Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8817 |
| ensemblid | ENSG00000156427.8 |
| hgncid | 3674 |
| symbol | FGF18 |
| name | fibroblast growth factor 18 |
| refseq_nuc | NM_003862.3 |
| refseq_prot | NP_003853.1 |
| ensembl_nuc | ENST00000274625.6 |
| ensembl_prot | ENSP00000274625.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 171419647 |
| end | 171457626 |
| strand | + |
| ver | v1.2 |
| region | chr5:171419647-171457626 |
| region5000 | chr5:171414647-171462626 |
| regionname0 | FGF18_chr5_171419647_171457626 |
| regionname5000 | FGF18_chr5_171414647_171462626 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 207 | 387 | 90 | 74 | 162 | 18 | 41 | 118 | FGF18_chr5_171414647_171462626 | FGF18 | MYSAP others(202): Show |
chr5 | 171414647 | 171462626 |
| a0002 | 0/0 | 207 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | MYSAP others(202): Show |
chr5 | 171414647 | 171462626 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 621 | 355 | 90 | 69 | 141 | 15 | 38 | FGF18_chr5_171414647_171462626 | FGF18 | ATGTA others(616): Show |
chr5 | 171414647 | 171462626 | ||
| a0001c0002 | 0/0 | 621 | 29 | 0 | 5 | 18 | 3 | 3 | FGF18_chr5_171414647_171462626 | FGF18 | ATGTA others(616): Show |
chr5 | 171414647 | 171462626 | ||
| a0001c0003 | 0/0 | 621 | 3 | 0 | 0 | 3 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | ATGTA others(616): Show |
chr5 | 171414647 | 171462626 | ||
| a0002c0004 | 0/0 | 621 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | ATGTA others(616): Show |
chr5 | 171414647 | 171462626 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1998 | 326 | 82 | 62 | 130 | 15 | 35 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0002 | 0/0 | 1999 | 19 | 5 | 4 | 9 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1994): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0003 | 0/0 | 1998 | 2 | 1 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0004 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0005 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0006 | 0/0 | 1999 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1994): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0007 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0008 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0009 | 0/0 | 1998 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0010 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0001t0011 | 0/0 | 1998 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0002t0001 | 0/0 | 1998 | 29 | 0 | 5 | 18 | 3 | 3 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0001c0003t0001 | 0/0 | 1998 | 3 | 0 | 0 | 3 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| a0002c0004t0001 | 0/0 | 1998 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | GGGAG others(1993): Show |
chr5 | 171414647 | 171462626 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 2 | 0 | 5 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0339 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0003g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0009g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0010g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| a0002c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | FIN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0098 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0148 | EUR | IBS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | IBS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0021 | EUR | IBS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | IBS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0021 | EUR | IBS | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0265 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | CDX | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0119 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0273 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0340 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0324 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03710 | hp1 | a0002 | c0004 | t0001 | g0151 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03942 | hp2 | a0001 | c0001 | t0011 | g0252 | SAS | BEB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG04228 | hp2 | a0001 | c0001 | t0009 | g0222 | SAS | STU | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | CHB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0088 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18993 | hp2 | a0001 | c0001 | t0010 | g0049 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | LWK | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | YRI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ASW | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ASW | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | GIH | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | GIH | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | USA | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | USA | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | LWK | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0215 | REF | REF | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0339 | REF | REF | FGF18_chr5_171414647_171462626 | FGF18 | chr5 | 171414647 | 171462626 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:171436169 | G | A | 1 | a0002 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.146G>A | p.Arg49His | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/5 | 699/1998 | 146/624 | 49/207 | chr5 | 171436169 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:171456664 | G | A | 1 | a0001c0003 | 3 | HG02129.hp2 HG02155.hp2 NA18994.hp1 |
synonymous_variant | LOW | c.483G>A | p.Lys161Lys | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 5/5 | 1036/1998 | 483/624 | 161/207 | chr5 | 171456664 | |||
| chr5:171456730 | G | A | 1 | a0001c0002 | 29 | HG00735.hp1 HG01081.hp2 HG01496.hp2 others(26): Show |
synonymous_variant | LOW | c.549G>A | p.Pro183Pro | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 5/5 | 1102/1998 | 549/624 | 183/207 | chr5 | 171456730 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:171419679 | C | T | 1 | a0001c0001t0011 | 1 | HG03942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-521C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 521 | chr5 | 171419679 | ||||||
| chr5:171419860 | C | A | 1 | a0001c0001t0004 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-340C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 340 | chr5 | 171419860 | ||||||
| chr5:171419880 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-320C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 320 | chr5 | 171419880 | ||||||
| chr5:171419882 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-318C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 318 | chr5 | 171419882 | ||||||
| chr5:171419885 | A | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-315A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 315 | chr5 | 171419885 | ||||||
| chr5:171419887 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-313G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | chr5 | 171419887 | |||||||
| chr5:171419889 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-311C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 311 | chr5 | 171419889 | ||||||
| chr5:171419890 | C | A | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-310C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 310 | chr5 | 171419890 | ||||||
| chr5:171419891 | G | A | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-309G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 309 | chr5 | 171419891 | ||||||
| chr5:171419904 | T | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-296T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 296 | chr5 | 171419904 | ||||||
| chr5:171419905 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-295G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 295 | chr5 | 171419905 | ||||||
| chr5:171419906 | A | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-294A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 294 | chr5 | 171419906 | ||||||
| chr5:171419910 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-290A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 290 | chr5 | 171419910 | ||||||
| chr5:171419911 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-289G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 289 | chr5 | 171419911 | ||||||
| chr5:171419914 | T | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-286T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 286 | chr5 | 171419914 | ||||||
| chr5:171419918 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-282C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 282 | chr5 | 171419918 | ||||||
| chr5:171419921 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-279A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 279 | chr5 | 171419921 | ||||||
| chr5:171419923 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-277C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 277 | chr5 | 171419923 | ||||||
| chr5:171419927 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-273C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 273 | chr5 | 171419927 | ||||||
| chr5:171419928 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-272A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 272 | chr5 | 171419928 | ||||||
| chr5:171419931 | C | A | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-269C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 269 | chr5 | 171419931 | ||||||
| chr5:171419934 | C | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-266C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 266 | chr5 | 171419934 | ||||||
| chr5:171419935 | T | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-265T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 265 | chr5 | 171419935 | ||||||
| chr5:171419937 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-263C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 263 | chr5 | 171419937 | ||||||
| chr5:171419942 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-258C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 258 | chr5 | 171419942 | ||||||
| chr5:171419943 | A | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-257A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 257 | chr5 | 171419943 | ||||||
| chr5:171419947 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-253G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 253 | chr5 | 171419947 | ||||||
| chr5:171419949 | T | A | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-251T>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 251 | chr5 | 171419949 | ||||||
| chr5:171419955 | C | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-245C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 245 | chr5 | 171419955 | ||||||
| chr5:171419959 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-241C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 241 | chr5 | 171419959 | ||||||
| chr5:171419960 | A | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-240A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 240 | chr5 | 171419960 | ||||||
| chr5:171419964 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-236C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 236 | chr5 | 171419964 | ||||||
| chr5:171419965 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-235C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 235 | chr5 | 171419965 | ||||||
| chr5:171419966 | T | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-234T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 234 | chr5 | 171419966 | ||||||
| chr5:171419972 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-228A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 228 | chr5 | 171419972 | ||||||
| chr5:171419974 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-226C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 226 | chr5 | 171419974 | ||||||
| chr5:171419976 | C | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-224C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | chr5 | 171419976 | |||||||
| chr5:171419978 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-222G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 222 | chr5 | 171419978 | ||||||
| chr5:171419981 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-219G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 219 | chr5 | 171419981 | ||||||
| chr5:171419985 | C | A | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-215C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 215 | chr5 | 171419985 | ||||||
| chr5:171419993 | G | C | 2 | a0001c0001t0005 a0001c0001t0010 |
2 | HG01496.hp1 NA18993.hp2 |
