Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2254 |
| ensemblid | ENSG00000102678.7 |
| hgncid | 3687 |
| symbol | FGF9 |
| name | fibroblast growth factor 9 |
| refseq_nuc | NM_002010.3 |
| refseq_prot | NP_002001.1 |
| ensembl_nuc | ENST00000382353.6 |
| ensembl_prot | ENSP00000371790.5 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 21671073 |
| end | 21704498 |
| strand | + |
| ver | v1.2 |
| region | chr13:21671073-21704498 |
| region5000 | chr13:21666073-21709498 |
| regionname0 | FGF9_chr13_21671073_21704498 |
| regionname5000 | FGF9_chr13_21666073_21709498 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 624 | 295 | 52 | 54 | 147 | 10 | 31 | FGF9_chr13_21666073_21709498 | FGF9 | ATGGC others(619): Show |
chr13 | 21666073 | 21709498 | ||
| a0001c0002 | 1/0 | 624 | 64 | 34 | 15 | 3 | 4 | 7 | FGF9_chr13_21666073_21709498 | FGF9 | ATGGC others(619): Show |
chr13 | 21666073 | 21709498 | ||
| a0001c0003 | 0/0 | 624 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | ATGGC others(619): Show |
chr13 | 21666073 | 21709498 | ||
| a0001c0004 | 0/0 | 624 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | ATGGC others(619): Show |
chr13 | 21666073 | 21709498 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4530 | 144 | 26 | 26 | 75 | 4 | 12 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0002 | 0/0 | 4532 | 93 | 1 | 20 | 55 | 5 | 12 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0004 | 0/0 | 4531 | 12 | 9 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0006 | 0/0 | 4531 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0009 | 0/0 | 4530 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0010 | 0/0 | 4531 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0011 | 0/0 | 4532 | 3 | 0 | 0 | 0 | 0 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0012 | 0/0 | 4532 | 3 | 0 | 1 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0013 | 0/0 | 4530 | 2 | 0 | 0 | 1 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0014 | 0/0 | 4530 | 2 | 0 | 0 | 0 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0015 | 0/0 | 4529 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4524): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0016 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0017 | 0/0 | 4530 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0019 | 0/0 | 4530 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0021 | 0/0 | 4532 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0024 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0025 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0027 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0028 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0029 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0030 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0031 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0032 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0034 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0038 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0039 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0041 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0042 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0043 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0044 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0046 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0047 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0048 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0001t0050 | 0/0 | 4530 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0001 | 0/0 | 4530 | 7 | 1 | 5 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0003 | 0/0 | 4530 | 16 | 12 | 2 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0005 | 0/0 | 4531 | 11 | 4 | 2 | 1 | 1 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0006 | 0/0 | 4531 | 6 | 6 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0007 | 0/0 | 4531 | 4 | 3 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0008 | 0/0 | 4532 | 4 | 0 | 2 | 0 | 1 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0016 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0018 | 0/0 | 4530 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0020 | 0/0 | 4527 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4522): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0022 | 0/0 | 4531 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0023 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4528): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0026 | 0/0 | 4531 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4526): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0033 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0035 | 0/0 | 4526 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4521): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0036 | 1/0 | 4530 | 1 | 0 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0037 | 0/0 | 4530 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0040 | 0/0 | 4533 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4528): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0045 | 0/0 | 4534 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4529): Show |
chr13 | 21666073 | 21709498 |
| a0001c0002t0049 | 0/0 | 4532 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4527): Show |
chr13 | 21666073 | 21709498 |
| a0001c0003t0001 | 0/0 | 4530 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| a0001c0004t0001 | 0/0 | 4530 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | GCCAC others(4525): Show |
