AATATTAT others(47): Show |
A | 3 | a0001c0001t0002g0146a0001c0001t0003g0139a0001c0001t0007g0145 | 3 | NA18973.hp1 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.345-1025_345-972de others(55): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631316 | ||||||
| chr15:92631319
|
AT | A | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-975delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631319 | ||||||
| chr15:92631321
|
T | A | 15 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0002g0101others(12): Show | 15 | HG00741.hp1 HG01978.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-976A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631321 | ||||||
| chr15:92631322
|
A | T | 11 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0002g0101others(8): Show | 11 | HG00741.hp1 HG01978.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-977T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631322 | ||||||
| chr15:92631328
|
A | T | 109 | a0001c0001t0001g0058a0001c0001t0001g0153a0001c0001t0001g0157others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.345-983T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631328 | ||||||
| chr15:92631329
|
A | T | 9 | a0001c0001t0001g0083a0001c0001t0002g0101a0001c0001t0003g0116others(6): Show | 9 | HG00741.hp1 HG02074.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.345-984T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631329 | ||||||
| chr15:92631333
|
A | T | 4 | a0001c0001t0004g0131a0001c0001t0006g0243a0001c0001t0011g0132others(1): Show | 4 | HG00642.hp1 HG01361.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-988T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631333 | ||||||
| chr15:92631334
|
T | A | 4 | a0001c0001t0004g0131a0001c0001t0006g0243a0001c0001t0011g0132others(1): Show | 4 | HG00642.hp1 HG01361.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-989A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631334 | ||||||
| chr15:92631334
|
TTA | T | 106 | a0001c0001t0001g0058a0001c0001t0001g0083a0001c0001t0001g0153others(103): Show | 107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.345-991_345-990del others(2): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631334 | ||||||
| chr15:92631335
|
T | A | 7 | a0001c0001t0002g0005a0001c0001t0003g0124a0001c0001t0004g0048others(4): Show | 8 | HG00741.hp1 HG02559.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-990A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631335 | ||||||
| chr15:92631336
|
A | ATATAT | 64 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0068others(61): Show | 64 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.345-996_345-992dup others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631336 | ||||||
| chr15:92631336
|
A | T | 3 | a0001c0001t0004g0048a0001c0001t0018g0247a0001c0001t0021g0185 | 3 | HG00741.hp1 HG02735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.345-991T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631336 | ||||||
| chr15:92631338
|
A | G | 11 | a0001c0001t0001g0153a0001c0001t0001g0222a0001c0001t0005g0201others(8): Show | 12 | HG01346.hp2 HG01496.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-993T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631338 | ||||||
| chr15:92631342
|
T | A | 7 | a0001c0001t0001g0099a0001c0001t0003g0116a0001c0001t0007g0111others(4): Show | 7 | HG00733.hp1 HG01975.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-997A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631342 | ||||||
| chr15:92631345
|
A | ATAT | 4 | a0001c0001t0001g0082a0001c0001t0003g0149a0001c0001t0006g0078others(1): Show | 4 | HG02071.hp1 HG03130.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1003_345-1001d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631345 | ||||||
| chr15:92631348
|
TAATATAT others(2): Show |
T | 37 | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0107others(34): Show | 37 | HG00423.hp1 HG00673.hp2 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.345-1012_345-1004d others(11): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631348 | ||||||
| chr15:92631349
|
A | T | 89 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0001g0150others(86): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.345-1004T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631349 | ||||||
| chr15:92631349
|
AATATATT others(59): Show |
A | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-1070_345-1005d others(68): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631349 | ||||||
| chr15:92631350
|
A | T | 5 | a0001c0001t0001g0082a0001c0001t0003g0149a0001c0001t0006g0078others(2): Show | 5 | HG02071.hp1 HG03130.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-1005T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631350 | ||||||
| chr15:92631355
|
TTA | T | 3 | a0001c0001t0001g0083a0001c0001t0002g0101a0001c0001t0006g0091 | 3 | HG02074.hp2 NA18983.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.345-1012_345-1011d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631355 | ||||||
| chr15:92631356
|
T | A | 6 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0029g0158others(3): Show | 6 | HG00642.hp1 HG02630.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1011A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631356 | ||||||
| chr15:92631357
|
A | ATATAT | 5 | a0001c0001t0001g0099a0001c0001t0003g0116a0001c0001t0007g0111others(2): Show | 5 | HG01978.hp1 HG03017.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-1017_345-1013d others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631357
|
A | ATATATAA others(5): Show |
3 | a0001c0001t0001g0082a0001c0001t0003g0149a0001c0001t0006g0078 | 3 | HG02071.hp1 NA18747.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.345-1013_345-1012i others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631357
|
A | ATATATAA others(19): Show |
1 | a0001c0001t0009g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.345-1013_345-1012i others(28): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631357
|
A | ATATATTA others(5): Show |
31 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0001g0096others(28): Show | 31 | HG00558.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-1013_345-1012i others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631357
|
A | ATATATTA others(29): Show |
1 | a0001c0001t0002g0092 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.345-1013_345-1012i others(38): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631357
|
A | ATATATTA others(31): Show |
26 | a0001c0001t0001g0068a0001c0001t0001g0276a0001c0001t0001g0281others(23): Show | 26 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.345-1050_345-1013d others(40): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631357
|
A | ATATATTA others(83): Show |
1 | a0001c0001t0002g0311 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.345-1013_345-1012i others(92): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631357
|
A | ATATATTA others(123): Show |
1 | a0001c0001t0003g0080 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.345-1013_345-1012i others(132): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631357
|
A | T | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1012T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631357 | ||||||
| chr15:92631361
|
A | T | 3 | a0001c0001t0009g0187a0001c0001t0015g0189a0001c0001t0065g0385 | 3 | HG02970.hp1 NA18961.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.345-1016T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631361 | ||||||
| chr15:92631362
|
T | A | 12 | a0001c0001t0002g0022a0001c0001t0008g0015a0001c0001t0008g0052others(9): Show | 12 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-1017A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631362 | ||||||
| chr15:92631363
|
T | A | 6 | a0001c0001t0001g0346a0001c0001t0004g0347a0001c0001t0010g0349others(3): Show | 6 | HG00733.hp1 HG01175.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1018A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631363 | ||||||
| chr15:92631368
|
T | A | 11 | a0001c0001t0001g0346a0001c0001t0002g0005a0001c0001t0004g0347others(8): Show | 12 | HG00423.hp2 HG00733.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-1023A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631368 | ||||||
| chr15:92631369
|
A | T | 4 | a0001c0001t0005g0211a0001c0001t0005g0323a0001c0001t0008g0012others(1): Show | 4 | HG00423.hp2 HG03225.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1024T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631369 | ||||||
| chr15:92631370
|
T | A | 2 | a0001c0001t0008g0012a0001c0001t0032g0032 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-1025A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631370 | ||||||
| chr15:92631374
|
TAA | T | 4 | a0001c0001t0005g0323a0001c0001t0009g0187a0001c0001t0015g0189others(1): Show | 4 | HG02970.hp1 HG04204.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1031_345-1030d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631374 | ||||||
| chr15:92631375
|
A | ATT | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1031_345-1030i others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631375 | ||||||
| chr15:92631375
|
A | T | 77 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(74): Show | 79 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.345-1030T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631375 | ||||||
| chr15:92631375
|
AATATATT others(52): Show |
A | 5 | a0001c0001t0001g0346a0001c0001t0004g0347a0001c0001t0010g0349others(2): Show | 5 | HG00733.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-1089_345-1031d others(61): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631375 | ||||||
| chr15:92631376
|
A | T | 3 | a0001c0001t0005g0211a0001c0001t0008g0012a0001c0001t0032g0032 | 3 | HG00423.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-1031T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631376 | ||||||
| chr15:92631381
|
T | A | 1 | a0001c0001t0059g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-1036A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631381 | ||||||
| chr15:92631382
|
T | A | 7 | a0001c0001t0004g0131a0001c0001t0008g0012a0001c0001t0011g0132others(4): Show | 7 | HG00642.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-1037A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631382 | ||||||
| chr15:92631382
|
T | C | 1 | a0001c0001t0060g0322 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.345-1037A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631382 | ||||||
| chr15:92631383
|
ATATATTA others(10): Show |
A | 1 | a0001c0001t0034g0031 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.345-1055_345-1039d others(19): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631383 | ||||||
| chr15:92631387
|
A | T | 75 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(72): Show | 77 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.345-1042T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631387 | ||||||
| chr15:92631388
|
T | A | 77 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(74): Show | 79 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.345-1043A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631388 | ||||||
| chr15:92631388
|
TTA | T | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1045_345-1044d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631388 | ||||||
| chr15:92631389
|
T | A | 2 | a0001c0001t0005g0323a0001c0001t0021g0361 | 2 | HG04204.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.345-1044A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631389 | ||||||
| chr15:92631390
|
ATATAT | A | 8 | a0001c0001t0001g0049a0001c0001t0003g0324a0001c0001t0003g0326others(5): Show | 8 | HG00423.hp2 HG00735.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-1050_345-1046d others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631390 | ||||||
| chr15:92631390
|
ATATATTA others(3): Show |
A | 8 | a0001c0001t0002g0022a0001c0001t0008g0015a0001c0001t0008g0052others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-1055_345-1046d others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631390 | ||||||
| chr15:92631391
|
T | C | 1 | a0001c0001t0005g0071 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.345-1046A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631391 | ||||||
| chr15:92631392
|
ATAT | A | 14 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0003g0334others(11): Show | 15 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-1050_345-1048d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631392 | ||||||
| chr15:92631393
|
T | A | 1 | a0001c0001t0003g0320 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.345-1048A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631393 | ||||||