5_prime_UTR_variant | MODIFIER | c.-207G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 207 | chr5 | 171419993 | ||||||
| chr5:171419996 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-204A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 204 | chr5 | 171419996 | ||||||
| chr5:171419997 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-203G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 203 | chr5 | 171419997 | ||||||
| chr5:171419999 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-201A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 201 | chr5 | 171419999 | ||||||
| chr5:171420000 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-200G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 200 | chr5 | 171420000 | ||||||
| chr5:171420005 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-195G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 195 | chr5 | 171420005 | ||||||
| chr5:171420007 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-193G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | chr5 | 171420007 | |||||||
| chr5:171420014 | T | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-186T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 186 | chr5 | 171420014 | ||||||
| chr5:171420015 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-185G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 185 | chr5 | 171420015 | ||||||
| chr5:171420016 | A | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-184A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 184 | chr5 | 171420016 | ||||||
| chr5:171420017 | T | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-183T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 183 | chr5 | 171420017 | ||||||
| chr5:171420019 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-181C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 181 | chr5 | 171420019 | ||||||
| chr5:171420021 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-179G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 179 | chr5 | 171420021 | ||||||
| chr5:171420024 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-176G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | chr5 | 171420024 | |||||||
| chr5:171420026 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-174G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 174 | chr5 | 171420026 | ||||||
| chr5:171420028 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-172G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 172 | chr5 | 171420028 | ||||||
| chr5:171420030 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-170G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 170 | chr5 | 171420030 | ||||||
| chr5:171420036 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-164G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 164 | chr5 | 171420036 | ||||||
| chr5:171420037 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-163A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 163 | chr5 | 171420037 | ||||||
| chr5:171420038 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-162G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 162 | chr5 | 171420038 | ||||||
| chr5:171420040 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 160 | chr5 | 171420040 | ||||||
| chr5:171420043 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-157C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 157 | chr5 | 171420043 | ||||||
| chr5:171420045 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-155G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 155 | chr5 | 171420045 | ||||||
| chr5:171420047 | A | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-153A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 153 | chr5 | 171420047 | ||||||
| chr5:171420050 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-150A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 150 | chr5 | 171420050 | ||||||
| chr5:171420054 | G | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-146G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 146 | chr5 | 171420054 | ||||||
| chr5:171420055 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-145A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 145 | chr5 | 171420055 | ||||||
| chr5:171420057 | T | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-143T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 143 | chr5 | 171420057 | ||||||
| chr5:171420059 | T | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 141 | chr5 | 171420059 | ||||||
| chr5:171420062 | A | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 138 | chr5 | 171420062 | ||||||
| chr5:171420063 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 137 | chr5 | 171420063 | ||||||
| chr5:171420066 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-134G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 134 | chr5 | 171420066 | ||||||
| chr5:171420069 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 131 | chr5 | 171420069 | ||||||
| chr5:171420070 | C | T | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 130 | chr5 | 171420070 | ||||||
| chr5:171420071 | A | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-129A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 129 | chr5 | 171420071 | ||||||
| chr5:171420074 | C | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-126C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 126 | chr5 | 171420074 | ||||||
| chr5:171420075 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 125 | chr5 | 171420075 | ||||||
| chr5:171420081 | G | C | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-119G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 119 | chr5 | 171420081 | ||||||
| chr5:171420082 | A | G | 1 | a0001c0001t0010 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 1/5 | 118 | chr5 | 171420082 | ||||||
| chr5:171456817 | G | A | 1 | a0001c0001t0006 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 5/5 | 12 | chr5 | 171456817 | ||||||
| chr5:171457036 | A | C | 1 | a0001c0001t0003 | 2 | HG01243.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*231A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 5/5 | 231 | chr5 | 171457036 | ||||||
| chr5:171457148 | G | T | 1 | a0001c0001t0009 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*343G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 5/5 | 343 | chr5 | 171457148 | ||||||
| chr5:171457158 | G | GA | 2 | a0001c0001t0002 a0001c0001t0006 |
20 | HG00673.hp2 HG01109.hp2 HG01346.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*367dupA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 5/5 | 368 | INFO_REALIGN_3_PRIME | chr5 | 171457158 | |||||
| chr5:171457173 | C | A | 2 | a0001c0001t0007 a0001c0001t0008 |
2 | NA18957.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*368C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 5/5 | 368 | chr5 | 171457173 | ||||||
| chr5:171457174 | A | C | 1 | a0001c0001t0008 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*369A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 5/5 | 369 | chr5 | 171457174 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:171420551 | T | C | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(327): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.69+108T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171420551 | |||||||
| chr5:171420573 | A | G | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.69+130A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171420573 | |||||||
| chr5:171420700 | G | T | 1 | a0001c0001t0001g0329 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69+257G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171420700 | |||||||
| chr5:171420996 | G | T | 1 | a0001c0001t0001g0328 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+553G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171420996 | |||||||
| chr5:171421083 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.69+640G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171421083 | |||||||
| chr5:171421120 | G | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.69+677G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171421120 | |||||||
| chr5:171421177 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.69+734G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171421177 | |||||||
| chr5:171421205 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.69+762C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171421205 | |||||||
| chr5:171421529 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.69+1086G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171421529 | |||||||
| chr5:171421556 | GA | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0207 a0001c0001t0001g0208 others(6): Show |
11 | HG02145.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+1116delA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171421556 | ||||||
| chr5:171421801 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.69+1358C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171421801 | |||||||
| chr5:171421812 | A | T | 1 | a0001c0002t0001g0326 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.69+1369A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171421812 | |||||||
| chr5:171421890 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.69+1447G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171421890 | |||||||
| chr5:171422213 | G | T | 1 | a0001c0001t0001g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.69+1770G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422213 | |||||||
| chr5:171422288 | G | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+1845G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422288 | |||||||
| chr5:171422424 | G | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0207 a0001c0001t0001g0208 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+1981G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422424 | |||||||
| chr5:171422443 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.69+2000T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422443 | |||||||
| chr5:171422517 | C | T | 19 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0196 others(16): Show |
21 | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.69+2074C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422517 | |||||||
| chr5:171422635 | G | A | 1 | a0001c0001t0003g0026 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.69+2192G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422635 | |||||||
| chr5:171422771 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.69+2328G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422771 | |||||||
| chr5:171422773 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.69+2330G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422773 | |||||||
| chr5:171422783 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+2340G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422783 | |||||||
| chr5:171422787 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.69+2344C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422787 | |||||||
| chr5:171422951 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.69+2508T>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171422951 | |||||||
| chr5:171423025 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.69+2582C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171423025 | |||||||
| chr5:171423291 | A | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18953.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.69+2848A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171423291 | |||||||
| chr5:171423441 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.69+2998G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171423441 | |||||||
| chr5:171423657 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.69+3214C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171423657 | |||||||
| chr5:171423711 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.69+3268G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171423711 | |||||||
| chr5:171423773 | C | CT | 31 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(28): Show |
31 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.69+3354dupT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171423773 | ||||||
| chr5:171423773 | CT | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(114): Show |
131 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.69+3354delT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171423773 | ||||||
| chr5:171423773 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+3344_69+3354del others(11): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171423773 | ||||||
| chr5:171423793 | T | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