chr13 | 21666073 | 21709498 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 3 | 9 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0002 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0009g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0010g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0010g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0011g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0012g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0012g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0013g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0014g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0017g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0019g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0019g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0021g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0021g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0024g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0025g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0027g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0028g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0029g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0030g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0031g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0032g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0034g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0038g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0039g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0041g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0042g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0043g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0044g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0046g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0047g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0048g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0001t0050g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0001g0004 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0005g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0007g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0008g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0008g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0016g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0018g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0018g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0020g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0020g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0022g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0022g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0023g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0026g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0033g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0035g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0036g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0037g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0040g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0045g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0002t0049g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0083 | EUR | GBR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00280 | hp1 | a0001 | c0002 | t0008 | g0039 | EUR | FIN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00280 | hp2 | a0001 | c0002 | t0005 | g0193 | EUR | FIN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | FIN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00323 | hp2 | a0001 | c0001 | t0012 | g0210 | EUR | FIN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0189 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00558 | hp1 | a0001 | c0002 | t0045 | g0224 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0144 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0021 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00738 | hp2 | a0001 | c0002 | t0008 | g0217 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00741 | hp1 | a0001 | c0002 | t0035 | g0067 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01069 | hp2 | a0001 | c0002 | t0022 | g0184 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01070 | hp2 | a0001 | c0002 | t0005 | g0006 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01071 | hp2 | a0001 | c0002 | t0005 | g0006 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01074 | hp2 | a0001 | c0001 | t0019 | g0164 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01081 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01099 | hp2 | a0001 | c0002 | t0020 | g0196 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01243 | hp1 | a0001 | c0002 | t0007 | g0033 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0034 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01358 | hp1 | a0001 | c0001 | t0031 | g0110 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01361 | hp2 | a0001 | c0002 | t0008 | g0039 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01433 | hp1 | a0001 | c0001 | t0032 | g0167 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | IBS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | IBS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0249 | EUR | IBS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | IBS | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01891 | hp2 | a0001 | c0001 | t0027 | g0119 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01934 | hp2 | a0001 | c0001 | t0028 | g0102 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02055 | hp1 | a0001 | c0002 | t0003 | g0116 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02055 | hp2 | a0001 | c0002 | t0026 | g0165 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02056 | hp2 | a0001 | c0001 | t0047 | g0030 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02071 | hp2 | a0001 | c0001 | t0050 | g0136 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02083 | hp1 | a0001 | c0001 | t0044 | g0240 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02129 | hp1 | a0001 | c0001 | t0013 | g0139 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02132 | hp1 | a0001 | c0002 | t0005 | g0006 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0137 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02145 | hp2 | a0001 | c0002 | t0007 | g0033 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0057 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02257 | hp2 | a0001 | c0001 | t0034 | g0086 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0032 