| geneid | 8823 |
|---|---|
| ensemblid | ENSG00000196468.8 |
| hgncid | 3672 |
| symbol | FGF16 |
| name | fibroblast growth factor 16 |
| refseq_nuc | NM_003868.3 |
| refseq_prot | NP_003859.1 |
| ensembl_nuc | ENST00000439435.3 |
| ensembl_prot | ENSP00000399324.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 77447389 |
| end | 77457278 |
| strand | + |
| ver | v1.2 |
| region | chrX:77447389-77457278 |
| region5000 | chrX:77442389-77462278 |
| regionname0 | FGF16_chrX_77447389_77457278 |
| regionname5000 | FGF16_chrX_77442389_77462278 |
| 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 | 1/1 | 207 | 307 | 74 | 48 | 140 | 13 | 30 | 116 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0002 | 0/0 | 207 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0003 | 0/0 | 55 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| 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 | 624 | 304 | 74 | 46 | 140 | 13 | 30 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| c0002 | 0/0 | 624 | 2 | 0 | 2 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| c0003 | 0/0 | 623 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| c0004 | 1/0 | 624 | 1 | 0 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| c0005 | 0/0 | 624 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| 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 | 1/1 | 1043 | 259 | 53 | 31 | 138 | 9 | 26 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| t0002 | 0/0 | 1043 | 42 | 18 | 16 | 0 | 4 | 4 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| t0003 | 0/0 | 1043 | 3 | 3 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| t0004 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| t0005 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| t0006 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| t0007 | 0/0 | 1043 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| t0008 | 0/0 | 1043 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| 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 | 0/1 | 56 | 3 | 17 | 25 | 4 | 6 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0002 | 0/0 | 41 | 0 | 2 | 34 | 0 | 5 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0003 | 0/0 | 22 | 0 | 4 | 12 | 1 | 5 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0004 | 0/0 | 14 | 6 | 4 | 0 | 2 | 2 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0005 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0006 | 0/0 | 12 | 4 | 7 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0007 | 1/0 | 10 | 0 | 2 | 7 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0009 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0010 | 0/0 | 5 | 3 | 0 | 2 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0011 | 0/0 | 5 | 2 | 1 | 0 | 0 | 2 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0013 | 0/0 | 5 | 1 | 0 | 2 | 0 | 2 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0018 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| 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 | 624 | 304 | 74 | 46 | 140 | 13 | 30 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0002 | 0/0 | 624 | 2 | 0 | 2 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0004 | 1/0 | 624 | 1 | 0 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0002c0005 | 0/0 | 624 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0003c0003 | 0/0 | 623 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1666 | 257 | 53 | 31 | 137 | 9 | 26 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0001t0002 | 0/0 | 1666 | 40 | 18 | 14 | 0 | 4 | 4 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0001t0003 | 0/0 | 1666 | 3 | 3 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0001t0005 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0001t0006 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0001t0007 | 0/0 | 1666 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0001t0008 | 0/0 | 1666 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0002t0002 | 0/0 | 1666 | 2 | 0 | 2 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0001c0004t0001 | 1/0 | 1666 | 1 | 0 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0002c0005t0001 | 0/0 | 1666 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| a0003c0003t0004 | 0/0 | 1664 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | copy fasta | chrX | 77442389 | 77462278 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 55 | 3 | 16 | 25 | 4 | 6 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0002 | 0/0 | 41 | 0 | 2 | 34 | 0 | 5 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0003 | 0/0 | 22 | 0 | 4 | 12 | 1 | 5 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0005 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0009 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0010 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0011 | 0/0 | 5 | 2 | 1 | 0 | 0 | 2 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0013 | 0/0 | 5 | 1 | 0 | 2 | 0 | 2 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0004 | 0/0 | 14 | 6 | 4 | 0 | 2 | 2 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0006 | 0/0 | 12 | 4 | 7 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0018 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0001t0008g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0001c0004t0001g0007 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0002c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| a0003c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0091 | EUR | IBS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | IBS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0055 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | YRI | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18949 | hp1 | a0002 | c0005 | t0001 | g0010 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | LWK | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19059 | hp1 | a0003 | c0003 | t0004 | g0041 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19067 | hp1 | a0001 | c0001 | t0006 | g0076 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0007 | REF | REF | FGF16_chrX_77442389_77462278 | FGF16 | chrX | 77442389 | 77462278 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:77447834
|
GC | G | 1 | a0003 | 1 | NA19059.hp1 | frameshift_variant | HIGH | c.163delC | p.His55fs | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/3 | 449/1666 | 163/624 | 55/207 | INFO_REALIGN_3_PRIME | chrX | 77447834 | |