88 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.69+3350T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171423793 | |||||||
| chr5:171424009 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.69+3566C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424009 | |||||||
| chr5:171424021 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.69+3578T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424021 | |||||||
| chr5:171424022 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.69+3579C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424022 | |||||||
| chr5:171424128 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.69+3685G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424128 | |||||||
| chr5:171424196 | G | T | 1 | a0001c0003t0001g0204 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.69+3753G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424196 | |||||||
| chr5:171424473 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0002g0340 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.69+4030C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424473 | |||||||
| chr5:171424474 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.69+4031G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424474 | |||||||
| chr5:171424513 | T | C | 6 | a0001c0001t0001g0117 a0001c0001t0001g0233 a0001c0001t0002g0118 others(3): Show |
7 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+4070T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424513 | |||||||
| chr5:171424549 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0029 others(68): Show |
79 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.69+4106C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424549 | |||||||
| chr5:171424620 | A | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(212): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.69+4177A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424620 | |||||||
| chr5:171424794 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.69+4351G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424794 | |||||||
| chr5:171424801 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+4358G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171424801 | |||||||
| chr5:171424853 | GGGGGAGG others(4): Show |
G | 1 | a0001c0001t0001g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+4421_69+4431del others(11): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171424853 | ||||||
| chr5:171425216 | A | G | 2 | a0001c0001t0001g0311 a0001c0001t0002g0171 |
2 | HG00673.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.69+4773A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171425216 | |||||||
| chr5:171425267 | G | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0233 a0001c0001t0002g0118 others(2): Show |
6 | HG01109.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+4824G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171425267 | |||||||
| chr5:171425383 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.69+4940G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171425383 | |||||||
| chr5:171425529 | C | CT | 95 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(92): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.69+5105dupT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171425529 | ||||||
| chr5:171425529 | C | CTT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0116 a0001c0001t0001g0156 others(7): Show |
11 | HG00642.hp1 HG00738.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+5104_69+5105dup others(2): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171425529 | ||||||
| chr5:171425669 | T | A | 78 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
87 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.69+5226T>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171425669 | |||||||
| chr5:171425678 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0212 |
2 | HG04115.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.69+5235G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171425678 | |||||||
| chr5:171425855 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.69+5412A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171425855 | |||||||
| chr5:171425992 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.69+5549G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171425992 | |||||||
| chr5:171426144 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0232 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.69+5701C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426144 | |||||||
| chr5:171426171 | T | C | 4 | a0001c0001t0001g0233 a0001c0001t0002g0118 a0001c0001t0002g0120 others(1): Show |
4 | HG01109.hp2 HG02257.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+5728T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426171 | |||||||
| chr5:171426252 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+5809G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426252 | |||||||
| chr5:171426393 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.69+5950T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426393 | |||||||
| chr5:171426569 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.69+6126G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426569 | |||||||
| chr5:171426734 | C | T | 1 | a0001c0001t0006g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.69+6291C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426734 | |||||||
| chr5:171426753 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.69+6310C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426753 | |||||||
| chr5:171426797 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.69+6354G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426797 | |||||||
| chr5:171426825 | T | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0332 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.69+6382T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171426825 | |||||||
| chr5:171427138 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0003g0026 |
3 | HG01243.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.69+6695C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427138 | |||||||
| chr5:171427158 | G | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
18 | HG00099.hp2 HG00642.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.69+6715G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427158 | |||||||
| chr5:171427163 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.69+6720C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427163 | |||||||
| chr5:171427195 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+6752G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427195 | |||||||
| chr5:171427206 | G | GA | 7 | a0001c0001t0001g0093 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | HG00673.hp1 HG01167.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+6778dupA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171427206 | ||||||
| chr5:171427206 | GA | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0212 a0001c0001t0001g0309 others(3): Show |
6 | HG01123.hp1 HG02129.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+6778delA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171427206 | ||||||
| chr5:171427208 | A | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0332 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.69+6765A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427208 | |||||||
| chr5:171427311 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.69+6868G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427311 | |||||||
| chr5:171427385 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
91 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.69+6942G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427385 | |||||||
| chr5:171427393 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.69+6950A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427393 | |||||||
| chr5:171427516 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.69+7073G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427516 | |||||||
| chr5:171427534 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0176 |
2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.69+7091C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427534 | |||||||
| chr5:171427696 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.69+7253C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427696 | |||||||
| chr5:171427697 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.69+7254T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427697 | |||||||
| chr5:171427753 | A | C | 59 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0091 others(56): Show |
62 | HG00544.hp1 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.69+7310A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427753 | |||||||
| chr5:171427829 | G | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG01978.hp1 HG03688.hp1 HG04199.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+7386G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427829 | |||||||
| chr5:171427834 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(47): Show |
56 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.69+7391G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427834 | |||||||
| chr5:171427858 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+7415G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171427858 | |||||||
| chr5:171428122 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(45): Show |
54 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.69+7679C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171428122 | |||||||
| chr5:171428242 | G | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0317 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.69+7799G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171428242 | |||||||
| chr5:171428331 | C | T | 77 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(74): Show |
84 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.70-7762C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171428331 | |||||||
| chr5:171428814 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.70-7279A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171428814 | |||||||
| chr5:171429030 | G | A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0001t0001g0317 others(1): Show |
4 | HG03041.hp1 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-7063G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429030 | |||||||
| chr5:171429079 | T | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.70-7014T>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429079 | |||||||
| chr5:171429086 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70-7007C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429086 | |||||||
| chr5:171429173 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.70-6920G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429173 | |||||||
| chr5:171429329 | G | A | 16 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(13): Show |
19 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-6764G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429329 | |||||||
| chr5:171429541 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.70-6552G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429541 | |||||||
| chr5:171429629 | G | T | 1 | a0001c0002t0001g0201 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.70-6464G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429629 | |||||||
| chr5:171429735 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0159 |
3 | HG00639.hp1 HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.70-6358G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429735 | |||||||
| chr5:171429856 | A | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0317 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-6237A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429856 | |||||||
| chr5:171429856 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | NA18946.hp1 NA18949.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-6237A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171429856 | |||||||
| chr5:171430186 | GTC | G | 20 | a0001c0001t0001g0193 a0001c0001t0001g0196 a0001c0002t0001g0005 others(17): Show |
23 | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-5903_70-5902del others(2): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430186 | ||||||
| chr5:171430221 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70-5872G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430221 | |||||||
| chr5:171430221 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.70-5872G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430221 | |||||||
| chr5:171430273 | A | G | 87 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(84): Show |