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02451 | hp2 | a0001 | c0002 | t0016 | g0015 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02572 | hp1 | a0001 | c0001 | t0046 | g0183 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0159 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02622 | hp2 | a0001 | c0001 | t0017 | g0143 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0037 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02647 | hp1 | a0001 | c0001 | t0015 | g0059 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02683 | hp2 | a0001 | c0002 | t0023 | g0190 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02698 | hp1 | a0001 | c0002 | t0040 | g0192 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0050 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02723 | hp2 | a0001 | c0002 | t0033 | g0113 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0180 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0233 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0054 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0124 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02970 | hp1 | a0001 | c0002 | t0007 | g0092 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0082 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0175 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0037 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0173 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0162 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03209 | hp2 | a0001 | c0001 | t0039 | g0158 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03225 | hp1 | a0001 | c0002 | t0022 | g0185 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03239 | hp2 | a0001 | c0001 | t0013 | g0001 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03486 | hp1 | a0001 | c0001 | t0024 | g0117 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0006 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03492 | hp2 | a0001 | c0002 | t0005 | g0006 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0149 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0120 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03710 | hp2 | a0001 | c0001 | t0012 | g0226 | SAS | PJL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03927 | hp2 | a0001 | c0002 | t0005 | g0195 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03942 | hp1 | a0001 | c0001 | t0011 | g0040 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03942 | hp2 | a0001 | c0001 | t0014 | g0181 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04115 | hp2 | a0001 | c0001 | t0011 | g0223 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04204 | hp1 | a0001 | c0002 | t0008 | g0063 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04204 | hp2 | a0001 | c0001 | t0014 | g0001 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | YRI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0081 | AFR | YRI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CHB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18612 | hp2 | a0001 | c0002 | t0049 | g0135 | EAS | CHB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0076 | AFR | YRI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18906 | hp2 | a0001 | c0002 | t0018 | g0074 | AFR | YRI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18944 | hp1 | a0001 | c0001 | t0043 | g0045 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18949 | hp1 | a0001 | c0001 | t0030 | g0094 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18960 | hp1 | a0001 | c0001 | t0025 | g0239 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18965 | hp2 | a0001 | c0001 | t0048 | g0128 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18988 | hp1 | a0001 | c0001 | t0042 | g0228 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19000 | hp2 | a0001 | c0001 | t0010 | g0187 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19006 | hp2 | a0001 | c0001 | t0021 | g0235 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19030 | hp1 | a0001 | c0001 | t0017 | g0112 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0073 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19070 | hp2 | a0001 | c0001 | t0041 | g0252 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19074 | hp1 | a0001 | c0001 | t0010 | g0191 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19083 | hp1 | a0001 | c0001 | t0021 | g0234 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19086 | hp1 | a0001 | c0001 | t0029 | g0155 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20129 | hp1 | a0001 | c0002 | t0037 | g0148 | AFR | ASW | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | ASW | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | TSI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | TSI | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | GIH | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0131 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02486 | hp2 | a0001 | c0002 | t0020 | g0194 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02559 | hp1 | a0001 | c0001 | t0038 | g0176 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0032 | AFR | ACB | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG03471 | hp2 | a0001 | c0001 | t0019 | g0157 | AFR | MSL | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | USA | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| HG06807 | hp2 | a0001 | c0002 | t0018 | g0118 | AFR | USA | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | USA | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | USA | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA21309 | hp1 | a0001 | c0002 | t0006 | g0174 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | LWK | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0109 | REF | REF | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0036 | g0004 | REF | REF | FGF9_chr13_21666073_21709498 | FGF9 | chr13 | 21666073 | 21709498 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21681091 | C | T | 1 | a0001c0003 | 2 | HG03579.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.327C>T | p.Gly109Gly | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/3 | 1167/4530 | 327/627 | 109/208 | chr13 | 21681091 | |||