| chrX:77454201
|
C | T | 1 | a0002 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.319C>T | p.Arg107Trp | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/3 | 605/1666 | 319/624 | 107/207 | chrX | 77454201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:77447818
|
C | T | 1 | a0001c0002 | 2 | HG01070.hp1 HG01071.hp2 |
synonymous_variant | LOW | c.144C>T | p.Gly48Gly | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/3 | 430/1666 | 144/624 | 48/207 | chrX | 77447818 | ||
| chrX:77447842
|
A | G | 4 | a0001c0001a0001c0002a0002c0005others(1): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
synonymous_variant | LOW | c.168A>G | p.Leu56Leu | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/3 | 454/1666 | 168/624 | 56/207 | chrX | 77447842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:77447427
|
C | A | 2 | a0001c0001t0002a0001c0002t0002 | 42 | HG00323.hp2 HG00733.hp2 HG00735.hp2 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-248C>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/3 | 248 | chrX | 77447427 | |||||
| chrX:77447430
|
AG | A | 1 | a0003c0003t0004 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-241delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/3 | 241 | INFO_REALIGN_3_PRIME | chrX | 77447430 | ||||
| chrX:77456731
|
C | G | 1 | a0001c0001t0008 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*209C>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 3/3 | 209 | chrX | 77456731 | |||||
| chrX:77456733
|
AG | A | 1 | a0001c0001t0005 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*214delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 3/3 | 214 | INFO_REALIGN_3_PRIME | chrX | 77456733 | ||||
| chrX:77456745
|
A | AG | 1 | a0001c0001t0006 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223_*224insG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 3/3 | 224 | chrX | 77456745 | |||||
| chrX:77456823
|
G | T | 1 | a0001c0001t0007 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301G>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 3/3 | 301 | chrX | 77456823 | |||||
| chrX:77457207
|
G | T | 1 | a0001c0001t0003 | 3 | HG02615.hp1 HG02630.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*685G>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 3/3 | 685 | chrX | 77457207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:77447971
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.274+23G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77447971 | ||||||
| chrX:77448031
|
C | T | 12 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0018others(9): Show | 41 | HG00323.hp2 HG00733.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.274+83C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77448031 | ||||||
| chrX:77448055
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.274+107G>C | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77448055 | ||||||
| chrX:77448073
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0036 | 7 | HG01243.hp1 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+125G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77448073 | ||||||
| chrX:77448215
|
G | GT | 1 | a0001c0001t0001g0089 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.274+269dupT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77448215 | |||||
| chrX:77448229
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.274+281A>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77448229 | ||||||
| chrX:77448282
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.274+334G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77448282 | ||||||
| chrX:77449077
|
TC | T | 1 | a0001c0001t0001g0089 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.274+1131delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77449077 | |||||
| chrX:77449098
|
C | A | 1 | a0001c0001t0001g0020 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.274+1150C>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77449098 | ||||||
| chrX:77449466
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.274+1518C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77449466 | ||||||
| chrX:77449508
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0038 | 4 | NA18954.hp2 NA18962.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+1560T>C | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77449508 | ||||||
| chrX:77449523
|
C | CA | 1 | a0001c0001t0001g0039 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.274+1584dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77449523 | |||||
| chrX:77449561
|
T | TG | 1 | a0001c0001t0001g0040 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.274+1618dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77449561 | |||||
| chrX:77449614
|
AT | A | 1 | a0003c0003t0004g0041 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.274+1671delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77449614 | |||||
| chrX:77449718
|
C | CA | 1 | a0001c0001t0001g0089 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.274+1771dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77449718 | |||||
| chrX:77449757
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.274+1809G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77449757 | ||||||
| chrX:77449776
|
A | ACTTAACA others(27): Show |
1 | a0001c0001t0001g0087 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274+1829_274+1830i others(36): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77449776 | |||||
| chrX:77449782
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | NA18955.hp1 NA18990.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.274+1834G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77449782 | ||||||
| chrX:77449857
|
GA | G | 1 | a0001c0001t0001g0045 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.274+1914delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77449857 | |||||
| chrX:77449989
|
C | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0095a0001c0001t0002g0096 | 4 | HG01891.hp1 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.274+2041C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77449989 | ||||||
| chrX:77450238
|
AG | A | 1 | a0001c0001t0001g0046 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.274+2291delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77450238 | ||||||