96 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.70-5820A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430273 | |||||||
| chr5:171430357 | C | CA | 95 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
106 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.70-5717dupA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430357 | ||||||
| chr5:171430357 | CA | C | 13 | a0001c0001t0001g0091 a0001c0001t0001g0112 a0001c0001t0001g0113 others(10): Show |
13 | HG00323.hp2 HG01070.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-5717delA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430357 | ||||||
| chr5:171430421 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0234 |
2 | HG00673.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.70-5672C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430421 | |||||||
| chr5:171430469 | C | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0235 |
2 | HG02155.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.70-5624C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430469 | |||||||
| chr5:171430493 | TAAAGAAA others(313): Show |
T | 9 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-5586_70-5267del | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430493 | ||||||
| chr5:171430494 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.70-5599A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430494 | |||||||
| chr5:171430597 | G | C | 1 | a0001c0001t0001g0254 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.70-5496G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430597 | |||||||
| chr5:171430705 | G | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.70-5388G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430705 | |||||||
| chr5:171430794 | C | CA | 17 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0124 others(14): Show |
17 | HG00099.hp1 HG00423.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.70-5277dupA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430794 | ||||||
| chr5:171430794 | CA | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(46): Show |
55 | HG00280.hp1 HG00609.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.70-5277delA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430794 | ||||||
| chr5:171430794 | CAAAAAAA others(5): Show |
C | 24 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0001c0001t0001g0126 others(21): Show |
24 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.70-5288_70-5277del others(12): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430794 | ||||||
| chr5:171430807 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.70-5279_70-5270del others(10): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430807 | ||||||
| chr5:171430809 | AAAAAAAA others(1): Show |
A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
82 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.70-5277_70-5270del others(8): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171430809 | ||||||
| chr5:171430810 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70-5283A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430810 | |||||||
| chr5:171430813 | A | G | 1 | a0001c0002t0001g0032 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.70-5280A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171430813 | |||||||
| chr5:171431021 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.70-5072T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431021 | |||||||
| chr5:171431131 | G | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.70-4962G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431131 | |||||||
| chr5:171431190 | C | A | 76 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(73): Show |
83 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.70-4903C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431190 | |||||||
| chr5:171431209 | G | C | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70-4884G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431209 | |||||||
| chr5:171431211 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.70-4882T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431211 | |||||||
| chr5:171431240 | C | T | 1 | a0001c0002t0001g0324 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.70-4853C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431240 | |||||||
| chr5:171431304 | A | AAGGATGA others(19): Show |
1 | a0001c0001t0001g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.70-4788_70-4763dup others(26): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171431304 | ||||||
| chr5:171431337 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.70-4756G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431337 | |||||||
| chr5:171431402 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0272 |
2 | HG02735.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.70-4691C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431402 | |||||||
| chr5:171431521 | T | C | 9 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-4572T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431521 | |||||||
| chr5:171431527 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.70-4566C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431527 | |||||||
| chr5:171431636 | G | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.70-4457G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431636 | |||||||
| chr5:171431756 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70-4337C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431756 | |||||||
| chr5:171431808 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0230 |
2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70-4285C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431808 | |||||||
| chr5:171431875 | C | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0314 |
2 | NA18944.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.70-4218C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431875 | |||||||
| chr5:171431957 | G | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0232 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.70-4136G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431957 | |||||||
| chr5:171431997 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.70-4096C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431997 | |||||||
| chr5:171431998 | G | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.70-4095G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171431998 | |||||||
| chr5:171432006 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0317 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-4087G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432006 | |||||||
| chr5:171432204 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.70-3889C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432204 | |||||||
| chr5:171432224 | G | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(215): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.70-3869G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432224 | |||||||
| chr5:171432347 | T | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.70-3746T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432347 | |||||||
| chr5:171432359 | T | TTTC | 140 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(137): Show |
155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.70-3716_70-3714dup others(3): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171432359 | ||||||
| chr5:171432380 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.70-3713T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432380 | |||||||
| chr5:171432396 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0219 a0001c0001t0003g0026 |
4 | HG01243.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-3697T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432396 | |||||||
| chr5:171432516 | C | A | 6 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0112 others(3): Show |
6 | HG00280.hp1 HG01256.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-3577C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432516 | |||||||
| chr5:171432520 | G | A | 9 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-3573G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432520 | |||||||
| chr5:171432660 | C | A | 1 | a0001c0001t0001g0278 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.70-3433C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432660 | |||||||
| chr5:171432677 | ACCTCGGC others(22): Show |
A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0073 |
2 | NA19084.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.70-3414_70-3386del others(29): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171432677 | ||||||
| chr5:171432682 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.70-3411G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432682 | |||||||
| chr5:171432712 | A | G | 9 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-3381A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432712 | |||||||
| chr5:171432779 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.70-3314A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432779 | |||||||
| chr5:171432843 | A | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(45): Show |
54 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.70-3250A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432843 | |||||||
| chr5:171432870 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.70-3223G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432870 | |||||||
| chr5:171432963 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.70-3130G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171432963 | |||||||
| chr5:171433013 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70-3080G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433013 | |||||||
| chr5:171433017 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG00323.hp2 HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.70-3076G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433017 | |||||||
| chr5:171433052 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.70-3041C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433052 | |||||||
| chr5:171433165 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.70-2928A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433165 | |||||||
| chr5:171433246 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.70-2847C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433246 | |||||||
| chr5:171433299 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.70-2794C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433299 | |||||||
| chr5:171433359 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.70-2734C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433359 | |||||||
| chr5:171433365 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70-2728G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433365 | |||||||
| chr5:171433405 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.70-2688G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433405 | |||||||
| chr5:171433413 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0258 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-2680C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433413 | |||||||
| chr5:171433515 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70-2578C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171433515 | |||||||
| chr5:171434260 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.70-1833A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171434260 | |||||||
| chr5:171434433 | C | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(7): Show |
13 | HG00099.hp2 HG00642.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-1660C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171434433 | |||||||
| chr5:171434446 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.70-1647A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171434446 | |||||||
| chr5:171434458 | G | C | 1 | a0001c0001t0001g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.70-1635G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171434458 | |||||||
| chr5:171434478 | G | A | 2 | a0001c0001t0002g0120 a0001c0001t0002g0125 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.70-1615G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171434478 | |||||||
| chr5:171434769 | T | C | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.70-1324T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171434769 | |||||||
| chr5:171434809 | C | CT | 79 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0018 others(76): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.70-1268dupT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 171434809 | ||||||