| chr13:21701231 | A | G | 1 | a0001c0004 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.423A>G | p.Glu141Glu | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1263/4530 | 423/627 | 141/208 | chr13 | 21701231 | |||
| chr13:21701255 | A | G | 3 | a0001c0001 a0001c0003 a0001c0004 |
297 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(294): Show |
synonymous_variant | LOW | c.447A>G | p.Ser149Ser | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1287/4530 | 447/627 | 149/208 | chr13 | 21701255 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21671081 | G | A | 1 | a0001c0002t0023 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-832G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 832 | chr13 | 21671081 | ||||||
| chr13:21671104 | G | C | 1 | a0001c0001t0024 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-809G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 809 | chr13 | 21671104 | ||||||
| chr13:21671138 | G | C | 1 | a0001c0001t0025 | 1 | NA18960.hp1 | 5_prime_UTR_variant | MODIFIER | c.-775G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 775 | chr13 | 21671138 | ||||||
| chr13:21671187 | C | T | 1 | a0001c0001t0050 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-726C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 726 | chr13 | 21671187 | ||||||
| chr13:21671201 | C | T | 2 | a0001c0001t0050 a0001c0002t0049 |
2 | HG02071.hp2 NA18612.hp2 |
5_prime_UTR_variant | MODIFIER | c.-712C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 712 | chr13 | 21671201 | ||||||
| chr13:21671210 | C | T | 1 | a0001c0001t0048 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-703C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 703 | chr13 | 21671210 | ||||||
| chr13:21671484 | G | A | 1 | a0001c0002t0026 | 1 | HG02055.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-429G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | chr13 | 21671484 | |||||||
| chr13:21671592 | G | A | 1 | a0001c0001t0027 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-321G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 321 | chr13 | 21671592 | ||||||
| chr13:21671703 | A | G | 1 | a0001c0001t0047 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 210 | chr13 | 21671703 | ||||||
| chr13:21671742 | A | G | 2 | a0001c0001t0046 a0001c0002t0022 |
3 | HG01069.hp2 HG02572.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-171A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 171 | chr13 | 21671742 | ||||||
| chr13:21671788 | C | CT | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(11): Show |
48 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-117dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 116 | INFO_REALIGN_3_PRIME | chr13 | 21671788 | |||||
| chr13:21671788 | C | CTT | 11 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0012 others(8): Show |
111 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-118_-117dupTT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 116 | INFO_REALIGN_3_PRIME | chr13 | 21671788 | |||||
| chr13:21671795 | T | TC | 2 | a0001c0001t0046 a0001c0002t0022 |
3 | HG01069.hp2 HG02572.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-118_-117insC | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/3 | 117 | chr13 | 21671795 | ||||||
| chr13:21701444 | G | A | 52 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(49): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*9G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 9 | chr13 | 21701444 | ||||||
| chr13:21701458 | G | A | 1 | a0001c0001t0028 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 23 | chr13 | 21701458 | ||||||
| chr13:21701643 | G | A | 1 | a0001c0001t0013 | 2 | HG02129.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*208G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 208 | chr13 | 21701643 | ||||||
| chr13:21701700 | A | AGT | 4 | a0001c0002t0023 a0001c0002t0040 a0001c0002t0045 others(1): Show |
4 | HG00558.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*272_*273dupGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 274 | INFO_REALIGN_3_PRIME | chr13 | 21701700 | |||||
| chr13:21701705 | GTGTA | G | 2 | a0001c0002t0020 a0001c0002t0035 |
3 | HG00741.hp1 HG01099.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*274_*277delATGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 274 | INFO_REALIGN_3_PRIME | chr13 | 21701705 | |||||
| chr13:21701707 | GTA | G | 1 | a0001c0002t0005 | 5 | HG01070.hp2 HG01071.hp2 HG02132.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*274_*275delAT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 274 | INFO_REALIGN_3_PRIME | chr13 | 21701707 | |||||
| chr13:21701709 | A | ATG | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(5): Show |
17 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*304_*305dupGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701709 | A | ATGTG | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(9): Show |
30 | HG00642.hp1 HG01109.hp2 HG01192.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*302_*305dupGTGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701709 | A | ATGTGTG | 7 | a0001c0001t0002 a0001c0001t0034 a0001c0002t0003 others(4): Show |
25 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*300_*305dupGTGTGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701709 | A | ATGTGTGT others(1): Show |
4 | a0001c0001t0001 a0001c0002t0005 a0001c0002t0022 others(1): Show |
7 | HG02257.hp1 HG03225.hp1 HG03225.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*298_*305dupGTGTGT others(2): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701709 | A | ATGTGTGT others(3): Show |
1 | a0001c0002t0007 | 4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*296_*305dupGTGTGT others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701709 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0009 | 3 | HG00735.hp1 HG02451.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290_*305dupGTGTGT others(10): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701709 | A | G | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0017 others(4): Show |