| chrX:77450295
|
AC | A | 1 | a0001c0001t0001g0089 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.274+2350delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77450295 | |||||
| chrX:77450868
|
AG | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.274+2924delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77450868 | |||||
| chrX:77450934
|
AC | A | 1 | a0003c0003t0004g0041 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.274+2990delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77450934 | |||||
| chrX:77451202
|
A | AG | 1 | a0001c0001t0001g0089 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.275-2952dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451202 | |||||
| chrX:77451214
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.275-2943G>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77451214 | ||||||
| chrX:77451378
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2777delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451378 | |||||
| chrX:77451385
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.275-2772C>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77451385 | ||||||
| chrX:77451406
|
C | CA | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2748dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451406 | |||||
| chrX:77451506
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.275-2651C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77451506 | ||||||
| chrX:77451521
|
GCT | G | 2 | a0001c0001t0003g0031a0001c0001t0003g0083 | 3 | HG02615.hp1 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.275-2633_275-2632d others(4): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451521 | |||||
| chrX:77451567
|
AC | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2588delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451567 | |||||
| chrX:77451600
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2556dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451600 | |||||
| chrX:77451671
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2479delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451671 | |||||
| chrX:77451770
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2386dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451770 | |||||
| chrX:77451842
|
TG | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2312delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451842 | |||||
| chrX:77451972
|
TA | T | 1 | a0001c0001t0001g0089 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.275-2182delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77451972 | |||||
| chrX:77451993
|
C | G | 2 | a0001c0002t0002g0093a0001c0002t0002g0094 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.275-2164C>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77451993 | ||||||
| chrX:77452107
|
T | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0048 | 3 | HG02280.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.275-2050T>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77452107 | ||||||
| chrX:77452115
|
G | GT | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2042_275-2041i others(3): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77452115 | ||||||
| chrX:77452147
|
TA | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-2008delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452147 | |||||
| chrX:77452158
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1998dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452158 | |||||
| chrX:77452206
|
A | AT | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1950dupT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452206 | |||||
| chrX:77452259
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(32): Show | 121 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.275-1898G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77452259 | ||||||
| chrX:77452303
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(25): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.275-1854C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77452303 | ||||||
| chrX:77452326
|
G | A | 1 | a0001c0001t0001g0023 | 2 | HG02135.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.275-1831G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77452326 | ||||||
| chrX:77452351
|
GT | G | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1804delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452351 | |||||
| chrX:77452391
|
TG | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1763delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452391 | |||||
| chrX:77452636
|
GC | G | 1 | a0003c0003t0004g0041 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.275-1518delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452636 | |||||
| chrX:77452653
|
AC | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1503delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77452653 | ||||||
| chrX:77452703
|
AT | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1452delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452703 | |||||
| chrX:77452730
|
GA | G | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1423delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452730 | |||||
| chrX:77452745
|
TC | T | 1 | a0001c0001t0001g0062 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.275-1409delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452745 | |||||
| chrX:77452835
|
TG | T | 1 | a0003c0003t0004g0041 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.275-1319delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452835 | |||||
| chrX:77452904
|
C | CT | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1251dupT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77452904 | |||||
| chrX:77452951
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.275-1206C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77452951 | ||||||
| chrX:77453001
|
T | TG | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1152dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453001 | |||||
| chrX:77453076
|
T | TC | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1080dupC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453076 | |||||
| chrX:77453092
|
C | CA | 2 | a0001c0001t0001g0062a0001c0001t0001g0089 | 2 | NA19059.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.275-1058dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453092 | |||||