| chr5:171434960 | T | G | 12 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0001t0001g0233 others(9): Show |
12 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-1133T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171434960 | |||||||
| chr5:171434989 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.70-1104G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171434989 | |||||||
| chr5:171435130 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG03579.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.70-963G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435130 | |||||||
| chr5:171435292 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0334 |
2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.70-801G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435292 | |||||||
| chr5:171435337 | T | C | 12 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0001t0001g0233 others(9): Show |
12 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-756T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435337 | |||||||
| chr5:171435412 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.70-681G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435412 | |||||||
| chr5:171435731 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0043 |
3 | HG01255.hp2 HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.70-362C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435731 | |||||||
| chr5:171435781 | C | A | 1 | a0001c0001t0006g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.70-312C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435781 | |||||||
| chr5:171435834 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.70-259G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435834 | |||||||
| chr5:171435973 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.70-120C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435973 | |||||||
| chr5:171435990 | G | A | 9 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-103G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171435990 | |||||||
| chr5:171436013 | T | G | 1 | a0001c0001t0001g0022 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-80T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171436013 | |||||||
| chr5:171436038 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.70-55A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 2/4 | chr5 | 171436038 | |||||||
| chr5:171436431 | G | T | 1 | a0001c0001t0001g0072 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.250+158G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171436431 | |||||||
| chr5:171436505 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(216): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.250+232C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171436505 | |||||||
| chr5:171436649 | A | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(218): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.250+376A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171436649 | |||||||
| chr5:171436663 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.250+390G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171436663 | |||||||
| chr5:171436668 | A | T | 1 | a0001c0001t0001g0072 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.250+395A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171436668 | |||||||
| chr5:171436669 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.250+396A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171436669 | |||||||
| chr5:171436670 | A | T | 1 | a0001c0001t0001g0072 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.250+397A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171436670 | |||||||
| chr5:171436935 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0308 |
2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.250+662C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171436935 | |||||||
| chr5:171437017 | G | T | 86 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(83): Show |
93 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.250+744G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437017 | |||||||
| chr5:171437128 | G | A | 1 | a0001c0001t0001g0321 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.250+855G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437128 | |||||||
| chr5:171437165 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.250+892C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437165 | |||||||
| chr5:171437235 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(220): Show |
245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.250+962A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437235 | |||||||
| chr5:171437479 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.250+1206C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437479 | |||||||
| chr5:171437486 | G | A | 7 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG00639.hp2 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+1213G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437486 | |||||||
| chr5:171437544 | T | C | 91 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(88): Show |
98 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.250+1271T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437544 | |||||||
| chr5:171437597 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.250+1324C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437597 | |||||||
| chr5:171437849 | G | C | 1 | a0001c0001t0006g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.250+1576G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171437849 | |||||||
| chr5:171438084 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.250+1811T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438084 | |||||||
| chr5:171438099 | C | CT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0152 a0001c0001t0001g0184 others(3): Show |
7 | HG01192.hp1 HG03516.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+1843dupT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171438099 | ||||||
| chr5:171438099 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.250+1826C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438099 | |||||||
| chr5:171438099 | CT | C | 93 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(90): Show |
101 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.250+1843delT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171438099 | ||||||
| chr5:171438100 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.250+1827T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438100 | |||||||
| chr5:171438159 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.250+1886T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438159 | |||||||
| chr5:171438160 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.250+1887G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438160 | |||||||
| chr5:171438205 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.250+1932G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438205 | |||||||
| chr5:171438225 | C | T | 80 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(77): Show |
87 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.250+1952C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438225 | |||||||
| chr5:171438312 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0002g0249 |
5 | HG01884.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+2039G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438312 | |||||||
| chr5:171438348 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.250+2075C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438348 | |||||||
| chr5:171438400 | G | A | 1 | a0001c0001t0008g0088 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.250+2127G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438400 | |||||||
| chr5:171438618 | G | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0247 a0001c0001t0001g0334 |
3 | HG02647.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.250+2345G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438618 | |||||||
| chr5:171438647 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.250+2374C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171438647 | |||||||
| chr5:171439187 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250+2914C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439187 | |||||||
| chr5:171439270 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.250+2997C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439270 | |||||||
| chr5:171439292 | C | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | HG01106.hp2 HG02258.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.250+3019C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439292 | |||||||
| chr5:171439332 | C | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0176 |
2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.250+3059C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439332 | |||||||
| chr5:171439495 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.250+3222G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439495 | |||||||
| chr5:171439707 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.250+3434C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439707 | |||||||
| chr5:171439754 | G | C | 96 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(93): Show |
103 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.250+3481G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439754 | |||||||
| chr5:171439755 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG01070.hp1 HG01071.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.250+3482G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439755 | |||||||
| chr5:171439792 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.250+3519C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439792 | |||||||
| chr5:171439891 | G | GA | 7 | a0001c0001t0001g0196 a0001c0002t0001g0005 a0001c0002t0001g0192 others(4): Show |
9 | HG00735.hp1 HG01496.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+3627dupA | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171439891 | ||||||
| chr5:171439922 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.250+3649C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171439922 | |||||||
| chr5:171440217 | TGGGTGTG others(29): Show |
T | 1 | a0001c0001t0001g0245 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.250+3947_250+3982d others(38): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171440217 | ||||||
| chr5:171440225 | T | TG | 62 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
70 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.250+3961dupG | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171440225 | ||||||
| chr5:171440225 | TG | T | 92 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(89): Show |
99 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.250+3961delG | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171440225 | ||||||
| chr5:171440227 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(48): Show |
57 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.250+3954G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171440227 | |||||||
| chr5:171440228 | G | C | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.250+3955G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171440228 | |||||||
| chr5:171440273 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.250+4000G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171440273 | |||||||
| chr5:171440343 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250+4070C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171440343 | |||||||
| chr5:171440371 | T | G | 94 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(91): Show |
101 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.250+4098T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171440371 | |||||||
| chr5:171440573 | A | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(221): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.250+4300A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171440573 | |||||||
| chr5:171440632 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0247 a0001c0001t0001g0334 |
3 | HG02647.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.250+4359A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171440632 | |||||||
| chr5:171440825 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.250+4552C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171440825 | |||||||
| chr5:171441055 | C | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
87 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.250+4782C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171441055 | |||||||
| chr5:171441095 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.250+4822G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171441095 | |||||||