| chr15:92631394
|
A | T | 74 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(71): Show | 76 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.345-1049T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631394 | ||||||
| chr15:92631395
|
T | A | 80 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(77): Show | 82 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.345-1050A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631395 | ||||||
| chr15:92631396
|
T | A | 2 | a0001c0001t0021g0361a0001c0001t0032g0032 | 2 | NA18954.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.345-1051A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631396 | ||||||
| chr15:92631400
|
T | A | 15 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0002g0005others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-1055A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631400 | ||||||
| chr15:92631400
|
T | TTA | 5 | a0001c0001t0008g0012a0001c0001t0009g0123a0001c0001t0009g0187others(2): Show | 5 | HG01109.hp2 HG02970.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-1057_345-1056d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631400 | ||||||
| chr15:92631401
|
T | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-1056A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631401 | ||||||
| chr15:92631406
|
T | A | 13 | a0001c0001t0002g0022a0001c0001t0004g0328a0001c0001t0004g0329others(10): Show | 13 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-1061A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631406 | ||||||
| chr15:92631407
|
A | T | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0059g0055 | 3 | HG02145.hp2 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.345-1062T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631407 | ||||||
| chr15:92631408
|
T | A | 1 | a0001c0001t0059g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-1063A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631408 | ||||||
| chr15:92631410
|
T | C | 1 | a0001c0001t0021g0361 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.345-1065A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631410 | ||||||
| chr15:92631413
|
A | T | 3 | a0001c0001t0040g0335a0001c0001t0060g0322a0003c0004t0037g0367 | 3 | HG02280.hp1 HG03130.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.345-1068T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631413 | ||||||
| chr15:92631413
|
AAT | A | 19 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0002g0092others(16): Show | 20 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.345-1070_345-1069d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631413 | ||||||
| chr15:92631414
|
A | T | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-1069T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631414 | ||||||
| chr15:92631415
|
T | A | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-1070A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631415 | ||||||
| chr15:92631415
|
T | C | 2 | a0001c0001t0047g0364a0001c0001t0050g0363 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.345-1070A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631415 | ||||||
| chr15:92631420
|
A | T | 11 | a0001c0001t0002g0146a0001c0001t0003g0067a0001c0001t0003g0139others(8): Show | 11 | HG01258.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-1075T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631420 | ||||||
| chr15:92631420
|
AAT | A | 13 | a0001c0001t0002g0022a0001c0001t0003g0163a0001c0001t0003g0164others(10): Show | 13 | HG00323.hp1 HG01109.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-1077_345-1076d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631420 | ||||||
| chr15:92631421
|
A | T | 1 | a0001c0001t0021g0361 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.345-1076T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631421 | ||||||
| chr15:92631422
|
TA | T | 7 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(4): Show | 9 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-1078delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631422 | ||||||
| chr15:92631427
|
A | AAT | 7 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0008g0191others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-1084_345-1083d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631427 | ||||||
| chr15:92631427
|
A | T | 3 | a0001c0001t0010g0036a0001c0001t0036g0381a0001c0001t0036g0382 | 3 | HG02280.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-1082T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631427 | ||||||
| chr15:92631427
|
AAT | A | 4 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(1): Show | 5 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-1084_345-1083d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631427 | ||||||
| chr15:92631427
|
AATATAAT | A | 15 | a0001c0001t0001g0344a0001c0001t0002g0005a0001c0001t0002g0188others(12): Show | 16 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.345-1089_345-1083d others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631427 | ||||||
| chr15:92631428
|
A | AT | 3 | a0001c0003t0002g0002a0001c0003t0002g0016a0001c0003t0002g0021 | 4 | HG02809.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1084dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631428 | ||||||
| chr15:92631432
|
A | G | 2 | a0001c0001t0004g0131a0001c0001t0011g0132 | 2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1087T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631432 | ||||||
| chr15:92631432
|
A | T | 7 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(4): Show | 8 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-1087T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631432 | ||||||
| chr15:92631433
|
A | AT | 3 | a0001c0003t0002g0002a0001c0003t0002g0016a0001c0003t0002g0021 | 4 | HG02809.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1089dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631433 | ||||||
| chr15:92631433
|
A | T | 88 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(85): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.345-1088T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631433 | ||||||
| chr15:92631434
|
T | A | 88 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(85): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.345-1089A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631434 | ||||||
| chr15:92631434
|
T | TATATA | 4 | a0001c0001t0001g0040a0001c0001t0008g0012a0001c0001t0024g0057others(1): Show | 4 | HG02615.hp1 HG03225.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-1090_345-1089i others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631434 | ||||||
| chr15:92631435
|
A | T | 1 | a0001c0001t0021g0361 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.345-1090T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631435 | ||||||
| chr15:92631435
|
AT | A | 5 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(2): Show | 6 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1091delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631435 | ||||||
| chr15:92631436
|
T | TA | 3 | a0001c0003t0002g0002a0001c0003t0002g0016a0001c0003t0002g0021 | 4 | HG02809.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1092dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631436 | ||||||
| chr15:92631437
|
A | T | 6 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0008g0191others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1092T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631437 | ||||||
| chr15:92631438
|
T | A | 6 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0008g0191others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1093A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631438 | ||||||
| chr15:92631439
|
T | A | 2 | a0001c0001t0001g0296a0001c0001t0021g0361 | 2 | HG01981.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.345-1094A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631439 | ||||||
| chr15:92631443
|
T | A | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1098A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631443 | ||||||
| chr15:92631444
|
A | T | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1099T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631444 | ||||||
| chr15:92631448
|
AACAT | A | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1107_345-1104d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631448 | ||||||
| chr15:92631450
|
C | T | 2 | a0001c0001t0016g0112a0001c0006t0024g0113 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.345-1105G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631450 | ||||||
| chr15:92631454
|
A | T | 10 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(7): Show | 12 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-1109T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631454 | ||||||
| chr15:92631459
|
T | A | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1114A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631459 | ||||||
| chr15:92631465
|
A | AAT | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-1121_345-1120i others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631465 | ||||||
| chr15:92631469
|
A | T | 107 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(104): Show | 107 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.345-1124T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631469 | ||||||
| chr15:92631482
|
T | TTA | 339 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0058others(336): Show | 344 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.345-1139_345-1138d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631482 | ||||||
| chr15:92631482
|
T | TTATA | 7 | a0001c0001t0004g0131a0001c0001t0004g0165a0001c0001t0011g0132others(4): Show | 7 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-1141_345-1138d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631482 | ||||||
| chr15:92631482
|
T | TTGTA | 30 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-1138_345-1137i others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631482 | ||||||
| chr15:92631500
|
C | CT | 7 | a0001c0001t0001g0301a0001c0001t0001g0308a0001c0001t0002g0313others(4): Show | 7 | HG00673.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-1156dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631500 | ||||||
| chr15:92631500
|
CT | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0209a0001c0001t0001g0287others(9): Show | 12 | HG01975.hp2 HG02451.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-1156delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631500 | ||||||
| chr15:92631552
|
T | C | 239 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0058others(236): Show | 240 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.345-1207A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631552 | ||||||
| chr15:92631564
|
G | A | 1 | a0001c0001t0059g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-1219C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631564 | ||||||
| chr15:92631590
|
G | A | 7 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0008g0191others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-1245C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631590 | ||||||
| chr15:92631591
|
T | C | 2 | a0001c0001t0009g0123a0001c0001t0024g0057 | 2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.345-1246A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631591 | ||||||
| chr15:92631596
|
A | G | 4 | a0001c0001t0010g0333a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02055.hp1 HG02886.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-1251T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631596 | ||||||
| chr15:92631656
|
G | A | 1 | a0001c0001t0026g0218 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.345-1311C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631656 | ||||||
| chr15:92631678
|
T | C | 1 | a0001c0001t0016g0341 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.345-1333A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631678 | ||||||
| chr15:92631791
|
C | T | 1 | a0001c0001t0038g0274 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.345-1446G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631791 | ||||||
| chr15:92631801
|
C | T | 226 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(223): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.345-1456G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631801 | ||||||
| chr15:92631833
|
TA | T | 374 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(371): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.345-1489delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631833 | ||||||
