Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2246 |
|---|---|
| ensemblid | ENSG00000113578.18 |
| hgncid | 3665 |
| symbol | FGF1 |
| name | fibroblast growth factor 1 |
| refseq_nuc | NM_000800.5 |
| refseq_prot | NP_000791.1 |
| ensembl_nuc | ENST00000337706.7 |
| ensembl_prot | ENSP00000338548.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 142592178 |
| end | 142686090 |
| strand | - |
| ver | v1.2 |
| region | chr5:142592178-142686090 |
| region5000 | chr5:142587178-142691090 |
| regionname0 | FGF1_chr5_142592178_142686090 |
| regionname5000 | FGF1_chr5_142587178_142691090 |
| 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 | 155 | 340 | 92 | 64 | 140 | 12 | 30 | 106 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| 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 | 1/1 | 468 | 340 | 92 | 64 | 140 | 12 | 30 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| 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 | 1/0 | 3281 | 73 | 8 | 11 | 30 | 3 | 20 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0002 | 0/0 | 3282 | 72 | 7 | 14 | 40 | 4 | 7 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0003 | 0/1 | 3281 | 36 | 5 | 16 | 12 | 2 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0004 | 0/0 | 3282 | 24 | 16 | 4 | 4 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0005 | 0/0 | 3282 | 16 | 3 | 2 | 9 | 1 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0006 | 0/0 | 3282 | 12 | 9 | 1 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0007 | 0/0 | 3282 | 11 | 0 | 0 | 11 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0008 | 0/0 | 3282 | 7 | 0 | 0 | 5 | 1 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0009 | 0/0 | 3282 | 7 | 3 | 0 | 4 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0010 | 0/0 | 3282 | 6 | 6 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0011 | 0/0 | 3282 | 6 | 4 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0012 | 0/0 | 3282 | 6 | 4 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0013 | 0/0 | 3282 | 5 | 5 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0014 | 0/0 | 3282 | 5 | 4 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0015 | 0/0 | 3282 | 4 | 4 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0016 | 0/0 | 3282 | 3 | 1 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0017 | 0/0 | 3282 | 3 | 0 | 0 | 3 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0018 | 0/0 | 3282 | 3 | 0 | 0 | 3 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0019 | 0/0 | 3282 | 3 | 0 | 2 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0020 | 0/0 | 3282 | 2 | 0 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0021 | 0/0 | 3282 | 2 | 1 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0022 | 0/0 | 3282 | 2 | 2 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0023 | 0/0 | 3281 | 2 | 0 | 0 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0024 | 0/0 | 3282 | 2 | 0 | 0 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0025 | 0/0 | 3282 | 2 | 1 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0026 | 0/0 | 3282 | 2 | 0 | 0 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0027 | 0/0 | 3282 | 2 | 1 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0028 | 0/0 | 3281 | 2 | 0 | 0 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0029 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0030 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0031 | 0/0 | 3281 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0032 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0033 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0034 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0035 | 0/0 | 3281 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0036 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0037 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0038 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0039 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0040 | 0/0 | 3281 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0041 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0042 | 0/0 | 3281 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0043 | 0/0 | 3281 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0044 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0045 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0046 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0047 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| t0048 | 0/0 | 3281 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| 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 | 1/1 | 468 | 340 | 92 | 64 | 140 | 12 | 30 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3748 | 73 | 8 | 11 | 30 | 3 | 20 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0002 | 0/0 | 3749 | 72 | 7 | 14 | 40 | 4 | 7 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0003 | 0/1 | 3748 | 36 | 5 | 16 | 12 | 2 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0004 | 0/0 | 3749 | 24 | 16 | 4 | 4 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0005 | 0/0 | 3749 | 16 | 3 | 2 | 9 | 1 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0006 | 0/0 | 3749 | 12 | 9 | 1 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0007 | 0/0 | 3749 | 11 | 0 | 0 | 11 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0008 | 0/0 | 3749 | 7 | 0 | 0 | 5 | 1 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0009 | 0/0 | 3749 | 7 | 3 | 0 | 4 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0010 | 0/0 | 3749 | 6 | 6 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0011 | 0/0 | 3749 | 6 | 4 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0012 | 0/0 | 3749 | 6 | 4 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0013 | 0/0 | 3749 | 5 | 5 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0014 | 0/0 | 3749 | 5 | 4 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0015 | 0/0 | 3749 | 4 | 4 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0016 | 0/0 | 3749 | 3 | 1 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0017 | 0/0 | 3749 | 3 | 0 | 0 | 3 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0018 | 0/0 | 3749 | 3 | 0 | 0 | 3 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0019 | 0/0 | 3749 | 3 | 0 | 2 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0020 | 0/0 | 3749 | 2 | 0 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0021 | 0/0 | 3749 | 2 | 1 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0022 | 0/0 | 3749 | 2 | 2 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0023 | 0/0 | 3748 | 2 | 0 | 0 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0024 | 0/0 | 3749 | 2 | 0 | 0 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0025 | 0/0 | 3749 | 2 | 1 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0026 | 0/0 | 3749 | 2 | 0 | 0 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0027 | 0/0 | 3749 | 2 | 1 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0028 | 0/0 | 3748 | 2 | 0 | 0 | 2 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0029 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0030 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0031 | 0/0 | 3748 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0032 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0033 | 0/0 | 3749 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0034 | 0/0 | 3749 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0035 | 0/0 | 3748 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0036 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0037 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0038 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0039 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0040 | 0/0 | 3748 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0041 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0042 | 0/0 | 3748 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0043 | 0/0 | 3748 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0044 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0045 | 0/0 | 3749 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0046 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0047 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| a0001c0001t0048 | 0/0 | 3748 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | copy fasta | chr5 | 142587178 | 142691090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0007g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0008g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0009g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0009g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0009g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0011g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0012g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0012g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0013g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0013g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0014g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0014g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0014g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0015g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0015g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0015g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0016g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0016g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0017g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0017g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0017g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0018g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0018g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0018g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0019g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0019g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0020g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0020g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0021g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0021g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0022g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0022g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0023g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0023g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0024g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0024g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0025g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0025g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0026g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0026g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0027g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0027g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0028g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0028g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0029g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0030g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0031g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0032g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0033g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0034g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0035g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0036g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0037g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0038g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0039g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0040g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0041g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0042g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0043g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0044g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0045g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0046g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0047g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| a0001c0001t0048g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | GBR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | GBR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0213 | EUR | GBR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | GBR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0225 | EUR | FIN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00408 | hp1 | a0001 | c0001 | t0019 | g0297 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0141 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00558 | hp2 | a0001 | c0001 | t0008 | g0250 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0299 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00639 | hp2 | a0001 | c0001 | t0011 | g0081 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00642 | hp2 | a0001 | c0001 | t0034 | g0069 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0223 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0082 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01099 | hp1 | a0001 | c0001 | t0020 | g0286 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0334 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0327 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01168 | hp1 | a0001 | c0001 | t0020 | g0288 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0292 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0287 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01175 | hp1 | a0001 | c0001 | t0016 | g0074 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01192 | hp2 | a0001 | c0001 | t0016 | g0073 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01243 | hp2 | a0001 | c0001 | t0025 | g0270 | AMR | PUR | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0220 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01256 | hp1 | a0001 | c0001 | t0043 | g0140 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01256 | hp2 | a0001 | c0001 | t0019 | g0001 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01258 | hp2 | a0001 | c0001 | t0019 | g0001 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01496 | hp1 | a0001 | c0001 | t0033 | g0048 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0335 | EUR | IBS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0040 | EUR | IBS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01517 | hp1 | a0001 | c0001 | t0021 | g0041 | EUR | IBS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0336 | EUR | IBS | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0308 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01884 | hp2 | a0001 | c0001 | t0015 | g0279 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0284 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01934 | hp1 | a0001 | c0001 | t0014 | g0164 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02015 | hp2 | a0001 | c0001 | t0024 | g0117 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0153 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02056 | hp2 | a0001 | c0001 | t0026 | g0114 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02074 | hp2 | a0001 | c0001 | t0017 | g0087 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02132 | hp1 | a0001 | c0001 | t0017 | g0259 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02135 | hp1 | a0001 | c0001 | t0017 | g0168 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02135 | hp2 | a0001 | c0001 | t0008 | g0091 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02145 | hp1 | a0001 | c0001 | t0037 | g0008 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0090 | EAS | CDX | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02165 | hp2 | a0001 | c0001 | t0024 | g0244 | EAS | CDX | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0272 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0329 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02273 | hp1 | a0001 | c0001 | t0048 | g0338 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02280 | hp1 | a0001 | c0001 | t0041 | g0070 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02523 | hp1 | a0001 | c0001 | t0038 | g0255 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0067 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02572 | hp2 | a0001 | c0001 | t0013 | g0061 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0129 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0173 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0311 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0263 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0307 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0315 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0184 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0137 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02723 | hp2 | a0001 | c0001 | t0013 | g0174 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0282 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02818 | hp1 | a0001 | c0001 | t0029 | g0032 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0136 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02886 | hp1 | a0001 | c0001 | t0022 | g0208 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0320 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0054 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02922 | hp2 | a0001 | c0001 | t0039 | g0271 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0171 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0065 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0316 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0314 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0177 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03130 | hp1 | a0001 | c0001 | t0025 | g0328 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0176 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0175 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03209 | hp1 | a0001 | c0001 | t0027 | g0162 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03209 | hp2 | a0001 | c0001 | t0015 | g0130 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0303 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0324 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0071 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0261 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0262 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0278 | AFR | ESN | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03540 | hp1 | a0001 | c0001 | t0042 | g0056 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | GWD | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0323 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | MSL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0245 | SAS | PJL | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG04199 | hp2 | a0001 | c0001 | t0008 | g0150 | SAS | STU | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG04204 | hp1 | a0001 | c0001 | t0040 | g0283 | SAS | STU | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | STU | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | YRI | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18747 | hp1 | a0001 | c0001 | t0007 | g0202 | EAS | CHB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18747 | hp2 | a0001 | c0001 | t0027 | g0238 | EAS | CHB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0007 | AFR | YRI | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18906 | hp2 | a0001 | c0001 | t0045 | g0331 | AFR | YRI | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18939 | hp2 | a0001 | c0001 | t0047 | g0093 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18941 | hp1 | a0001 | c0001 | t0023 | g0333 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18956 | hp1 | a0001 | c0001 | t0009 | g0035 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18960 | hp1 | a0001 | c0001 | t0009 | g0142 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18962 | hp2 | a0001 | c0001 | t0044 | g0210 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18965 | hp1 | a0001 | c0001 | t0032 | g0295 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18966 | hp1 | a0001 | c0001 | t0008 | g0305 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0120 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18968 | hp1 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18972 | hp1 | a0001 | c0001 | t0023 | g0024 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18974 | hp2 | a0001 | c0001 | t0007 | g0332 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0100 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18979 | hp2 | a0001 | c0001 | t0018 | g0105 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18991 | hp1 | a0001 | c0001 | t0046 | g0095 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18994 | hp1 | a0001 | c0001 | t0009 | g0194 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18995 | hp1 | a0001 | c0001 | t0028 | g0052 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0099 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19007 | hp2 | a0001 | c0001 | t0018 | g0121 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19011 | hp1 | a0001 | c0001 | t0018 | g0268 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19011 | hp2 | a0001 | c0001 | t0026 | g0304 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19030 | hp1 | a0001 | c0001 | t0036 | g0163 | AFR | LWK | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0161 | AFR | LWK | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0132 | AFR | LWK | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | LWK | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19062 | hp1 | a0001 | c0001 | t0028 | g0011 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19065 | hp1 | a0001 | c0001 | t0031 | g0023 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19077 | hp1 | a0001 | c0001 | t0035 | g0197 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0267 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19085 | hp2 | a0001 | c0001 | t0009 | g0189 | EAS | JPT | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19240 | hp1 | a0001 | c0001 | t0030 | g0064 | AFR | YRI | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0057 | AFR | YRI | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0053 | EUR | TSI | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0337 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02486 | hp2 | a0001 | c0001 | t0022 | g0138 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0281 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0276 | AFR | ACB | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | USA | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | USA | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA20300 | hp2 | a0001 | c0001 | t0021 | g0058 | AFR | USA | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | LWK | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0183 | AFR | LWK | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0249 | REF | REF | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0212 | REF | REF | FGF1_chr5_142587178_142691090 | FGF1 | chr5 | 142587178 | 142691090 |
| 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 |
|---|
| 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 |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:142592539
|
G | A | 1 | a0001c0001t0032 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2751C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 2751 | chr5 | 142592539 | |||||
| chr5:142592563
|
C | T | 17 | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(14): Show | 71 | HG00544.hp1 HG00673.hp1 HG01099.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2727G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 2727 | chr5 | 142592563 | |||||
| chr5:142592804
|
T | TG | 38 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(35): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*2485dupC | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 2485 | chr5 | 142592804 | |||||
| chr5:142592984
|
G | A | 1 | a0001c0001t0037 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2306C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 2306 | chr5 | 142592984 | |||||
| chr5:142593101
|
C | T | 3 | a0001c0001t0025a0001c0001t0036a0001c0001t0041 | 4 | HG01243.hp2 HG02280.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2189G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 2189 | chr5 | 142593101 | |||||
| chr5:142593148
|
T | C | 6 | a0001c0001t0003a0001c0001t0031a0001c0001t0043others(3): Show | 41 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2142A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 2142 | chr5 | 142593148 | |||||
| chr5:142593422
|
G | A | 1 | a0001c0001t0047 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1868C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1868 | chr5 | 142593422 | |||||
| chr5:142593659
|
A | G | 3 | a0001c0001t0013a0001c0001t0024a0001c0001t0032 | 8 | HG02015.hp2 HG02165.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1631T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1631 | chr5 | 142593659 | |||||
| chr5:142593731
|
A | G | 1 | a0001c0001t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1559T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1559 | chr5 | 142593731 | |||||
| chr5:142593784
|
C | G | 20 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(17): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1506G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1506 | chr5 | 142593784 | |||||
| chr5:142593936
|
T | C | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(27): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*1354A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1354 | chr5 | 142593936 | |||||
| chr5:142593991
|
G | T | 1 | a0001c0001t0016 | 3 | HG01175.hp1 HG01192.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1299C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1299 | chr5 | 142593991 | |||||
| chr5:142594034
|
C | A | 29 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(26): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1256G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1256 | chr5 | 142594034 | |||||
| chr5:142594064
|
T | A | 2 | a0001c0001t0007a0001c0001t0047 | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1226A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1226 | chr5 | 142594064 | |||||
| chr5:142594128
|
G | T | 1 | a0001c0001t0030 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1162C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 1162 | chr5 | 142594128 | |||||
| chr5:142594387
|
A | G | 1 | a0001c0001t0040 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 903 | chr5 | 142594387 | |||||
| chr5:142594468
|
C | T | 1 | a0001c0001t0029 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*822G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 822 | chr5 | 142594468 | |||||
| chr5:142594505
|
C | T | 1 | a0001c0001t0008 | 7 | HG00558.hp2 HG01516.hp2 HG02135.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*785G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 785 | chr5 | 142594505 | |||||
| chr5:142594517
|
C | G | 15 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(12): Show | 79 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*773G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 773 | chr5 | 142594517 | |||||
| chr5:142594651
|
A | G | 1 | a0001c0001t0039 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 639 | chr5 | 142594651 | |||||
| chr5:142594720
|
T | C | 2 | a0001c0001t0007a0001c0001t0047 | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*570A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 570 | chr5 | 142594720 | |||||
| chr5:142594790
|
T | C | 1 | a0001c0001t0028 | 2 | NA18995.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*500A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 500 | chr5 | 142594790 | |||||
| chr5:142594968
|
C | T | 8 | a0001c0001t0008a0001c0001t0010a0001c0001t0016others(5): Show | 24 | HG00558.hp2 HG01099.hp1 HG01168.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*322G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 322 | chr5 | 142594968 | |||||
| chr5:142594999
|
T | G | 1 | a0001c0001t0038 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*291A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 291 | chr5 | 142594999 | |||||
| chr5:142595007
|
G | T | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(27): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*283C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 283 | chr5 | 142595007 | |||||
| chr5:142595088
|
T | G | 2 | a0001c0001t0007a0001c0001t0047 | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*202A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 4/4 | 202 | chr5 | 142595088 | |||||
| chr5:142686000
|
G | C | 1 | a0001c0001t0048 | 1 | HG02273.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/4 | 71873 | chr5 | 142686000 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:142595502
|
A | C | 207 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.274-18T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142595502 | ||||||
| chr5:142595560
|
G | A | 2 | a0001c0001t0004g0131a0001c0001t0004g0307 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.274-76C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142595560 | ||||||
| chr5:142595782
|
T | C | 1 | a0001c0001t0030g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.274-298A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142595782 | ||||||
| chr5:142595842
|
G | A | 1 | a0001c0001t0036g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.274-358C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142595842 | ||||||
| chr5:142596092
|
G | A | 85 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.274-608C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596092 | ||||||
| chr5:142596139
|
T | G | 29 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(26): Show | 29 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.274-655A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596139 | ||||||
| chr5:142596264
|
GTTTGAGG others(128): Show |
G | 4 | a0001c0001t0012g0007a0001c0001t0012g0071a0001c0001t0012g0282others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-915_274-781del | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596264 | ||||||
| chr5:142596305
|
ACAATTTT others(129): Show |
A | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274-957_274-822del | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596305 | ||||||
| chr5:142596308
|
ATTTTTTT others(129): Show |
A | 2 | a0001c0001t0009g0262a0001c0001t0029g0032 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.274-960_274-825del | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596308 | ||||||
| chr5:142596352
|
C | CACAACAC others(131): Show |
28 | a0001c0001t0004g0036a0001c0001t0005g0022a0001c0001t0005g0098others(25): Show | 28 | HG00280.hp2 HG00423.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.274-1006_274-869du others(139): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596352 | ||||||
| chr5:142596405
|
G | A | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-921C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596405 | ||||||
| chr5:142596443
|
A | AT | 9 | a0001c0001t0001g0157a0001c0001t0001g0231a0001c0001t0011g0067others(6): Show | 9 | HG00639.hp2 HG00735.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-960dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596443 | ||||||
| chr5:142596444
|
T | A | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274-960A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596444 | ||||||
| chr5:142596444
|
TTTTTTTT others(130): Show |
T | 4 | a0001c0001t0001g0077a0001c0001t0001g0146a0001c0001t0001g0207others(1): Show | 4 | HG03669.hp2 HG03704.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-1097_274-961de others(1): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596444 | ||||||
| chr5:142596554
|
G | A | 1 | a0001c0001t0002g0125 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.274-1070C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596554 | ||||||
| chr5:142596581
|
AT | A | 7 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0012g0007others(4): Show | 7 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-1098delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596581 | ||||||
| chr5:142596593
|
T | A | 1 | a0001c0001t0025g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-1109A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596593 | ||||||
| chr5:142596655
|
G | T | 2 | a0001c0001t0001g0072a0001c0001t0027g0162 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.274-1171C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596655 | ||||||
| chr5:142596674
|
GTTTGAGG others(97): Show |
G | 7 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0012g0007others(4): Show | 7 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-1294_274-1191d others(2): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596674 | ||||||
| chr5:142596709
|
C | T | 1 | a0001c0001t0042g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.274-1225G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596709 | ||||||
| chr5:142596903
|
C | G | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-1419G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596903 | ||||||
| chr5:142596903
|
C | T | 1 | a0001c0001t0003g0313 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.274-1419G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142596903 | ||||||
| chr5:142597018
|
G | T | 7 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(4): Show | 7 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-1534C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597018 | ||||||
| chr5:142597062
|
A | G | 8 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0011g0067others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-1578T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597062 | ||||||
| chr5:142597093
|
G | T | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.274-1609C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597093 | ||||||
| chr5:142597094
|
A | G | 1 | a0001c0001t0025g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-1610T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597094 | ||||||
| chr5:142597113
|
A | G | 10 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0012g0007others(7): Show | 10 | HG01175.hp1 HG01192.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-1629T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597113 | ||||||
| chr5:142597196
|
T | A | 1 | a0001c0001t0003g0258 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.274-1712A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597196 | ||||||
| chr5:142597300
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.274-1816T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597300 | ||||||
| chr5:142597362
|
A | C | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.274-1878T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597362 | ||||||
| chr5:142597376
|
G | T | 1 | a0001c0001t0044g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.274-1892C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597376 | ||||||
| chr5:142597380
|
G | A | 200 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(197): Show | 201 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.274-1896C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597380 | ||||||
| chr5:142597441
|
G | C | 1 | a0001c0001t0003g0258 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.274-1957C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597441 | ||||||
| chr5:142597442
|
C | G | 1 | a0001c0001t0003g0258 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.274-1958G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597442 | ||||||
| chr5:142597555
|
G | A | 2 | a0001c0001t0020g0286a0001c0001t0020g0288 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.274-2071C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597555 | ||||||
| chr5:142597649
|
T | A | 1 | a0001c0001t0003g0092 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.274-2165A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597649 | ||||||
| chr5:142597727
|
T | C | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-2243A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597727 | ||||||
| chr5:142597921
|
C | A | 1 | a0001c0001t0025g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-2437G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597921 | ||||||
| chr5:142597940
|
G | C | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-2456C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142597940 | ||||||
| chr5:142598031
|
A | G | 8 | a0001c0001t0011g0067a0001c0001t0011g0081a0001c0001t0011g0082others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-2547T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598031 | ||||||
| chr5:142598208
|
G | T | 1 | a0001c0001t0025g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.273+2494C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598208 | ||||||
| chr5:142598238
|
C | T | 1 | a0001c0001t0009g0315 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.273+2464G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598238 | ||||||
| chr5:142598258
|
C | G | 1 | a0001c0001t0004g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.273+2444G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598258 | ||||||
| chr5:142598293
|
A | G | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+2409T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598293 | ||||||
| chr5:142598548
|
T | C | 1 | a0001c0001t0002g0326 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.273+2154A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598548 | ||||||
| chr5:142598623
|
C | T | 53 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(50): Show | 53 | HG00544.hp1 HG00673.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.273+2079G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598623 | ||||||
| chr5:142598678
|
A | G | 328 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(325): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.273+2024T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598678 | ||||||
| chr5:142598712
|
A | C | 1 | a0001c0001t0002g0018 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.273+1990T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598712 | ||||||
| chr5:142598755
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.273+1947G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598755 | ||||||
| chr5:142598822
|
G | T | 27 | a0001c0001t0004g0036a0001c0001t0005g0022a0001c0001t0005g0098others(24): Show | 27 | HG00280.hp2 HG00423.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.273+1880C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598822 | ||||||
| chr5:142598867
|
A | G | 7 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0012g0007others(4): Show | 7 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+1835T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598867 | ||||||
| chr5:142598902
|
C | G | 3 | a0001c0001t0012g0002a0001c0001t0025g0270a0001c0001t0036g0163 | 4 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+1800G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598902 | ||||||
| chr5:142598921
|
A | G | 13 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(10): Show | 13 | HG00544.hp1 HG00673.hp1 HG03130.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+1781T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598921 | ||||||
| chr5:142598990
|