7 | HG00558.hp1 HG00639.hp2 HG00733.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*274A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 274 | chr13 | 21701709 | ||||||
| chr13:21701709 | ATG | A | 2 | a0001c0001t0001 a0001c0001t0002 |
6 | HG01496.hp1 HG02109.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*304_*305delGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 304 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701709 | ATGTG | A | 2 | a0001c0001t0001 a0001c0001t0042 |
6 | HG00408.hp1 HG00609.hp1 NA18954.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*302_*305delGTGT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 302 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701709 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292_*305delGTGTGT others(8): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 292 | INFO_REALIGN_3_PRIME | chr13 | 21701709 | |||||
| chr13:21701741 | A | G | 2 | a0001c0002t0018 a0001c0002t0026 |
2 | HG02055.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*306A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 306 | chr13 | 21701741 | ||||||
| chr13:21701753 | G | A | 1 | a0001c0001t0041 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 318 | chr13 | 21701753 | ||||||
| chr13:21701768 | G | T | 1 | a0001c0001t0044 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 333 | chr13 | 21701768 | ||||||
| chr13:21701786 | C | T | 2 | a0001c0002t0018 a0001c0002t0026 |
3 | HG02055.hp2 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*351C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 351 | chr13 | 21701786 | ||||||
| chr13:21701807 | A | T | 21 | a0001c0001t0006 a0001c0001t0017 a0001c0001t0027 others(18): Show |
62 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*372A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 372 | chr13 | 21701807 | ||||||
| chr13:21701877 | T | C | 1 | a0001c0002t0040 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 442 | chr13 | 21701877 | ||||||
| chr13:21701918 | C | T | 2 | a0001c0002t0018 a0001c0002t0026 |
3 | HG02055.hp2 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*483C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 483 | chr13 | 21701918 | ||||||
| chr13:21701931 | C | T | 2 | a0001c0001t0012 a0001c0001t0032 |
4 | HG00323.hp2 HG01081.hp1 HG01433.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*496C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 496 | chr13 | 21701931 | ||||||
| chr13:21701976 | C | A | 1 | a0001c0001t0021 | 2 | NA19006.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*541C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 541 | chr13 | 21701976 | ||||||
| chr13:21702001 | T | A | 1 | a0001c0001t0042 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*566T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 566 | chr13 | 21702001 | ||||||
| chr13:21702304 | C | T | 1 | a0001c0001t0031 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*869C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 869 | chr13 | 21702304 | ||||||
| chr13:21702431 | A | G | 2 | a0001c0001t0017 a0001c0001t0027 |
3 | HG01891.hp2 HG02622.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*996A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 996 | chr13 | 21702431 | ||||||
| chr13:21702529 | C | T | 27 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0015 others(24): Show |
72 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1094 | chr13 | 21702529 | ||||||
| chr13:21702701 | A | G | 1 | a0001c0001t0034 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1266A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1266 | chr13 | 21702701 | ||||||
| chr13:21702827 | T | A | 2 | a0001c0002t0018 a0001c0002t0026 |
3 | HG02055.hp2 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1392T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1392 | chr13 | 21702827 | ||||||
| chr13:21702828 | C | T | 2 | a0001c0002t0018 a0001c0002t0026 |
3 | HG02055.hp2 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1393C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1393 | chr13 | 21702828 | ||||||
| chr13:21702846 | T | C | 1 | a0001c0001t0029 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1411T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1411 | chr13 | 21702846 | ||||||
| chr13:21702953 | A | G | 1 | a0001c0001t0024 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1518A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1518 | chr13 | 21702953 | ||||||
| chr13:21702972 | A | G | 1 | a0001c0002t0033 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1537A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1537 | chr13 | 21702972 | ||||||
| chr13:21703059 | T | C | 1 | a0001c0001t0039 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1624 | chr13 | 21703059 | ||||||
| chr13:21703106 | A | G | 1 | a0001c0001t0043 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 1671 | chr13 | 21703106 | ||||||
| chr13:21703760 | A | G | 2 | a0001c0001t0010 a0001c0001t0030 |
4 | HG00438.hp2 NA18949.hp1 NA19000.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2325A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2325 | chr13 | 21703760 | ||||||
| chr13:21703930 | AT | A | 2 | a0001c0001t0015 a0001c0001t0019 |
4 | HG01074.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2497delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2497 | INFO_REALIGN_3_PRIME | chr13 | 21703930 | |||||
| chr13:21703998 | G | C | 24 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0016 others(21): Show |
67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2563G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2563 | chr13 | 21703998 | ||||||
| chr13:21704020 | C | T | 3 | a0001c0001t0006 a0001c0001t0009 a0001c0002t0006 |
11 | HG00735.hp1 HG01891.hp1 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2585C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2585 | chr13 | 21704020 | ||||||