| chr15:92631836
|
A | G | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-1491T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631836 | ||||||
| chr15:92631873
|
C | T | 2 | a0001c0001t0009g0123a0001c0001t0024g0057 | 2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.345-1528G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631873 | ||||||
| chr15:92631874
|
G | C | 1 | a0001c0001t0049g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.345-1529C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92631874 | ||||||
| chr15:92632013
|
C | CCAAATTG others(20): Show |
3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-1669_345-1668i others(29): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632013 | ||||||
| chr15:92632027
|
A | G | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-1682T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632027 | ||||||
| chr15:92632093
|
G | T | 1 | a0001c0001t0003g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.345-1748C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632093 | ||||||
| chr15:92632283
|
G | A | 2 | a0001c0001t0009g0123a0001c0001t0024g0057 | 2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.345-1938C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632283 | ||||||
| chr15:92632340
|
A | C | 4 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0048g0122others(1): Show | 4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1995T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632340 | ||||||
| chr15:92632487
|
A | T | 3 | a0001c0001t0001g0296a0001c0001t0002g0297a0001c0001t0006g0298 | 3 | HG01934.hp1 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.345-2142T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632487 | ||||||
| chr15:92632584
|
G | A | 2 | a0001c0001t0001g0344a0001c0001t0012g0343 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.345-2239C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632584 | ||||||
| chr15:92632680
|
T | G | 1 | a0001c0001t0001g0296 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-2335A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632680 | ||||||
| chr15:92632681
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-2336C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632681 | ||||||
| chr15:92632681
|
GT | G | 89 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(86): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.345-2337delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632681 | ||||||
| chr15:92632684
|
T | G | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-2339A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632684 | ||||||
| chr15:92632717
|
T | C | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-2372A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632717 | ||||||
| chr15:92632723
|
T | C | 1 | a0001c0001t0059g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345-2378A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632723 | ||||||
| chr15:92632759
|
C | T | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-2414G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632759 | ||||||
| chr15:92632796
|
G | A | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-2451C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632796 | ||||||
| chr15:92632858
|
T | A | 1 | a0001c0001t0007g0348 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.345-2513A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632858 | ||||||
| chr15:92632914
|
ACT | A | 117 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0153others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.345-2571_345-2570d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632914 | ||||||
| chr15:92632934
|
G | A | 1 | a0001c0001t0013g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.345-2589C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632934 | ||||||
| chr15:92632968
|
C | T | 102 | a0001c0001t0001g0058a0001c0001t0001g0153a0001c0001t0001g0157others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.345-2623G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92632968 | ||||||
| chr15:92633009
|
TTTG | T | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-2667_345-2665d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633009 | ||||||
| chr15:92633051
|
C | CTT | 3 | a0001c0001t0006g0261a0001c0001t0006g0262a0001c0001t0006g0265 | 3 | NA18940.hp2 NA19002.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.345-2708_345-2707d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633051 | ||||||
| chr15:92633100
|
A | T | 2 | a0001c0001t0002g0272a0001c0001t0002g0273 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.345-2755T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633100 | ||||||
| chr15:92633181
|
C | A | 4 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0048g0122others(1): Show | 4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-2836G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633181 | ||||||
| chr15:92633203
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.345-2858G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633203 | ||||||
| chr15:92633263
|
G | A | 34 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.345-2918C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633263 | ||||||
| chr15:92633319
|
C | T | 88 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(85): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.345-2974G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633319 | ||||||
| chr15:92633334
|
C | G | 10 | a0001c0001t0002g0146a0001c0001t0003g0067a0001c0001t0003g0139others(7): Show | 10 | HG00642.hp1 HG01109.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.345-2989G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633334 | ||||||
| chr15:92633385
|
A | T | 1 | a0002c0002t0015g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.345-3040T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633385 | ||||||
| chr15:92633498
|
T | C | 9 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(6): Show | 11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-3153A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633498 | ||||||
| chr15:92633576
|
G | A | 1 | a0001c0001t0054g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.345-3231C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633576 | ||||||
| chr15:92633753
|
C | A | 4 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0048g0122others(1): Show | 4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-3408G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633753 | ||||||
| chr15:92633786
|
C | T | 1 | a0001c0001t0024g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.345-3441G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633786 | ||||||
| chr15:92633795
|
A | T | 48 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0344others(45): Show | 49 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.345-3450T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633795 | ||||||
| chr15:92633998
|
C | T | 1 | a0001c0006t0002g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.345-3653G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92633998 | ||||||
| chr15:92634000
|
A | T | 1 | a0001c0001t0002g0312 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.345-3655T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634000 | ||||||
| chr15:92634134
|
C | G | 4 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0048g0122others(1): Show | 4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-3789G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634134 | ||||||
| chr15:92634141
|
G | A | 1 | a0001c0006t0024g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.345-3796C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634141 | ||||||
| chr15:92634158
|
C | T | 7 | a0001c0001t0001g0104a0001c0001t0009g0117a0001c0001t0015g0118others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-3813G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634158 | ||||||
| chr15:92634341
|
A | T | 1 | a0001c0001t0049g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.345-3996T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634341 | ||||||
| chr15:92634369
|
A | G | 221 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(218): Show | 222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.345-4024T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634369 | ||||||
| chr15:92634377
|
A | T | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-4032T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634377 | ||||||
| chr15:92634420
|
T | C | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-4075A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634420 | ||||||
| chr15:92634563
|
A | G | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-4218T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634563 | ||||||
| chr15:92634568
|
C | T | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-4223G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634568 | ||||||
| chr15:92634598
|
T | C | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-4253A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634598 | ||||||
| chr15:92634712
|
G | A | 9 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(6): Show | 11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-4367C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634712 | ||||||
| chr15:92634738
|
C | T | 2 | a0001c0001t0004g0131a0001c0001t0011g0132 | 2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-4393G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634738 | ||||||
| chr15:92634873
|
A | G | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-4528T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634873 | ||||||
| chr15:92634878
|
T | C | 1 | a0001c0001t0006g0243 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.345-4533A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634878 | ||||||
| chr15:92634922
|
G | GT | 18 | a0001c0001t0002g0188a0001c0001t0002g0353a0001c0001t0002g0354others(15): Show | 19 | HG01346.hp1 HG01515.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.345-4578dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634922 | ||||||
| chr15:92634952
|
C | A | 4 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0048g0122others(1): Show | 4 | HG00642.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-4607G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634952 | ||||||
| chr15:92634985
|
G | C | 32 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.345-4640C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92634985 | ||||||
| chr15:92635047
|
T | C | 372 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(369): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.345-4702A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635047 | ||||||
| chr15:92635077
|
A | G | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-4732T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635077 | ||||||
| chr15:92635096
|
G | GCC | 32 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.345-4753_345-4752d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635096 | ||||||
| chr15:92635120
|
GTC | G | 225 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0059others(222): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.345-4777_345-4776d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635120 | ||||||
| chr15:92635136
|
CCT | C | 4 | a0001c0003t0002g0002a0001c0003t0002g0016a0001c0003t0002g0017others(1): Show | 5 | HG02630.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-4793_345-4792d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635136 | ||||||
| chr15:92635158
|
TCCACACA others(3): Show |
T | 93 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0109others(90): Show | 95 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.345-4823_345-4814d others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635158 | ||||||
| chr15:92635159
|
CCACACAC others(5): Show |
C | 62 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(59): Show | 64 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.345-4826_345-4815d others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635159 | ||||||
| chr15:92635159
|
CCACACAC others(7): Show |
C | 6 | a0001c0001t0001g0027a0001c0001t0005g0258a0001c0001t0009g0029others(3): Show | 6 | HG01258.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.345-4828_345-4815d others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635159 | ||||||
| chr15:92635161
|
ACACACAC others(1): Show |