T | C | 68 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(65): Show | 69 | HG00544.hp1 HG00673.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.273+1712A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142598990 | ||||||
| chr5:142599040
|
G | A | 1 | a0001c0001t0025g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.273+1662C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599040 | ||||||
| chr5:142599042
|
A | G | 336 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(333): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.273+1660T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599042 | ||||||
| chr5:142599069
|
T | C | 146 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(143): Show | 147 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.273+1633A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599069 | ||||||
| chr5:142599191
|
G | A | 192 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(189): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.273+1511C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599191 | ||||||
| chr5:142599236
|
C | T | 7 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(4): Show | 7 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+1466G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599236 | ||||||
| chr5:142599272
|
C | T | 1 | a0001c0001t0008g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.273+1430G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599272 | ||||||
| chr5:142599451
|
C | T | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 50 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.273+1251G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599451 | ||||||
| chr5:142599460
|
T | A | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 50 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.273+1242A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599460 | ||||||
| chr5:142599491
|
A | C | 1 | a0001c0001t0041g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.273+1211T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599491 | ||||||
| chr5:142599635
|
A | G | 27 | a0001c0001t0004g0036a0001c0001t0005g0022a0001c0001t0005g0098others(24): Show | 27 | HG00280.hp2 HG00423.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.273+1067T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599635 | ||||||
| chr5:142599652
|
C | A | 11 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0012g0002others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+1050G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599652 | ||||||
| chr5:142599839
|
AT | A | 39 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(36): Show | 39 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.273+862delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599839 | ||||||
| chr5:142599944
|
T | C | 4 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(1): Show | 4 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+758A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142599944 | ||||||
| chr5:142600063
|
G | A | 1 | a0001c0001t0022g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.273+639C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600063 | ||||||
| chr5:142600141
|
C | T | 11 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0012g0002others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+561G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600141 | ||||||
| chr5:142600145
|
C | T | 1 | a0001c0001t0011g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.273+557G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600145 | ||||||
| chr5:142600218
|
T | C | 51 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(48): Show | 51 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.273+484A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600218 | ||||||
| chr5:142600224
|
T | G | 1 | a0001c0001t0025g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.273+478A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600224 | ||||||
| chr5:142600266
|
G | T | 4 | a0001c0001t0012g0007a0001c0001t0012g0071a0001c0001t0012g0282others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+436C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600266 | ||||||
| chr5:142600327
|
A | C | 42 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(39): Show | 42 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+375T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600327 | ||||||
| chr5:142600340
|
C | T | 2 | a0001c0001t0012g0071a0001c0001t0012g0311 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.273+362G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600340 | ||||||
| chr5:142600476
|
A | C | 42 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(39): Show | 42 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+226T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600476 | ||||||
| chr5:142600506
|
A | T | 42 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(39): Show | 42 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+196T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 3/3 | chr5 | 142600506 | ||||||
| chr5:142600877
|
C | T | 2 | a0001c0001t0003g0199a0001c0001t0003g0249 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.170-72G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142600877 | ||||||
| chr5:142600912
|
C | T | 3 | a0001c0001t0016g0073a0001c0001t0016g0074a0001c0001t0016g0177 | 3 | HG01175.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.170-107G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142600912 | ||||||
| chr5:142600969
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0251 | 2 | NA18981.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.170-164A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142600969 | ||||||
| chr5:142601000
|
G | A | 1 | a0001c0001t0003g0249 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.170-195C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601000 | ||||||
| chr5:142601034
|
G | T | 8 | a0001c0001t0013g0054a0001c0001t0013g0061a0001c0001t0013g0171others(5): Show | 8 | HG02015.hp2 HG02165.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-229C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601034 | ||||||
| chr5:142601077
|
C | T | 1 | a0001c0001t0002g0125 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.170-272G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601077 | ||||||
| chr5:142601156
|
A | T | 3 | a0001c0001t0016g0073a0001c0001t0016g0074a0001c0001t0016g0177 | 3 | HG01175.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.170-351T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601156 | ||||||
| chr5:142601167
|
C | G | 1 | a0001c0001t0007g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.170-362G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601167 | ||||||
| chr5:142601201
|
G | A | 1 | a0001c0001t0006g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.170-396C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601201 | ||||||
| chr5:142601250
|
C | T | 4 | a0001c0001t0013g0054a0001c0001t0024g0117a0001c0001t0024g0244others(1): Show | 4 | HG02015.hp2 HG02165.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-445G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601250 | ||||||
| chr5:142601255
|
G | T | 85 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.170-450C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601255 | ||||||
| chr5:142601285
|
A | G | 1 | a0001c0001t0002g0159 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.170-480T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601285 | ||||||
| chr5:142601304
|
G | A | 3 | a0001c0001t0006g0063a0001c0001t0006g0303a0001c0001t0015g0130 | 3 | HG02886.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.170-499C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601304 | ||||||
| chr5:142601312
|
T | C | 1 | a0001c0001t0043g0140 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.170-507A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601312 | ||||||
| chr5:142601400
|
G | T | 85 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.170-595C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601400 | ||||||
| chr5:142601414
|
A | G | 1 | a0001c0001t0003g0313 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.170-609T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601414 | ||||||
| chr5:142601493
|
G | A | 41 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(38): Show | 41 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.170-688C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601493 | ||||||
| chr5:142601525
|
A | C | 9 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0012g0007others(6): Show | 9 | HG02280.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-720T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601525 | ||||||
| chr5:142601536
|
C | CTCAACTG others(1): Show |
3 | a0001c0001t0006g0063a0001c0001t0006g0303a0001c0001t0015g0130 | 3 | HG02886.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.170-732_170-731ins others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601536 | ||||||
| chr5:142601537
|
A | G | 3 | a0001c0001t0006g0063a0001c0001t0006g0303a0001c0001t0015g0130 | 3 | HG02886.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.170-732T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601537 | ||||||
| chr5:142601637
|
C | T | 1 | a0001c0001t0046g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.170-832G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601637 | ||||||
| chr5:142601904
|
G | C | 10 | a0001c0001t0010g0065a0001c0001t0010g0137a0001c0001t0010g0173others(7): Show | 10 | HG01934.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.170-1099C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142601904 | ||||||
| chr5:142602144
|
G | A | 41 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(38): Show | 41 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.170-1339C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602144 | ||||||
| chr5:142602176
|
C | CT | 7 | a0001c0001t0004g0027a0001c0001t0004g0062a0001c0001t0004g0186others(4): Show | 7 | HG02040.hp1 NA18962.hp1 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.170-1372dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602176 | ||||||
| chr5:142602176
|
CT | C | 28 | a0001c0001t0002g0115a0001c0001t0004g0036a0001c0001t0005g0022others(25): Show | 28 | HG00280.hp2 HG00423.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.170-1372delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602176 | ||||||
| chr5:142602269
|
C | T | 1 | a0001c0001t0004g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.170-1464G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602269 | ||||||
| chr5:142602278
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0040g0283 | 2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.170-1473C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602278 | ||||||
| chr5:142602352
|
T | G | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.170-1547A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602352 | ||||||
| chr5:142602369
|
G | T | 3 | a0001c0001t0016g0073a0001c0001t0016g0074a0001c0001t0016g0177 | 3 | HG01175.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.170-1564C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602369 | ||||||
| chr5:142602410
|
T | C | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.170-1605A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602410 | ||||||
| chr5:142602472
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.170-1667C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602472 | ||||||
| chr5:142602770
|
A | G | 3 | a0001c0001t0006g0063a0001c0001t0006g0303a0001c0001t0015g0130 | 3 | HG02886.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.170-1965T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602770 | ||||||
| chr5:142602861
|
T | C | 4 | a0001c0001t0004g0104a0001c0001t0004g0139a0001c0001t0004g0264others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-2056A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602861 | ||||||
| chr5:142602938
|
A | G | 8 | a0001c0001t0013g0054a0001c0001t0013g0061a0001c0001t0013g0171others(5): Show | 8 | HG02015.hp2 HG02165.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-2133T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142602938 | ||||||
| chr5:142603018
|
T | A | 1 | a0001c0001t0001g0319 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.170-2213A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603018 | ||||||
| chr5:142603103
|
C | T | 1 | a0001c0001t0012g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.170-2298G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603103 | ||||||
| chr5:142603104
|
G | A | 21 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0008g0040others(18): Show | 21 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.170-2299C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603104 | ||||||
| chr5:142603205
|
A | T | 1 | a0001c0001t0012g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.170-2400T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603205 | ||||||
| chr5:142603333
|
C | T | 3 | a0001c0001t0012g0002a0001c0001t0025g0270a0001c0001t0036g0163 | 4 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-2528G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603333 | ||||||
| chr5:142603357
|
C | T | 3 | a0001c0001t0015g0057a0001c0001t0015g0278a0001c0001t0015g0279 | 3 | HG01884.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-2552G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603357 | ||||||
| chr5:142603358
|
G | A | 71 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0013others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.170-2553C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603358 | ||||||
| chr5:142603395
|
A | G | 21 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0008g0040others(18): Show | 21 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.170-2590T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603395 | ||||||
| chr5:142603416
|
T | C | 181 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(178): Show | 182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.170-2611A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603416 | ||||||
| chr5:142603667
|
C | T | 21 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0008g0040others(18): Show | 21 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.170-2862G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603667 | ||||||
| chr5:142603876
|
C | A | 1 | a0001c0001t0035g0197 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.170-3071G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603876 | ||||||
| chr5:142603908
|
A | T | 21 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0008g0040others(18): Show | 21 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.170-3103T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142603908 | ||||||
| chr5:142604141
|
A | C | 53 | a0001c0001t0002g0089a0001c0001t0002g0096a0001c0001t0002g0198others(50): Show | 53 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(50): Show |
intron_variant | MODIFIER | c.170-3336T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604141 | ||||||
| chr5:142604328
|
A | G | 61 | a0001c0001t0002g0089a0001c0001t0002g0096a0001c0001t0002g0198others(58): Show | 62 | HG00544.hp1 HG00639.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.170-3523T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604328 | ||||||
| chr5:142604371
|
T | G | 7 | a0001c0001t0005g0147a0001c0001t0020g0286a0001c0001t0020g0288others(4): Show | 7 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-3566A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604371 | ||||||
| chr5:142604662
|
G | A | 17 | a0001c0001t0004g0036a0001c0001t0005g0147a0001c0001t0010g0065others(14): Show | 17 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-3857C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604662 | ||||||
| chr5:142604738
|
T | C | 89 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.170-3933A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604738 | ||||||
| chr5:142604743
|
T | C | 60 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(57): Show | 60 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.170-3938A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604743 | ||||||
| chr5:142604807
|
A | G | 4 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(1): Show | 4 | HG01891.hp2 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-4002T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604807 | ||||||
| chr5:142604916
|
T | C | 8 | a0001c0001t0013g0054a0001c0001t0013g0061a0001c0001t0013g0171others(5): Show | 8 | HG02015.hp2 HG02165.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-4111A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604916 | ||||||
| chr5:142604951
|
C | T | 65 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(62): Show | 66 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.170-4146G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604951 | ||||||
| chr5:142604958
|
C | T | 41 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(38): Show | 42 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.170-4153G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142604958 | ||||||
| chr5:142605002
|
A | G | 2 | a0001c0001t0025g0270a0001c0001t0036g0163 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.170-4197T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605002 | ||||||
| chr5:142605098
|
G | T | 2 | a0001c0001t0004g0131a0001c0001t0004g0307 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.170-4293C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605098 | ||||||
| chr5:142605110
|
C | G | 32 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0007g0100others(29): Show | 32 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.170-4305G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605110 | ||||||
| chr5:142605149
|
C | G | 21 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0008g0040others(18): Show | 21 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.170-4344G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605149 | ||||||
| chr5:142605253
|
C | T | 21 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0008g0040others(18): Show | 21 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.170-4448G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605253 | ||||||
| chr5:142605263
|
T | C | 61 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(58): Show | 61 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.170-4458A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605263 | ||||||
| chr5:142605273
|
G | GT | 26 | a0001c0001t0001g0047a0001c0001t0001g0285a0001c0001t0001g0290others(23): Show | 26 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.170-4469dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605273 | ||||||
| chr5:142605273
|
GT | G | 28 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(25): Show | 28 | HG00558.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.170-4469delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605273 | ||||||
| chr5:142605280
|
T | G | 1 | a0001c0001t0002g0151 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.170-4475A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605280 | ||||||
| chr5:142605356
|
G | A | 17 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0008g0040others(14): Show | 17 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-4551C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605356 | ||||||
| chr5:142605389
|
G | A | 17 | a0001c0001t0004g0036a0001c0001t0005g0147a0001c0001t0010g0065others(14): Show | 17 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-4584C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605389 | ||||||
| chr5:142605432
|
A | G | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.170-4627T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605432 | ||||||
| chr5:142605562
|
C | A | 1 | a0001c0001t0002g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.170-4757G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605562 | ||||||
| chr5:142605790
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.170-4985C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605790 | ||||||
| chr5:142605814
|
T | C | 328 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(325): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.170-5009A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605814 | ||||||
| chr5:142605940
|
G | A | 71 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0013others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.170-5135C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142605940 | ||||||
| chr5:142606021
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.170-5216C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606021 | ||||||
| chr5:142606036
|
TC | T | 82 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-5232delG | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606036 | ||||||
| chr5:142606064
|
C | T | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.170-5259G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606064 | ||||||
| chr5:142606081
|
GCA | G | 28 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(25): Show | 28 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.170-5278_170-5277d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606081 | ||||||
| chr5:142606210
|
TTC | T | 8 | a0001c0001t0013g0054a0001c0001t0013g0061a0001c0001t0013g0171others(5): Show | 8 | HG02015.hp2 HG02165.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-5407_170-5406d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606210 | ||||||
| chr5:142606212
|
C | CTGTGTGT others(5): Show |
2 | a0001c0001t0009g0262a0001c0001t0029g0032 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.170-5408_170-5407i others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606212 | ||||||
| chr5:142606212
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.170-5408_170-5407i others(18): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606212 | ||||||
| chr5:142606214
|
C | CTGTGTG | 4 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(1): Show | 4 | HG01891.hp2 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-5410_170-5409i others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606214 | ||||||
| chr5:142606214
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0036g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.170-5410_170-5409i others(18): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606214 | ||||||
| chr5:142606214
|
C | G | 4 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0025g0328others(1): Show | 4 | HG02615.hp1 HG02818.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-5409G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606214 | ||||||
| chr5:142606216
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0007g0202a0001c0001t0007g0332 | 2 | NA18747.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.170-5412_170-5411i others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606216 | ||||||
| chr5:142606216
|
C | CTGTGTGT others(7): Show |
8 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0122others(5): Show | 8 | HG00673.hp1 NA18939.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-5412_170-5411i others(16): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606216 | ||||||
| chr5:142606216
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0007g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.170-5412_170-5411i others(18): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606216 | ||||||
| chr5:142606216
|
C | G | 45 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(42): Show | 46 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.170-5411G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606216 | ||||||
| chr5:142606218
|
C | CTCTG | 3 | a0001c0001t0015g0057a0001c0001t0015g0278a0001c0001t0015g0279 | 3 | HG01884.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.170-5414_170-5413i others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTCTGTGT others(3): Show |
16 | a0001c0001t0002g0330a0001c0001t0004g0036a0001c0001t0005g0147others(13): Show | 16 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.170-5414_170-5413i others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTCTGTGT others(5): Show |
6 | a0001c0001t0010g0065a0001c0001t0010g0137a0001c0001t0010g0173others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.170-5414_170-5413i others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTCTGTGT others(7): Show |
3 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0010g0276 | 3 | HG01167.hp1 HG01169.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.170-5414_170-5413i others(16): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTGTG | 124 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0026others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.170-5417_170-5414d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTGTGTG | 18 | a0001c0001t0001g0014a0001c0001t0001g0075a0001c0001t0001g0079others(15): Show | 18 | HG00280.hp1 HG01070.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.170-5419_170-5414d others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTGTGTGT others(1): Show |
60 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0013others(57): Show | 60 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.170-5421_170-5414d others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTGTGTGT others(3): Show |
13 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(10): Show | 13 | HG00140.hp1 HG00642.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.170-5423_170-5414d others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTGTGTGT others(5): Show |
2 | a0001c0001t0002g0021a0001c0001t0002g0337 | 2 | HG00673.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.170-5425_170-5414d others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0007g0141 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.170-5427_170-5414d others(16): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | CTGTGTGT others(9): Show |
2 | a0001c0001t0002g0033a0001c0001t0002g0243 | 2 | NA18977.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.170-5429_170-5414d others(18): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606218
|
C | G | 68 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(65): Show | 69 | HG00558.hp2 HG00639.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.170-5413G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606218 | ||||||
| chr5:142606242
|
G | A | 8 | a0001c0001t0013g0054a0001c0001t0013g0061a0001c0001t0013g0171others(5): Show | 8 | HG02015.hp2 HG02165.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-5437C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606242 | ||||||
| chr5:142606242
|
G | GTA | 11 | a0001c0001t0008g0040a0001c0001t0008g0090a0001c0001t0008g0091others(8): Show | 11 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.170-5438_170-5437i others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606242 | ||||||
| chr5:142606242
|
G | GTGTA | 22 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(19): Show | 22 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.170-5441_170-5438d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606242 | ||||||
| chr5:142606242
|
G | GTGTGTGT others(1): Show |
3 | a0001c0001t0023g0024a0001c0001t0023g0333a0001c0001t0031g0023 | 3 | NA18941.hp1 NA18972.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.170-5438_170-5437i others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606242 | ||||||
| chr5:142606244
|
G | GTGTGTA | 6 | a0001c0001t0011g0067a0001c0001t0011g0081a0001c0001t0011g0082others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-5440_170-5439i others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606244 | ||||||
| chr5:142606244
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0012g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.170-5440_170-5439i others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606244 | ||||||
| chr5:142606250
|
A | AT | 3 | a0001c0001t0005g0133a0001c0001t0005g0135a0001c0001t0005g0291 | 3 | HG02040.hp1 NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.170-5446_170-5445i others(3): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606250 | ||||||
| chr5:142606251
|
GT | G | 45 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(42): Show | 45 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.170-5447delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606251 | ||||||
| chr5:142606252
|
T | TAG | 3 | a0001c0001t0005g0133a0001c0001t0005g0135a0001c0001t0005g0291 | 3 | HG02040.hp1 NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.170-5448_170-5447i others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606252 | ||||||
| chr5:142606262
|
T | A | 2 | a0001c0001t0025g0270a0001c0001t0036g0163 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.170-5457A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606262 | ||||||
| chr5:142606302
|
A | G | 4 | a0001c0001t0012g0007a0001c0001t0012g0071a0001c0001t0012g0282others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-5497T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606302 | ||||||
| chr5:142606383
|
G | A | 1 | a0001c0001t0002g0236 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.170-5578C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606383 | ||||||
| chr5:142606399
|
G | A | 3 | a0001c0001t0006g0063a0001c0001t0006g0303a0001c0001t0015g0130 | 3 | HG02886.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.170-5594C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606399 | ||||||
| chr5:142606460
|
C | CA | 9 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0008g0040others(6): Show | 9 | HG00558.hp2 HG01516.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.170-5656dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606460 | ||||||
| chr5:142606460
|
CA | C | 26 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(23): Show | 27 | HG00544.hp1 HG00639.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.170-5656delT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606460 | ||||||
| chr5:142606547
|
C | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0108others(21): Show | 24 | HG00544.hp2 HG00621.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.170-5742G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606547 | ||||||
| chr5:142606573
|
A | G | 2 | a0001c0001t0009g0129a0001c0001t0009g0262 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.170-5768T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606573 | ||||||
| chr5:142606617
|
A | G | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.170-5812T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606617 | ||||||
| chr5:142606669
|
C | T | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.170-5864G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606669 | ||||||
| chr5:142606718
|
A | T | 1 | a0001c0001t0008g0099 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.170-5913T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606718 | ||||||
| chr5:142606775
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.170-5970T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606775 | ||||||
| chr5:142606796
|
C | T | 3 | a0001c0001t0016g0073a0001c0001t0016g0074a0001c0001t0016g0177 | 3 | HG01175.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.170-5991G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606796 | ||||||
| chr5:142606832
|
C | A | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.170-6027G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606832 | ||||||
| chr5:142606924
|
C | T | 82 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-6119G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142606924 | ||||||
| chr5:142607046
|
G | A | 82 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-6241C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607046 | ||||||
| chr5:142607074
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.170-6269C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607074 | ||||||
| chr5:142607116
|
T | G | 49 | a0001c0001t0002g0042a0001c0001t0004g0009a0001c0001t0004g0027others(46): Show | 49 | HG00558.hp2 HG00642.hp2 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.170-6311A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607116 | ||||||
| chr5:142607150
|
C | T | 47 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(44): Show | 47 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.170-6345G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607150 | ||||||
| chr5:142607231
|
G | A | 5 | a0001c0001t0002g0148a0001c0001t0002g0165a0001c0001t0002g0335others(2): Show | 5 | HG01123.hp1 HG01175.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-6426C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607231 | ||||||
| chr5:142607275
|
C | T | 4 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(1): Show | 4 | HG01891.hp2 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-6470G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607275 | ||||||
| chr5:142607315
|
G | A | 3 | a0001c0001t0016g0073a0001c0001t0016g0074a0001c0001t0016g0177 | 3 | HG01175.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.170-6510C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607315 | ||||||
| chr5:142607323
|
G | A | 82 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.170-6518C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607323 | ||||||
| chr5:142607351
|
G | A | 75 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(72): Show | 76 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.170-6546C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607351 | ||||||
| chr5:142607446
|
G | A | 47 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(44): Show | 47 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.169+6513C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607446 | ||||||
| chr5:142607447
|
T | A | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.169+6512A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607447 | ||||||
| chr5:142607453
|
G | A | 3 | a0001c0001t0015g0057a0001c0001t0015g0278a0001c0001t0015g0279 | 3 | HG01884.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169+6506C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607453 | ||||||
| chr5:142607531
|
T | C | 1 | a0001c0001t0014g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.169+6428A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607531 | ||||||
| chr5:142607655
|
G | A | 47 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(44): Show | 47 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.169+6304C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607655 | ||||||
| chr5:142607890
|
G | C | 47 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(44): Show | 47 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.169+6069C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607890 | ||||||
| chr5:142607905
|
C | T | 7 | a0001c0001t0008g0040a0001c0001t0008g0090a0001c0001t0008g0091others(4): Show | 7 | HG00558.hp2 HG01516.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+6054G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607905 | ||||||
| chr5:142607944
|
T | C | 1 | a0001c0001t0004g0062 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.169+6015A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142607944 | ||||||
| chr5:142608153
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.169+5806G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608153 | ||||||
| chr5:142608216
|
T | C | 26 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(23): Show | 26 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+5743A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608216 | ||||||
| chr5:142608219
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0251 | 2 | NA18981.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.169+5740G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608219 | ||||||
| chr5:142608319
|
C | T | 2 | a0001c0001t0020g0286a0001c0001t0020g0288 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.169+5640G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608319 | ||||||
| chr5:142608382
|
A | T | 3 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0029g0032 | 3 | HG02615.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.169+5577T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608382 | ||||||
| chr5:142608497
|
A | AAT | 8 | a0001c0001t0013g0054a0001c0001t0013g0061a0001c0001t0013g0171others(5): Show | 8 | HG02015.hp2 HG02165.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+5460_169+5461d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608497 | ||||||
| chr5:142608497
|
A | AATAT | 3 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0037g0008 | 3 | HG02145.hp1 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.169+5458_169+5461d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608497 | ||||||
| chr5:142608498
|
ATATATAT others(74): Show |
A | 1 | a0001c0001t0001g0274 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.169+5380_169+5460d others(83): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608498 | ||||||
| chr5:142608526
|
A | T | 47 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(44): Show | 47 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.169+5433T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608526 | ||||||
| chr5:142608542
|
C | A | 2 | a0001c0001t0004g0143a0001c0001t0004g0334 | 2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.169+5417G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
C | CTA | 13 | a0001c0001t0001g0047a0001c0001t0001g0112a0001c0001t0001g0124others(10): Show | 13 | HG00621.hp2 HG00738.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.169+5415_169+5416d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
C | CTATA | 3 | a0001c0001t0001g0003a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG03017.hp1 NA18972.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.169+5413_169+5416d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTA | C | 37 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0037others(34): Show | 37 | HG00544.hp2 HG00738.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.169+5415_169+5416d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATA | C | 27 | a0001c0001t0001g0020a0001c0001t0001g0088a0001c0001t0001g0155others(24): Show | 27 | HG00408.hp1 HG00408.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.169+5413_169+5416d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATATA | C | 17 | a0001c0001t0001g0178a0001c0001t0001g0221a0001c0001t0001g0239others(14): Show | 17 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+5411_169+5416d others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATATAT others(1): Show |
C | 9 | a0001c0001t0001g0172a0001c0001t0003g0012a0001c0001t0003g0080others(6): Show | 9 | HG00642.hp2 HG01257.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+5409_169+5416d others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATATAT others(3): Show |
C | 4 | a0001c0001t0003g0029a0001c0001t0003g0193a0001c0001t0003g0195others(1): Show | 4 | HG00423.hp1 NA18956.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+5407_169+5416d others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATATAT others(5): Show |
C | 3 | a0001c0001t0001g0294a0001c0001t0001g0296a0001c0001t0003g0068 | 3 | HG00099.hp2 HG01123.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.169+5405_169+5416d others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATATAT others(7): Show |