| chr5:171441460 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.250+5187A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171441460 | |||||||
| chr5:171441472 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | NA19005.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.250+5199C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171441472 | |||||||
| chr5:171441473 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250+5200G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171441473 | |||||||
| chr5:171441547 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.250+5274G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171441547 | |||||||
| chr5:171441618 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(44): Show |
53 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.250+5345C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171441618 | |||||||
| chr5:171441890 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.250+5617C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171441890 | |||||||
| chr5:171442010 | C | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
87 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.250+5737C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442010 | |||||||
| chr5:171442169 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(12): Show |
20 | HG00140.hp1 HG00280.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.250+5896C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442169 | |||||||
| chr5:171442290 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.250+6017C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442290 | |||||||
| chr5:171442415 | T | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
88 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.250+6142T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442415 | |||||||
| chr5:171442449 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0325 |
2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.250+6176C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442449 | |||||||
| chr5:171442493 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0002g0168 |
2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.250+6220C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442493 | |||||||
| chr5:171442578 | T | C | 174 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(171): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.250+6305T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442578 | |||||||
| chr5:171442702 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0242 |
2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.250+6429G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442702 | |||||||
| chr5:171442793 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
88 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.251-6354C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171442793 | |||||||
| chr5:171443135 | C | CTTT | 92 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(89): Show |
99 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.251-6001_251-5999d others(5): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443135 | ||||||
| chr5:171443278 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.251-5869T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443278 | |||||||
| chr5:171443279 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.251-5868G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443279 | |||||||
| chr5:171443296 | A | AT | 96 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(93): Show |
103 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.251-5843dupT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443296 | ||||||
| chr5:171443296 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.251-5851A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443296 | |||||||
| chr5:171443455 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0159 |
3 | HG00639.hp1 HG00741.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.251-5692G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443455 | |||||||
| chr5:171443473 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.251-5674G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443473 | |||||||
| chr5:171443500 | C | CTTTTTTT others(1): Show |
15 | a0001c0001t0001g0023 a0001c0001t0001g0107 a0001c0001t0001g0116 others(12): Show |
16 | HG00639.hp2 HG01069.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.251-5647_251-5646i others(10): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | C | CTTTTTTT others(2): Show |
23 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0108 others(20): Show |
28 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.251-5647_251-5646i others(11): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | C | CTTTTTTT others(3): Show |
22 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0132 others(19): Show |
22 | HG01109.hp2 HG01952.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.251-5647_251-5646i others(12): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | C | CTTTTTTT others(4): Show |
9 | a0001c0001t0001g0126 a0001c0001t0001g0181 a0001c0001t0001g0264 others(6): Show |
9 | HG01069.hp1 HG01884.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.251-5647_251-5646i others(13): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | C | CTTTTTTT others(5): Show |
6 | a0001c0001t0001g0091 a0001c0001t0001g0127 a0001c0001t0001g0141 others(3): Show |
6 | HG01071.hp1 HG02027.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-5647_251-5646i others(14): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.251-5647_251-5646i others(16): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | C | CTTTTTTT others(9): Show |
5 | a0001c0001t0001g0109 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG00544.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-5647_251-5646i others(18): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | CAT | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0178 a0001c0001t0001g0269 others(1): Show |
4 | HG01071.hp2 HG01099.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-5646_251-5645d others(4): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | CATTTTTT others(6): Show |
C | 1 | a0001c0001t0003g0026 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.251-5646_251-5634d others(15): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443500 | CATTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.251-5646_251-5633d others(16): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443500 | |||||||
| chr5:171443501 | A | ATTTTT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0029 others(24): Show |
33 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.251-5619_251-5615d others(7): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443501 | ||||||
| chr5:171443501 | A | ATTTTTT | 19 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0163 others(16): Show |
19 | HG00741.hp2 HG01123.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.251-5620_251-5615d others(8): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443501 | ||||||
| chr5:171443501 | A | ATTTTTTT | 6 | a0001c0001t0001g0147 a0001c0001t0001g0166 a0001c0001t0001g0301 others(3): Show |
6 | HG00099.hp1 HG00544.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-5621_251-5615d others(9): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443501 | ||||||
| chr5:171443501 | A | ATTTTTTT others(1): Show |
6 | a0001c0001t0001g0033 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
8 | NA18747.hp1 NA18945.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.251-5622_251-5615d others(10): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443501 | ||||||
| chr5:171443501 | A | T | 85 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(82): Show |
91 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.251-5646A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443501 | |||||||
| chr5:171443501 | AT | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0028 others(28): Show |
38 | HG00642.hp2 HG00735.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.251-5615delT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443501 | ||||||
| chr5:171443501 | ATT | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0121 a0001c0001t0001g0218 others(3): Show |
6 | HG01167.hp1 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-5616_251-5615d others(4): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443501 | ||||||
| chr5:171443501 | ATTT | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0045 others(9): Show |
13 | HG00280.hp2 HG00438.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-5617_251-5615d others(5): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443501 | ||||||
| chr5:171443501 | ATTTT | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(110): Show |
127 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.251-5618_251-5615d others(6): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171443501 | ||||||
| chr5:171443542 | A | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(221): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.251-5605A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443542 | |||||||
| chr5:171443641 | C | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
87 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.251-5506C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443641 | |||||||
| chr5:171443645 | T | C | 174 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(171): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.251-5502T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443645 | |||||||
| chr5:171443843 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(44): Show |
51 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.251-5304C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443843 | |||||||
| chr5:171443917 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.251-5230G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171443917 | |||||||
| chr5:171444059 | T | TC | 220 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(217): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.251-5085dupC | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171444059 | ||||||
| chr5:171444068 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(136): Show |
150 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.251-5079C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171444068 | |||||||
| chr5:171444070 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(217): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.251-5077G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171444070 | |||||||
| chr5:171444742 | A | G | 2 | a0001c0002t0001g0299 a0001c0002t0001g0318 |
2 | NA18747.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.251-4405A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171444742 | |||||||
| chr5:171444842 | G | A | 12 | a0001c0001t0001g0185 a0001c0001t0001g0233 a0001c0001t0001g0244 others(9): Show |
12 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-4305G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171444842 | |||||||
| chr5:171444977 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.251-4170G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171444977 | |||||||
| chr5:171445147 | C | T | 22 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0045 others(19): Show |
23 | HG00558.hp1 HG00621.hp2 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.251-4000C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445147 | |||||||
| chr5:171445176 | C | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0116 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-3971C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445176 | |||||||
| chr5:171445274 | A | G | 1 | a0001c0003t0001g0265 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.251-3873A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445274 | |||||||
| chr5:171445279 | A | C | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-3868A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445279 | |||||||
| chr5:171445328 | A | G | 71 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
78 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.251-3819A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445328 | |||||||
| chr5:171445344 | A | G | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.251-3803A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445344 | |||||||
| chr5:171445534 | G | GT | 76 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(73): Show |
85 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.251-3602dupT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 171445534 | ||||||