A | 29 | a0001c0001t0001g0040a0001c0001t0001g0275a0001c0001t0001g0276others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.345-4824_345-4817d others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635161 | ||||||
| chr15:92635163
|
ACACACC | A | 176 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0128others(173): Show | 178 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.345-4824_345-4819d others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635163 | ||||||
| chr15:92635165
|
ACACC | A | 5 | a0001c0001t0003g0130a0001c0001t0004g0048a0001c0001t0005g0214others(2): Show | 5 | HG01099.hp2 HG02622.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-4824_345-4821d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635165 | ||||||
| chr15:92635169
|
C | A | 1 | a0001c0001t0022g0260 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.345-4824G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635169 | ||||||
| chr15:92635169
|
C | CCACA | 7 | a0001c0001t0010g0362a0002c0002t0004g0372a0002c0002t0004g0375others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-4828_345-4825d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635169 | ||||||
| chr15:92635180
|
C | A | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-4835G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635180 | ||||||
| chr15:92635199
|
C | A | 1 | a0001c0001t0003g0318 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.345-4854G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635199 | ||||||
| chr15:92635359
|
T | C | 5 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-5014A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635359 | ||||||
| chr15:92635579
|
C | CT | 26 | a0001c0001t0001g0058a0001c0001t0001g0104a0001c0001t0001g0128others(23): Show | 27 | HG00438.hp2 HG01074.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.345-5235dupA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635579 | ||||||
| chr15:92635579
|
CT | C | 45 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0241others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.345-5235delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635579 | ||||||
| chr15:92635772
|
G | T | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(4): Show | 7 | HG01346.hp2 HG01928.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-5427C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635772 | ||||||
| chr15:92635862
|
T | C | 3 | a0001c0001t0010g0036a0001c0001t0036g0381a0001c0001t0036g0382 | 3 | HG02280.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-5517A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635862 | ||||||
| chr15:92635870
|
C | T | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-5525G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635870 | ||||||
| chr15:92635871
|
G | A | 1 | a0001c0001t0005g0325 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.345-5526C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635871 | ||||||
| chr15:92635923
|
G | T | 1 | a0001c0001t0009g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345-5578C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635923 | ||||||
| chr15:92635924
|
C | T | 1 | a0001c0001t0009g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.345-5579G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635924 | ||||||
| chr15:92635945
|
T | C | 33 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.345-5600A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92635945 | ||||||
| chr15:92636035
|
C | G | 1 | a0001c0001t0007g0126 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.345-5690G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636035 | ||||||
| chr15:92636150
|
A | T | 112 | a0001c0001t0001g0027a0001c0001t0001g0128a0001c0001t0001g0150others(109): Show | 116 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.345-5805T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636150 | ||||||
| chr15:92636271
|
G | A | 3 | a0001c0001t0004g0131a0001c0001t0011g0132a0003c0004t0004g0368 | 3 | HG00642.hp1 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-5926C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636271 | ||||||
| chr15:92636315
|
AAAT | A | 5 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-5973_345-5971d others(5): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636315 | ||||||
| chr15:92636338
|
A | G | 2 | a0001c0001t0007g0081a0001c0001t0013g0110 | 2 | NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.345-5993T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636338 | ||||||
| chr15:92636354
|
C | T | 33 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.345-6009G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636354 | ||||||
| chr15:92636369
|
G | A | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.345-6024C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636369 | ||||||
| chr15:92636572
|
G | A | 1 | a0001c0001t0005g0225 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.345-6227C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636572 | ||||||
| chr15:92636628
|
A | AGGCT | 33 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.345-6287_345-6284d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636628 | ||||||
| chr15:92636632
|
T | C | 19 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0001g0096others(16): Show | 19 | HG00558.hp1 HG01106.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.345-6287A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636632 | ||||||
| chr15:92636749
|
C | T | 14 | a0001c0001t0001g0241a0001c0001t0006g0004a0001c0001t0006g0183others(11): Show | 15 | HG01099.hp1 HG01255.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-6404G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636749 | ||||||
| chr15:92636750
|
G | A | 1 | a0001c0001t0016g0351 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345-6405C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92636750 | ||||||
| chr15:92637000
|
A | G | 8 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0016g0112others(5): Show | 8 | HG00642.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-6655T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637000 | ||||||
| chr15:92637012
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.345-6667G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637012 | ||||||
| chr15:92637268
|
G | A | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-6923C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637268 | ||||||
| chr15:92637484
|
G | A | 1 | a0001c0001t0003g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.345-7139C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637484 | ||||||
| chr15:92637684
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.345-7339G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637684 | ||||||
| chr15:92637688
|
G | A | 7 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0016g0112others(4): Show | 7 | HG00642.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-7343C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637688 | ||||||
| chr15:92637727
|
C | T | 4 | a0001c0001t0002g0146a0001c0001t0003g0067a0001c0001t0003g0139others(1): Show | 4 | HG01258.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-7382G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637727 | ||||||
| chr15:92637730
|
C | A | 1 | a0003c0004t0004g0368 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.345-7385G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637730 | ||||||
| chr15:92637735
|
G | A | 5 | a0001c0001t0009g0117a0001c0001t0015g0118a0001c0001t0015g0119others(2): Show | 5 | HG01243.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-7390C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637735 | ||||||
| chr15:92637881
|
G | C | 1 | a0009c0007t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.345-7536C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637881 | ||||||
| chr15:92637890
|
A | G | 379 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(376): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.345-7545T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637890 | ||||||
| chr15:92637993
|
G | A | 3 | a0001c0001t0002g0092a0001c0001t0006g0078a0001c0001t0006g0091 | 3 | HG00544.hp1 NA18983.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.345-7648C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92637993 | ||||||
| chr15:92638139
|
C | T | 1 | a0001c0001t0016g0352 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.345-7794G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638139 | ||||||
| chr15:92638254
|
C | T | 2 | a0001c0001t0036g0381a0001c0001t0036g0382 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.345-7909G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638254 | ||||||
| chr15:92638265
|
G | A | 245 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0001g0128others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.345-7920C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638265 | ||||||
| chr15:92638433
|
C | T | 1 | a0001c0001t0013g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.345-8088G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638433 | ||||||
| chr15:92638467
|
G | C | 1 | a0001c0001t0003g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.345-8122C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638467 | ||||||
| chr15:92638471
|
G | A | 1 | a0001c0001t0003g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.345-8126C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638471 | ||||||
| chr15:92638471
|
G | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0226a0001c0001t0025g0227 | 3 | HG00438.hp2 HG02523.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.345-8126C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638471 | ||||||
| chr15:92638475
|
C | A | 1 | a0001c0001t0001g0319 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.345-8130G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638475 | ||||||
| chr15:92638498
|
C | T | 7 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0016g0112others(4): Show | 7 | HG00642.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-8153G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638498 | ||||||
| chr15:92638582
|
G | A | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.345-8237C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638582 | ||||||
| chr15:92638654
|
C | T | 134 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0059others(131): Show | 136 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.345-8309G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638654 | ||||||
| chr15:92638706
|
G | A | 1 | a0001c0001t0004g0093 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.345-8361C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638706 | ||||||
| chr15:92638819
|
G | A | 12 | a0001c0001t0004g0131a0001c0001t0004g0328a0001c0001t0004g0329others(9): Show | 12 | HG00642.hp1 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.345-8474C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638819 | ||||||
| chr15:92638874
|
A | G | 124 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0068others(121): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.345-8529T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638874 | ||||||
| chr15:92638904
|
G | A | 5 | a0001c0001t0001g0344a0001c0001t0010g0036a0001c0001t0012g0343others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-8559C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638904 | ||||||
| chr15:92638918
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.345-8573A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638918 | ||||||
| chr15:92638955
|
C | T | 4 | a0001c0001t0002g0146a0001c0001t0003g0067a0001c0001t0003g0139others(1): Show | 4 | HG01258.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-8610G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92638955 | ||||||
| chr15:92639099
|
G | A | 1 | a0001c0001t0002g0125 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.345-8754C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639099 | ||||||
| chr15:92639192
|
C | T | 215 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0150others(212): Show | 218 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.345-8847G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639192 | ||||||
| chr15:92639233
|
G | C | 1 | a0001c0001t0002g0079 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.345-8888C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639233 | ||||||
| chr15:92639235
|
AAGTT | A | 11 | a0001c0001t0002g0022a0001c0001t0008g0012a0001c0001t0008g0015others(8): Show | 11 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-8894_345-8891d others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639235 | ||||||
| chr15:92639241
|