C | 2 | a0001c0001t0014g0183a0001c0001t0025g0270 | 2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.169+5403_169+5416d others(16): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATATAT others(9): Show |
C | 3 | a0001c0001t0014g0132a0001c0001t0014g0284a0001c0001t0036g0163 | 3 | HG01891.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.169+5401_169+5416d others(18): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATATAT others(11): Show |
C | 18 | a0001c0001t0001g0083a0001c0001t0005g0022a0001c0001t0005g0098others(15): Show | 18 | HG00280.hp2 HG00423.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.169+5399_169+5416d others(20): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608542
|
CTATATAT others(25): Show |
C | 2 | a0001c0001t0001g0086a0001c0001t0001g0157 | 2 | HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.169+5385_169+5416d others(34): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608542 | ||||||
| chr5:142608551
|
T | TAA | 13 | a0001c0001t0004g0322a0001c0001t0010g0065a0001c0001t0010g0137others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+5407_169+5408i others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608551 | ||||||
| chr5:142608553
|
T | A | 7 | a0001c0001t0004g0036a0001c0001t0004g0308a0001c0001t0005g0147others(4): Show | 7 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+5406A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608553 | ||||||
| chr5:142608559
|
TATATATA others(19): Show |
T | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.169+5374_169+5399d others(28): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608559 | ||||||
| chr5:142608561
|
T | C | 13 | a0001c0001t0004g0322a0001c0001t0010g0065a0001c0001t0010g0137others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+5398A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608561 | ||||||
| chr5:142608561
|
TATATATA others(17): Show |
T | 2 | a0001c0001t0004g0131a0001c0001t0004g0307 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.169+5374_169+5397d others(26): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608561 | ||||||
| chr5:142608561
|
TATATATA others(19): Show |
T | 23 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(20): Show | 23 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+5372_169+5397d others(28): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608561 | ||||||
| chr5:142608563
|
T | C | 19 | a0001c0001t0004g0036a0001c0001t0004g0322a0001c0001t0005g0147others(16): Show | 20 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.169+5396A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608563 | ||||||
| chr5:142608563
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0025g0328a0001c0001t0041g0070 | 2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.169+5374_169+5395d others(24): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608563 | ||||||
| chr5:142608563
|
TATATATA others(17): Show |
T | 12 | a0001c0001t0005g0133a0001c0001t0005g0135a0001c0001t0005g0291others(9): Show | 12 | HG01175.hp1 HG01192.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+5372_169+5395d others(26): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608563 | ||||||
| chr5:142608564
|
A | C | 1 | a0001c0001t0004g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169+5395T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608564 | ||||||
| chr5:142608565
|
T | C | 6 | a0001c0001t0004g0036a0001c0001t0005g0147a0001c0001t0020g0286others(3): Show | 6 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+5394A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608565 | ||||||
| chr5:142608565
|
TATATATA others(13): Show |
T | 5 | a0001c0001t0007g0100a0001c0001t0007g0141a0001c0001t0007g0202others(2): Show | 5 | HG00544.hp1 HG02818.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5374_169+5393d others(22): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608565 | ||||||
| chr5:142608565
|
TATATATA others(15): Show |
T | 8 | a0001c0001t0013g0054a0001c0001t0013g0061a0001c0001t0013g0171others(5): Show | 8 | HG02015.hp2 HG02165.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+5372_169+5393d others(24): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608565 | ||||||
| chr5:142608566
|
A | C | 13 | a0001c0001t0004g0322a0001c0001t0010g0065a0001c0001t0010g0137others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+5393T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608566 | ||||||
| chr5:142608567
|
TATATATA others(11): Show |
T | 8 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0007g0122others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+5374_169+5391d others(20): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608567 | ||||||
| chr5:142608567
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0008g0250 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.169+5372_169+5391d others(22): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608567 | ||||||
| chr5:142608568
|
A | C | 6 | a0001c0001t0004g0036a0001c0001t0005g0147a0001c0001t0020g0286others(3): Show | 6 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+5391T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608568 | ||||||
| chr5:142608569
|
TATATATA others(9): Show |
T | 4 | a0001c0001t0007g0120a0001c0001t0007g0223a0001c0001t0007g0224others(1): Show | 4 | HG00673.hp1 NA18944.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+5374_169+5389d others(18): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608569 | ||||||
| chr5:142608573
|
TATATATA others(5): Show |
T | 2 | a0001c0001t0007g0116a0001c0001t0038g0255 | 2 | HG02523.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.169+5374_169+5385d others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608573 | ||||||
| chr5:142608575
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046 | 3 | HG00733.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.169+5374_169+5383d others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608575 | ||||||
| chr5:142608577
|
TATATATA others(1): Show |
T | 23 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0021others(20): Show | 23 | HG00673.hp2 HG01496.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+5374_169+5381d others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608577 | ||||||
| chr5:142608577
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0012g0282 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.169+5372_169+5381d others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608577 | ||||||
| chr5:142608579
|
TATATAC | T | 33 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0010others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.169+5374_169+5379d others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608579 | ||||||
| chr5:142608581
|
TATAC | T | 13 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0025others(10): Show | 13 | HG00140.hp1 HG00558.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.169+5374_169+5377d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608581 | ||||||
| chr5:142608583
|
T | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0078a0001c0001t0001g0079others(15): Show | 18 | HG00280.hp2 HG00423.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.169+5376A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608583 | ||||||
| chr5:142608583
|
T | TAC | 3 | a0001c0001t0001g0102a0001c0001t0001g0234a0001c0001t0001g0306 | 3 | HG02257.hp2 HG04184.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.169+5374_169+5375d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608583 | ||||||
| chr5:142608583
|
TAC | T | 7 | a0001c0001t0001g0319a0001c0001t0002g0170a0001c0001t0002g0226others(4): Show | 7 | HG01106.hp2 HG01934.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5374_169+5375d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608583 | ||||||
| chr5:142608585
|
C | T | 21 | a0001c0001t0002g0248a0001c0001t0004g0036a0001c0001t0004g0308others(18): Show | 22 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.169+5374G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608585 | ||||||
| chr5:142608587
|
C | T | 20 | a0001c0001t0004g0036a0001c0001t0004g0308a0001c0001t0004g0322others(17): Show | 21 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.169+5372G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608587 | ||||||
| chr5:142608616
|
G | GA | 13 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0078others(10): Show | 13 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.169+5342dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608616 | ||||||
| chr5:142608616
|
GAA | G | 47 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(44): Show | 47 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.169+5341_169+5342d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608616 | ||||||
| chr5:142608662
|
G | C | 1 | a0001c0001t0021g0041 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.169+5297C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608662 | ||||||
| chr5:142608688
|
A | G | 2 | a0001c0001t0002g0019a0001c0001t0002g0097 | 2 | NA18954.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.169+5271T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608688 | ||||||
| chr5:142608708
|
C | CATATAT | 19 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0008g0040others(16): Show | 19 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.169+5245_169+5250d others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608708 | ||||||
| chr5:142608708
|
C | CATATATA others(5): Show |
26 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(23): Show | 26 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+5250_169+5251i others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608708 | ||||||
| chr5:142608720
|
C | T | 170 | a0001c0001t0001g0319a0001c0001t0002g0004a0001c0001t0002g0005others(167): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.169+5239G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608720 | ||||||
| chr5:142608740
|
ATATATAT others(2): Show |
A | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.169+5210_169+5218d others(11): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608740 | ||||||
| chr5:142608748
|
A | G | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169+5211T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608748 | ||||||
| chr5:142608797
|
A | ATG | 10 | a0001c0001t0005g0022a0001c0001t0005g0245a0001c0001t0008g0040others(7): Show | 10 | HG00423.hp2 HG00558.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.169+5160_169+5161d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608797 | ||||||
| chr5:142608797
|
ATG | A | 240 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.169+5160_169+5161d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608797 | ||||||
| chr5:142608797
|
ATGTG | A | 3 | a0001c0001t0024g0117a0001c0001t0024g0244a0001c0001t0032g0295 | 3 | HG02015.hp2 HG02165.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.169+5158_169+5161d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608797 | ||||||
| chr5:142608900
|
A | G | 1 | a0001c0001t0023g0024 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.169+5059T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608900 | ||||||
| chr5:142608943
|
T | C | 1 | a0001c0001t0039g0271 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169+5016A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608943 | ||||||
| chr5:142608952
|
C | T | 48 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(45): Show | 48 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.169+5007G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608952 | ||||||
| chr5:142608976
|
T | C | 48 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(45): Show | 48 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.169+4983A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142608976 | ||||||
| chr5:142609021
|
A | G | 47 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(44): Show | 47 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.169+4938T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609021 | ||||||
| chr5:142609096
|
G | A | 25 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0088others(22): Show | 25 | HG02015.hp1 HG02074.hp1 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.169+4863C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609096 | ||||||
| chr5:142609245
|
C | T | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.169+4714G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609245 | ||||||
| chr5:142609319
|
C | T | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.169+4640G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609319 | ||||||
| chr5:142609365
|
G | A | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.169+4594C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609365 | ||||||
| chr5:142609374
|
G | A | 1 | a0001c0001t0043g0140 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.169+4585C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609374 | ||||||
| chr5:142609558
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.169+4401A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609558 | ||||||
| chr5:142609637
|
G | A | 1 | a0001c0001t0006g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.169+4322C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609637 | ||||||
| chr5:142609806
|
C | T | 3 | a0001c0001t0006g0063a0001c0001t0006g0303a0001c0001t0015g0130 | 3 | HG02886.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.169+4153G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609806 | ||||||
| chr5:142609920
|
C | T | 32 | a0001c0001t0005g0022a0001c0001t0005g0098a0001c0001t0005g0106others(29): Show | 32 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.169+4039G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142609920 | ||||||
| chr5:142610004
|
G | A | 19 | a0001c0001t0005g0022a0001c0001t0005g0098a0001c0001t0005g0106others(16): Show | 19 | HG00280.hp2 HG00423.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.169+3955C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610004 | ||||||
| chr5:142610105
|
G | C | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.169+3854C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610105 | ||||||
| chr5:142610217
|
A | T | 49 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(46): Show | 49 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.169+3742T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610217 | ||||||
| chr5:142610256
|
C | G | 1 | a0001c0001t0005g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.169+3703G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610256 | ||||||
| chr5:142610285
|
A | G | 336 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(333): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.169+3674T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610285 | ||||||
| chr5:142610400
|
G | A | 4 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(1): Show | 4 | HG01891.hp2 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+3559C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610400 | ||||||
| chr5:142610509
|
T | C | 48 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(45): Show | 48 | HG00558.hp2 HG01109.hp2 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.169+3450A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610509 | ||||||
| chr5:142610685
|
A | G | 23 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0060others(20): Show | 23 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+3274T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610685 | ||||||
| chr5:142610762
|
C | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0246 | 2 | HG02257.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.169+3197G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142610762 | ||||||
| chr5:142611037
|
G | T | 5 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0025g0328others(2): Show | 5 | HG02280.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+2922C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611037 | ||||||
| chr5:142611075
|
C | G | 5 | a0001c0001t0001g0240a0001c0001t0001g0274a0001c0001t0001g0290others(2): Show | 5 | HG00621.hp1 HG02165.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+2884G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611075 | ||||||
| chr5:142611076
|
T | C | 103 | a0001c0001t0004g0009a0001c0001t0004g0027a0001c0001t0004g0036others(100): Show | 104 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.169+2883A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611076 | ||||||
| chr5:142611203
|
T | C | 1 | a0001c0001t0036g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169+2756A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611203 | ||||||
| chr5:142611205
|
A | C | 10 | a0001c0001t0005g0133a0001c0001t0005g0135a0001c0001t0005g0291others(7): Show | 10 | HG00558.hp2 HG01516.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+2754T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611205 | ||||||
| chr5:142611243
|
T | C | 3 | a0001c0001t0024g0117a0001c0001t0024g0244a0001c0001t0032g0295 | 3 | HG02015.hp2 HG02165.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.169+2716A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611243 | ||||||
| chr5:142611303
|
C | T | 2 | a0001c0001t0025g0328a0001c0001t0041g0070 | 2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.169+2656G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611303 | ||||||
| chr5:142611354
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.169+2605C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611354 | ||||||
| chr5:142611371
|
A | C | 27 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(24): Show | 27 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.169+2588T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611371 | ||||||
| chr5:142611379
|
G | A | 1 | a0001c0001t0011g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169+2580C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611379 | ||||||
| chr5:142611389
|
C | T | 74 | a0001c0001t0001g0319a0001c0001t0002g0004a0001c0001t0002g0005others(71): Show | 75 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.169+2570G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611389 | ||||||
| chr5:142611437
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.169+2522T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611437 | ||||||
| chr5:142611510
|
C | G | 4 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(1): Show | 4 | HG01891.hp2 NA19030.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+2449G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611510 | ||||||
| chr5:142611550
|
C | A | 14 | a0001c0001t0005g0022a0001c0001t0005g0098a0001c0001t0005g0106others(11): Show | 14 | HG00280.hp2 HG00423.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.169+2409G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611550 | ||||||
| chr5:142611550
|
C | T | 1 | a0001c0001t0047g0093 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.169+2409G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611550 | ||||||
| chr5:142611603
|
C | T | 2 | a0001c0001t0017g0168a0001c0001t0017g0259 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.169+2356G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611603 | ||||||
| chr5:142611640
|
G | T | 24 | a0001c0001t0004g0036a0001c0001t0004g0308a0001c0001t0004g0322others(21): Show | 25 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.169+2319C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611640 | ||||||
| chr5:142611843
|
C | A | 24 | a0001c0001t0004g0036a0001c0001t0004g0308a0001c0001t0004g0322others(21): Show | 25 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.169+2116G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611843 | ||||||
| chr5:142611918
|
G | A | 1 | a0001c0001t0036g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169+2041C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611918 | ||||||
| chr5:142611975
|
C | T | 24 | a0001c0001t0004g0036a0001c0001t0004g0308a0001c0001t0004g0322others(21): Show | 25 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.169+1984G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142611975 | ||||||
| chr5:142612013
|
C | T | 6 | a0001c0001t0005g0147a0001c0001t0020g0286a0001c0001t0020g0288others(3): Show | 6 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+1946G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612013 | ||||||
| chr5:142612049
|
A | C | 14 | a0001c0001t0005g0022a0001c0001t0005g0098a0001c0001t0005g0106others(11): Show | 14 | HG00280.hp2 HG00423.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.169+1910T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612049 | ||||||
| chr5:142612065
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.169+1894C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612065 | ||||||
| chr5:142612072
|
G | A | 1 | a0001c0001t0036g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169+1887C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612072 | ||||||
| chr5:142612141
|
C | A | 1 | a0001c0001t0013g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169+1818G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612141 | ||||||
| chr5:142612212
|
C | G | 1 | a0001c0001t0007g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.169+1747G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612212 | ||||||
| chr5:142612294
|
C | T | 3 | a0001c0001t0016g0073a0001c0001t0016g0074a0001c0001t0016g0177 | 3 | HG01175.hp1 HG01192.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.169+1665G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612294 | ||||||
| chr5:142612314
|
T | C | 1 | a0001c0001t0025g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.169+1645A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612314 | ||||||
| chr5:142612482
|
A | C | 1 | a0001c0001t0002g0115 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.169+1477T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612482 | ||||||
| chr5:142612547
|
A | T | 1 | a0001c0001t0002g0033 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.169+1412T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612547 | ||||||
| chr5:142612617
|
C | CT | 32 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(29): Show | 32 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.169+1341dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612617 | ||||||
| chr5:142612617
|
CT | C | 17 | a0001c0001t0001g0293a0001c0001t0001g0312a0001c0001t0005g0022others(14): Show | 17 | HG00280.hp2 HG00423.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+1341delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612617 | ||||||
| chr5:142612664
|
A | G | 41 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(38): Show | 41 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.169+1295T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612664 | ||||||
| chr5:142612710
|
A | T | 41 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(38): Show | 41 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.169+1249T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612710 | ||||||
| chr5:142612724
|
G | A | 10 | a0001c0001t0005g0022a0001c0001t0005g0098a0001c0001t0005g0106others(7): Show | 10 | HG00280.hp2 HG00423.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+1235C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612724 | ||||||
| chr5:142612756
|
TC | T | 41 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(38): Show | 41 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.169+1202delG | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612756 | ||||||
| chr5:142612791
|
G | C | 3 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0029g0032 | 3 | HG02615.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.169+1168C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612791 | ||||||
| chr5:142612801
|
C | T | 36 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(33): Show | 36 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.169+1158G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612801 | ||||||
| chr5:142612824
|
A | G | 180 | a0001c0001t0001g0190a0001c0001t0001g0319a0001c0001t0002g0004others(177): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.169+1135T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612824 | ||||||
| chr5:142612910
|
G | A | 40 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(37): Show | 40 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.169+1049C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612910 | ||||||
| chr5:142612933
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.169+1026G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612933 | ||||||
| chr5:142612960
|
AAGTG | A | 15 | a0001c0001t0005g0022a0001c0001t0005g0098a0001c0001t0005g0106others(12): Show | 15 | HG00280.hp2 HG00423.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.169+995_169+998del others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142612960 | ||||||
| chr5:142613086
|
C | T | 1 | a0001c0001t0039g0271 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169+873G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613086 | ||||||
| chr5:142613129
|
C | A | 21 | a0001c0001t0004g0009a0001c0001t0004g0060a0001c0001t0004g0104others(18): Show | 21 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.169+830G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613129 | ||||||
| chr5:142613176
|
T | C | 1 | a0001c0001t0025g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.169+783A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613176 | ||||||
| chr5:142613258
|
A | T | 5 | a0001c0001t0011g0067a0001c0001t0011g0081a0001c0001t0011g0082others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+701T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613258 | ||||||
| chr5:142613366
|
C | T | 3 | a0001c0001t0015g0057a0001c0001t0015g0278a0001c0001t0015g0279 | 3 | HG01884.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.169+593G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613366 | ||||||
| chr5:142613441
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.169+518C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613441 | ||||||
| chr5:142613485
|
C | T | 1 | a0001c0001t0004g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.169+474G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613485 | ||||||
| chr5:142613563
|
A | G | 1 | a0001c0001t0039g0271 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169+396T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613563 | ||||||
| chr5:142613593
|
T | G | 1 | a0001c0001t0001g0239 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.169+366A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613593 | ||||||
| chr5:142613697
|
C | G | 3 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0029g0032 | 3 | HG02615.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.169+262G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613697 | ||||||
| chr5:142613756
|
G | A | 4 | a0001c0001t0012g0007a0001c0001t0012g0071a0001c0001t0012g0282others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+203C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613756 | ||||||
| chr5:142613829
|
C | A | 36 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(33): Show | 36 | HG00558.hp2 HG01175.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.169+130G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613829 | ||||||
| chr5:142613933
|
G | T | 1 | a0001c0001t0034g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.169+26C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 2/3 | chr5 | 142613933 | ||||||
| chr5:142614190
|
G | C | 5 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(2): Show | 5 | HG01891.hp2 NA19030.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-29C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614190 | ||||||
| chr5:142614269
|
T | A | 1 | a0001c0001t0014g0284 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-34-108A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614269 | ||||||
| chr5:142614302
|
C | T | 21 | a0001c0001t0005g0022a0001c0001t0005g0098a0001c0001t0005g0106others(18): Show | 21 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.-34-141G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614302 | ||||||
| chr5:142614386
|
A | G | 2 | a0001c0001t0001g0325a0001c0001t0004g0264 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-225T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614386 | ||||||
| chr5:142614544
|
G | A | 21 | a0001c0001t0005g0022a0001c0001t0005g0098a0001c0001t0005g0106others(18): Show | 21 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.-34-383C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614544 | ||||||
| chr5:142614617
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0004g0186 | 2 | HG00673.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-34-456G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614617 | ||||||
| chr5:142614645
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-34-484C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614645 | ||||||
| chr5:142614798
|
T | C | 2 | a0001c0001t0002g0031a0001c0001t0002g0219 | 2 | NA18995.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-34-637A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614798 | ||||||
| chr5:142614908
|
G | A | 97 | a0001c0001t0001g0319a0001c0001t0002g0004a0001c0001t0002g0005others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-34-747C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614908 | ||||||
| chr5:142614984
|
A | G | 3 | a0001c0001t0009g0129a0001c0001t0009g0262a0001c0001t0029g0032 | 3 | HG02615.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-34-823T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614984 | ||||||
| chr5:142614986
|
C | T | 1 | a0001c0001t0021g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-34-825G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142614986 | ||||||
| chr5:142615001
|
A | T | 2 | a0001c0001t0004g0143a0001c0001t0004g0334 | 2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-34-840T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615001 | ||||||
| chr5:142615032
|
A | ACAAACTT others(349): Show |
1 | a0001c0001t0002g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-34-872_-34-871ins others(356): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615032 | ||||||
| chr5:142615089
|
C | T | 7 | a0001c0001t0002g0028a0001c0001t0002g0111a0001c0001t0002g0118others(4): Show | 7 | HG00558.hp1 NA18947.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-928G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615089 | ||||||
| chr5:142615094
|
C | A | 4 | a0001c0001t0013g0054a0001c0001t0024g0117a0001c0001t0024g0244others(1): Show | 4 | HG02015.hp2 HG02165.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-933G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615094 | ||||||
| chr5:142615101
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-34-940C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615101 | ||||||
| chr5:142615372
|
C | T | 1 | a0001c0001t0018g0105 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-34-1211G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615372 | ||||||
| chr5:142615412
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-34-1251A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615412 | ||||||
| chr5:142615425
|
T | C | 6 | a0001c0001t0011g0067a0001c0001t0011g0081a0001c0001t0011g0082others(3): Show | 6 | HG00639.hp2 HG00735.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-1264A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615425 | ||||||
| chr5:142615486
|
TGCTGGGA others(3571): Show |
T | 2 | a0001c0001t0004g0027a0001c0001t0004g0062 | 2 | NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-34-4903_-34-1326d others(2): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615486 | ||||||
| chr5:142615493
|
A | T | 1 | a0001c0001t0006g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-34-1332T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615493 | ||||||
| chr5:142615512
|
G | A | 98 | a0001c0001t0001g0319a0001c0001t0002g0004a0001c0001t0002g0005others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-34-1351C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615512 | ||||||
| chr5:142615591
|
T | C | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-1430A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615591 | ||||||
| chr5:142615674
|
G | A | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-1513C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615674 | ||||||
| chr5:142615825
|
G | T | 1 | a0001c0001t0001g0187 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-34-1664C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615825 | ||||||
| chr5:142615947
|
G | A | 5 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(2): Show | 5 | HG01891.hp2 NA19030.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-1786C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142615947 | ||||||
| chr5:142616060
|
T | C | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-1899A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142616060 | ||||||
| chr5:142616209
|
C | G | 1 | a0001c0001t0004g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-34-2048G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142616209 | ||||||
| chr5:142616212
|
A | G | 142 | a0001c0001t0001g0217a0001c0001t0001g0319a0001c0001t0002g0004others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-34-2051T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142616212 | ||||||
| chr5:142616377
|
A | G | 2 | a0001c0001t0028g0011a0001c0001t0028g0052 | 2 | NA18995.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-34-2216T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142616377 | ||||||
| chr5:142616407
|
C | T | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-34-2246G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142616407 | ||||||
| chr5:142616796
|
T | G | 1 | a0001c0001t0001g0273 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-34-2635A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142616796 | ||||||
| chr5:142616899
|
C | A | 7 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-2738G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142616899 | ||||||
| chr5:142617217
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-34-3056A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617217 | ||||||
| chr5:142617296
|
C | T | 9 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(6): Show | 9 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34-3135G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617296 | ||||||
| chr5:142617351
|
C | T | 9 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(6): Show | 9 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34-3190G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617351 | ||||||
| chr5:142617364
|
C | CA | 9 | a0001c0001t0011g0067a0001c0001t0011g0081a0001c0001t0011g0082others(6): Show | 9 | HG00639.hp2 HG00735.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-3204dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617364 | ||||||
| chr5:142617375
|
A | G | 1 | a0001c0001t0006g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34-3214T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617375 | ||||||
| chr5:142617574
|
G | C | 5 | a0001c0001t0014g0132a0001c0001t0014g0161a0001c0001t0014g0183others(2): Show | 5 | HG01891.hp2 NA19030.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-3413C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617574 | ||||||
| chr5:142617628
|
G | C | 24 | a0001c0001t0004g0036a0001c0001t0004g0308a0001c0001t0004g0322others(21): Show | 24 | HG01099.hp1 HG01168.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.-34-3467C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617628 | ||||||
| chr5:142617793
|
C | G | 12 | a0001c0001t0004g0009a0001c0001t0004g0060a0001c0001t0004g0104others(9): Show | 12 | HG01168.hp2 HG01169.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-34-3632G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617793 | ||||||
| chr5:142617988
|
T | A | 2 | a0001c0001t0025g0328a0001c0001t0041g0070 | 2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-34-3827A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142617988 | ||||||
| chr5:142618141
|
G | A | 1 | a0001c0001t0025g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-34-3980C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618141 | ||||||
| chr5:142618462
|
C | T | 1 | a0001c0001t0002g0237 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-34-4301G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618462 | ||||||
| chr5:142618463
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-34-4302C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618463 | ||||||
| chr5:142618615
|
A | G | 2 | a0001c0001t0003g0049a0001c0001t0003g0181 | 2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-34-4454T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618615 | ||||||
| chr5:142618801
|
G | A | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-34-4640C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618801 | ||||||
| chr5:142618815
|
A | T | 289 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0039others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-34-4654T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618815 | ||||||
| chr5:142618883
|
A | G | 1 | a0001c0001t0004g0334 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-34-4722T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618883 | ||||||
| chr5:142618921
|
G | GT | 5 | a0001c0001t0005g0133a0001c0001t0005g0135a0001c0001t0005g0291others(2): Show | 5 | HG01516.hp2 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-4761dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
G | GTT | 3 | a0001c0001t0008g0099a0001c0001t0008g0150a0001c0001t0008g0250 | 3 | HG00558.hp2 HG04199.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-34-4762_-34-4761d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0024g0244 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-34-4761_-34-4760i others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0013g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-34-4761_-34-4760i others(13): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0013g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-34-4761_-34-4760i others(17): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0024g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-34-4761_-34-4760i others(20): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
GTTGTT | G | 15 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0033others(12): Show | 15 | HG01175.hp2 HG02074.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34-4765_-34-4761d others(7): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
GTTGTTTT others(3): Show |
G | 4 | a0001c0001t0011g0067a0001c0001t0011g0081a0001c0001t0011g0261others(1): Show | 4 | HG00639.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-4770_-34-4761d others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
GTTGTTTT others(5): Show |
G | 3 | a0001c0001t0004g0131a0001c0001t0004g0307a0001c0001t0037g0008 | 3 | HG02145.hp1 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-34-4772_-34-4761d others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618921
|
GTTGTTTT others(8): Show |
G | 6 | a0001c0001t0004g0036a0001c0001t0009g0129a0001c0001t0009g0262others(3): Show | 6 | HG01243.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-4775_-34-4761d others(17): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618921 | ||||||
| chr5:142618923
|