| chrX:77453097
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.275-1060A>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453097 | ||||||
| chrX:77453144
|
AT | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-1010delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453144 | |||||
| chrX:77453203
|
C | G | 49 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(46): Show | 151 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.275-954C>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453203 | ||||||
| chrX:77453204
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-951dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453204 | |||||
| chrX:77453220
|
G | A | 1 | a0001c0001t0001g0022 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.275-937G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453220 | ||||||
| chrX:77453237
|
AT | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-918delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453237 | |||||
| chrX:77453272
|
TG | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-882delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453272 | |||||
| chrX:77453318
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.275-839G>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453318 | ||||||
| chrX:77453319
|
TC | T | 1 | a0001c0001t0001g0081 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.275-836delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453319 | |||||
| chrX:77453334
|
AG | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-821delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453334 | |||||
| chrX:77453360
|
AT | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-793delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453360 | |||||
| chrX:77453496
|
TA | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-657delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453496 | |||||
| chrX:77453582
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0085 | 3 | HG02040.hp1 NA18950.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.275-575C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453582 | ||||||
| chrX:77453606
|
AG | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-546delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453606 | |||||
| chrX:77453637
|
C | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(33): Show | 122 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.275-520C>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453637 | ||||||
| chrX:77453668
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.275-489G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453668 | ||||||
| chrX:77453691
|
TG | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-461delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453691 | |||||
| chrX:77453748
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0063 | 4 | HG02258.hp1 HG02922.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-409G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453748 | ||||||
| chrX:77453822
|
TTC | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-333_275-332del others(2): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453822 | |||||
| chrX:77453825
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-332T>C | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453825 | ||||||
| chrX:77453846
|
C | CA | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-311_275-310ins others(1): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77453846 | ||||||
| chrX:77453926
|
G | GC | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275-230dupC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chrX | 77453926 | |||||
| chrX:77454053
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0074 | 3 | HG00099.hp1 HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.275-104G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 1/2 | chrX | 77454053 | ||||||
| chrX:77454272
|
G | GT | 39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(36): Show | 133 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.378+42dupT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454272 | |||||
| chrX:77454272
|
G | GTT | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(11): Show | 42 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.378+41_378+42dupTT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454272 | |||||
| chrX:77454272
|
G | GTTT | 5 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0080others(2): Show | 7 | HG00733.hp2 HG00735.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+40_378+42dupTT others(1): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454272 | |||||
| chrX:77454272
|
G | GTTTTT | 1 | a0001c0001t0001g0022 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.378+38_378+42dupTT others(3): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454272 | |||||
| chrX:77454272
|
GT | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0002g0095others(1): Show | 5 | HG01256.hp1 HG01891.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+42delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454272 | |||||
| chrX:77454272
|
GTTTTT | G | 1 | a0001c0001t0001g0063 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.378+38_378+42delTT others(3): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454272 | |||||
| chrX:77454278
|
T | TG | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.378+18_378+19insG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454278 | ||||||
| chrX:77454279
|
T | G | 1 | a0001c0001t0001g0012 | 5 | HG02559.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+19T>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454279 | ||||||
| chrX:77454350
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.378+90A>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454350 | ||||||
| chrX:77454465
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.378+205A>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454465 | ||||||
| chrX:77454484
|
A | AC | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+225dupC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454484 | |||||
| chrX:77454512
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.378+252G>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454512 | ||||||