T | C | 11 | a0001c0001t0002g0022a0001c0001t0008g0012a0001c0001t0008g0015others(8): Show | 11 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-8896A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639241 | ||||||
| chr15:92639243
|
T | C | 11 | a0001c0001t0002g0022a0001c0001t0008g0012a0001c0001t0008g0015others(8): Show | 11 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.345-8898A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639243 | ||||||
| chr15:92639263
|
G | T | 1 | a0001c0001t0002g0354 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.345-8918C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639263 | ||||||
| chr15:92639319
|
G | A | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-8974C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639319 | ||||||
| chr15:92639329
|
AG | A | 5 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-8985delC | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639329 | ||||||
| chr15:92639398
|
G | C | 1 | a0001c0001t0052g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.345-9053C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639398 | ||||||
| chr15:92639485
|
G | T | 1 | a0001c0001t0004g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.345-9140C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639485 | ||||||
| chr15:92639715
|
T | A | 75 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(72): Show | 75 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.345-9370A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639715 | ||||||
| chr15:92639829
|
A | C | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.345-9484T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639829 | ||||||
| chr15:92639889
|
C | G | 5 | a0001c0001t0011g0033a0001c0001t0011g0035a0001c0001t0032g0032others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-9544G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639889 | ||||||
| chr15:92639908
|
C | T | 1 | a0001c0001t0005g0211 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.345-9563G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639908 | ||||||
| chr15:92639992
|
G | C | 1 | a0001c0001t0003g0178 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.345-9647C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92639992 | ||||||
| chr15:92640200
|
C | A | 1 | a0009c0007t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.345-9855G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640200 | ||||||
| chr15:92640268
|
T | C | 358 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(355): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.345-9923A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640268 | ||||||
| chr15:92640285
|
C | T | 5 | a0001c0001t0011g0033a0001c0001t0011g0035a0001c0001t0032g0032others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-9940G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640285 | ||||||
| chr15:92640444
|
C | T | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-10099G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640444 | ||||||
| chr15:92640539
|
G | A | 2 | a0001c0001t0047g0364a0001c0001t0050g0363 | 2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.345-10194C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640539 | ||||||
| chr15:92640551
|
CAA | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0294a0001c0001t0001g0344others(6): Show | 9 | HG01258.hp1 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-10208_345-1020 others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | ||||||
| chr15:92640551
|
CAAA | C | 30 | a0001c0001t0001g0155a0001c0001t0001g0229a0001c0001t0001g0292others(27): Show | 31 | HG01109.hp1 HG01175.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.345-10209_345-1020 others(7): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | ||||||
| chr15:92640551
|
CAAAA | C | 101 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0099others(98): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.345-10210_345-1020 others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | ||||||
| chr15:92640551
|
CAAAAA | C | 130 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0098others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.345-10211_345-1020 others(9): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | ||||||
| chr15:92640551
|
CAAAAAA | C | 87 | a0001c0001t0001g0027a0001c0001t0001g0068a0001c0001t0001g0082others(84): Show | 88 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.345-10212_345-1020 others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | ||||||
| chr15:92640551
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0004g0316a0001c0001t0052g0317 | 2 | HG00642.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.345-10220_345-1020 others(18): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | ||||||
| chr15:92640551
|
CAAAAAAA others(11): Show |
C | 9 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(6): Show | 11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-10224_345-1020 others(22): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | ||||||
| chr15:92640551
|
CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-10226_345-1020 others(24): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640551 | ||||||
| chr15:92640656
|
T | A | 9 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(6): Show | 11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-10311A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640656 | ||||||
| chr15:92640674
|
A | C | 1 | a0001c0001t0003g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.345-10329T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640674 | ||||||
| chr15:92640731
|
G | T | 9 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(6): Show | 11 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-10386C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640731 | ||||||
| chr15:92640760
|
T | G | 5 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-10415A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640760 | ||||||
| chr15:92640780
|
G | A | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.345-10435C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640780 | ||||||
| chr15:92640892
|
G | A | 1 | a0003c0004t0037g0367 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.345-10547C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640892 | ||||||
| chr15:92640934
|
C | T | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.345-10589G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92640934 | ||||||
| chr15:92641062
|
T | TCA | 126 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(123): Show | 126 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.345-10719_345-1071 others(6): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641062 | ||||||
| chr15:92641201
|
A | C | 1 | a0009c0007t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.345-10856T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641201 | ||||||
| chr15:92641394
|
G | A | 5 | a0001c0001t0002g0146a0001c0001t0003g0067a0001c0001t0003g0139others(2): Show | 5 | HG01258.hp1 NA18973.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-11049C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641394 | ||||||
| chr15:92641439
|
A | C | 7 | a0001c0001t0002g0005a0001c0001t0003g0334a0001c0001t0009g0338others(4): Show | 8 | HG00099.hp1 HG00140.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.345-11094T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641439 | ||||||
| chr15:92641514
|
A | G | 362 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(359): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.345-11169T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641514 | ||||||
| chr15:92641518
|
A | G | 363 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(360): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.345-11173T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641518 | ||||||
| chr15:92641547
|
A | C | 365 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(362): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.345-11202T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641547 | ||||||
| chr15:92641558
|
T | C | 17 | a0001c0001t0001g0049a0001c0001t0001g0330a0001c0001t0004g0046others(14): Show | 17 | HG01884.hp1 HG02965.hp2 HG03041.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-11213A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641558 | ||||||
| chr15:92641560
|
T | G | 2 | a0001c0001t0004g0131a0001c0001t0011g0132 | 2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.345-11215A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641560 | ||||||
| chr15:92641578
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.345-11233C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641578 | ||||||
| chr15:92641658
|
C | T | 1 | a0001c0003t0002g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.345-11313G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641658 | ||||||
| chr15:92641702
|
G | A | 1 | a0001c0001t0018g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.345-11357C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641702 | ||||||
| chr15:92641716
|
G | T | 1 | a0001c0001t0004g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.345-11371C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641716 | ||||||
| chr15:92641760
|
C | A | 1 | a0001c0001t0007g0126 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.345-11415G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641760 | ||||||
| chr15:92641776
|
C | G | 5 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-11431G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641776 | ||||||
| chr15:92641816
|
G | T | 7 | a0001c0001t0004g0131a0001c0001t0011g0132a0001c0001t0016g0112others(4): Show | 7 | HG00642.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.345-11471C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641816 | ||||||
| chr15:92641850
|
G | T | 4 | a0001c0001t0002g0146a0001c0001t0003g0067a0001c0001t0003g0139others(1): Show | 4 | HG01258.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-11505C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641850 | ||||||
| chr15:92641867
|
T | G | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.345-11522A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92641867 | ||||||
| chr15:92642083
|
A | G | 1 | a0001c0001t0021g0185 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.345-11738T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642083 | ||||||
| chr15:92642283
|
C | G | 1 | a0001c0001t0005g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.345-11938G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642283 | ||||||
| chr15:92642417
|
C | G | 357 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(354): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.345-12072G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642417 | ||||||
| chr15:92642548
|
T | C | 1 | a0001c0001t0010g0036 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.345-12203A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642548 | ||||||
| chr15:92642654
|
C | T | 181 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0150others(178): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.345-12309G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642654 | ||||||
| chr15:92642683
|
T | C | 4 | a0001c0001t0003g0124a0001c0001t0009g0123a0001c0001t0024g0057others(1): Show | 4 | HG01109.hp2 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-12338A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642683 | ||||||
| chr15:92642798
|
A | G | 5 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.345-12453T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642798 | ||||||
| chr15:92642867
|
C | T | 376 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(373): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.344+12449G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642867 | ||||||
| chr15:92642899
|
C | T | 55 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0344others(52): Show | 58 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.344+12417G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642899 | ||||||
| chr15:92642939
|
T | G | 2 | a0001c0001t0001g0344a0001c0001t0012g0343 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.344+12377A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642939 | ||||||
| chr15:92642981
|
T | C | 2 | a0001c0001t0003g0182a0001c0001t0004g0181 | 2 | HG00733.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.344+12335A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642981 | ||||||
| chr15:92642995
|