TGTTTTG | T | 57 | a0001c0001t0001g0319a0001c0001t0002g0004a0001c0001t0002g0005others(54): Show | 58 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.-34-4768_-34-4763d others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618923 | ||||||
| chr5:142618924
|
G | GT | 11 | a0001c0001t0003g0260a0001c0001t0004g0308a0001c0001t0004g0322others(8): Show | 11 | HG01884.hp1 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34-4764dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618924 | ||||||
| chr5:142618924
|
G | GTT | 16 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0084others(13): Show | 17 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-34-4765_-34-4764d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618924 | ||||||
| chr5:142618924
|
G | GTTT | 4 | a0001c0001t0002g0205a0001c0001t0005g0232a0001c0001t0005g0245others(1): Show | 4 | HG02109.hp2 HG03710.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-4766_-34-4764d others(5): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618924 | ||||||
| chr5:142618924
|
G | T | 23 | a0001c0001t0002g0031a0001c0001t0002g0219a0001c0001t0005g0133others(20): Show | 23 | HG00558.hp2 HG01516.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34-4763C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618924 | ||||||
| chr5:142618924
|
GTTTTGTT others(7): Show |
G | 12 | a0001c0001t0007g0100a0001c0001t0007g0116a0001c0001t0007g0120others(9): Show | 12 | HG00544.hp1 HG00673.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-4777_-34-4764d others(16): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618924 | ||||||
| chr5:142618925
|
TTTTG | T | 20 | a0001c0001t0004g0060a0001c0001t0004g0104a0001c0001t0004g0139others(17): Show | 20 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.-34-4768_-34-4765d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618925 | ||||||
| chr5:142618928
|
TG | T | 8 | a0001c0001t0006g0063a0001c0001t0006g0303a0001c0001t0012g0071others(5): Show | 8 | HG01099.hp1 HG01168.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-4768delC | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618928 | ||||||
| chr5:142618929
|
G | GT | 53 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0066others(50): Show | 53 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-34-4769dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618929 | ||||||
| chr5:142618929
|
G | T | 82 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0016others(79): Show | 83 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-34-4768C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618929 | ||||||
| chr5:142618986
|
T | G | 2 | a0001c0001t0002g0211a0001c0001t0014g0161 | 2 | HG02523.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-34-4825A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618986 | ||||||
| chr5:142618990
|
A | T | 1 | a0001c0001t0036g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-34-4829T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142618990 | ||||||
| chr5:142619030
|
G | A | 2 | a0001c0001t0004g0131a0001c0001t0004g0307 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-34-4869C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619030 | ||||||
| chr5:142619035
|
C | T | 10 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0180others(7): Show | 10 | HG01975.hp1 HG02074.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-4874G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619035 | ||||||
| chr5:142619101
|
A | AT | 10 | a0001c0001t0002g0125a0001c0001t0002g0134a0001c0001t0007g0116others(7): Show | 10 | HG00673.hp1 NA18939.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-4941dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619101 | ||||||
| chr5:142619128
|
G | A | 5 | a0001c0001t0002g0016a0001c0001t0002g0018a0001c0001t0002g0188others(2): Show | 5 | NA18942.hp2 NA18950.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-4967C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619128 | ||||||
| chr5:142619136
|
G | A | 1 | a0001c0001t0008g0250 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-34-4975C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619136 | ||||||
| chr5:142619146
|
A | G | 25 | a0001c0001t0001g0003a0001c0001t0001g0108a0001c0001t0001g0112others(22): Show | 25 | HG00544.hp2 HG00621.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.-34-4985T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619146 | ||||||
| chr5:142619156
|
G | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(243): Show | 247 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.-34-4995C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619156 | ||||||
| chr5:142619169
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(242): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-34-5008G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619169 | ||||||
| chr5:142619177
|
A | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(242): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-34-5016T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619177 | ||||||
| chr5:142619178
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(242): Show | 246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-34-5017G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619178 | ||||||
| chr5:142619186
|
A | G | 1 | a0001c0001t0005g0098 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-34-5025T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619186 | ||||||
| chr5:142619224
|
A | G | 2 | a0001c0001t0004g0186a0001c0001t0004g0265 | 2 | NA18994.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-34-5063T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619224 | ||||||
| chr5:142619232
|
C | G | 108 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0037others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-34-5071G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619232 | ||||||
| chr5:142619269
|
C | G | 1 | a0001c0001t0010g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-34-5108G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619269 | ||||||
| chr5:142619401
|
G | A | 127 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0037others(124): Show | 128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-34-5240C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619401 | ||||||
| chr5:142619477
|
C | A | 1 | a0001c0001t0023g0333 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-34-5316G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619477 | ||||||
| chr5:142619575
|
G | A | 5 | a0001c0001t0001g0157a0001c0001t0002g0044a0001c0001t0002g0045others(2): Show | 5 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-5414C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619575 | ||||||
| chr5:142619662
|
C | T | 98 | a0001c0001t0001g0072a0001c0001t0001g0079a0001c0001t0001g0112others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-34-5501G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619662 | ||||||
| chr5:142619687
|
G | A | 274 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(271): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.-34-5526C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619687 | ||||||
| chr5:142619701
|
C | T | 37 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0001g0088others(34): Show | 37 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-34-5540G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619701 | ||||||
| chr5:142619703
|
C | T | 32 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0001g0088others(29): Show | 32 | HG00621.hp1 HG01106.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.-34-5542G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619703 | ||||||
| chr5:142619704
|
A | G | 64 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0039others(61): Show | 64 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.-34-5543T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619704 | ||||||
| chr5:142619837
|
A | G | 14 | a0001c0001t0002g0330a0001c0001t0004g0308a0001c0001t0006g0209others(11): Show | 14 | HG01175.hp1 HG01192.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-34-5676T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619837 | ||||||
| chr5:142619851
|
G | GA | 40 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0079others(37): Show | 41 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.-34-5691dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619851 | ||||||
| chr5:142619901
|
AAAAG | A | 12 | a0001c0001t0001g0179a0001c0001t0002g0005a0001c0001t0002g0013others(9): Show | 12 | HG01255.hp2 HG02004.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.-34-5744_-34-5741d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142619901 | ||||||
| chr5:142620014
|
T | C | 1 | a0001c0001t0003g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-34-5853A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620014 | ||||||
| chr5:142620047
|
A | T | 42 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0072others(39): Show | 42 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-34-5886T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620047 | ||||||
| chr5:142620118
|
C | T | 33 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0149others(30): Show | 34 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(31): Show |
intron_variant | MODIFIER | c.-34-5957G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620118 | ||||||
| chr5:142620133
|
C | T | 3 | a0001c0001t0018g0105a0001c0001t0018g0121a0001c0001t0018g0268 | 3 | NA18979.hp2 NA19007.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-34-5972G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620133 | ||||||
| chr5:142620144
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(115): Show | 118 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-34-5983C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620144 | ||||||
| chr5:142620155
|
C | T | 3 | a0001c0001t0004g0287a0001c0001t0004g0292a0001c0001t0014g0183 | 3 | HG01168.hp2 HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-34-5994G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620155 | ||||||
| chr5:142620169
|
C | G | 1 | a0001c0001t0002g0021 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-34-6008G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620169 | ||||||
| chr5:142620192
|
C | T | 43 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0112others(40): Show | 44 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.-34-6031G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620192 | ||||||
| chr5:142620205
|
A | C | 15 | a0001c0001t0001g0026a0001c0001t0001g0113a0001c0001t0001g0290others(12): Show | 15 | HG02004.hp2 HG03710.hp2 NA18950.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34-6044T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620205 | ||||||
| chr5:142620240
|
A | C | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-6079T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620240 | ||||||
| chr5:142620241
|
C | A | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-6080G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620241 | ||||||
| chr5:142620286
|
T | C | 4 | a0001c0001t0002g0335a0001c0001t0002g0336a0001c0001t0002g0337others(1): Show | 4 | HG01123.hp1 HG01516.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-6125A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620286 | ||||||
| chr5:142620350
|
G | A | 4 | a0001c0001t0006g0209a0001c0001t0006g0272a0001c0001t0006g0303others(1): Show | 4 | HG01167.hp2 HG02257.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-6189C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620350 | ||||||
| chr5:142620375
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0252a0001c0001t0003g0049 | 3 | HG00735.hp2 HG01361.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-34-6214C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620375 | ||||||
| chr5:142620512
|
A | G | 5 | a0001c0001t0006g0209a0001c0001t0006g0272a0001c0001t0006g0303others(2): Show | 5 | HG01167.hp2 HG01243.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-6351T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620512 | ||||||
| chr5:142620521
|
G | A | 1 | a0001c0001t0039g0271 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-34-6360C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620521 | ||||||
| chr5:142620574
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-34-6413G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620574 | ||||||
| chr5:142620598
|
A | G | 1 | a0001c0001t0002g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-34-6437T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620598 | ||||||
| chr5:142620903
|
A | T | 5 | a0001c0001t0006g0209a0001c0001t0006g0272a0001c0001t0006g0303others(2): Show | 5 | HG01167.hp2 HG01243.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-6742T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620903 | ||||||
| chr5:142620970
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(150): Show | 153 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.-34-6809A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620970 | ||||||
| chr5:142620980
|
C | T | 149 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(146): Show | 149 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.-34-6819G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142620980 | ||||||
| chr5:142621354
|
T | TTC | 137 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(134): Show | 137 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.-34-7195_-34-7194d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621354 | ||||||
| chr5:142621473
|
A | G | 1 | a0001c0001t0003g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-34-7312T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621473 | ||||||
| chr5:142621484
|
G | A | 1 | a0001c0001t0041g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-34-7323C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621484 | ||||||
| chr5:142621491
|
C | A | 2 | a0001c0001t0001g0228a0001c0001t0003g0298 | 2 | HG00408.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.-34-7330G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621491 | ||||||
| chr5:142621574
|
C | CT | 3 | a0001c0001t0001g0072a0001c0001t0015g0278a0001c0001t0015g0279 | 3 | HG01884.hp2 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-34-7414dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621574 | ||||||
| chr5:142621588
|
C | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0312a0001c0001t0002g0241others(5): Show | 8 | HG00642.hp2 HG01256.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-7427G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621588 | ||||||
| chr5:142621589
|
A | G | 51 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0172others(48): Show | 51 | HG00642.hp2 HG01168.hp2 HG01169.hp2 others(48): Show |
intron_variant | MODIFIER | c.-34-7428T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621589 | ||||||
| chr5:142621609
|
C | T | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-7448G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621609 | ||||||
| chr5:142621764
|
C | G | 4 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0282others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-7603G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621764 | ||||||
| chr5:142621986
|
A | G | 8 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0002g0084others(5): Show | 8 | HG01496.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-7825T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142621986 | ||||||
| chr5:142622141
|
G | A | 14 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0002g0084others(11): Show | 14 | HG01168.hp2 HG01169.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34-7980C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622141 | ||||||
| chr5:142622146
|
A | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(119): Show | 122 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.-34-7985T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622146 | ||||||
| chr5:142622422
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-34-8261C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622422 | ||||||
| chr5:142622667
|
T | A | 31 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0149others(28): Show | 32 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.-34-8506A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622667 | ||||||
| chr5:142622684
|
G | C | 8 | a0001c0001t0001g0112a0001c0001t0002g0151a0001c0001t0006g0017others(5): Show | 8 | NA18747.hp1 NA18747.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-8523C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622684 | ||||||
| chr5:142622770
|
A | G | 2 | a0001c0001t0011g0261a0001c0001t0011g0281 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-34-8609T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622770 | ||||||
| chr5:142622777
|
T | C | 223 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(220): Show | 225 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-34-8616A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622777 | ||||||
| chr5:142622863
|
C | T | 3 | a0001c0001t0014g0161a0001c0001t0014g0284a0001c0001t0036g0163 | 3 | HG01891.hp2 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-34-8702G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622863 | ||||||
| chr5:142622935
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-34-8774T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622935 | ||||||
| chr5:142622939
|
G | C | 16 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0002g0084others(13): Show | 16 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-34-8778C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142622939 | ||||||
| chr5:142623032
|
T | A | 1 | a0001c0001t0003g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-34-8871A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623032 | ||||||
| chr5:142623101
|
A | C | 2 | a0001c0001t0015g0130a0001c0001t0030g0064 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-34-8940T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623101 | ||||||
| chr5:142623106
|
T | C | 1 | a0001c0001t0011g0281 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-34-8945A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623106 | ||||||
| chr5:142623108
|
C | CT | 4 | a0001c0001t0002g0156a0001c0001t0012g0002a0001c0001t0025g0328others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-8948dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623108 | ||||||
| chr5:142623116
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-34-8955A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623116 | ||||||
| chr5:142623347
|
C | CT | 15 | a0001c0001t0001g0037a0001c0001t0001g0309a0001c0001t0004g0131others(12): Show | 15 | HG02615.hp2 HG02622.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34-9187dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623347 | ||||||
| chr5:142623347
|
CT | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(115): Show | 118 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-34-9187delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623347 | ||||||
| chr5:142623366
|
A | G | 1 | a0001c0001t0003g0094 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-34-9205T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623366 | ||||||
| chr5:142623375
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-34-9214G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623375 | ||||||
| chr5:142623537
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-34-9376C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623537 | ||||||
| chr5:142623713
|
T | G | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-34-9552A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623713 | ||||||
| chr5:142623723
|
T | C | 16 | a0001c0001t0001g0253a0001c0001t0001g0312a0001c0001t0002g0156others(13): Show | 17 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-34-9562A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623723 | ||||||
| chr5:142623745
|
A | AT | 3 | a0001c0001t0011g0263a0001c0001t0015g0130a0001c0001t0030g0064 | 3 | HG02630.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-34-9585_-34-9584i others(3): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623745 | ||||||
| chr5:142623746
|
A | AT | 142 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(139): Show | 142 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.-34-9586dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623746 | ||||||
| chr5:142623746
|
A | ATT | 51 | a0001c0001t0001g0051a0001c0001t0001g0149a0001c0001t0001g0234others(48): Show | 52 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34-9587_-34-9586d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623746 | ||||||
| chr5:142623746
|
A | T | 3 | a0001c0001t0011g0263a0001c0001t0015g0130a0001c0001t0030g0064 | 3 | HG02630.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-34-9585T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623746 | ||||||
| chr5:142623795
|
G | A | 6 | a0001c0001t0001g0112a0001c0001t0002g0151a0001c0001t0007g0100others(3): Show | 6 | NA18747.hp1 NA18944.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-9634C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623795 | ||||||
| chr5:142623801
|
A | G | 18 | a0001c0001t0001g0253a0001c0001t0001g0312a0001c0001t0001g0325others(15): Show | 19 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-34-9640T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142623801 | ||||||
| chr5:142624197
|
G | T | 38 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0149others(35): Show | 39 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.-34-10036C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624197 | ||||||
| chr5:142624200
|
G | A | 5 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0205others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-10039C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624200 | ||||||
| chr5:142624213
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-34-10052G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624213 | ||||||
| chr5:142624289
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-10128T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624289 | ||||||
| chr5:142624404
|
T | A | 3 | a0001c0001t0002g0335a0001c0001t0002g0336a0001c0001t0002g0337 | 3 | HG01123.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-34-10243A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624404 | ||||||
| chr5:142624478
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34-10317G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624478 | ||||||
| chr5:142624502
|
A | G | 1 | a0001c0001t0007g0116 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-34-10341T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624502 | ||||||
| chr5:142624717
|
C | T | 1 | a0001c0001t0004g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-34-10556G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624717 | ||||||
| chr5:142624718
|
A | C | 1 | a0001c0001t0004g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-10557T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624718 | ||||||
| chr5:142624743
|
T | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(215): Show | 220 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-34-10582A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624743 | ||||||
| chr5:142624857
|
C | T | 73 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0051others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-34-10696G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142624857 | ||||||
| chr5:142625029
|
C | T | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-10868G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625029 | ||||||
| chr5:142625181
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-34-11020T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625181 | ||||||
| chr5:142625292
|
G | A | 34 | a0001c0001t0001g0037a0001c0001t0001g0172a0001c0001t0001g0178others(31): Show | 34 | HG00642.hp2 HG01168.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-34-11131C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625292 | ||||||
| chr5:142625307
|
C | G | 1 | a0001c0001t0005g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-11146G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625307 | ||||||
| chr5:142625313
|
G | GAC | 5 | a0001c0001t0001g0112a0001c0001t0002g0084a0001c0001t0006g0063others(2): Show | 5 | HG02723.hp2 HG02886.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-11154_-34-1115 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625313 | ||||||
| chr5:142625313
|
G | GACAC | 7 | a0001c0001t0001g0072a0001c0001t0001g0325a0001c0001t0002g0044others(4): Show | 7 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-11156_-34-1115 others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625313 | ||||||
| chr5:142625313
|
GAC | G | 72 | a0001c0001t0001g0075a0001c0001t0001g0127a0001c0001t0001g0155others(69): Show | 72 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.-34-11154_-34-1115 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625313 | ||||||
| chr5:142625313
|
GACAC | G | 50 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0149others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-34-11156_-34-1115 others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625313 | ||||||
| chr5:142625313
|
GACACAC | G | 44 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0001g0086others(41): Show | 44 | HG01167.hp2 HG01975.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.-34-11158_-34-1115 others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625313 | ||||||
| chr5:142625313
|
GACACACA others(1): Show |
G | 125 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0026others(122): Show | 126 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.-34-11160_-34-1115 others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625313 | ||||||
| chr5:142625313
|
GACACACA others(3): Show |
G | 10 | a0001c0001t0001g0246a0001c0001t0001g0293a0001c0001t0002g0042others(7): Show | 10 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-11162_-34-1115 others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625313 | ||||||
| chr5:142625313
|
GACACACA others(5): Show |
G | 4 | a0001c0001t0001g0285a0001c0001t0008g0040a0001c0001t0011g0081others(1): Show | 4 | HG00639.hp2 HG00735.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-11164_-34-1115 others(16): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625313 | ||||||
| chr5:142625552
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0102others(63): Show | 66 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-34-11391C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625552 | ||||||
| chr5:142625601
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34-11440G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625601 | ||||||
| chr5:142625608
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-34-11447G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625608 | ||||||
| chr5:142625665
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0003g0249 | 2 | HG03492.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-34-11504G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625665 | ||||||
| chr5:142625702
|
A | C | 5 | a0001c0001t0001g0325a0001c0001t0004g0307a0001c0001t0005g0152others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-11541T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625702 | ||||||
| chr5:142625703
|
A | G | 21 | a0001c0001t0001g0037a0001c0001t0001g0172a0001c0001t0001g0178others(18): Show | 21 | HG01168.hp2 HG01169.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-34-11542T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625703 | ||||||
| chr5:142625834
|
T | C | 2 | a0001c0001t0003g0076a0001c0001t0003g0229 | 2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-34-11673A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625834 | ||||||
| chr5:142625873
|
A | G | 3 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0041g0070 | 3 | HG02055.hp1 HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-34-11712T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625873 | ||||||
| chr5:142625938
|
T | C | 4 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0282others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-11777A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625938 | ||||||
| chr5:142625948
|
T | G | 47 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0001g0086others(44): Show | 48 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.-34-11787A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625948 | ||||||
| chr5:142625994
|
T | C | 44 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0001g0086others(41): Show | 44 | HG00280.hp2 HG01167.hp2 HG01975.hp1 others(41): Show |
intron_variant | MODIFIER | c.-34-11833A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142625994 | ||||||
| chr5:142626012
|
A | C | 43 | a0001c0001t0001g0020a0001c0001t0001g0083a0001c0001t0001g0086others(40): Show | 43 | HG00280.hp2 HG01167.hp2 HG01975.hp1 others(40): Show |
intron_variant | MODIFIER | c.-34-11851T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626012 | ||||||
| chr5:142626129
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-34-11968A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626129 | ||||||
| chr5:142626149
|
A | G | 10 | a0001c0001t0001g0325a0001c0001t0004g0036a0001c0001t0004g0277others(7): Show | 10 | HG02055.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-11988T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626149 | ||||||
| chr5:142626152
|
ATTTTTG | A | 8 | a0001c0001t0001g0253a0001c0001t0001g0312a0001c0001t0002g0241others(5): Show | 8 | HG00642.hp2 HG01256.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-11997_-34-1199 others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626152 | ||||||
| chr5:142626174
|
T | G | 2 | a0001c0001t0015g0278a0001c0001t0015g0279 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-34-12013A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626174 | ||||||
| chr5:142626232
|
G | C | 10 | a0001c0001t0004g0104a0001c0001t0004g0139a0001c0001t0004g0264others(7): Show | 10 | HG01167.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34-12071C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626232 | ||||||
| chr5:142626370
|
A | T | 1 | a0001c0001t0005g0022 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-34-12209T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626370 | ||||||
| chr5:142626433
|
G | A | 4 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0282others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-12272C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626433 | ||||||
| chr5:142626439
|
G | T | 1 | a0001c0001t0004g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-34-12278C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626439 | ||||||
| chr5:142626491
|
T | G | 8 | a0001c0001t0004g0060a0001c0001t0004g0128a0001c0001t0004g0308others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-12330A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626491 | ||||||
| chr5:142626553
|
C | G | 15 | a0001c0001t0001g0253a0001c0001t0001g0312a0001c0001t0002g0241others(12): Show | 15 | HG00642.hp2 HG01243.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.-34-12392G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626553 | ||||||
| chr5:142626555
|
A | C | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-34-12394T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626555 | ||||||
| chr5:142626578
|
C | T | 1 | a0001c0001t0009g0262 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34-12417G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626578 | ||||||
| chr5:142626617
|
A | G | 1 | a0001c0001t0046g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-34-12456T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626617 | ||||||
| chr5:142626657
|
C | A | 1 | a0001c0001t0001g0325 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34-12496G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626657 | ||||||
| chr5:142626689
|
G | A | 1 | a0001c0001t0025g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-34-12528C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142626689 | ||||||
| chr5:142627094
|
T | C | 1 | a0001c0001t0023g0333 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-34-12933A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142627094 | ||||||
| chr5:142627424
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0252a0001c0001t0001g0266others(2): Show | 5 | HG00735.hp2 HG00741.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-13263G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142627424 | ||||||
| chr5:142627488
|
C | T | 3 | a0001c0001t0005g0098a0001c0001t0005g0107a0001c0001t0005g0267 | 3 | NA19065.hp2 NA19080.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-34-13327G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142627488 | ||||||
| chr5:142627561
|
C | A | 7 | a0001c0001t0004g0277a0001c0001t0004g0307a0001c0001t0005g0152others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-13400G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142627561 | ||||||
| chr5:142627896
|
A | G | 7 | a0001c0001t0004g0277a0001c0001t0009g0129a0001c0001t0012g0071others(4): Show | 7 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-13735T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142627896 | ||||||
| chr5:142627946
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-34-13785G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142627946 | ||||||
| chr5:142628027
|
G | A | 2 | a0001c0001t0004g0314a0001c0001t0006g0323 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-34-13866C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628027 | ||||||
| chr5:142628237
|
G | A | 30 | a0001c0001t0001g0026a0001c0001t0001g0191a0001c0001t0001g0228others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34-14076C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628237 | ||||||
| chr5:142628304
|
T | G | 7 | a0001c0001t0004g0060a0001c0001t0004g0128a0001c0001t0004g0308others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-14143A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628304 | ||||||
| chr5:142628327
|
G | C | 67 | a0001c0001t0001g0077a0001c0001t0001g0102a0001c0001t0001g0108others(64): Show | 67 | HG00408.hp2 HG00733.hp2 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.-34-14166C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628327 | ||||||
| chr5:142628360
|
A | T | 8 | a0001c0001t0004g0060a0001c0001t0004g0128a0001c0001t0004g0308others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-14199T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628360 | ||||||
| chr5:142628458
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-34-14297G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628458 | ||||||
| chr5:142628524
|
A | G | 7 | a0001c0001t0004g0060a0001c0001t0004g0128a0001c0001t0004g0308others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-14363T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628524 | ||||||
| chr5:142628544
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-34-14383T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628544 | ||||||
| chr5:142628681
|
C | T | 1 | a0001c0001t0025g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-34-14520G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628681 | ||||||
| chr5:142628823
|
G | A | 113 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0051others(110): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.-34-14662C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628823 | ||||||
| chr5:142628852
|
G | A | 2 | a0001c0001t0004g0314a0001c0001t0006g0323 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-34-14691C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628852 | ||||||
| chr5:142628895
|
A | G | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-14734T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628895 | ||||||
| chr5:142628916
|
G | C | 1 | a0001c0001t0001g0003 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-34-14755C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628916 | ||||||
| chr5:142628948
|
C | T | 5 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0311others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-14787G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628948 | ||||||
| chr5:142628960
|
T | C | 151 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0051others(148): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-34-14799A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628960 | ||||||
| chr5:142628993
|
G | C | 2 | a0001c0001t0023g0024a0001c0001t0031g0023 | 2 | NA18972.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-34-14832C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142628993 | ||||||
| chr5:142629092
|
C | A | 71 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0102others(68): Show | 71 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-34-14931G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629092 | ||||||
| chr5:142629313
|
G | C | 27 | a0001c0001t0001g0077a0001c0001t0001g0102a0001c0001t0001g0108others(24): Show | 27 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-34-15152C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629313 | ||||||
| chr5:142629360
|
C | T | 25 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0252others(22): Show | 25 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-34-15199G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629360 | ||||||
| chr5:142629379
|
G | C | 36 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0191others(33): Show | 36 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-34-15218C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629379 | ||||||
| chr5:142629414
|
C | T | 222 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0039others(219): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-34-15253G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629414 | ||||||
| chr5:142629482
|
A | C | 144 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0051others(141): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-34-15321T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629482 | ||||||
| chr5:142629628
|
T | A | 143 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0051others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-34-15467A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629628 | ||||||
| chr5:142629738
|
A | G | 16 | a0001c0001t0001g0026a0001c0001t0001g0228a0001c0001t0001g0290others(13): Show | 16 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.-34-15577T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629738 | ||||||
| chr5:142629745
|
C | G | 3 | a0001c0001t0004g0314a0001c0001t0006g0055a0001c0001t0006g0323 | 3 | HG02809.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-34-15584G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629745 | ||||||
| chr5:142629754
|
T | C | 145 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0051others(142): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-34-15593A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629754 | ||||||
| chr5:142629755
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-34-15594G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629755 | ||||||
| chr5:142629877
|
T | TTA | 77 | a0001c0001t0001g0026a0001c0001t0001g0077a0001c0001t0001g0102others(74): Show | 77 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.-34-15718_-34-1571 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629877 | ||||||