| chr5:171445604 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.251-3543G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445604 | |||||||
| chr5:171445694 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.251-3453C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445694 | |||||||
| chr5:171445699 | G | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0187 |
4 | NA18952.hp1 NA18971.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-3448G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445699 | |||||||
| chr5:171445903 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
5 | HG01069.hp2 HG01346.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-3244G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445903 | |||||||
| chr5:171445903 | G | C | 1 | a0001c0001t0002g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.251-3244G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445903 | |||||||
| chr5:171445943 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.251-3204C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171445943 | |||||||
| chr5:171446072 | A | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(144): Show |
163 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.251-3075A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171446072 | |||||||
| chr5:171446073 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0113 |
2 | HG02683.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.251-3074C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171446073 | |||||||
| chr5:171446091 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.251-3056C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171446091 | |||||||
| chr5:171446146 | T | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
8 | HG01168.hp2 HG01169.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-3001T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171446146 | |||||||
| chr5:171446359 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.251-2788C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171446359 | |||||||
| chr5:171446391 | G | T | 12 | a0001c0001t0001g0185 a0001c0001t0001g0233 a0001c0001t0001g0244 others(9): Show |
12 | HG00639.hp2 HG01109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-2756G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171446391 | |||||||
| chr5:171446581 | G | A | 2 | a0001c0001t0001g0301 a0001c0001t0001g0308 |
2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.251-2566G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171446581 | |||||||
| chr5:171446829 | G | A | 1 | a0001c0002t0001g0324 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.251-2318G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171446829 | |||||||
| chr5:171447134 | T | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(133): Show |
149 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.251-2013T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447134 | |||||||
| chr5:171447282 | A | G | 1 | a0001c0001t0003g0026 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.251-1865A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447282 | |||||||
| chr5:171447285 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.251-1862A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447285 | |||||||
| chr5:171447296 | C | T | 1 | a0001c0001t0011g0252 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.251-1851C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447296 | |||||||
| chr5:171447405 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.251-1742A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447405 | |||||||
| chr5:171447465 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0176 |
2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.251-1682C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447465 | |||||||
| chr5:171447605 | G | A | 3 | a0001c0001t0001g0259 a0001c0001t0001g0314 a0001c0001t0002g0340 |
3 | HG03225.hp2 NA18944.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.251-1542G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447605 | |||||||
| chr5:171447713 | A | C | 1 | a0001c0001t0002g0050 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.251-1434A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447713 | |||||||
| chr5:171447831 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0002g0140 |
2 | HG01978.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.251-1316G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447831 | |||||||
| chr5:171447912 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.251-1235C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171447912 | |||||||
| chr5:171448047 | G | A | 26 | a0001c0001t0002g0249 a0001c0002t0001g0005 a0001c0002t0001g0021 others(23): Show |
30 | HG00735.hp1 HG01081.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.251-1100G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448047 | |||||||
| chr5:171448093 | A | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(90): Show |
103 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.251-1054A>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448093 | |||||||
| chr5:171448147 | A | T | 5 | a0001c0001t0001g0185 a0001c0001t0002g0118 a0001c0001t0002g0120 others(2): Show |
5 | HG01109.hp2 HG02257.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-1000A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448147 | |||||||
| chr5:171448172 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0020 others(44): Show |
51 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.251-975T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448172 | |||||||
| chr5:171448215 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.251-932G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448215 | |||||||
| chr5:171448258 | C | G | 1 | a0001c0001t0001g0297 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.251-889C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448258 | |||||||
| chr5:171448652 | T | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0031 others(2): Show |
8 | HG00140.hp2 HG01074.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-495T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448652 | |||||||
| chr5:171448691 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.251-456T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448691 | |||||||
| chr5:171448754 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0142 |
2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.251-393T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448754 | |||||||
| chr5:171448981 | T | C | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.251-166T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448981 | |||||||
| chr5:171448982 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.251-165G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448982 | |||||||
| chr5:171448983 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.251-164G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 3/4 | chr5 | 171448983 | |||||||
| chr5:171449286 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.357+33G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449286 | |||||||
| chr5:171449360 | C | CGT | 18 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0094 others(15): Show |
18 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.357+147_357+148dup others(2): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | C | CGTGT | 46 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0034 others(43): Show |
50 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.357+145_357+148dup others(4): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | C | CGTGTGT | 35 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0025 others(32): Show |
40 | HG00423.hp1 HG00544.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.357+143_357+148dup others(6): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | C | CGTGTGTG others(1): Show |
63 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(60): Show |
74 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.357+141_357+148dup others(8): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | C | CGTGTGTG others(3): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(42): Show |
55 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.357+139_357+148dup others(10): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | C | CGTGTGTG others(5): Show |
24 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0059 others(21): Show |
24 | HG00323.hp1 HG01256.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.357+137_357+148dup others(12): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | C | CGTGTGTG others(7): Show |
12 | a0001c0001t0001g0051 a0001c0001t0001g0147 a0001c0001t0001g0157 others(9): Show |
12 | HG00099.hp1 HG01106.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.357+135_357+148dup others(14): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | C | CGTGTGTG others(9): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0177 a0001c0001t0001g0301 |
3 | HG00642.hp2 HG01070.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.357+133_357+148dup others(16): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0329 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.357+139_357+148del others(10): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449360 | CGTGTGTG others(11): Show |
C | 2 | a0001c0001t0002g0340 a0001c0001t0003g0026 |
3 | HG01243.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.357+131_357+148del others(18): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449360 | ||||||
| chr5:171449387 | G | T | 1 | a0001c0001t0002g0340 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.357+134G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449387 | |||||||
| chr5:171449390 | TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0006g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.357+139_357+152del others(14): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449390 | ||||||
| chr5:171449396 | TGTGTGA | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0258 a0001c0001t0001g0317 |
3 | HG02717.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.357+145_357+150del others(6): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449396 | ||||||
| chr5:171449398 | TGTGAGA | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0277 a0001c0002t0001g0194 |
3 | HG02055.hp1 NA18952.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.357+147_357+152del others(6): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449398 | ||||||
| chr5:171449400 | T | A | 2 | a0001c0001t0002g0340 a0001c0001t0003g0026 |
3 | HG01243.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.357+147T>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449400 | |||||||
| chr5:171449400 | T | TGTGTGTG others(1): Show |
3 | a0001c0001t0001g0067 a0001c0001t0002g0090 a0001c0001t0007g0213 |
3 | HG01361.hp2 NA19090.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.357+148_357+149ins others(8): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449400 | ||||||
| chr5:171449400 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0013 | 2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.357+148_357+149ins others(10): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449400 | ||||||
| chr5:171449400 | T | TGTGTGTG others(3): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0043 others(3): Show |
7 | HG01106.hp2 HG01192.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.357+148_357+149ins others(10): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449400 | ||||||
| chr5:171449400 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0036 |
2 | HG00280.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.357+148_357+149ins others(12): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449400 | ||||||
| chr5:171449400 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0012 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.357+148_357+149ins others(14): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449400 | ||||||
| chr5:171449400 | TGA | T | 42 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(39): Show |
48 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.357+170_357+171del others(2): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449400 | ||||||
| chr5:171449400 | TGAGA | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0116 others(1): Show |
4 | HG02896.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+168_357+171del others(4): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449400 | ||||||
| chr5:171449402 | A | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.357+149A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449402 | |||||||
| chr5:171449404 | A | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(137): Show |