A | G | 2 | a0001c0001t0048g0122a0002c0002t0015g0379 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.344+12321T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92642995 | ||||||
| chr15:92643001
|
A | G | 361 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(358): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.344+12315T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643001 | ||||||
| chr15:92643136
|
GT | G | 369 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(366): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.344+12179delA | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643136 | ||||||
| chr15:92643141
|
T | A | 14 | a0001c0001t0001g0241a0001c0001t0006g0004a0001c0001t0006g0183others(11): Show | 15 | HG01099.hp1 HG01255.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.344+12175A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643141 | ||||||
| chr15:92643157
|
TG | T | 187 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0150others(184): Show | 190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.344+12158delC | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643157 | ||||||
| chr15:92643167
|
C | G | 1 | a0001c0001t0043g0184 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.344+12149G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643167 | ||||||
| chr15:92643285
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0168 | 2 | NA18947.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.344+12031C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643285 | ||||||
| chr15:92643304
|
G | C | 1 | a0001c0001t0020g0345 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.344+12012C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643304 | ||||||
| chr15:92643343
|
A | AGTGTGTG others(3): Show |
7 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | HG00558.hp1 HG01106.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+11972_344+1197 others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643343 | ||||||
| chr15:92643344
|
A | ATATGTGT others(5): Show |
1 | a0001c0001t0024g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.344+11971_344+1197 others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | ATGTG | 23 | a0001c0001t0001g0040a0001c0001t0001g0104a0001c0001t0003g0267others(20): Show | 23 | HG00642.hp1 HG00733.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.344+11968_344+1197 others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | ATGTGTG | 11 | a0001c0001t0001g0049a0001c0001t0003g0318a0001c0001t0004g0316others(8): Show | 11 | HG00639.hp2 HG00642.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.344+11966_344+1197 others(10): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | ATGTGTGT others(1): Show |
34 | a0001c0001t0001g0027a0001c0001t0001g0277a0001c0001t0001g0310others(31): Show | 34 | HG01109.hp1 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.344+11964_344+1197 others(12): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | ATGTGTGT others(3): Show |
40 | a0001c0001t0001g0100a0001c0001t0001g0128a0001c0001t0001g0246others(37): Show | 41 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.344+11962_344+1197 others(14): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | ATGTGTGT others(5): Show |
167 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0106others(164): Show | 170 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.344+11960_344+1197 others(16): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | ATGTGTGT others(7): Show |
51 | a0001c0001t0001g0058a0001c0001t0001g0171a0001c0001t0001g0288others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.344+11958_344+1197 others(18): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | ATGTGTGT others(9): Show |
22 | a0001c0001t0001g0068a0001c0001t0001g0278a0001c0001t0001g0302others(19): Show | 22 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(19): Show |
intron_variant | MODIFIER | c.344+11956_344+1197 others(20): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | ATGTGTGT others(11): Show |
2 | a0001c0001t0002g0159a0001c0001t0016g0351 | 2 | HG01934.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.344+11954_344+1197 others(22): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
A | G | 8 | a0001c0001t0001g0059a0001c0001t0001g0095a0001c0001t0001g0096others(5): Show | 8 | HG00558.hp1 HG01106.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+11972T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643344
|
ATGTG | A | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+11968_344+1197 others(8): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643344 | ||||||
| chr15:92643378
|
A | G | 1 | a0001c0001t0008g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.344+11938T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643378 | ||||||
| chr15:92643447
|
T | C | 3 | a0001c0001t0010g0362a0001c0001t0047g0364a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+11869A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643447 | ||||||
| chr15:92643499
|
T | A | 32 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.344+11817A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643499 | ||||||
| chr15:92643543
|
T | C | 365 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(362): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.344+11773A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643543 | ||||||
| chr15:92643569
|
T | A | 4 | a0001c0001t0003g0124a0001c0001t0009g0123a0001c0001t0024g0057others(1): Show | 4 | HG01109.hp2 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+11747A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643569 | ||||||
| chr15:92643572
|
A | G | 2 | a0001c0001t0009g0123a0001c0001t0024g0057 | 2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344+11744T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643572 | ||||||
| chr15:92643652
|
C | T | 1 | a0001c0001t0007g0268 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.344+11664G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643652 | ||||||
| chr15:92643758
|
G | A | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344+11558C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643758 | ||||||
| chr15:92643798
|
A | G | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+11518T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643798 | ||||||
| chr15:92643826
|
G | A | 96 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(93): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.344+11490C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643826 | ||||||
| chr15:92643955
|
G | A | 16 | a0001c0001t0001g0049a0001c0001t0001g0330a0001c0001t0004g0046others(13): Show | 16 | HG01884.hp1 HG02602.hp2 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.344+11361C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643955 | ||||||
| chr15:92643989
|
G | A | 2 | a0001c0001t0036g0381a0001c0001t0036g0382 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.344+11327C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643989 | ||||||
| chr15:92643999
|
A | G | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+11317T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92643999 | ||||||
| chr15:92644023
|
T | C | 1 | a0001c0001t0005g0129 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.344+11293A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644023 | ||||||
| chr15:92644046
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(2): Show | 5 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+11270G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644046 | ||||||
| chr15:92644105
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.344+11211G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644105 | ||||||
| chr15:92644125
|
A | G | 1 | a0001c0001t0029g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.344+11191T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644125 | ||||||
| chr15:92644363
|
G | C | 2 | a0001c0001t0011g0050a0001c0001t0063g0051 | 2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.344+10953C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644363 | ||||||
| chr15:92644367
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.344+10949A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644367 | ||||||
| chr15:92644413
|
T | C | 2 | a0001c0001t0009g0123a0001c0001t0024g0057 | 2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.344+10903A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644413 | ||||||
| chr15:92644482
|
C | T | 1 | a0001c0001t0019g0300 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.344+10834G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644482 | ||||||
| chr15:92644499
|
C | T | 5 | a0001c0001t0002g0146a0001c0001t0003g0067a0001c0001t0003g0139others(2): Show | 5 | HG01258.hp1 NA18970.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+10817G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644499 | ||||||
| chr15:92644573
|
C | A | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.344+10743G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644573 | ||||||
| chr15:92644587
|
G | A | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+10729C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644587 | ||||||
| chr15:92644712
|
T | C | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+10604A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644712 | ||||||
| chr15:92644769
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.344+10547G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644769 | ||||||
| chr15:92644803
|
G | A | 1 | a0002c0002t0030g0373 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.344+10513C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644803 | ||||||
| chr15:92644890
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.344+10426G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92644890 | ||||||
| chr15:92645121
|
C | G | 7 | a0001c0001t0001g0040a0001c0001t0002g0022a0001c0001t0008g0012others(4): Show | 7 | HG02257.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.344+10195G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645121 | ||||||
| chr15:92645152
|
G | A | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344+10164C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645152 | ||||||
| chr15:92645211
|
T | C | 364 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(361): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.344+10105A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645211 | ||||||
| chr15:92645281
|
T | C | 8 | a0001c0001t0001g0296a0001c0001t0002g0297a0001c0001t0002g0311others(5): Show | 8 | HG00558.hp2 HG01934.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+10035A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645281 | ||||||
| chr15:92645368
|
T | C | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+9948A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645368 | ||||||
| chr15:92645473
|
T | C | 1 | a0001c0001t0003g0269 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.344+9843A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645473 | ||||||
| chr15:92645482
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.344+9834G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645482 | ||||||
| chr15:92645506
|
A | G | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0153others(4): Show | 7 | HG01346.hp2 HG01928.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.344+9810T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645506 | ||||||
| chr15:92645641
|
A | G | 108 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.344+9675T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645641 | ||||||
| chr15:92645653
|
T | C | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+9663A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645653 | ||||||
| chr15:92645726
|
C | A | 187 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0150others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.344+9590G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645726 | ||||||
| chr15:92645747
|
C | T | 187 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0150others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.344+9569G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645747 | ||||||
| chr15:92645797
|
G | A | 255 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.344+9519C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645797 | ||||||
| chr15:92645869
|
C | A | 1 | a0001c0001t0003g0271 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.344+9447G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645869 | ||||||
| chr15:92645992
|
C | T | 2 | a0002c0002t0004g0372a0002c0002t0030g0373 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.344+9324G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645992 | ||||||