| chr5:142629877
|
T | TTATA | 5 | a0001c0001t0004g0287a0001c0001t0004g0292a0001c0001t0014g0183others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-15720_-34-1571 others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629877 | ||||||
| chr5:142629878
|
T | A | 12 | a0001c0001t0001g0039a0001c0001t0001g0266a0001c0001t0001g0325others(9): Show | 12 | HG00741.hp1 HG01099.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-15717A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629878 | ||||||
| chr5:142629879
|
A | T | 2 | a0001c0001t0005g0152a0001c0001t0005g0153 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-34-15718T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629879 | ||||||
| chr5:142629892
|
TA | T | 3 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0004g0036 | 3 | HG01243.hp1 HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-34-15732delT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629892 | ||||||
| chr5:142629893
|
A | ATT | 14 | a0001c0001t0001g0285a0001c0001t0002g0154a0001c0001t0002g0200others(11): Show | 15 | HG01069.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-34-15733_-34-1573 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629893 | ||||||
| chr5:142629894
|
TA | T | 22 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0252others(19): Show | 22 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-34-15734delT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629894 | ||||||
| chr5:142629895
|
A | ATAT | 10 | a0001c0001t0001g0113a0001c0001t0001g0155a0001c0001t0003g0034others(7): Show | 10 | HG00423.hp1 HG00621.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34-15735_-34-1573 others(7): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629895 | ||||||
| chr5:142629895
|
A | ATT | 31 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0083others(28): Show | 31 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-34-15736_-34-1573 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629895 | ||||||
| chr5:142629895
|
A | T | 25 | a0001c0001t0001g0158a0001c0001t0001g0285a0001c0001t0002g0154others(22): Show | 26 | HG00741.hp2 HG01069.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.-34-15734T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629895 | ||||||
| chr5:142629895
|
AT | A | 29 | a0001c0001t0002g0236a0001c0001t0003g0260a0001c0001t0003g0300others(26): Show | 29 | HG00733.hp2 HG01070.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-34-15735delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629895 | ||||||
| chr5:142629896
|
T | TA | 6 | a0001c0001t0001g0190a0001c0001t0001g0317a0001c0001t0005g0133others(3): Show | 6 | HG00738.hp1 HG02074.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-15736_-34-1573 others(5): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629896 | ||||||
| chr5:142629897
|
T | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0039others(84): Show | 87 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-34-15736A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629897 | ||||||
| chr5:142629898
|
T | A | 7 | a0001c0001t0004g0139a0001c0001t0004g0264a0001c0001t0004g0320others(4): Show | 7 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-15737A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629898 | ||||||
| chr5:142629899
|
T | A | 6 | a0001c0001t0001g0269a0001c0001t0004g0314a0001c0001t0006g0063others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-15738A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629899 | ||||||
| chr5:142629917
|
A | G | 146 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0051others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-34-15756T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142629917 | ||||||
| chr5:142630274
|
GTTAGCTG others(14): Show |
G | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-16134_-34-1611 others(25): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630274 | ||||||
| chr5:142630297
|
G | T | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-16136C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630297 | ||||||
| chr5:142630366
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-34-16205A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630366 | ||||||
| chr5:142630551
|
C | G | 2 | a0001c0001t0013g0061a0001c0001t0013g0171 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-34-16390G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630551 | ||||||
| chr5:142630578
|
C | A | 36 | a0001c0001t0001g0026a0001c0001t0001g0191a0001c0001t0001g0228others(33): Show | 36 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-34-16417G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630578 | ||||||
| chr5:142630667
|
A | G | 4 | a0001c0001t0004g0287a0001c0001t0004g0292a0001c0001t0015g0130others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-16506T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630667 | ||||||
| chr5:142630680
|
T | C | 1 | a0001c0001t0006g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-34-16519A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630680 | ||||||
| chr5:142630815
|
G | A | 224 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0039others(221): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.-34-16654C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630815 | ||||||
| chr5:142630920
|
G | A | 12 | a0001c0001t0001g0037a0001c0001t0001g0172a0001c0001t0001g0178others(9): Show | 12 | HG01496.hp2 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-16759C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630920 | ||||||
| chr5:142630982
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-16821T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142630982 | ||||||
| chr5:142631017
|
G | A | 5 | a0001c0001t0002g0097a0001c0001t0005g0232a0001c0001t0007g0120others(2): Show | 5 | NA18947.hp1 NA18954.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-16856C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631017 | ||||||
| chr5:142631029
|
A | G | 1 | a0001c0001t0009g0035 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-34-16868T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631029 | ||||||
| chr5:142631165
|
G | C | 1 | a0001c0001t0012g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-34-17004C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631165 | ||||||
| chr5:142631205
|
C | G | 11 | a0001c0001t0001g0020a0001c0001t0001g0124a0001c0001t0001g0158others(8): Show | 11 | HG00558.hp2 HG00621.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34-17044G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631205 | ||||||
| chr5:142631499
|
G | A | 7 | a0001c0001t0004g0060a0001c0001t0004g0128a0001c0001t0004g0308others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-17338C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631499 | ||||||
| chr5:142631779
|
C | CT | 36 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0078others(33): Show | 36 | HG00408.hp1 HG01516.hp1 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.-34-17619dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631779 | ||||||
| chr5:142631779
|
CT | C | 99 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0075others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-34-17619delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631779 | ||||||
| chr5:142631779
|
CTT | C | 76 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0083others(73): Show | 77 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.-34-17620_-34-1761 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631779 | ||||||
| chr5:142631779
|
CTTT | C | 23 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0001g0126others(20): Show | 23 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34-17621_-34-1761 others(7): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631779 | ||||||
| chr5:142631878
|
G | A | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-17717C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142631878 | ||||||
| chr5:142632027
|
C | T | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-17866G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632027 | ||||||
| chr5:142632061
|
A | G | 10 | a0001c0001t0002g0154a0001c0001t0002g0302a0001c0001t0003g0038others(7): Show | 10 | HG01069.hp2 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-17900T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632061 | ||||||
| chr5:142632388
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34-18227G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632388 | ||||||
| chr5:142632396
|
A | G | 1 | a0001c0001t0003g0199 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-34-18235T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632396 | ||||||
| chr5:142632405
|
A | G | 6 | a0001c0001t0002g0097a0001c0001t0005g0232a0001c0001t0007g0116others(3): Show | 6 | NA18947.hp1 NA18954.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-18244T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632405 | ||||||
| chr5:142632483
|
A | G | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-18322T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632483 | ||||||
| chr5:142632795
|
C | G | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-18634G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632795 | ||||||
| chr5:142632922
|
CT | C | 172 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0039others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-34-18762delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632922 | ||||||
| chr5:142632929
|
T | C | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-18768A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142632929 | ||||||
| chr5:142633065
|
G | A | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-18904C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142633065 | ||||||
| chr5:142633112
|
G | T | 1 | a0001c0001t0005g0245 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-34-18951C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142633112 | ||||||
| chr5:142633657
|
A | C | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-19496T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142633657 | ||||||
| chr5:142633684
|
T | C | 1 | a0001c0001t0026g0114 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-34-19523A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142633684 | ||||||
| chr5:142633837
|
G | T | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-19676C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142633837 | ||||||
| chr5:142633838
|
T | G | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-19677A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142633838 | ||||||
| chr5:142633889
|
T | C | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-19728A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142633889 | ||||||
| chr5:142633955
|
C | T | 5 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0311others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-19794G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142633955 | ||||||
| chr5:142634000
|
C | T | 6 | a0001c0001t0001g0266a0001c0001t0001g0325a0001c0001t0002g0170others(3): Show | 6 | HG00741.hp1 HG01099.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-19839G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634000 | ||||||
| chr5:142634028
|
C | CA | 111 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0047others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-34-19868_-34-1986 others(5): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634028 | ||||||
| chr5:142634028
|
C | CAA | 12 | a0001c0001t0001g0072a0001c0001t0001g0146a0001c0001t0004g0060others(9): Show | 12 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-19868_-34-1986 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634028 | ||||||
| chr5:142634029
|
C | A | 151 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0047others(148): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-34-19868G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634029 | ||||||
| chr5:142634029
|
C | CA | 8 | a0001c0001t0002g0097a0001c0001t0005g0152a0001c0001t0005g0153others(5): Show | 8 | HG02055.hp1 HG02486.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-19869dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634029 | ||||||
| chr5:142634192
|
C | CA | 13 | a0001c0001t0001g0083a0001c0001t0001g0290a0001c0001t0002g0125others(10): Show | 13 | HG00140.hp2 HG01123.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-34-20032dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634192 | ||||||
| chr5:142634193
|
AAG | A | 51 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0252others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-34-20034_-34-2003 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634193 | ||||||
| chr5:142634194
|
AG | A | 41 | a0001c0001t0001g0072a0001c0001t0001g0102a0001c0001t0001g0108others(38): Show | 41 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.-34-20034delC | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634194 | ||||||
| chr5:142634195
|
G | A | 127 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0047others(124): Show | 128 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.-34-20034C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634195 | ||||||
| chr5:142634195
|
G | GA | 7 | a0001c0001t0001g0158a0001c0001t0001g0251a0001c0001t0002g0015others(4): Show | 7 | NA18939.hp2 NA18950.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-20035dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634195 | ||||||
| chr5:142634220
|
C | G | 12 | a0001c0001t0001g0037a0001c0001t0001g0172a0001c0001t0002g0006others(9): Show | 12 | HG01496.hp2 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34-20059G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634220 | ||||||
| chr5:142634327
|
G | A | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34-20166C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634327 | ||||||
| chr5:142634472
|
G | A | 6 | a0001c0001t0004g0277a0001c0001t0009g0129a0001c0001t0012g0071others(3): Show | 6 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-20311C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634472 | ||||||
| chr5:142634730
|
C | G | 2 | a0001c0001t0004g0314a0001c0001t0006g0323 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-34-20569G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634730 | ||||||
| chr5:142634787
|
G | C | 1 | a0001c0001t0028g0011 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-34-20626C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634787 | ||||||
| chr5:142634875
|
T | C | 4 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0311others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-20714A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634875 | ||||||
| chr5:142634886
|
T | C | 8 | a0001c0001t0001g0039a0001c0001t0001g0266a0001c0001t0001g0325others(5): Show | 8 | HG00741.hp1 HG01099.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-20725A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634886 | ||||||
| chr5:142634972
|
G | T | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-20811C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142634972 | ||||||
| chr5:142635261
|
T | C | 1 | a0001c0001t0003g0029 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-34-21100A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142635261 | ||||||
| chr5:142635313
|
G | C | 4 | a0001c0001t0004g0287a0001c0001t0004g0292a0001c0001t0015g0130others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-21152C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142635313 | ||||||
| chr5:142635465
|
G | C | 1 | a0001c0001t0002g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-34-21304C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142635465 | ||||||
| chr5:142635780
|
T | G | 48 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0191others(45): Show | 48 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.-34-21619A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142635780 | ||||||
| chr5:142635824
|
C | T | 55 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0146others(52): Show | 56 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.-34-21663G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142635824 | ||||||
| chr5:142635992
|
C | T | 5 | a0001c0001t0002g0097a0001c0001t0005g0232a0001c0001t0007g0120others(2): Show | 5 | NA18947.hp1 NA18954.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-21831G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142635992 | ||||||
| chr5:142636037
|
T | A | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-21876A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636037 | ||||||
| chr5:142636069
|
A | G | 15 | a0001c0001t0001g0158a0001c0001t0001g0242a0001c0001t0001g0251others(12): Show | 15 | HG00408.hp1 HG01255.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34-21908T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636069 | ||||||
| chr5:142636127
|
T | A | 21 | a0001c0001t0001g0077a0001c0001t0001g0102a0001c0001t0001g0108others(18): Show | 21 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.-34-21966A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636127 | ||||||
| chr5:142636150
|
G | A | 78 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0102others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.-34-21989C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636150 | ||||||
| chr5:142636315
|
A | T | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-22154T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636315 | ||||||
| chr5:142636329
|
T | C | 1 | a0001c0001t0003g0181 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-34-22168A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636329 | ||||||
| chr5:142636738
|
G | A | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-22577C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636738 | ||||||
| chr5:142636807
|
A | G | 6 | a0001c0001t0002g0097a0001c0001t0005g0232a0001c0001t0007g0116others(3): Show | 6 | NA18947.hp1 NA18954.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-22646T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636807 | ||||||
| chr5:142636898
|
C | T | 2 | a0001c0001t0005g0152a0001c0001t0005g0153 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-34-22737G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636898 | ||||||
| chr5:142636905
|
A | C | 3 | a0001c0001t0004g0314a0001c0001t0006g0055a0001c0001t0006g0323 | 3 | HG02809.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-34-22744T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142636905 | ||||||
| chr5:142637128
|
C | T | 1 | a0001c0001t0005g0107 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-34-22967G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637128 | ||||||
| chr5:142637138
|
C | T | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-22977G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637138 | ||||||
| chr5:142637148
|
G | C | 4 | a0001c0001t0002g0330a0001c0001t0011g0281a0001c0001t0014g0284others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-22987C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637148 | ||||||
| chr5:142637174
|
G | A | 6 | a0001c0001t0001g0266a0001c0001t0001g0325a0001c0001t0002g0170others(3): Show | 6 | HG00741.hp1 HG01099.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-23013C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637174 | ||||||
| chr5:142637257
|
G | C | 2 | a0001c0001t0016g0073a0001c0001t0016g0074 | 2 | HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-34-23096C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637257 | ||||||
| chr5:142637266
|
A | T | 1 | a0001c0001t0002g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-34-23105T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637266 | ||||||
| chr5:142637314
|
C | T | 4 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0311others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-23153G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637314 | ||||||
| chr5:142637324
|
GT | G | 222 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0037others(219): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-34-23164delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637324 | ||||||
| chr5:142637358
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-34-23197G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637358 | ||||||
| chr5:142637359
|
G | A | 56 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0252others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-34-23198C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637359 | ||||||
| chr5:142637383
|
G | A | 6 | a0001c0001t0001g0266a0001c0001t0001g0325a0001c0001t0002g0170others(3): Show | 6 | HG00741.hp1 HG01099.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-23222C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637383 | ||||||
| chr5:142637570
|
C | T | 54 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0146others(51): Show | 55 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.-34-23409G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637570 | ||||||
| chr5:142637652
|
G | A | 46 | a0001c0001t0001g0026a0001c0001t0001g0191a0001c0001t0001g0228others(43): Show | 46 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-34-23491C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637652 | ||||||
| chr5:142637857
|
T | C | 8 | a0001c0001t0001g0072a0001c0001t0004g0060a0001c0001t0004g0128others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-23696A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142637857 | ||||||
| chr5:142638075
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-34-23914G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638075 | ||||||
| chr5:142638171
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-34-24010G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638171 | ||||||
| chr5:142638295
|
C | T | 54 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0146others(51): Show | 55 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.-34-24134G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638295 | ||||||
| chr5:142638464
|
T | G | 8 | a0001c0001t0001g0072a0001c0001t0004g0060a0001c0001t0004g0128others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-24303A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638464 | ||||||
| chr5:142638572
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-34-24411A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638572 | ||||||
| chr5:142638599
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-34-24438C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638599 | ||||||
| chr5:142638696
|
A | G | 26 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0252others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-34-24535T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638696 | ||||||
| chr5:142638744
|
T | C | 139 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0072others(136): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-34-24583A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638744 | ||||||
| chr5:142638803
|
A | G | 20 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0252others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.-34-24642T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638803 | ||||||
| chr5:142638859
|
T | G | 229 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0037others(226): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.-34-24698A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142638859 | ||||||
| chr5:142639085
|
T | C | 8 | a0001c0001t0001g0072a0001c0001t0004g0060a0001c0001t0004g0128others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-24924A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639085 | ||||||
| chr5:142639115
|
T | C | 54 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0146others(51): Show | 55 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.-34-24954A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639115 | ||||||
| chr5:142639213
|
T | G | 12 | a0001c0001t0001g0072a0001c0001t0004g0060a0001c0001t0004g0128others(9): Show | 12 | HG01884.hp1 HG02280.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-34-25052A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639213 | ||||||
| chr5:142639330
|
T | C | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-25169A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639330 | ||||||
| chr5:142639519
|
T | C | 4 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0311others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-25358A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639519 | ||||||
| chr5:142639621
|
G | A | 106 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0083others(103): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-34-25460C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639621 | ||||||
| chr5:142639631
|
G | C | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-34-25470C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639631 | ||||||
| chr5:142639641
|
A | T | 1 | a0001c0001t0027g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-34-25480T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639641 | ||||||
| chr5:142639647
|
C | T | 57 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0252others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.-34-25486G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639647 | ||||||
| chr5:142639671
|
G | A | 5 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0311others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-25510C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639671 | ||||||
| chr5:142639803
|
G | T | 104 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0083others(101): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-34-25642C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142639803 | ||||||
| chr5:142640025
|
T | A | 1 | a0001c0001t0032g0295 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-34-25864A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640025 | ||||||
| chr5:142640031
|
G | A | 88 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0072others(85): Show | 88 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.-34-25870C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640031 | ||||||
| chr5:142640092
|
G | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0075others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.-34-25931C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640092 | ||||||
| chr5:142640384
|
C | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0037others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.-34-26223G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640384 | ||||||
| chr5:142640426
|
T | TG | 43 | a0001c0001t0001g0039a0001c0001t0001g0079a0001c0001t0001g0088others(40): Show | 43 | HG00408.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-34-26266dupC | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640426 | ||||||
| chr5:142640426
|
T | TGG | 48 | a0001c0001t0001g0078a0001c0001t0001g0146a0001c0001t0001g0217others(45): Show | 49 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-34-26267_-34-2626 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640426 | ||||||
| chr5:142640426
|
T | TGGG | 56 | a0001c0001t0001g0026a0001c0001t0001g0051a0001c0001t0001g0083others(53): Show | 56 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-34-26268_-34-2626 others(7): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640426 | ||||||
| chr5:142640427
|
G | C | 2 | a0001c0001t0012g0007a0001c0001t0014g0164 | 2 | HG01934.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-34-26266C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640427 | ||||||
| chr5:142640432
|
G | T | 2 | a0001c0001t0004g0287a0001c0001t0004g0292 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-34-26271C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640432 | ||||||
| chr5:142640493
|
T | C | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-26332A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640493 | ||||||
| chr5:142640586
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-34-26425G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640586 | ||||||
| chr5:142640815
|
C | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0037others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-34-26654G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640815 | ||||||
| chr5:142640873
|
A | G | 57 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0146others(54): Show | 58 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-34-26712T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640873 | ||||||
| chr5:142640943
|
T | G | 111 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0047others(108): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-34-26782A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640943 | ||||||
| chr5:142640950
|
T | C | 4 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0311others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-26789A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142640950 | ||||||
| chr5:142641035
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0124 | 2 | NA18987.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-34-26874T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142641035 | ||||||
| chr5:142641253
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0172a0001c0001t0001g0178 | 3 | HG03098.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-34-27092A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142641253 | ||||||
| chr5:142641559
|
T | G | 1 | a0001c0001t0005g0184 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-34-27398A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142641559 | ||||||
| chr5:142641808
|
A | G | 1 | a0001c0001t0015g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34-27647T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142641808 | ||||||
| chr5:142641812
|
G | A | 21 | a0001c0001t0001g0075a0001c0001t0001g0157a0001c0001t0001g0252others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-34-27651C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142641812 | ||||||
| chr5:142641899
|
C | T | 4 | a0001c0001t0004g0277a0001c0001t0012g0071a0001c0001t0012g0311others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-27738G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142641899 | ||||||
| chr5:142641943
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-34-27782A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142641943 | ||||||
| chr5:142641956
|
T | G | 6 | a0001c0001t0002g0097a0001c0001t0005g0232a0001c0001t0007g0116others(3): Show | 6 | NA18947.hp1 NA18954.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-27795A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142641956 | ||||||
| chr5:142642021
|
T | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0077others(45): Show | 48 | HG00408.hp2 HG01168.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.-34-27860A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142642021 | ||||||
| chr5:142642022
|
A | G | 2 | a0001c0001t0011g0263a0001c0001t0014g0161 | 2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-34-27861T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142642022 | ||||||
| chr5:142642182
|
G | C | 3 | a0001c0001t0004g0314a0001c0001t0006g0055a0001c0001t0006g0323 | 3 | HG02809.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-34-28021C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142642182 | ||||||
| chr5:142642537
|
G | C | 1 | a0001c0001t0003g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-34-28376C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142642537 | ||||||
| chr5:142642683
|
G | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0077others(45): Show | 48 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-34-28522C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142642683 | ||||||
| chr5:142642736
|
A | C | 19 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0157others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.-34-28575T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142642736 | ||||||
| chr5:142642958
|
C | G | 1 | a0001c0001t0024g0117 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-34-28797G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142642958 | ||||||
| chr5:142642979
|
G | T | 7 | a0001c0001t0002g0330a0001c0001t0004g0036a0001c0001t0005g0152others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-28818C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142642979 | ||||||
| chr5:142643143
|
G | A | 1 | a0001c0001t0002g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-34-28982C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643143 | ||||||
| chr5:142643212
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0066others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34-29051C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643212 | ||||||
| chr5:142643246
|
A | G | 1 | a0001c0001t0002g0302 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-34-29085T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643246 | ||||||
| chr5:142643296
|
TAC | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0066others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.-34-29137_-34-2913 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643296 | ||||||
| chr5:142643564
|
T | C | 1 | a0001c0001t0004g0062 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-34-29403A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643564 | ||||||
| chr5:142643664
|
A | C | 13 | a0001c0001t0001g0072a0001c0001t0004g0060a0001c0001t0004g0307others(10): Show | 13 | HG01884.hp1 HG02280.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-34-29503T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643664 | ||||||
| chr5:142643723
|
C | G | 1 | a0001c0001t0013g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-34-29562G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643723 | ||||||
| chr5:142643880
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-34-29719A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643880 | ||||||
| chr5:142643978
|
C | T | 1 | a0001c0001t0004g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34-29817G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142643978 | ||||||
| chr5:142644013
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-34-29852G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142644013 | ||||||
| chr5:142644122
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-34-29961G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142644122 | ||||||
| chr5:142644197
|
A | C | 1 | a0001c0001t0004g0186 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-34-30036T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142644197 | ||||||
| chr5:142644261
|
C | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0207a0001c0001t0001g0221others(17): Show | 20 | HG00741.hp1 HG01099.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-34-30100G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142644261 | ||||||
| chr5:142644370
|
G | A | 1 | a0001c0001t0046g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-34-30209C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142644370 | ||||||
| chr5:142644464
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0008g0099 | 2 | NA19002.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-34-30303G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142644464 | ||||||
| chr5:142644530
|
G | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0075others(51): Show | 54 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-34-30369C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142644530 | ||||||
| chr5:142644691
|
T | C | 122 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0051others(119): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-34-30530A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142644691 | ||||||
| chr5:142645093
|
T | TA | 195 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0037others(192): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.-34-30933dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645093 | ||||||
| chr5:142645220
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-34-31059A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645220 | ||||||
| chr5:142645230
|
C | T | 3 | a0001c0001t0002g0335a0001c0001t0002g0336a0001c0001t0002g0337 | 3 | HG01123.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-34-31069G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645230 | ||||||
| chr5:142645457
|
A | G | 24 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0157others(21): Show | 25 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.-34-31296T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645457 | ||||||
| chr5:142645899
|
T | G | 2 | a0001c0001t0006g0272a0001c0001t0006g0327 | 2 | HG01167.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-34-31738A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645899 | ||||||
| chr5:142645926
|
T | G | 2 | a0001c0001t0006g0272a0001c0001t0006g0327 | 2 | HG01167.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-34-31765A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645926 | ||||||
| chr5:142645944
|
T | C | 6 | a0001c0001t0004g0060a0001c0001t0009g0315a0001c0001t0012g0007others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-31783A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645944 | ||||||
| chr5:142645948
|
G | A | 30 | a0001c0001t0001g0078a0001c0001t0001g0088a0001c0001t0001g0126others(27): Show | 30 | HG00280.hp2 HG00408.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34-31787C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645948 | ||||||
| chr5:142645985
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0002g0185a0001c0001t0003g0193others(1): Show | 4 | NA18947.hp2 NA18956.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-31824A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142645985 | ||||||
| chr5:142646003
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-34-31842G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646003 | ||||||
| chr5:142646145
|
G | A | 7 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(4): Show | 7 | HG00642.hp1 HG00733.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-31984C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646145 | ||||||
| chr5:142646180
|
A | G | 7 | a0001c0001t0001g0178a0001c0001t0004g0036a0001c0001t0004g0060others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-32019T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646180 | ||||||
| chr5:142646189
|
G | A | 142 | a0001c0001t0001g0020a0001c0001t0001g0066a0001c0001t0001g0075others(139): Show | 143 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-34-32028C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646189 | ||||||
| chr5:142646205
|
G | A | 2 | a0001c0001t0002g0330a0001c0001t0036g0163 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-34-32044C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646205 | ||||||
| chr5:142646208
|
C | CT | 71 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0066others(68): Show | 71 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-34-32048dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646208 | ||||||
| chr5:142646208
|
C | CTT | 49 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0158others(46): Show | 50 | HG00280.hp1 HG00544.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.-34-32049_-34-3204 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646208 | ||||||