153 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.357+151A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449404 | |||||||
| chr5:171449406 | A | T | 60 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(57): Show |
66 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.357+153A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449406 | |||||||
| chr5:171449451 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.357+198C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449451 | |||||||
| chr5:171449470 | C | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.357+217C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449470 | |||||||
| chr5:171449492 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.357+239G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449492 | |||||||
| chr5:171449567 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.357+314G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449567 | |||||||
| chr5:171449802 | AT | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0095 a0001c0001t0001g0102 others(2): Show |
6 | HG00609.hp2 NA18946.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.357+552delT | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171449802 | ||||||
| chr5:171449855 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.357+602C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449855 | |||||||
| chr5:171449970 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.357+717T>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171449970 | |||||||
| chr5:171450201 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0055 others(43): Show |
49 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.357+948T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171450201 | |||||||
| chr5:171450242 | T | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
104 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.357+989T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171450242 | |||||||
| chr5:171450433 | G | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(330): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.357+1180G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171450433 | |||||||
| chr5:171450677 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.357+1424C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171450677 | |||||||
| chr5:171450679 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.357+1426C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171450679 | |||||||
| chr5:171450846 | T | C | 1 | a0001c0001t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.357+1593T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171450846 | |||||||
| chr5:171450916 | A | G | 2 | a0001c0001t0002g0340 a0001c0001t0003g0026 |
3 | HG01243.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.357+1663A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171450916 | |||||||
| chr5:171450996 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(124): Show |
138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.357+1743T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171450996 | |||||||
| chr5:171451038 | G | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.357+1785G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451038 | |||||||
| chr5:171451243 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0011g0252 |
2 | HG01257.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.357+1990G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451243 | |||||||
| chr5:171451250 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.357+1997C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451250 | |||||||
| chr5:171451293 | C | T | 4 | a0001c0001t0002g0118 a0001c0001t0002g0120 a0001c0001t0002g0125 others(1): Show |
4 | HG01109.hp2 HG02257.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+2040C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451293 | |||||||
| chr5:171451321 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.357+2068A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451321 | |||||||
| chr5:171451610 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.357+2357C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451610 | |||||||
| chr5:171451613 | T | C | 43 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0047 others(40): Show |
43 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.357+2360T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451613 | |||||||
| chr5:171451645 | C | T | 1 | a0001c0001t0003g0026 | 2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.357+2392C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451645 | |||||||
| chr5:171451717 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.357+2464C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451717 | |||||||
| chr5:171451747 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.357+2494C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451747 | |||||||
| chr5:171451748 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.357+2495G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451748 | |||||||
| chr5:171451786 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.357+2533G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171451786 | |||||||
| chr5:171452218 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(130): Show |
145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.357+2965A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452218 | |||||||
| chr5:171452260 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.357+3007G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452260 | |||||||
| chr5:171452297 | C | T | 5 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0322 others(2): Show |
5 | HG01346.hp2 HG01981.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.357+3044C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452297 | |||||||
| chr5:171452320 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.357+3067A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452320 | |||||||
| chr5:171452411 | T | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(126): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.357+3158T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452411 | |||||||
| chr5:171452658 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0317 |
2 | HG01167.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.357+3405C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452658 | |||||||
| chr5:171452701 | G | A | 3 | a0001c0002t0001g0021 a0001c0002t0001g0148 a0001c0002t0001g0199 |
4 | HG01081.hp2 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+3448G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452701 | |||||||
| chr5:171452709 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.357+3456A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452709 | |||||||
| chr5:171452763 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.357+3510G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171452763 | |||||||
| chr5:171453611 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(123): Show |
138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.358-2928C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171453611 | |||||||
| chr5:171453620 | G | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(115): Show |
129 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.358-2919G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171453620 | |||||||
| chr5:171453805 | T | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): Show |
77 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.358-2734T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171453805 | |||||||
| chr5:171453929 | C | T | 2 | a0001c0001t0002g0118 a0001c0001t0006g0119 |
2 | HG01109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.358-2610C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171453929 | |||||||
| chr5:171453959 | T | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0082 others(2): Show |
5 | NA18977.hp1 NA18991.hp2 NA19084.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-2580T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171453959 | |||||||
| chr5:171453960 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.358-2579C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171453960 | |||||||
| chr5:171454168 | G | C | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.358-2371G>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454168 | |||||||
| chr5:171454268 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.358-2271T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454268 | |||||||
| chr5:171454376 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.358-2163G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454376 | |||||||
| chr5:171454400 | C | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0233 a0001c0001t0001g0247 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-2139C>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454400 | |||||||
| chr5:171454481 | G | A | 2 | a0001c0001t0002g0340 a0001c0001t0003g0026 |
3 | HG01243.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.358-2058G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454481 | |||||||
| chr5:171454520 | AG | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0330 others(1): Show |
4 | HG01070.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-2017delG | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171454520 | ||||||
| chr5:171454523 | T | C | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0330 others(1): Show |
4 | HG01070.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-2016T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454523 | |||||||
| chr5:171454530 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.358-2009A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454530 | |||||||
| chr5:171454740 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.358-1799G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454740 | |||||||
| chr5:171454768 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.358-1771G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454768 | |||||||
| chr5:171454884 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.358-1655G>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454884 | |||||||
| chr5:171454922 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.358-1617C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454922 | |||||||
| chr5:171454954 | A | T | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.358-1585A>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454954 | |||||||
| chr5:171454981 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.358-1558G>A | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171454981 | |||||||
| chr5:171455023 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0187 |
4 | NA18952.hp1 NA18971.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-1516A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171455023 | |||||||
| chr5:171455077 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.358-1462T>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171455077 | |||||||
| chr5:171455147 | A | G | 3 | a0001c0002t0001g0021 a0001c0002t0001g0148 a0001c0002t0001g0199 |
4 | HG01081.hp2 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-1392A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171455147 | |||||||
| chr5:171455603 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(225): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.358-936A>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171455603 | |||||||
| chr5:171455771 | T | TGC | 4 | a0001c0001t0002g0118 a0001c0001t0002g0120 a0001c0001t0002g0125 others(1): Show |
4 | HG01109.hp2 HG02257.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-767_358-766dup others(2): Show |
FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 171455771 | ||||||
| chr5:171456165 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.358-374C>T | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171456165 | |||||||
| chr5:171456302 | C | G | 5 | a0001c0001t0002g0118 a0001c0001t0002g0120 a0001c0001t0002g0125 others(2): Show |
5 | HG01109.hp2 HG02257.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-237C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171456302 | |||||||
| chr5:171456374 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.358-165T>C | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171456374 | |||||||
| chr5:171456408 | C | G | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0047 others(38): Show |
41 | HG00544.hp1 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.358-131C>G | FGF18 | ENSG00000156427.8 | transcript | ENST00000274625.6 | protein_coding | 4/4 | chr5 | 171456408 |