| chr15:92645995
|
T | C | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344+9321A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92645995 | ||||||
| chr15:92646168
|
G | A | 2 | a0001c0001t0002g0272a0001c0001t0002g0273 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.344+9148C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646168 | ||||||
| chr15:92646188
|
G | C | 1 | a0001c0001t0038g0274 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.344+9128C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646188 | ||||||
| chr15:92646222
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.344+9094T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646222 | ||||||
| chr15:92646298
|
T | C | 174 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(171): Show | 175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.344+9018A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646298 | ||||||
| chr15:92646299
|
C | T | 29 | a0001c0001t0001g0040a0001c0001t0001g0344a0001c0001t0001g0346others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.344+9017G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646299 | ||||||
| chr15:92646301
|
T | C | 1 | a0002c0002t0015g0379 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344+9015A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646301 | ||||||
| chr15:92646318
|
T | A | 195 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0150others(192): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.344+8998A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646318 | ||||||
| chr15:92646323
|
T | G | 107 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(104): Show | 107 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.344+8993A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646323 | ||||||
| chr15:92646459
|
A | G | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.344+8857T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646459 | ||||||
| chr15:92646670
|
A | C | 90 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(87): Show | 90 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.344+8646T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646670 | ||||||
| chr15:92646688
|
C | T | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+8628G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646688 | ||||||
| chr15:92646714
|
A | T | 6 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(3): Show | 6 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.344+8602T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646714 | ||||||
| chr15:92646889
|
A | G | 1 | a0001c0001t0018g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.344+8427T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92646889 | ||||||
| chr15:92647062
|
G | A | 13 | a0001c0001t0001g0040a0001c0001t0001g0109a0001c0001t0002g0022others(10): Show | 13 | HG01109.hp1 HG02257.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.344+8254C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647062 | ||||||
| chr15:92647106
|
T | C | 3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0059g0055 | 3 | HG02145.hp2 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.344+8210A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647106 | ||||||
| chr15:92647174
|
C | G | 1 | a0001c0001t0049g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.344+8142G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647174 | ||||||
| chr15:92647227
|
T | C | 2 | a0001c0001t0016g0351a0001c0001t0016g0352 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.344+8089A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647227 | ||||||
| chr15:92647271
|
G | C | 1 | a0001c0001t0001g0278 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.344+8045C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647271 | ||||||
| chr15:92647285
|
G | A | 2 | a0001c0001t0003g0124a0002c0002t0015g0377 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.344+8031C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647285 | ||||||
| chr15:92647299
|
C | T | 73 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(70): Show | 73 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.344+8017G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647299 | ||||||
| chr15:92647445
|
C | A | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | NA18963.hp1 NA18968.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+7871G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647445 | ||||||
| chr15:92647586
|
C | A | 80 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0082others(77): Show | 80 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.344+7730G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647586 | ||||||
| chr15:92647619
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.344+7697C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647619 | ||||||
| chr15:92647691
|
C | T | 376 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(373): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.344+7625G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647691 | ||||||
| chr15:92647833
|
A | C | 236 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0128others(233): Show | 239 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.344+7483T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647833 | ||||||
| chr15:92647834
|
G | C | 1 | a0001c0001t0013g0110 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.344+7482C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92647834 | ||||||
| chr15:92648005
|
A | G | 1 | a0001c0001t0007g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.344+7311T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648005 | ||||||
| chr15:92648099
|
T | C | 2 | a0001c0001t0004g0328a0001c0001t0004g0329 | 2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.344+7217A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648099 | ||||||
| chr15:92648439
|
G | A | 1 | a0001c0001t0007g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.344+6877C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648439 | ||||||
| chr15:92648463
|
C | T | 1 | a0001c0001t0049g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.344+6853G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648463 | ||||||
| chr15:92648489
|
G | C | 4 | a0001c0001t0016g0112a0001c0006t0024g0113a0003c0004t0004g0368others(1): Show | 4 | HG00642.hp1 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+6827C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648489 | ||||||
| chr15:92648520
|
T | C | 47 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0344others(44): Show | 50 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.344+6796A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648520 | ||||||
| chr15:92648529
|
G | A | 194 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0150others(191): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.344+6787C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648529 | ||||||
| chr15:92648531
|
C | A | 8 | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(5): Show | 10 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+6785G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648531 | ||||||
| chr15:92648597
|
C | A | 228 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0150others(225): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.344+6719G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648597 | ||||||
| chr15:92648633
|
T | A | 1 | a0001c0001t0009g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.344+6683A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648633 | ||||||
| chr15:92648786
|
G | A | 195 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0128others(192): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.344+6530C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648786 | ||||||
| chr15:92648809
|
C | T | 327 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0058others(324): Show | 330 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.344+6507G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648809 | ||||||
| chr15:92648810
|
G | A | 1 | a0001c0001t0004g0131 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.344+6506C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648810 | ||||||
| chr15:92648880
|
T | G | 1 | a0001c0001t0009g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.344+6436A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648880 | ||||||
| chr15:92648943
|
G | A | 1 | a0001c0001t0064g0030 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.344+6373C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92648943 | ||||||
| chr15:92649118
|
C | G | 104 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0068others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.344+6198G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649118 | ||||||
| chr15:92649121
|
A | G | 4 | a0001c0001t0010g0333a0001c0001t0011g0037a0001c0001t0011g0038others(1): Show | 4 | HG02055.hp1 HG02886.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+6195T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649121 | ||||||
| chr15:92649255
|
G | A | 1 | a0001c0001t0025g0289 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.344+6061C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649255 | ||||||
| chr15:92649267
|
G | A | 2 | a0002c0002t0010g0378a0002c0002t0015g0379 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.344+6049C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649267 | ||||||
| chr15:92649293
|
G | A | 181 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0001g0151others(178): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.344+6023C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649293 | ||||||
| chr15:92649527
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0009g0029a0001c0001t0031g0028others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+5789A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649527 | ||||||
| chr15:92649586
|
T | C | 3 | a0001c0001t0010g0362a0001c0001t0047g0364a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+5730A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649586 | ||||||
| chr15:92649615
|
T | C | 1 | a0001c0001t0013g0290 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.344+5701A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649615 | ||||||
| chr15:92649646
|
A | C | 14 | a0001c0001t0002g0022a0001c0001t0007g0023a0001c0001t0007g0025others(11): Show | 14 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.344+5670T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649646 | ||||||
| chr15:92649678
|
G | A | 3 | a0001c0001t0010g0362a0001c0001t0047g0364a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+5638C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649678 | ||||||
| chr15:92649733
|
C | T | 22 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0330others(19): Show | 22 | HG01884.hp1 HG02280.hp2 HG02896.hp1 others(19): Show |
intron_variant | MODIFIER | c.344+5583G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649733 | ||||||
| chr15:92649757
|
C | G | 1 | a0001c0001t0049g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.344+5559G>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649757 | ||||||
| chr15:92649782
|
A | G | 324 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(321): Show | 327 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.344+5534T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649782 | ||||||
| chr15:92649836
|
G | C | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.344+5480C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92649836 | ||||||
| chr15:92650037
|
C | A | 1 | a0001c0001t0004g0291 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.344+5279G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650037 | ||||||
| chr15:92650201
|
G | A | 1 | a0001c0001t0024g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.344+5115C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650201 | ||||||
| chr15:92650336
|
G | C | 99 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0068others(96): Show | 99 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.344+4980C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650336 | ||||||
| chr15:92650337
|
G | A | 3 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0004g0293 | 3 | NA18965.hp2 NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.344+4979C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650337 | ||||||
| chr15:92650509
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0003g0139a0001c0001t0007g0126 | 3 | NA18970.hp2 NA18973.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.344+4807G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650509 | ||||||