| chr5:142646208
|
C | CTTT | 46 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0001t0001g0078others(43): Show | 46 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-34-32050_-34-3204 others(7): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646208 | ||||||
| chr5:142646208
|
C | CTTTT | 30 | a0001c0001t0001g0088a0001c0001t0001g0126a0001c0001t0001g0157others(27): Show | 31 | HG00280.hp2 HG00642.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.-34-32051_-34-3204 others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646208 | ||||||
| chr5:142646208
|
C | CTTTTT | 10 | a0001c0001t0001g0254a0001c0001t0001g0317a0001c0001t0002g0115others(7): Show | 10 | HG00738.hp1 HG00738.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-32052_-34-3204 others(9): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646208 | ||||||
| chr5:142646208
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0325a0001c0001t0006g0323a0001c0001t0037g0008 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-32058_-34-3204 others(15): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646208 | ||||||
| chr5:142646208
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0330a0001c0001t0036g0163 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-34-32059_-34-3204 others(16): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646208 | ||||||
| chr5:142646302
|
T | C | 1 | a0001c0001t0006g0299 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-34-32141A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646302 | ||||||
| chr5:142646347
|
C | T | 15 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0002g0330others(12): Show | 16 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34-32186G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646347 | ||||||
| chr5:142646349
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0027g0162 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-34-32188C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646349 | ||||||
| chr5:142646372
|
G | T | 3 | a0001c0001t0001g0325a0001c0001t0006g0323a0001c0001t0037g0008 | 3 | HG02145.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-34-32211C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646372 | ||||||
| chr5:142646414
|
G | A | 1 | a0001c0001t0014g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-34-32253C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646414 | ||||||
| chr5:142646444
|
C | G | 9 | a0001c0001t0001g0172a0001c0001t0002g0084a0001c0001t0004g0104others(6): Show | 9 | HG01934.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34-32283G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646444 | ||||||
| chr5:142646484
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-34-32323G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646484 | ||||||
| chr5:142646567
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0009g0142 | 2 | NA18612.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-34-32406T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646567 | ||||||
| chr5:142646597
|
C | T | 10 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0002g0084others(7): Show | 10 | HG01934.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34-32436G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646597 | ||||||
| chr5:142646709
|
G | A | 1 | a0001c0001t0014g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-34-32548C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646709 | ||||||
| chr5:142646728
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-34-32567C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646728 | ||||||
| chr5:142646770
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-34-32609C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646770 | ||||||
| chr5:142646780
|
C | G | 1 | a0001c0001t0007g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-34-32619G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646780 | ||||||
| chr5:142646790
|
C | A | 1 | a0001c0001t0008g0090 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-34-32629G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646790 | ||||||
| chr5:142646936
|
A | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0217a0001c0001t0001g0309others(7): Show | 10 | HG01891.hp2 HG02273.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-32775T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646936 | ||||||
| chr5:142646983
|
A | T | 1 | a0001c0001t0002g0042 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-34-32822T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142646983 | ||||||
| chr5:142647010
|
C | A | 9 | a0001c0001t0001g0325a0001c0001t0003g0182a0001c0001t0004g0308others(6): Show | 9 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-32849G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647010 | ||||||
| chr5:142647076
|
G | C | 3 | a0001c0001t0010g0324a0001c0001t0016g0073a0001c0001t0016g0074 | 3 | HG01175.hp1 HG01192.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-34-32915C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647076 | ||||||
| chr5:142647090
|
G | A | 1 | a0001c0001t0010g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-34-32929C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647090 | ||||||
| chr5:142647270
|
A | G | 3 | a0001c0001t0004g0128a0001c0001t0009g0129a0001c0001t0015g0130 | 3 | HG02615.hp1 HG02896.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-34-33109T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647270 | ||||||
| chr5:142647320
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-34-33159A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647320 | ||||||
| chr5:142647399
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(120): Show | 124 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-34-33238C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647399 | ||||||
| chr5:142647431
|
G | A | 1 | a0001c0001t0003g0313 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-34-33270C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647431 | ||||||
| chr5:142647551
|
G | T | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-34-33390C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647551 | ||||||
| chr5:142647559
|
T | G | 1 | a0001c0001t0002g0125 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-34-33398A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647559 | ||||||
| chr5:142647571
|
C | T | 1 | a0001c0001t0013g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-34-33410G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647571 | ||||||
| chr5:142647603
|
T | C | 1 | a0001c0001t0004g0009 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-34-33442A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647603 | ||||||
| chr5:142647685
|
T | A | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-34-33524A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647685 | ||||||
| chr5:142647958
|
A | G | 185 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-34-33797T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647958 | ||||||
| chr5:142647982
|
G | A | 1 | a0001c0001t0005g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-34-33821C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647982 | ||||||
| chr5:142647988
|
A | G | 100 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(97): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-34-33827T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142647988 | ||||||
| chr5:142648039
|
C | T | 1 | a0001c0001t0006g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34-33878G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648039 | ||||||
| chr5:142648189
|
C | T | 8 | a0001c0001t0003g0260a0001c0001t0003g0301a0001c0001t0004g0264others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34-34028G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648189 | ||||||
| chr5:142648282
|
TA | T | 83 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0037others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-34-34122delT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648282 | ||||||
| chr5:142648478
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-34-34317T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648478 | ||||||
| chr5:142648506
|
G | A | 5 | a0001c0001t0001g0325a0001c0001t0002g0160a0001c0001t0006g0323others(2): Show | 5 | HG01496.hp2 HG03579.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-34345C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648506 | ||||||
| chr5:142648530
|
A | ATAGCAT | 10 | a0001c0001t0001g0172a0001c0001t0004g0128a0001c0001t0004g0131others(7): Show | 10 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34-34375_-34-3437 others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648530 | ||||||
| chr5:142648689
|
C | CA | 96 | a0001c0001t0001g0086a0001c0001t0001g0108a0001c0001t0001g0126others(93): Show | 97 | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.-34-34529dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648689 | ||||||
| chr5:142648689
|
C | CAA | 41 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(38): Show | 41 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-34-34530_-34-3452 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648689 | ||||||
| chr5:142648689
|
CA | C | 27 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(24): Show | 27 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.-34-34529delT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648689 | ||||||
| chr5:142648689
|
CAA | C | 9 | a0001c0001t0001g0285a0001c0001t0002g0006a0001c0001t0004g0060others(6): Show | 9 | HG02148.hp2 HG02572.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34-34530_-34-3452 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648689 | ||||||
| chr5:142648720
|
G | C | 1 | a0001c0001t0005g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-34-34559C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648720 | ||||||
| chr5:142648868
|
C | T | 19 | a0001c0001t0001g0172a0001c0001t0002g0006a0001c0001t0004g0060others(16): Show | 19 | HG01934.hp1 HG02572.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.-34-34707G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648868 | ||||||
| chr5:142648965
|
C | T | 3 | a0001c0001t0002g0185a0001c0001t0003g0094a0001c0001t0004g0186 | 3 | NA18939.hp1 NA18947.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-34-34804G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648965 | ||||||
| chr5:142648968
|
C | T | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-34-34807G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142648968 | ||||||
| chr5:142649154
|
C | T | 19 | a0001c0001t0001g0172a0001c0001t0002g0006a0001c0001t0004g0060others(16): Show | 19 | HG01934.hp1 HG02572.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.-34-34993G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649154 | ||||||
| chr5:142649179
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-34-35018T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649179 | ||||||
| chr5:142649318
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-34-35157T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649318 | ||||||
| chr5:142649412
|
GT | G | 73 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0066others(70): Show | 73 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-34-35252delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649412 | ||||||
| chr5:142649430
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-34-35269C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649430 | ||||||
| chr5:142649453
|
C | A | 2 | a0001c0001t0006g0063a0001c0001t0009g0262 | 2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-34-35292G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649453 | ||||||
| chr5:142649468
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-34-35307C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649468 | ||||||
| chr5:142649628
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-34-35467G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649628 | ||||||
| chr5:142649639
|
C | A | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-34-35478G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649639 | ||||||
| chr5:142649650
|
G | A | 13 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(10): Show | 14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.-34-35489C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649650 | ||||||
| chr5:142649702
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-34-35541G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649702 | ||||||
| chr5:142649789
|
G | A | 75 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0066others(72): Show | 75 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.-34-35628C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649789 | ||||||
| chr5:142649824
|
C | T | 1 | a0001c0001t0010g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-34-35663G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649824 | ||||||
| chr5:142649935
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0002g0018 | 2 | NA18989.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-34-35774T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649935 | ||||||
| chr5:142649938
|
A | G | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-34-35777T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142649938 | ||||||
| chr5:142650170
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+35787C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650170 | ||||||
| chr5:142650171
|
T | C | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+35786A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650171 | ||||||
| chr5:142650182
|
C | T | 12 | a0001c0001t0001g0108a0001c0001t0001g0266a0001c0001t0001g0269others(9): Show | 12 | HG00741.hp1 HG02165.hp1 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+35775G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650182 | ||||||
| chr5:142650185
|
G | T | 19 | a0001c0001t0001g0172a0001c0001t0002g0006a0001c0001t0004g0060others(16): Show | 19 | HG01934.hp1 HG02572.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.-35+35772C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650185 | ||||||
| chr5:142650303
|
T | C | 1 | a0001c0001t0040g0283 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-35+35654A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650303 | ||||||
| chr5:142650393
|
C | A | 1 | a0001c0001t0003g0257 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-35+35564G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650393 | ||||||
| chr5:142650582
|
G | A | 1 | a0001c0001t0011g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-35+35375C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650582 | ||||||
| chr5:142650648
|
C | G | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-35+35309G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650648 | ||||||
| chr5:142650650
|
C | G | 8 | a0001c0001t0001g0187a0001c0001t0001g0325a0001c0001t0002g0185others(5): Show | 8 | HG03579.hp1 NA18939.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+35307G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650650 | ||||||
| chr5:142650650
|
C | T | 66 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(63): Show | 66 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-35+35307G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650650 | ||||||
| chr5:142650668
|
G | A | 77 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(74): Show | 77 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.-35+35289C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650668 | ||||||
| chr5:142650673
|
T | TAC | 3 | a0001c0001t0002g0031a0001c0001t0023g0024a0001c0001t0031g0023 | 3 | NA18972.hp1 NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-35+35283_-35+3528 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650673 | ||||||
| chr5:142650675
|
T | C | 50 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(47): Show | 50 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-35+35282A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650675 | ||||||
| chr5:142650675
|
T | TAC | 12 | a0001c0001t0001g0172a0001c0001t0003g0260a0001c0001t0003g0301others(9): Show | 12 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+35280_-35+3528 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650675 | ||||||
| chr5:142650730
|
T | C | 1 | a0001c0001t0003g0053 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-35+35227A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650730 | ||||||
| chr5:142650776
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-35+35181G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650776 | ||||||
| chr5:142650777
|
G | A | 49 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-35+35180C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650777 | ||||||
| chr5:142650972
|
G | A | 3 | a0001c0001t0005g0135a0001c0001t0017g0259a0001c0001t0044g0210 | 3 | HG02040.hp1 HG02132.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-35+34985C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142650972 | ||||||
| chr5:142651033
|
C | T | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+34924G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651033 | ||||||
| chr5:142651043
|
A | G | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+34914T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651043 | ||||||
| chr5:142651262
|
T | C | 84 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-35+34695A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651262 | ||||||
| chr5:142651387
|
G | A | 1 | a0001c0001t0013g0316 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-35+34570C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651387 | ||||||
| chr5:142651403
|
G | A | 32 | a0001c0001t0001g0108a0001c0001t0001g0266a0001c0001t0001g0269others(29): Show | 32 | HG00099.hp2 HG00741.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.-35+34554C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651403 | ||||||
| chr5:142651616
|
T | C | 6 | a0001c0001t0001g0290a0001c0001t0003g0029a0001c0001t0003g0298others(3): Show | 6 | HG00408.hp2 HG00621.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+34341A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651616 | ||||||
| chr5:142651728
|
T | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0289 | 2 | NA18974.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-35+34229A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651728 | ||||||
| chr5:142651787
|
C | A | 40 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(37): Show | 40 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-35+34170G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651787 | ||||||
| chr5:142651829
|
AT | A | 82 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(79): Show | 83 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-35+34127delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651829 | ||||||
| chr5:142651829
|
ATT | A | 10 | a0001c0001t0001g0187a0001c0001t0001g0325a0001c0001t0002g0185others(7): Show | 10 | HG02818.hp1 HG03579.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35+34126_-35+3412 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651829 | ||||||
| chr5:142651850
|
G | T | 40 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(37): Show | 40 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-35+34107C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651850 | ||||||
| chr5:142651866
|
T | C | 6 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0031others(3): Show | 6 | NA18960.hp2 NA18962.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+34091A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651866 | ||||||
| chr5:142651947
|
G | A | 12 | a0001c0001t0001g0172a0001c0001t0003g0260a0001c0001t0003g0301others(9): Show | 12 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+34010C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651947 | ||||||
| chr5:142651954
|
C | T | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+34003G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142651954 | ||||||
| chr5:142652045
|
T | C | 4 | a0001c0001t0001g0072a0001c0001t0016g0073a0001c0001t0016g0074others(1): Show | 4 | HG01175.hp1 HG01192.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+33912A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652045 | ||||||
| chr5:142652186
|
T | G | 84 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-35+33771A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652186 | ||||||
| chr5:142652196
|
T | A | 1 | a0001c0001t0007g0332 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-35+33761A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652196 | ||||||
| chr5:142652324
|
T | C | 1 | a0001c0001t0012g0282 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-35+33633A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652324 | ||||||
| chr5:142652354
|
T | C | 8 | a0001c0001t0001g0187a0001c0001t0001g0325a0001c0001t0002g0185others(5): Show | 8 | HG03579.hp1 NA18939.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+33603A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652354 | ||||||
| chr5:142652709
|
T | G | 84 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(81): Show | 84 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-35+33248A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652709 | ||||||
| chr5:142652719
|
G | A | 1 | a0001c0001t0036g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-35+33238C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652719 | ||||||
| chr5:142652757
|
G | A | 1 | a0001c0001t0006g0209 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-35+33200C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652757 | ||||||
| chr5:142652785
|
G | A | 10 | a0001c0001t0001g0086a0001c0001t0001g0126a0001c0001t0002g0109others(7): Show | 10 | HG00544.hp1 HG01109.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35+33172C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652785 | ||||||
| chr5:142652915
|
T | G | 81 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.-35+33042A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652915 | ||||||
| chr5:142652953
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+33004A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142652953 | ||||||
| chr5:142653291
|
C | G | 2 | a0001c0001t0001g0217a0001c0001t0003g0216 | 2 | NA19055.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-35+32666G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653291 | ||||||
| chr5:142653398
|
T | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(36): Show | 39 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.-35+32559A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653398 | ||||||
| chr5:142653451
|
C | T | 1 | a0001c0001t0007g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-35+32506G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653451 | ||||||
| chr5:142653498
|
G | A | 1 | a0001c0001t0002g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-35+32459C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653498 | ||||||
| chr5:142653531
|
G | A | 49 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-35+32426C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653531 | ||||||
| chr5:142653535
|
C | T | 1 | a0001c0001t0002g0196 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-35+32422G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653535 | ||||||
| chr5:142653617
|
C | T | 1 | a0001c0001t0004g0334 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-35+32340G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653617 | ||||||
| chr5:142653708
|
C | T | 3 | a0001c0001t0004g0277a0001c0001t0012g0002a0001c0001t0012g0311 | 4 | HG01069.hp1 HG01071.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+32249G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653708 | ||||||
| chr5:142653722
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+32235C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653722 | ||||||
| chr5:142653743
|
T | G | 333 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(330): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-35+32214A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653743 | ||||||
| chr5:142653761
|
T | C | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-35+32196A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653761 | ||||||
| chr5:142653814
|
C | T | 2 | a0001c0001t0010g0276a0001c0001t0012g0282 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-35+32143G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653814 | ||||||
| chr5:142653908
|
A | G | 6 | a0001c0001t0002g0330a0001c0001t0006g0272a0001c0001t0006g0327others(3): Show | 6 | HG01167.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+32049T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142653908 | ||||||
| chr5:142654013
|
A | G | 10 | a0001c0001t0001g0172a0001c0001t0004g0128a0001c0001t0004g0131others(7): Show | 10 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35+31944T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654013 | ||||||
| chr5:142654027
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-35+31930C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654027 | ||||||
| chr5:142654130
|
T | G | 193 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-35+31827A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654130 | ||||||
| chr5:142654322
|
T | A | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+31635A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654322 | ||||||
| chr5:142654422
|
G | A | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+31535C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654422 | ||||||
| chr5:142654424
|
A | G | 2 | a0001c0001t0002g0006a0001c0001t0027g0162 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-35+31533T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654424 | ||||||
| chr5:142654438
|
C | A | 8 | a0001c0001t0002g0006a0001c0001t0004g0060a0001c0001t0006g0055others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-35+31519G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654438 | ||||||
| chr5:142654542
|
G | A | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+31415C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654542 | ||||||
| chr5:142654675
|
G | A | 8 | a0001c0001t0004g0128a0001c0001t0004g0131a0001c0001t0006g0176others(5): Show | 8 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+31282C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654675 | ||||||
| chr5:142654730
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0003g0080a0001c0001t0011g0081others(1): Show | 4 | HG00639.hp2 HG00735.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+31227G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654730 | ||||||
| chr5:142654754
|
T | C | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+31203A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654754 | ||||||
| chr5:142654759
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0038g0255 | 2 | HG02523.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-35+31198A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654759 | ||||||
| chr5:142654795
|
C | A | 1 | a0001c0001t0006g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-35+31162G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654795 | ||||||
| chr5:142654822
|
A | T | 19 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0004g0009others(16): Show | 19 | HG01934.hp1 HG02145.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-35+31135T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654822 | ||||||
| chr5:142654973
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0014g0183 | 2 | HG02683.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-35+30984G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142654973 | ||||||
| chr5:142655164
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+30793C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655164 | ||||||
| chr5:142655323
|
G | A | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+30634C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655323 | ||||||
| chr5:142655371
|
T | C | 6 | a0001c0001t0002g0330a0001c0001t0006g0272a0001c0001t0006g0327others(3): Show | 6 | HG01167.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+30586A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655371 | ||||||
| chr5:142655478
|
C | T | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+30479G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655478 | ||||||
| chr5:142655542
|
C | T | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+30415G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655542 | ||||||
| chr5:142655724
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-35+30233C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655724 | ||||||
| chr5:142655768
|
T | C | 1 | a0001c0001t0006g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-35+30189A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655768 | ||||||
| chr5:142655790
|
G | C | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+30167C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655790 | ||||||
| chr5:142655902
|
G | A | 12 | a0001c0001t0001g0187a0001c0001t0001g0325a0001c0001t0002g0185others(9): Show | 12 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+30055C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142655902 | ||||||
| chr5:142656040
|
A | C | 1 | a0001c0001t0006g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-35+29917T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656040 | ||||||
| chr5:142656218
|
T | TAGAAAAT others(280): Show |
9 | a0001c0001t0001g0187a0001c0001t0001g0325a0001c0001t0002g0185others(6): Show | 9 | HG02886.hp2 HG03579.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.-35+29738_-35+2973 others(291): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656218 | ||||||
| chr5:142656287
|
T | G | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+29670A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656287 | ||||||
| chr5:142656345
|
T | TA | 79 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-35+29611dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656345 | ||||||
| chr5:142656346
|
A | T | 1 | a0001c0001t0005g0245 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-35+29611T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656346 | ||||||
| chr5:142656371
|
G | A | 9 | a0001c0001t0004g0128a0001c0001t0004g0131a0001c0001t0006g0176others(6): Show | 9 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35+29586C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656371 | ||||||
| chr5:142656516
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+29441C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656516 | ||||||
| chr5:142656546
|
T | A | 2 | a0001c0001t0001g0306a0001c0001t0003g0101 | 2 | HG01928.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-35+29411A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656546 | ||||||
| chr5:142656631
|
C | A | 78 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(75): Show | 78 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-35+29326G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656631 | ||||||
| chr5:142656631
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-35+29326G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656631 | ||||||
| chr5:142656719
|
T | G | 1 | a0001c0001t0002g0243 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-35+29238A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656719 | ||||||
| chr5:142656784
|
A | T | 79 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-35+29173T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656784 | ||||||
| chr5:142656843
|
C | T | 1 | a0001c0001t0028g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-35+29114G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656843 | ||||||
| chr5:142656904
|
A | AT | 67 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(64): Show | 67 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-35+29052dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656904 | ||||||
| chr5:142656904
|
A | ATT | 11 | a0001c0001t0001g0172a0001c0001t0004g0128a0001c0001t0004g0131others(8): Show | 11 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35+29051_-35+2905 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656904 | ||||||
| chr5:142656971
|
G | A | 8 | a0001c0001t0001g0072a0001c0001t0002g0160a0001c0001t0012g0071others(5): Show | 8 | HG01175.hp1 HG01192.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+28986C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656971 | ||||||
| chr5:142656972
|
C | A | 8 | a0001c0001t0001g0072a0001c0001t0002g0160a0001c0001t0012g0071others(5): Show | 8 | HG01175.hp1 HG01192.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+28985G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656972 | ||||||
| chr5:142656991
|
C | T | 1 | a0001c0001t0003g0038 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-35+28966G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142656991 | ||||||
| chr5:142657004
|
A | G | 85 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(82): Show | 85 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-35+28953T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657004 | ||||||
| chr5:142657060
|
GGCATGTG others(7): Show |
G | 4 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+28883_-35+2889 others(18): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657060 | ||||||
| chr5:142657097
|
A | G | 1 | a0001c0001t0034g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-35+28860T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657097 | ||||||
| chr5:142657196
|
T | C | 79 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-35+28761A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657196 | ||||||
| chr5:142657217
|
C | T | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+28740G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657217 | ||||||
| chr5:142657306
|
C | T | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+28651G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657306 | ||||||
| chr5:142657311
|
C | T | 79 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-35+28646G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657311 | ||||||
| chr5:142657364
|
C | T | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+28593G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657364 | ||||||
| chr5:142657416
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-35+28541G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657416 | ||||||
| chr5:142657452
|
C | A | 1 | a0001c0001t0001g0014 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-35+28505G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657452 | ||||||
| chr5:142657455
|
C | T | 5 | a0001c0001t0004g0036a0001c0001t0004g0139a0001c0001t0005g0152others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+28502G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657455 | ||||||
| chr5:142657526
|
G | A | 79 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-35+28431C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657526 | ||||||
| chr5:142657555
|
A | G | 79 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-35+28402T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657555 | ||||||
| chr5:142657673
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+28284C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657673 | ||||||
| chr5:142657746
|
C | T | 1 | a0001c0001t0012g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-35+28211G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657746 | ||||||
| chr5:142657843
|
T | C | 83 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-35+28114A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657843 | ||||||
| chr5:142657926
|
A | G | 83 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-35+28031T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657926 | ||||||
| chr5:142657931
|
T | C | 83 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-35+28026A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142657931 | ||||||
| chr5:142658264
|
G | A | 1 | a0001c0001t0006g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-35+27693C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658264 | ||||||
| chr5:142658343
|
A | G | 89 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(86): Show | 89 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.-35+27614T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658343 | ||||||
| chr5:142658388
|
C | G | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+27569G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658388 | ||||||
| chr5:142658482
|
C | CT | 4 | a0001c0001t0002g0330a0001c0001t0006g0327a0001c0001t0006g0329others(1): Show | 4 | HG01167.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+27474dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658482 | ||||||
| chr5:142658496
|
A | G | 1 | a0001c0001t0004g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-35+27461T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658496 | ||||||
| chr5:142658806
|
G | A | 11 | a0001c0001t0001g0172a0001c0001t0004g0128a0001c0001t0004g0131others(8): Show | 11 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35+27151C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658806 | ||||||
| chr5:142658848
|
C | T | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+27109G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658848 | ||||||
| chr5:142658849
|
G | A | 4 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+27108C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658849 | ||||||
| chr5:142658855
|
A | G | 7 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0160others(4): Show | 7 | HG01496.hp2 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35+27102T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658855 | ||||||
| chr5:142658941
|
C | G | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+27016G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142658941 | ||||||
| chr5:142659013
|
A | G | 6 | a0001c0001t0004g0060a0001c0001t0006g0055a0001c0001t0013g0061others(3): Show | 6 | HG02572.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+26944T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659013 | ||||||
| chr5:142659018
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0005g0245 | 2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-35+26939G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659018 | ||||||
| chr5:142659042
|
G | A | 3 | a0001c0001t0001g0325a0001c0001t0006g0063a0001c0001t0006g0323 | 3 | HG02886.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+26915C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659042 | ||||||
| chr5:142659122
|
G | A | 4 | a0001c0001t0002g0006a0001c0001t0002g0160a0001c0001t0014g0161others(1): Show | 4 | HG01496.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+26835C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659122 | ||||||
| chr5:142659131
|
G | A | 83 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-35+26826C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659131 | ||||||
| chr5:142659152
|
AT | A | 22 | a0001c0001t0001g0172a0001c0001t0002g0006a0001c0001t0002g0010others(19): Show | 22 | HG01934.hp1 HG02145.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35+26804delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659152 | ||||||
| chr5:142659181
|