| chrX:77454513
|
G | T | 1 | a0001c0001t0008g0055 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.378+253G>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454513 | ||||||
| chrX:77454527
|
C | CA | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+268dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454527 | |||||
| chrX:77454536
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+276T>A | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454536 | ||||||
| chrX:77454537
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+277C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454537 | ||||||
| chrX:77454624
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.378+364C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454624 | ||||||
| chrX:77454654
|
C | CA | 1 | a0003c0003t0004g0041 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.378+404dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454654 | |||||
| chrX:77454665
|
GA | G | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+408delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454665 | |||||
| chrX:77454690
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+436delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454690 | |||||
| chrX:77454740
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.378+480A>G | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454740 | ||||||
| chrX:77454740
|
AG | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+483delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454740 | |||||
| chrX:77454781
|
CA | C | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+525delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454781 | |||||
| chrX:77454790
|
C | CT | 20 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(17): Show | 36 | HG00621.hp1 HG01243.hp1 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.378+549dupT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454790 | |||||
| chrX:77454790
|
C | CTTTT | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+546_378+549dup others(4): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454790 | |||||
| chrX:77454790
|
CT | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0051a0001c0001t0001g0052 | 5 | HG02258.hp1 HG02922.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+549delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454790 | |||||
| chrX:77454817
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.378+557G>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77454817 | ||||||
| chrX:77454824
|
T | TC | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+565dupC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454824 | |||||
| chrX:77454840
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+582dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454840 | |||||
| chrX:77454852
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+593dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454852 | |||||
| chrX:77454892
|
G | GT | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+634dupT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77454892 | |||||
| chrX:77455018
|
C | CT | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.378+758_378+759ins others(1): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77455018 | ||||||
| chrX:77455038
|
A | AG | 1 | a0001c0001t0001g0051 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.378+778_378+779ins others(1): Show |
FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77455038 | ||||||
| chrX:77455090
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.378+830C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77455090 | ||||||
| chrX:77455284
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.379-993C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77455284 | ||||||
| chrX:77455284
|
CA | C | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.379-988delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455284 | |||||
| chrX:77455370
|
G | GA | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.379-906dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455370 | |||||
| chrX:77455396
|
CA | C | 1 | a0001c0001t0001g0062 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.379-878delA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455396 | |||||
| chrX:77455423
|
TG | T | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.379-852delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455423 | |||||
| chrX:77455461
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.379-816C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77455461 | ||||||
| chrX:77455589
|
TG | T | 1 | a0001c0001t0001g0024 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.379-686delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455589 | |||||
| chrX:77455600
|
AC | A | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.379-673delC | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455600 | |||||
| chrX:77455612
|
C | CA | 1 | a0001c0001t0006g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.379-664dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455612 | |||||
| chrX:77455668
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(84): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.379-609T>C | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77455668 | ||||||
| chrX:77455767
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.379-509dupG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455767 | |||||
| chrX:77455783
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.379-490delT | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455783 | |||||
| chrX:77455972
|
TG | T | 1 | a0001c0001t0001g0062 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.379-302delG | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77455972 | |||||
| chrX:77456068
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0048 | 3 | HG02280.hp2 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.379-209C>T | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | chrX | 77456068 | ||||||
| chrX:77456274
|
C | CA | 1 | a0001c0001t0005g0077 | 1 | NA18967.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.379-2dupA | FGF16 | ENSG00000196468.8 | transcript | ENST00000439435.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chrX | 77456274 |