| chr15:92650544
|
C | A | 1 | a0001c0001t0045g0295 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.344+4772G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650544 | ||||||
| chr15:92650696
|
G | A | 121 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(118): Show | 121 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.344+4620C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650696 | ||||||
| chr15:92650750
|
C | CA | 8 | a0001c0001t0003g0124a0001c0001t0004g0328a0001c0001t0004g0329others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+4565dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650750 | ||||||
| chr15:92650949
|
T | C | 3 | a0001c0001t0010g0362a0001c0001t0047g0364a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+4367A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92650949 | ||||||
| chr15:92651025
|
A | T | 1 | a0001c0001t0010g0036 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.344+4291T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651025 | ||||||
| chr15:92651049
|
T | C | 1 | a0001c0001t0002g0314 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.344+4267A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651049 | ||||||
| chr15:92651065
|
G | A | 1 | a0001c0001t0059g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344+4251C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651065 | ||||||
| chr15:92651171
|
A | C | 2 | a0001c0001t0004g0131a0001c0001t0011g0132 | 2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.344+4145T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651171 | ||||||
| chr15:92651186
|
C | A | 4 | a0001c0001t0003g0318a0001c0001t0004g0316a0001c0001t0022g0315others(1): Show | 4 | HG00639.hp2 HG00642.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+4130G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651186 | ||||||
| chr15:92651439
|
C | A | 1 | a0001c0001t0003g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.344+3877G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651439 | ||||||
| chr15:92651441
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.344+3875A>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651441 | ||||||
| chr15:92651450
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.344+3866T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651450 | ||||||
| chr15:92651458
|
T | C | 324 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(321): Show | 327 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.344+3858A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651458 | ||||||
| chr15:92651524
|
T | C | 8 | a0001c0001t0003g0124a0001c0001t0004g0328a0001c0001t0004g0329others(5): Show | 8 | HG01109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+3792A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651524 | ||||||
| chr15:92651565
|
G | C | 5 | a0001c0001t0009g0117a0001c0001t0015g0118a0001c0001t0015g0119others(2): Show | 5 | HG01243.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+3751C>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651565 | ||||||
| chr15:92651692
|
A | C | 1 | a0001c0001t0002g0125 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.344+3624T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651692 | ||||||
| chr15:92651713
|
A | C | 1 | a0001c0001t0007g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.344+3603T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651713 | ||||||
| chr15:92651749
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.344+3567A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651749 | ||||||
| chr15:92651777
|
G | A | 3 | a0002c0002t0010g0378a0002c0002t0015g0377a0002c0002t0015g0379 | 3 | HG01243.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.344+3539C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651777 | ||||||
| chr15:92651865
|
GAC | G | 320 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(317): Show | 323 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.344+3449_344+3450d others(4): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651865 | ||||||
| chr15:92651958
|
A | C | 24 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(21): Show | 24 | HG01884.hp1 HG02280.hp2 HG02896.hp1 others(21): Show |
intron_variant | MODIFIER | c.344+3358T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651958 | ||||||
| chr15:92651972
|
C | T | 10 | a0001c0001t0003g0124a0001c0001t0004g0328a0001c0001t0004g0329others(7): Show | 10 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.344+3344G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92651972 | ||||||
| chr15:92652232
|
A | T | 322 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(319): Show | 325 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.344+3084T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652232 | ||||||
| chr15:92652572
|
A | G | 58 | a0001c0001t0001g0027a0001c0001t0001g0344a0001c0001t0001g0346others(55): Show | 61 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.344+2744T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652572 | ||||||
| chr15:92652575
|
G | A | 1 | a0001c0001t0003g0320 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.344+2741C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652575 | ||||||
| chr15:92652605
|
G | A | 317 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(314): Show | 320 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.344+2711C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652605 | ||||||
| chr15:92652655
|
A | T | 1 | a0001c0001t0048g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.344+2661T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652655 | ||||||
| chr15:92652713
|
T | C | 377 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(374): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.344+2603A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652713 | ||||||
| chr15:92652855
|
T | G | 237 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0128others(234): Show | 240 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.344+2461A>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92652855 | ||||||
| chr15:92653048
|
A | C | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.344+2268T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653048 | ||||||
| chr15:92653081
|
C | T | 1 | a0001c0001t0066g0387 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.344+2235G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653081 | ||||||
| chr15:92653115
|
G | A | 8 | a0001c0001t0002g0354a0001c0001t0002g0355a0001c0001t0005g0356others(5): Show | 8 | HG02071.hp2 HG02135.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+2201C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653115 | ||||||
| chr15:92653291
|
C | T | 1 | a0001c0001t0020g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.344+2025G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653291 | ||||||
| chr15:92653295
|
C | A | 1 | a0001c0001t0011g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.344+2021G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653295 | ||||||
| chr15:92653374
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0007g0023a0001c0001t0007g0025others(6): Show | 9 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.344+1942G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653374 | ||||||
| chr15:92653587
|
A | C | 327 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(324): Show | 330 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.344+1729T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653587 | ||||||
| chr15:92653832
|
G | A | 23 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0330others(20): Show | 23 | HG01884.hp1 HG02280.hp2 HG02896.hp1 others(20): Show |
intron_variant | MODIFIER | c.344+1484C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92653832 | ||||||
| chr15:92654069
|
A | G | 374 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(371): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.344+1247T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654069 | ||||||
| chr15:92654194
|
T | C | 326 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0049others(323): Show | 329 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.344+1122A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654194 | ||||||
| chr15:92654352
|
C | A | 1 | a0001c0001t0041g0321 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.344+964G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654352 | ||||||
| chr15:92654378
|
C | T | 1 | a0001c0001t0005g0135 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.344+938G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654378 | ||||||
| chr15:92654400
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.344+916A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654400 | ||||||
| chr15:92654446
|
A | G | 1 | a0001c0001t0010g0036 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.344+870T>C | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654446 | ||||||
| chr15:92654485
|
G | T | 1 | a0001c0001t0004g0340 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.344+831C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654485 | ||||||
| chr15:92654499
|
A | C | 1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.344+817T>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654499 | ||||||
| chr15:92654544
|
G | A | 1 | a0001c0001t0010g0339 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.344+772C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654544 | ||||||
| chr15:92654546
|
G | T | 1 | a0001c0001t0061g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.344+770C>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654546 | ||||||
| chr15:92654567
|
C | T | 7 | a0001c0001t0002g0005a0001c0001t0003g0334a0001c0001t0009g0338others(4): Show | 8 | HG00140.hp2 HG01167.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+749G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654567 | ||||||
| chr15:92654653
|
A | T | 1 | a0001c0001t0024g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.344+663T>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654653 | ||||||
| chr15:92654719
|
C | T | 3 | a0003c0004t0004g0368a0003c0004t0016g0366a0003c0004t0037g0367 | 3 | HG00642.hp1 HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.344+597G>A | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654719 | ||||||
| chr15:92654731
|
G | A | 1 | a0001c0001t0060g0322 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.344+585C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654731 | ||||||
| chr15:92654787
|
C | CA | 202 | a0001c0001t0001g0137a0001c0001t0001g0150a0001c0001t0001g0151others(199): Show | 205 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.344+528dupT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654787 | ||||||
| chr15:92654787
|
CA | C | 43 | a0001c0001t0001g0344a0001c0001t0001g0346a0001c0001t0002g0005others(40): Show | 46 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.344+528delT | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654787 | ||||||
| chr15:92654799
|
A | AAAG | 26 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0330others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.344+514_344+516dup others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654799 | ||||||
| chr15:92654799
|
AAAG | A | 12 | a0001c0001t0003g0324a0001c0001t0003g0326a0001c0001t0004g0328others(9): Show | 12 | HG01109.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.344+514_344+516del others(3): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92654799 | ||||||
| chr15:92655066
|
G | A | 317 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0058others(314): Show | 320 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.344+250C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655066 | ||||||
| chr15:92655067
|
G | A | 3 | a0001c0001t0001g0330a0001c0001t0006g0331a0001c0001t0006g0332 | 3 | NA18944.hp2 NA18977.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.344+249C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655067 | ||||||
| chr15:92655089
|
T | C | 1 | a0001c0001t0010g0333 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344+227A>G | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655089 | ||||||
| chr15:92655283
|
C | A | 29 | a0001c0001t0001g0344a0001c0001t0001g0346a0001c0001t0002g0005others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.344+33G>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655283 | ||||||
| chr15:92655304
|
G | A | 3 | a0001c0001t0010g0362a0001c0001t0047g0364a0001c0001t0050g0363 | 3 | HG02622.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.344+12C>T | FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | 92655304 |