A | AT | 19 | a0001c0001t0001g0172a0001c0001t0003g0258a0001c0001t0004g0060others(16): Show | 19 | HG01934.hp1 HG02572.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.-35+26775dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659181 | ||||||
| chr5:142659231
|
G | GT | 16 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0180others(13): Show | 16 | HG01109.hp1 HG02056.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-35+26725dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659231 | ||||||
| chr5:142659231
|
GT | G | 124 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0072others(121): Show | 126 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-35+26725delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659231 | ||||||
| chr5:142659231
|
GTT | G | 7 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0160others(4): Show | 7 | HG01496.hp2 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35+26724_-35+2672 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659231 | ||||||
| chr5:142659268
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA18954.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-35+26689G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659268 | ||||||
| chr5:142659270
|
C | T | 5 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0004g0009others(2): Show | 5 | HG02145.hp2 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+26687G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659270 | ||||||
| chr5:142659289
|
C | T | 3 | a0001c0001t0001g0325a0001c0001t0006g0063a0001c0001t0006g0323 | 3 | HG02886.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+26668G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659289 | ||||||
| chr5:142659331
|
C | G | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+26626G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659331 | ||||||
| chr5:142659382
|
C | T | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-35+26575G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659382 | ||||||
| chr5:142659463
|
G | A | 18 | a0001c0001t0001g0172a0001c0001t0004g0060a0001c0001t0004g0128others(15): Show | 18 | HG01934.hp1 HG02572.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.-35+26494C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659463 | ||||||
| chr5:142659523
|
T | C | 2 | a0001c0001t0010g0276a0001c0001t0012g0282 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-35+26434A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659523 | ||||||
| chr5:142659576
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-35+26381G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659576 | ||||||
| chr5:142659577
|
G | A | 1 | a0001c0001t0006g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-35+26380C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659577 | ||||||
| chr5:142659657
|
G | C | 25 | a0001c0001t0001g0172a0001c0001t0002g0006a0001c0001t0002g0010others(22): Show | 25 | HG01496.hp2 HG01934.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.-35+26300C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659657 | ||||||
| chr5:142659713
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-35+26244G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659713 | ||||||
| chr5:142659891
|
C | G | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+26066G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659891 | ||||||
| chr5:142659891
|
C | T | 1 | a0001c0001t0006g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-35+26066G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142659891 | ||||||
| chr5:142660018
|
G | A | 18 | a0001c0001t0001g0172a0001c0001t0004g0060a0001c0001t0004g0128others(15): Show | 18 | HG01934.hp1 HG02572.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.-35+25939C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660018 | ||||||
| chr5:142660051
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-35+25906C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660051 | ||||||
| chr5:142660055
|
A | G | 1 | a0001c0001t0011g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-35+25902T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660055 | ||||||
| chr5:142660089
|
A | C | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+25868T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660089 | ||||||
| chr5:142660119
|
T | C | 6 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(3): Show | 6 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+25838A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660119 | ||||||
| chr5:142660147
|
C | T | 1 | a0001c0001t0006g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-35+25810G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660147 | ||||||
| chr5:142660208
|
AG | A | 3 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0025 | 3 | NA18987.hp1 NA19075.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-35+25748delC | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660208 | ||||||
| chr5:142660320
|
G | T | 2 | a0001c0001t0002g0006a0001c0001t0027g0162 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-35+25637C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660320 | ||||||
| chr5:142660495
|
G | A | 1 | a0001c0001t0005g0107 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-35+25462C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660495 | ||||||
| chr5:142660518
|
A | G | 2 | a0001c0001t0002g0160a0001c0001t0014g0161 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+25439T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660518 | ||||||
| chr5:142660582
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-35+25375G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660582 | ||||||
| chr5:142660615
|
C | A | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-35+25342G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660615 | ||||||
| chr5:142660639
|
C | G | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+25318G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660639 | ||||||
| chr5:142660737
|
C | T | 2 | a0001c0001t0002g0006a0001c0001t0027g0162 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-35+25220G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660737 | ||||||
| chr5:142660762
|
C | T | 1 | a0001c0001t0017g0087 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-35+25195G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660762 | ||||||
| chr5:142660887
|
T | C | 5 | a0001c0001t0001g0172a0001c0001t0010g0175a0001c0001t0013g0171others(2): Show | 5 | HG01934.hp1 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+25070A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660887 | ||||||
| chr5:142660924
|
C | G | 5 | a0001c0001t0004g0036a0001c0001t0004g0139a0001c0001t0005g0152others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+25033G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142660924 | ||||||
| chr5:142661039
|
A | G | 5 | a0001c0001t0002g0330a0001c0001t0004g0314a0001c0001t0006g0327others(2): Show | 5 | HG01167.hp2 HG02258.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+24918T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661039 | ||||||
| chr5:142661259
|
T | A | 2 | a0001c0001t0004g0320a0001c0001t0004g0321 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-35+24698A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661259 | ||||||
| chr5:142661736
|
G | A | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-35+24221C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661736 | ||||||
| chr5:142661737
|
C | T | 5 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+24220G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661737 | ||||||
| chr5:142661762
|
G | A | 94 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(91): Show | 96 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-35+24195C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661762 | ||||||
| chr5:142661775
|
G | A | 12 | a0001c0001t0002g0330a0001c0001t0003g0260a0001c0001t0003g0301others(9): Show | 12 | HG01167.hp2 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+24182C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661775 | ||||||
| chr5:142661779
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-35+24178T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661779 | ||||||
| chr5:142661796
|
G | T | 213 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(210): Show | 215 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-35+24161C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661796 | ||||||
| chr5:142661937
|
A | G | 9 | a0001c0001t0001g0187a0001c0001t0002g0185a0001c0001t0002g0188others(6): Show | 9 | HG02886.hp2 HG02976.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35+24020T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661937 | ||||||
| chr5:142661970
|
A | C | 1 | a0001c0001t0002g0214 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-35+23987T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142661970 | ||||||
| chr5:142662039
|
A | C | 46 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(43): Show | 46 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.-35+23918T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662039 | ||||||
| chr5:142662144
|
C | T | 16 | a0001c0001t0002g0156a0001c0001t0002g0200a0001c0001t0002g0201others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-35+23813G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662144 | ||||||
| chr5:142662145
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-35+23812C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662145 | ||||||
| chr5:142662248
|
G | C | 86 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(83): Show | 86 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.-35+23709C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662248 | ||||||
| chr5:142662251
|
G | T | 1 | a0001c0001t0012g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35+23706C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662251 | ||||||
| chr5:142662302
|
C | T | 8 | a0001c0001t0001g0178a0001c0001t0004g0264a0001c0001t0006g0136others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+23655G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662302 | ||||||
| chr5:142662508
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-35+23449T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662508 | ||||||
| chr5:142662635
|
G | GTCAT | 134 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(131): Show | 134 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-35+23318_-35+2332 others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662635 | ||||||
| chr5:142662693
|
G | T | 44 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(41): Show | 44 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35+23264C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662693 | ||||||
| chr5:142662829
|
G | A | 11 | a0001c0001t0001g0172a0001c0001t0004g0128a0001c0001t0004g0131others(8): Show | 11 | HG01934.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35+23128C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662829 | ||||||
| chr5:142662888
|
A | G | 134 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(131): Show | 134 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-35+23069T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662888 | ||||||
| chr5:142662930
|
C | T | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+23027G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142662930 | ||||||
| chr5:142663249
|
G | GA | 15 | a0001c0001t0001g0072a0001c0001t0001g0325a0001c0001t0002g0006others(12): Show | 15 | HG01175.hp1 HG01192.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.-35+22707dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663249 | ||||||
| chr5:142663249
|
G | GAA | 79 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(76): Show | 79 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.-35+22706_-35+2270 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663249 | ||||||
| chr5:142663249
|
G | GAAA | 44 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(41): Show | 44 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35+22705_-35+2270 others(7): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663249 | ||||||
| chr5:142663257
|
A | G | 89 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(86): Show | 91 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-35+22700T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663257 | ||||||
| chr5:142663340
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+22617A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663340 | ||||||
| chr5:142663429
|
G | A | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+22528C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663429 | ||||||
| chr5:142663510
|
C | G | 5 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+22447G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663510 | ||||||
| chr5:142663649
|
T | C | 9 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0083others(6): Show | 10 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35+22308A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663649 | ||||||
| chr5:142663736
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-35+22221G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663736 | ||||||
| chr5:142663761
|
A | G | 32 | a0001c0001t0001g0088a0001c0001t0001g0112a0001c0001t0001g0113others(29): Show | 32 | HG00558.hp1 HG00621.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.-35+22196T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663761 | ||||||
| chr5:142663774
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-35+22183G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663774 | ||||||
| chr5:142663779
|
G | A | 44 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0172others(41): Show | 44 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35+22178C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142663779 | ||||||
| chr5:142664100
|
G | A | 1 | a0001c0001t0004g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35+21857C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664100 | ||||||
| chr5:142664131
|
A | C | 1 | a0001c0001t0009g0035 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-35+21826T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664131 | ||||||
| chr5:142664146
|
G | C | 1 | a0001c0001t0003g0258 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-35+21811C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664146 | ||||||
| chr5:142664154
|
A | C | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+21803T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664154 | ||||||
| chr5:142664187
|
A | G | 134 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(131): Show | 134 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.-35+21770T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664187 | ||||||
| chr5:142664365
|
G | T | 1 | a0001c0001t0024g0244 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-35+21592C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664365 | ||||||
| chr5:142664375
|
C | T | 1 | a0001c0001t0004g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35+21582G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664375 | ||||||
| chr5:142664445
|
C | T | 6 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0002g0145others(3): Show | 6 | HG01175.hp2 HG01192.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+21512G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664445 | ||||||
| chr5:142664446
|
G | A | 5 | a0001c0001t0004g0139a0001c0001t0005g0152a0001c0001t0005g0153others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+21511C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664446 | ||||||
| chr5:142664455
|
C | T | 3 | a0001c0001t0002g0160a0001c0001t0014g0161a0001c0001t0027g0162 | 3 | HG01496.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+21502G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664455 | ||||||
| chr5:142664467
|
G | A | 2 | a0001c0001t0002g0335a0001c0001t0002g0336 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-35+21490C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664467 | ||||||
| chr5:142664704
|
C | T | 20 | a0001c0001t0001g0172a0001c0001t0002g0330a0001c0001t0004g0128others(17): Show | 20 | HG01167.hp2 HG01934.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35+21253G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664704 | ||||||
| chr5:142664852
|
C | T | 1 | a0001c0001t0010g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-35+21105G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664852 | ||||||
| chr5:142664908
|
A | C | 4 | a0001c0001t0004g0128a0001c0001t0004g0131a0001c0001t0009g0129others(1): Show | 4 | HG02615.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+21049T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664908 | ||||||
| chr5:142664924
|
T | C | 1 | a0001c0001t0021g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-35+21033A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664924 | ||||||
| chr5:142664942
|
C | T | 2 | a0001c0001t0002g0109a0001c0001t0002g0110 | 2 | NA18975.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-35+21015G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664942 | ||||||
| chr5:142664972
|
A | G | 3 | a0001c0001t0002g0185a0001c0001t0003g0094a0001c0001t0004g0186 | 3 | NA18939.hp1 NA18947.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-35+20985T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142664972 | ||||||
| chr5:142665009
|
A | G | 23 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(20): Show | 23 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-35+20948T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142665009 | ||||||
| chr5:142665291
|
C | T | 5 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+20666G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142665291 | ||||||
| chr5:142665294
|
C | T | 1 | a0001c0001t0007g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-35+20663G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142665294 | ||||||
| chr5:142665365
|
A | G | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+20592T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142665365 | ||||||
| chr5:142665507
|
C | G | 1 | a0001c0001t0010g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-35+20450G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142665507 | ||||||
| chr5:142665722
|
C | G | 5 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+20235G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142665722 | ||||||
| chr5:142665831
|
A | T | 44 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(41): Show | 44 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35+20126T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142665831 | ||||||
| chr5:142665958
|
C | A | 1 | a0001c0001t0001g0294 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-35+19999G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142665958 | ||||||
| chr5:142666045
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-35+19912C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666045 | ||||||
| chr5:142666111
|
C | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19846G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666111 | ||||||
| chr5:142666112
|
T | C | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19845A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666112 | ||||||
| chr5:142666120
|
AAG | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19835_-35+1983 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666120 | ||||||
| chr5:142666123
|
T | G | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19834A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666123 | ||||||
| chr5:142666136
|
T | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19821A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666136 | ||||||
| chr5:142666141
|
C | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19816G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666141 | ||||||
| chr5:142666142
|
T | C | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19815A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666142 | ||||||
| chr5:142666146
|
C | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19811G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666146 | ||||||
| chr5:142666157
|
C | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19800G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666157 | ||||||
| chr5:142666178
|
A | G | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19779T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666178 | ||||||
| chr5:142666183
|
G | T | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19774C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666183 | ||||||
| chr5:142666184
|
A | G | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19773T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666184 | ||||||
| chr5:142666205
|
C | G | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19752G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666205 | ||||||
| chr5:142666208
|
T | C | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19749A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666208 | ||||||
| chr5:142666209
|
C | T | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19748G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666209 | ||||||
| chr5:142666212
|
G | A | 3 | a0001c0001t0002g0010a0001c0001t0004g0009a0001c0001t0004g0307 | 3 | HG02145.hp2 HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-35+19745C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666212 | ||||||
| chr5:142666216
|
A | T | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19741T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666216 | ||||||
| chr5:142666227
|
C | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19730G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666227 | ||||||
| chr5:142666239
|
AC | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19717delG | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666239 | ||||||
| chr5:142666242
|
C | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19715G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666242 | ||||||
| chr5:142666245
|
C | A | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19712G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666245 | ||||||
| chr5:142666249
|
A | G | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19708T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666249 | ||||||
| chr5:142666276
|
TAATA | T | 22 | a0001c0001t0001g0039a0001c0001t0001g0293a0001c0001t0001g0294others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35+19677_-35+1968 others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666276 | ||||||
| chr5:142666276
|
TAATACA | T | 4 | a0001c0001t0002g0042a0001c0001t0003g0043a0001c0001t0008g0040others(1): Show | 4 | HG00639.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+19675_-35+1968 others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666276 | ||||||
| chr5:142666277
|
A | C | 311 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(308): Show | 313 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-35+19680T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666277 | ||||||
| chr5:142666279
|
T | TAC | 84 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(81): Show | 86 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-35+19676_-35+1967 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666279 | ||||||
| chr5:142666279
|
T | TACAC | 67 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0047others(64): Show | 67 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-35+19674_-35+1967 others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666279 | ||||||
| chr5:142666279
|
T | TACACAC | 18 | a0001c0001t0001g0026a0001c0001t0001g0207a0001c0001t0001g0289others(15): Show | 18 | HG01123.hp2 HG01891.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.-35+19672_-35+1967 others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666279 | ||||||
| chr5:142666279
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0126a0001c0001t0005g0152a0001c0001t0005g0153others(1): Show | 4 | HG02055.hp1 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+19670_-35+1967 others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666279 | ||||||
| chr5:142666279
|
T | TACACACA others(3): Show |
6 | a0001c0001t0001g0051a0001c0001t0001g0072a0001c0001t0004g0139others(3): Show | 6 | HG00642.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+19668_-35+1967 others(14): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666279 | ||||||
| chr5:142666279
|
T | TACACACA others(5): Show |
6 | a0001c0001t0001g0325a0001c0001t0005g0291a0001c0001t0014g0132others(3): Show | 6 | HG01175.hp1 HG01192.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+19666_-35+1967 others(16): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666279 | ||||||
| chr5:142666279
|
TAC | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0127others(13): Show | 16 | HG00140.hp2 HG01243.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.-35+19676_-35+1967 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666279 | ||||||
| chr5:142666283
|
C | T | 22 | a0001c0001t0001g0039a0001c0001t0001g0293a0001c0001t0001g0294others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35+19674G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666283 | ||||||
| chr5:142666285
|
C | T | 4 | a0001c0001t0002g0042a0001c0001t0003g0043a0001c0001t0008g0040others(1): Show | 4 | HG00639.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+19672G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666285 | ||||||
| chr5:142666324
|
T | C | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19633A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666324 | ||||||
| chr5:142666331
|
T | C | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19626A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666331 | ||||||
| chr5:142666333
|
T | C | 337 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0020others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-35+19624A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666333 | ||||||
| chr5:142666377
|
A | G | 4 | a0001c0001t0002g0335a0001c0001t0002g0336a0001c0001t0002g0337others(1): Show | 4 | HG01109.hp2 HG01123.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+19580T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666377 | ||||||
| chr5:142666435
|
G | A | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+19522C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666435 | ||||||
| chr5:142666543
|
C | CA | 99 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(96): Show | 99 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.-35+19413dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666543 | ||||||
| chr5:142666551
|
A | C | 1 | a0001c0001t0001g0269 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-35+19406T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666551 | ||||||
| chr5:142666607
|
T | C | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+19350A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666607 | ||||||
| chr5:142666611
|
A | G | 47 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(44): Show | 47 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-35+19346T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666611 | ||||||
| chr5:142666618
|
G | T | 99 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(96): Show | 99 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.-35+19339C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666618 | ||||||
| chr5:142666918
|
A | AAAAAAC | 4 | a0001c0001t0002g0125a0001c0001t0005g0267a0001c0001t0007g0122others(1): Show | 4 | NA19011.hp1 NA19055.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+19033_-35+1903 others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142666918 | ||||||
| chr5:142667003
|
C | T | 2 | a0001c0001t0005g0267a0001c0001t0018g0268 | 2 | NA19011.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-35+18954G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667003 | ||||||
| chr5:142667058
|
C | G | 99 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(96): Show | 99 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.-35+18899G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667058 | ||||||
| chr5:142667158
|
C | G | 1 | a0001c0001t0009g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-35+18799G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667158 | ||||||
| chr5:142667312
|
C | A | 1 | a0001c0001t0012g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35+18645G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667312 | ||||||
| chr5:142667352
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-35+18605G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667352 | ||||||
| chr5:142667353
|
G | A | 4 | a0001c0001t0002g0330a0001c0001t0006g0327a0001c0001t0006g0329others(1): Show | 4 | HG01167.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+18604C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667353 | ||||||
| chr5:142667357
|
T | C | 102 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(99): Show | 102 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.-35+18600A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667357 | ||||||
| chr5:142667459
|
G | A | 3 | a0001c0001t0002g0160a0001c0001t0014g0161a0001c0001t0027g0162 | 3 | HG01496.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+18498C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667459 | ||||||
| chr5:142667512
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0006g0323 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+18445C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667512 | ||||||
| chr5:142667585
|
C | CA | 6 | a0001c0001t0001g0083a0001c0001t0002g0030a0001c0001t0003g0300others(3): Show | 6 | HG00733.hp2 HG02886.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+18371dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667585 | ||||||
| chr5:142667585
|
CA | C | 21 | a0001c0001t0001g0172a0001c0001t0001g0325a0001c0001t0002g0097others(18): Show | 21 | HG01167.hp2 HG01168.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.-35+18371delT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667585 | ||||||
| chr5:142667626
|
A | G | 227 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-35+18331T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667626 | ||||||
| chr5:142667633
|
G | A | 1 | a0001c0001t0038g0255 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-35+18324C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667633 | ||||||
| chr5:142667648
|
G | C | 93 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(90): Show | 93 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.-35+18309C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667648 | ||||||
| chr5:142667660
|
G | A | 55 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-35+18297C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667660 | ||||||
| chr5:142667738
|
G | A | 4 | a0001c0001t0001g0285a0001c0001t0004g0287a0001c0001t0020g0286others(1): Show | 4 | HG01099.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+18219C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667738 | ||||||
| chr5:142667790
|
G | C | 1 | a0001c0001t0001g0289 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-35+18167C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667790 | ||||||
| chr5:142667869
|
G | C | 13 | a0001c0001t0002g0160a0001c0001t0002g0330a0001c0001t0004g0139others(10): Show | 13 | HG01167.hp2 HG01496.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-35+18088C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667869 | ||||||
| chr5:142667949
|
C | T | 1 | a0001c0001t0013g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-35+18008G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142667949 | ||||||
| chr5:142668138
|
T | A | 1 | a0001c0001t0001g0256 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-35+17819A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142668138 | ||||||
| chr5:142668260
|
A | G | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+17697T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142668260 | ||||||
| chr5:142668266
|
A | G | 102 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(99): Show | 103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-35+17691T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142668266 | ||||||
| chr5:142668344
|
T | C | 29 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-35+17613A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142668344 | ||||||
| chr5:142668590
|
T | G | 1 | a0001c0001t0002g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-35+17367A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142668590 | ||||||
| chr5:142668704
|
C | T | 101 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(98): Show | 102 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-35+17253G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142668704 | ||||||
| chr5:142668742
|
A | G | 103 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(100): Show | 104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-35+17215T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142668742 | ||||||
| chr5:142669036
|
G | T | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+16921C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669036 | ||||||
| chr5:142669100
|
G | T | 2 | a0001c0001t0003g0203a0001c0001t0003g0204 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-35+16857C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669100 | ||||||
| chr5:142669150
|
T | C | 102 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(99): Show | 103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-35+16807A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669150 | ||||||
| chr5:142669283
|
C | T | 28 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0002g0042others(25): Show | 28 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35+16674G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669283 | ||||||
| chr5:142669335
|
T | C | 72 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(69): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-35+16622A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669335 | ||||||
| chr5:142669357
|
C | T | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+16600G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669357 | ||||||
| chr5:142669377
|
A | T | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+16580T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669377 | ||||||
| chr5:142669386
|
C | A | 50 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(47): Show | 50 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-35+16571G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669386 | ||||||
| chr5:142669461
|
A | G | 1 | a0001c0001t0007g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-35+16496T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669461 | ||||||
| chr5:142669541
|
T | A | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+16416A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669541 | ||||||
| chr5:142669571
|
C | CGGAAGGA others(32): Show |
1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+16385_-35+1638 others(43): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669571 | ||||||
| chr5:142669611
|
C | T | 53 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.-35+16346G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669611 | ||||||
| chr5:142669663
|
C | T | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-35+16294G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669663 | ||||||
| chr5:142669664
|
G | A | 28 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0002g0042others(25): Show | 28 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35+16293C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669664 | ||||||
| chr5:142669683
|
C | T | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+16274G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669683 | ||||||
| chr5:142669716
|
G | T | 2 | a0001c0001t0001g0325a0001c0001t0006g0323 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+16241C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669716 | ||||||
| chr5:142669721
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-35+16236C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669721 | ||||||
| chr5:142669783
|
T | C | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+16174A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669783 | ||||||
| chr5:142669856
|
C | T | 11 | a0001c0001t0002g0160a0001c0001t0002g0330a0001c0001t0004g0139others(8): Show | 11 | HG01167.hp2 HG01496.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35+16101G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142669856 | ||||||
| chr5:142670083
|
G | A | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+15874C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670083 | ||||||
| chr5:142670258
|
C | T | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+15699G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670258 | ||||||
| chr5:142670597
|
CATGGT | C | 4 | a0001c0001t0004g0139a0001c0001t0005g0152a0001c0001t0005g0153others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+15355_-35+1535 others(9): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670597 | ||||||
| chr5:142670600
|
G | A | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+15357C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670600 | ||||||
| chr5:142670626
|
A | G | 1 | a0001c0001t0003g0257 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-35+15331T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670626 | ||||||
| chr5:142670636
|
C | T | 6 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0003g0260others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+15321G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670636 | ||||||
| chr5:142670654
|
A | G | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+15303T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670654 | ||||||
| chr5:142670671
|
C | A | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+15286G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670671 | ||||||
| chr5:142670730
|
C | T | 1 | a0001c0001t0005g0106 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-35+15227G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670730 | ||||||
| chr5:142670791
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-35+15166C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670791 | ||||||
| chr5:142670847
|
G | C | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+15110C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670847 | ||||||
| chr5:142670861
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-35+15096G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670861 | ||||||
| chr5:142670866
|
G | A | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+15091C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670866 | ||||||
| chr5:142670934
|
T | G | 102 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(99): Show | 103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-35+15023A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142670934 | ||||||
| chr5:142671091
|
A | C | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+14866T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671091 | ||||||
| chr5:142671091
|
A | G | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+14866T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671091 | ||||||
| chr5:142671106
|
C | T | 2 | a0001c0001t0001g0325a0001c0001t0006g0323 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+14851G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671106 | ||||||
| chr5:142671109
|
T | C | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+14848A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671109 | ||||||
| chr5:142671122
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-35+14835G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671122 | ||||||
| chr5:142671140
|
A | C | 1 | a0001c0001t0003g0012 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-35+14817T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671140 | ||||||
| chr5:142671288
|
T | C | 1 | a0001c0001t0003g0034 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-35+14669A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671288 | ||||||
| chr5:142671452
|
A | C | 2 | a0001c0001t0003g0144a0001c0001t0004g0143 | 2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-35+14505T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671452 | ||||||
| chr5:142671460
|
C | A | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+14497G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671460 | ||||||
| chr5:142671530
|
T | C | 102 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(99): Show | 103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-35+14427A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671530 | ||||||
| chr5:142671553
|
G | C | 2 | a0001c0001t0004g0320a0001c0001t0004g0321 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-35+14404C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671553 | ||||||
| chr5:142671698
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-35+14259C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671698 | ||||||
| chr5:142671894
|
C | G | 1 | a0001c0001t0003g0199 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-35+14063G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142671894 | ||||||
| chr5:142672156
|
A | G | 4 | a0001c0001t0002g0096a0001c0001t0002g0196a0001c0001t0002g0198others(1): Show | 4 | NA18977.hp1 NA18979.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+13801T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672156 | ||||||
| chr5:142672295
|
C | T | 98 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(95): Show | 99 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-35+13662G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672295 | ||||||
| chr5:142672310
|
G | T | 97 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(94): Show | 98 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-35+13647C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672310 | ||||||
| chr5:142672386
|
C | T | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+13571G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672386 | ||||||
| chr5:142672399
|
T | C | 1 | a0001c0001t0004g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-35+13558A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672399 | ||||||
| chr5:142672430
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-35+13527G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672430 | ||||||
| chr5:142672471
|
A | G | 1 | a0001c0001t0004g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-35+13486T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672471 | ||||||
| chr5:142672500
|
G | GT | 16 | a0001c0001t0001g0178a0001c0001t0001g0192a0001c0001t0002g0042others(13): Show | 16 | HG00423.hp1 HG00621.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-35+13456dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672500 | ||||||
| chr5:142672500
|
GT | G | 6 | a0001c0001t0003g0257a0001c0001t0003g0258a0001c0001t0004g0264others(3): Show | 6 | HG02451.hp2 HG03098.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+13456delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672500 | ||||||
| chr5:142672500
|
GTT | G | 17 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(14): Show | 18 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-35+13455_-35+1345 others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672500 | ||||||
| chr5:142672500
|
GTTT | G | 49 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-35+13454_-35+1345 others(7): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672500 | ||||||
| chr5:142672565
|
T | C | 103 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(100): Show | 104 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-35+13392A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672565 | ||||||
| chr5:142672598
|
A | G | 101 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(98): Show | 102 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-35+13359T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672598 | ||||||
| chr5:142672641
|
A | T | 1 | a0001c0001t0011g0067 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-35+13316T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672641 | ||||||
| chr5:142672719
|
C | T | 16 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(13): Show | 17 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+13238G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672719 | ||||||
| chr5:142672956
|
G | T | 29 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0002g0042others(26): Show | 29 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-35+13001C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142672956 | ||||||
| chr5:142673075
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-35+12882C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673075 | ||||||
| chr5:142673151
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0006g0323 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+12806C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673151 | ||||||
| chr5:142673165
|
G | T | 16 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0002g0042others(13): Show | 16 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-35+12792C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673165 | ||||||
| chr5:142673396
|
C | G | 8 | a0001c0001t0002g0160a0001c0001t0004g0104a0001c0001t0004g0139others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+12561G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673396 | ||||||
| chr5:142673422
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-35+12535C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673422 | ||||||
| chr5:142673460
|
A | C | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+12497T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673460 | ||||||
| chr5:142673743
|
A | C | 2 | a0001c0001t0001g0192a0001c0001t0003g0193 | 2 | NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-35+12214T>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673743 | ||||||
| chr5:142673746
|
G | T | 4 | a0001c0001t0002g0330a0001c0001t0006g0327a0001c0001t0006g0329others(1): Show | 4 | HG01167.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+12211C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673746 | ||||||
| chr5:142673910
|
C | T | 16 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(13): Show | 17 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+12047G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673910 | ||||||
| chr5:142673940
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-35+12017C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142673940 | ||||||
| chr5:142674072
|
T | C | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+11885A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674072 | ||||||
| chr5:142674134
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-35+11823A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674134 | ||||||
| chr5:142674135
|
C | T | 1 | a0001c0001t0002g0125 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-35+11822G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674135 | ||||||
| chr5:142674199
|
T | A | 1 | a0001c0001t0001g0290 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-35+11758A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674199 | ||||||
| chr5:142674256
|
G | A | 1 | a0001c0001t0002g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-35+11701C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674256 | ||||||
| chr5:142674318
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-35+11639C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674318 | ||||||
| chr5:142674472
|
G | A | 1 | a0001c0001t0002g0337 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-35+11485C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674472 | ||||||
| chr5:142674527
|
A | G | 115 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(112): Show | 116 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-35+11430T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674527 | ||||||
| chr5:142674690
|
G | A | 15 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0002g0042others(12): Show | 15 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-35+11267C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674690 | ||||||
| chr5:142674814
|
A | G | 100 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(97): Show | 101 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-35+11143T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142674814 | ||||||
| chr5:142675014
|
G | A | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-35+10943C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675014 | ||||||
| chr5:142675089
|
C | A | 1 | a0001c0001t0015g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-35+10868G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675089 | ||||||
| chr5:142675118
|
C | A | 1 | a0001c0001t0002g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-35+10839G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675118 | ||||||
| chr5:142675121
|
C | T | 26 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0002g0042others(23): Show | 26 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+10836G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675121 | ||||||
| chr5:142675258
|
C | T | 1 | a0001c0001t0009g0315 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-35+10699G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675258 | ||||||
| chr5:142675276
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-35+10681G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675276 | ||||||
| chr5:142675565
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-35+10392T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675565 | ||||||
| chr5:142675590
|
G | A | 1 | a0001c0001t0033g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-35+10367C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675590 | ||||||
| chr5:142675638
|
G | A | 4 | a0001c0001t0004g0128a0001c0001t0004g0131a0001c0001t0009g0129others(1): Show | 4 | HG02615.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+10319C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675638 | ||||||
| chr5:142675769
|
C | A | 1 | a0001c0001t0002g0125 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-35+10188G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675769 | ||||||
| chr5:142675859
|
A | G | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+10098T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675859 | ||||||
| chr5:142675864
|
G | A | 1 | a0001c0001t0004g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-35+10093C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675864 | ||||||
| chr5:142675972
|
T | G | 101 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(98): Show | 102 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-35+9985A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675972 | ||||||
| chr5:142675999
|
C | T | 4 | a0001c0001t0002g0330a0001c0001t0006g0327a0001c0001t0006g0329others(1): Show | 4 | HG01167.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+9958G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142675999 | ||||||
| chr5:142676073
|
C | A | 28 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(25): Show | 28 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35+9884G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676073 | ||||||
| chr5:142676109
|
A | G | 5 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+9848T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676109 | ||||||
| chr5:142676306
|
G | A | 1 | a0001c0001t0005g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-35+9651C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676306 | ||||||
| chr5:142676344
|
C | A | 102 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(99): Show | 103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-35+9613G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676344 | ||||||
| chr5:142676362
|
T | C | 102 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(99): Show | 103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-35+9595A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676362 | ||||||
| chr5:142676372
|
T | C | 1 | a0001c0001t0017g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-35+9585A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676372 | ||||||
| chr5:142676408
|
G | C | 213 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(210): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-35+9549C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676408 | ||||||
| chr5:142676588
|
G | C | 1 | a0001c0001t0002g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-35+9369C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676588 | ||||||
| chr5:142676726
|
T | C | 4 | a0001c0001t0001g0126a0001c0001t0005g0291a0001c0001t0007g0141others(1): Show | 4 | HG00544.hp1 NA18960.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+9231A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676726 | ||||||
| chr5:142676769
|
G | A | 16 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(13): Show | 17 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+9188C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676769 | ||||||
| chr5:142676804
|
G | A | 7 | a0001c0001t0002g0160a0001c0001t0004g0139a0001c0001t0005g0152others(4): Show | 7 | HG01496.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+9153C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676804 | ||||||
| chr5:142676833
|
A | G | 86 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.-35+9124T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676833 | ||||||
| chr5:142676883
|
A | T | 1 | a0001c0001t0030g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-35+9074T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676883 | ||||||
| chr5:142676919
|
A | AAAC | 81 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.-35+9035_-35+9037d others(5): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676919 | ||||||
| chr5:142676919
|
A | AAACAAC | 4 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+9032_-35+9037d others(8): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676919 | ||||||
| chr5:142676989
|
C | A | 44 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(41): Show | 45 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-35+8968G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676989 | ||||||
| chr5:142676989
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-35+8968G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142676989 | ||||||
| chr5:142677035
|
G | C | 1 | a0001c0001t0002g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-35+8922C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677035 | ||||||
| chr5:142677082
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+8875C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677082 | ||||||
| chr5:142677098
|
G | A | 21 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(18): Show | 21 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-35+8859C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677098 | ||||||
| chr5:142677355
|
C | T | 1 | a0001c0001t0003g0049 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-35+8602G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677355 | ||||||
| chr5:142677439
|
A | G | 3 | a0001c0001t0002g0160a0001c0001t0014g0161a0001c0001t0027g0162 | 3 | HG01496.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-35+8518T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677439 | ||||||
| chr5:142677521
|
C | A | 1 | a0001c0001t0002g0302 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-35+8436G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677521 | ||||||
| chr5:142677595
|
G | T | 15 | a0001c0001t0001g0187a0001c0001t0001g0293a0001c0001t0001g0294others(12): Show | 15 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.-35+8362C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677595 | ||||||
| chr5:142677598
|
T | C | 16 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(13): Show | 17 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+8359A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677598 | ||||||
| chr5:142677694
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0003g0181 | 2 | HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-35+8263T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677694 | ||||||
| chr5:142677772
|
T | C | 6 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0296others(3): Show | 6 | HG00099.hp2 HG01168.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+8185A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677772 | ||||||
| chr5:142677798
|
A | T | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8159T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677798 | ||||||
| chr5:142677809
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8148A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677809 | ||||||
| chr5:142677815
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8142G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677815 | ||||||
| chr5:142677816
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8141G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677816 | ||||||
| chr5:142677819
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8138G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677819 | ||||||
| chr5:142677850
|
G | T | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8107C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677850 | ||||||
| chr5:142677867
|
T | A | 2 | a0001c0001t0004g0139a0001c0001t0004g0322 | 2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+8090A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677867 | ||||||
| chr5:142677874
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8083A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677874 | ||||||
| chr5:142677882
|
AAATTACG others(8): Show |
A | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8060_-35+8074d others(17): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677882 | ||||||
| chr5:142677898
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8059A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677898 | ||||||
| chr5:142677902
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8055G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677902 | ||||||
| chr5:142677932
|
G | T | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8025C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677932 | ||||||
| chr5:142677933
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-35+8024T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677933 | ||||||
| chr5:142677936
|
CAG | C | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+8019_-35+8020d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142677936 | ||||||
| chr5:142678012
|
G | T | 1 | a0001c0001t0029g0032 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-35+7945C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678012 | ||||||
| chr5:142678122
|
G | A | 1 | a0001c0001t0002g0031 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-35+7835C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678122 | ||||||
| chr5:142678161
|
C | G | 1 | a0001c0001t0006g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-35+7796G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678161 | ||||||
| chr5:142678332
|
T | A | 1 | a0001c0001t0006g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-35+7625A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678332 | ||||||
| chr5:142678398
|
T | C | 1 | a0001c0001t0016g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-35+7559A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678398 | ||||||
| chr5:142678452
|
C | G | 104 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(101): Show | 105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-35+7505G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678452 | ||||||
| chr5:142678553
|
C | T | 2 | a0001c0001t0007g0141a0001c0001t0009g0142 | 2 | HG00544.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-35+7404G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678553 | ||||||
| chr5:142678555
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-35+7402G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678555 | ||||||
| chr5:142678677
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-35+7280T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678677 | ||||||
| chr5:142678730
|
A | G | 1 | a0001c0001t0004g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-35+7227T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678730 | ||||||
| chr5:142678767
|
A | G | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+7190T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678767 | ||||||
| chr5:142678915
|
A | T | 16 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(13): Show | 17 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+7042T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142678915 | ||||||
| chr5:142679097
|
G | C | 1 | a0001c0001t0006g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-35+6860C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679097 | ||||||
| chr5:142679207
|
A | G | 21 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(18): Show | 22 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35+6750T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679207 | ||||||
| chr5:142679339
|
T | C | 104 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(101): Show | 105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-35+6618A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679339 | ||||||
| chr5:142679393
|
C | A | 4 | a0001c0001t0002g0330a0001c0001t0006g0327a0001c0001t0006g0329others(1): Show | 4 | HG01167.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+6564G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679393 | ||||||
| chr5:142679425
|
G | T | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+6532C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679425 | ||||||
| chr5:142679458
|
G | C | 1 | a0001c0001t0004g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35+6499C>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679458 | ||||||
| chr5:142679486
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-35+6471G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679486 | ||||||
| chr5:142679516
|
C | T | 9 | a0001c0001t0001g0172a0001c0001t0006g0176a0001c0001t0010g0173others(6): Show | 9 | HG01934.hp1 HG02622.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35+6441G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679516 | ||||||
| chr5:142679538
|
T | G | 3 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0322 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-35+6419A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679538 | ||||||
| chr5:142679769
|
A | T | 1 | a0001c0001t0002g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-35+6188T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679769 | ||||||
| chr5:142679835
|
T | C | 88 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-35+6122A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142679835 | ||||||
| chr5:142680028
|
T | A | 7 | a0001c0001t0002g0160a0001c0001t0004g0139a0001c0001t0005g0152others(4): Show | 7 | HG01496.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+5929A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680028 | ||||||
| chr5:142680120
|
G | T | 37 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(34): Show | 38 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-35+5837C>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680120 | ||||||
| chr5:142680172
|
C | T | 2 | a0001c0001t0003g0092a0001c0001t0047g0093 | 2 | HG00621.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.-35+5785G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680172 | ||||||
| chr5:142680275
|
C | T | 1 | a0001c0001t0008g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-35+5682G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680275 | ||||||
| chr5:142680413
|
G | A | 37 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(34): Show | 38 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-35+5544C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680413 | ||||||
| chr5:142680489
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0006g0323 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+5468C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680489 | ||||||
| chr5:142680504
|
A | T | 1 | a0001c0001t0004g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35+5453T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680504 | ||||||
| chr5:142680518
|
T | C | 37 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(34): Show | 38 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-35+5439A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680518 | ||||||
| chr5:142680563
|
TAA | T | 37 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(34): Show | 38 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-35+5392_-35+5393d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680563 | ||||||
| chr5:142680581
|
CT | C | 4 | a0001c0001t0002g0330a0001c0001t0006g0327a0001c0001t0006g0329others(1): Show | 4 | HG01167.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+5375delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680581 | ||||||
| chr5:142680926
|
G | A | 33 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(30): Show | 34 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-35+5031C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142680926 | ||||||
| chr5:142681448
|
C | T | 1 | a0001c0001t0004g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35+4509G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142681448 | ||||||
| chr5:142681748
|
C | T | 2 | a0001c0001t0008g0040a0001c0001t0021g0041 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-35+4209G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142681748 | ||||||
| chr5:142681839
|
T | C | 1 | a0001c0001t0010g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35+4118A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142681839 | ||||||
| chr5:142681950
|
G | A | 17 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(14): Show | 17 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-35+4007C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142681950 | ||||||
| chr5:142682003
|
T | C | 104 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(101): Show | 105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-35+3954A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682003 | ||||||
| chr5:142682085
|
A | AT | 10 | a0001c0001t0001g0155a0001c0001t0001g0166a0001c0001t0002g0160others(7): Show | 10 | HG01099.hp2 HG01496.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35+3871dupA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682085 | ||||||
| chr5:142682085
|
AT | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0002g0084others(16): Show | 19 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.-35+3871delA | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682085 | ||||||
| chr5:142682085
|
ATT | A | 31 | a0001c0001t0001g0047a0001c0001t0001g0072a0001c0001t0001g0075others(28): Show | 32 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.-35+3870_-35+3871d others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682085 | ||||||
| chr5:142682114
|
T | A | 1 | a0001c0001t0001g0306 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-35+3843A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682114 | ||||||
| chr5:142682138
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-35+3819G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682138 | ||||||
| chr5:142682171
|
T | C | 108 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(105): Show | 109 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-35+3786A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682171 | ||||||
| chr5:142682252
|
T | C | 1 | a0001c0001t0009g0035 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-35+3705A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682252 | ||||||
| chr5:142682441
|
G | A | 37 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(34): Show | 38 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-35+3516C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682441 | ||||||
| chr5:142682615
|
A | G | 1 | a0001c0001t0014g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-35+3342T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682615 | ||||||
| chr5:142682691
|
C | T | 4 | a0001c0001t0002g0330a0001c0001t0006g0327a0001c0001t0006g0329others(1): Show | 4 | HG01167.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+3266G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682691 | ||||||
| chr5:142682927
|
C | T | 7 | a0001c0001t0002g0160a0001c0001t0004g0139a0001c0001t0005g0152others(4): Show | 7 | HG01496.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+3030G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142682927 | ||||||
| chr5:142683269
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0002g0089a0001c0001t0008g0090others(2): Show | 5 | HG02074.hp2 HG02135.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35+2688G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683269 | ||||||
| chr5:142683821
|
C | CA | 6 | a0001c0001t0001g0149a0001c0001t0001g0309a0001c0001t0001g0325others(3): Show | 6 | HG01192.hp1 HG02622.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+2135dupT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683821 | ||||||
| chr5:142683821
|
C | CAAAA | 16 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0077others(13): Show | 17 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-35+2132_-35+2135d others(6): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683821 | ||||||
| chr5:142683821
|
C | CAAAAA | 13 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0002g0042others(10): Show | 13 | HG00639.hp1 HG00733.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-35+2131_-35+2135d others(7): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683821 | ||||||
| chr5:142683821
|
C | CAAAAAAA others(1): Show |
36 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(33): Show | 36 | HG00099.hp1 HG00423.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.-35+2128_-35+2135d others(10): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683821 | ||||||
| chr5:142683821
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0002g0033a0001c0001t0003g0034a0001c0001t0003g0068others(10): Show | 13 | HG00642.hp2 HG01123.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-35+2127_-35+2135d others(11): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683821 | ||||||
| chr5:142683821
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0014g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-35+2126_-35+2135d others(12): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683821 | ||||||
| chr5:142683821
|
CA | C | 11 | a0001c0001t0001g0086a0001c0001t0001g0155a0001c0001t0001g0157others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35+2135delT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683821 | ||||||
| chr5:142683857
|
AATCCTTT | A | 87 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+2093_-35+2099d others(9): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683857 | ||||||
| chr5:142683951
|
G | A | 6 | a0001c0001t0001g0066a0001c0001t0003g0068a0001c0001t0010g0065others(3): Show | 6 | HG00642.hp2 HG01109.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+2006C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142683951 | ||||||
| chr5:142684014
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-35+1943G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684014 | ||||||
| chr5:142684079
|
T | A | 2 | a0001c0001t0001g0325a0001c0001t0006g0323 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+1878A>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684079 | ||||||
| chr5:142684107
|
T | C | 2 | a0001c0001t0001g0325a0001c0001t0006g0323 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+1850A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684107 | ||||||
| chr5:142684140
|
C | T | 6 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0002g0145others(3): Show | 6 | HG01175.hp2 HG01192.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+1817G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684140 | ||||||
| chr5:142684164
|
T | C | 87 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+1793A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684164 | ||||||
| chr5:142684227
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-35+1730G>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684227 | ||||||
| chr5:142684401
|
A | G | 1 | a0001c0001t0028g0011 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-35+1556T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684401 | ||||||
| chr5:142684638
|
C | T | 87 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+1319G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684638 | ||||||
| chr5:142684659
|
A | G | 2 | a0001c0001t0003g0144a0001c0001t0004g0143 | 2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-35+1298T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684659 | ||||||
| chr5:142684739
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-35+1218C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684739 | ||||||
| chr5:142684751
|
C | T | 87 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+1206G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684751 | ||||||
| chr5:142684774
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-35+1183A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684774 | ||||||
| chr5:142684830
|
G | A | 1 | a0001c0001t0003g0313 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-35+1127C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684830 | ||||||
| chr5:142684839
|
A | G | 87 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+1118T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684839 | ||||||
| chr5:142684840
|
A | T | 87 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+1117T>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684840 | ||||||
| chr5:142684869
|
C | G | 2 | a0001c0001t0007g0141a0001c0001t0009g0142 | 2 | HG00544.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-35+1088G>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684869 | ||||||
| chr5:142684942
|
C | T | 87 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+1015G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684942 | ||||||
| chr5:142684961
|
G | A | 87 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-35+996C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142684961 | ||||||
| chr5:142685029
|
C | T | 33 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0047others(30): Show | 34 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-35+928G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685029 | ||||||
| chr5:142685053
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-35+904G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685053 | ||||||
| chr5:142685136
|
T | G | 1 | a0001c0001t0001g0325 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-35+821A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685136 | ||||||
| chr5:142685401
|
T | G | 1 | a0001c0001t0004g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35+556A>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685401 | ||||||
| chr5:142685535
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-35+422T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685535 | ||||||
| chr5:142685615
|
C | T | 1 | a0001c0001t0022g0138 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-35+342G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685615 | ||||||
| chr5:142685664
|
T | C | 2 | a0001c0001t0009g0315a0001c0001t0013g0316 | 2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-35+293A>G | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685664 | ||||||
| chr5:142685681
|
A | G | 5 | a0001c0001t0001g0072a0001c0001t0012g0071a0001c0001t0016g0073others(2): Show | 5 | HG01175.hp1 HG01192.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+276T>C | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685681 | ||||||
| chr5:142685759
|
C | T | 47 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(44): Show | 47 | HG00099.hp1 HG00423.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-35+198G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685759 | ||||||
| chr5:142685790
|
G | A | 2 | a0001c0001t0002g0050a0001c0001t0003g0049 | 2 | HG02004.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-35+167C>T | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685790 | ||||||
| chr5:142685871
|
CA | C | 3 | a0001c0001t0002g0134a0001c0001t0005g0133a0001c0001t0005g0135 | 3 | HG02040.hp1 NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-35+85delT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685871 | ||||||
| chr5:142685874
|
A | AAC | 80 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0075others(77): Show | 81 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-35+81_-35+82dupGT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685874 | ||||||
| chr5:142685874
|
A | AACAC | 41 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0026others(38): Show | 41 | HG00423.hp2 HG00639.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-35+79_-35+82dupGT others(2): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685874 | ||||||
| chr5:142685874
|
A | AACACAC | 7 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(4): Show | 7 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35+77_-35+82dupGT others(4): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685874 | ||||||
| chr5:142685874
|
A | AC | 3 | a0001c0001t0001g0051a0001c0001t0003g0053a0001c0001t0028g0052 | 3 | HG03927.hp1 NA18995.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-35+82_-35+83insG | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685874 | ||||||
| chr5:142685874
|
AAC | A | 9 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0325others(6): Show | 9 | HG00738.hp1 HG02040.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35+81_-35+82delGT | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685874 | ||||||
| chr5:142685874
|
AACAC | A | 12 | a0001c0001t0002g0326a0001c0001t0002g0330a0001c0001t0002g0335others(9): Show | 12 | HG01109.hp2 HG01123.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+79_-35+82delGT others(2): Show |
FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685874 | ||||||
| chr5:142685946
|
C | T | 1 | a0001c0001t0001g0003 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-35+11G>A | FGF1 | ENSG00000113578.18 | transcript | ENST00000337706.7 | protein_coding | 1/3 | chr5 | 142685946 |