| chr13:21704069 | C | T | 2 | a0001c0001t0011 a0001c0001t0014 |
5 | HG02738.hp1 HG03942.hp1 HG03942.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2634C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2634 | chr13 | 21704069 | ||||||
| chr13:21704372 | G | A | 1 | a0001c0002t0033 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2937G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 3/3 | 2937 | chr13 | 21704372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:21672318 | GTCTC | G | 1 | a0001c0001t0009g0021 | 3 | HG00735.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.277+141_277+144del others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21672318 | ||||||
| chr13:21672322 | C | G | 1 | a0001c0001t0001g0009 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.277+133C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672322 | |||||||
| chr13:21672505 | C | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0047 |
3 | HG00423.hp1 NA18950.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.277+316C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672505 | |||||||
| chr13:21672580 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.277+391G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672580 | |||||||
| chr13:21672581 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.277+392C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672581 | |||||||
| chr13:21672598 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.277+409C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672598 | |||||||
| chr13:21672650 | G | T | 78 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0017 others(75): Show |
105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.277+461G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672650 | |||||||
| chr13:21672875 | A | C | 11 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(8): Show |
15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+686A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672875 | |||||||
| chr13:21672902 | T | A | 11 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(8): Show |
15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+713T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672902 | |||||||
| chr13:21672903 | G | C | 11 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(8): Show |
15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+714G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21672903 | |||||||
| chr13:21673107 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.277+918A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673107 | |||||||
| chr13:21673656 | C | T | 3 | a0001c0001t0046g0183 a0001c0002t0022g0184 a0001c0002t0022g0185 |
3 | HG01069.hp2 HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.277+1467C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673656 | |||||||
| chr13:21673689 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.277+1500G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673689 | |||||||
| chr13:21673698 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.277+1509C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673698 | |||||||
| chr13:21673746 | G | A | 1 | a0001c0002t0003g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.277+1557G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673746 | |||||||
| chr13:21673800 | GCCAGGCG others(70): Show |
G | 1 | a0001c0001t0014g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.277+1613_277+1689d others(79): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21673800 | ||||||
| chr13:21673855 | G | T | 1 | a0001c0001t0004g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.277+1666G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673855 | |||||||
| chr13:21673928 | C | T | 1 | a0001c0002t0003g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.277+1739C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673928 | |||||||
| chr13:21673979 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.277+1790C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21673979 | |||||||
| chr13:21674330 | G | C | 4 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0053 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+2141G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674330 | |||||||
| chr13:21674428 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.277+2239G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674428 | |||||||
| chr13:21674432 | G | C | 1 | a0001c0001t0002g0197 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.277+2243G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674432 | |||||||
| chr13:21674505 | G | C | 4 | a0001c0001t0046g0183 a0001c0002t0005g0057 a0001c0002t0022g0184 others(1): Show |
4 | HG01069.hp2 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+2316G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674505 | |||||||
| chr13:21674515 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.277+2326G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674515 | |||||||
| chr13:21674527 | G | C | 1 | a0001c0001t0015g0059 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.277+2338G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674527 | |||||||
| chr13:21674562 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.277+2373G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674562 | |||||||
| chr13:21674589 | G | A | 1 | a0001c0001t0002g0038 | 2 | NA18948.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.277+2400G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674589 | |||||||
| chr13:21674594 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.277+2405T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674594 | |||||||
| chr13:21674707 | A | AT | 15 | a0001c0001t0002g0253 a0001c0001t0004g0177 a0001c0001t0004g0179 others(12): Show |
20 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.277+2530dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21674707 | ||||||
| chr13:21674802 | G | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0002t0008g0063 |
3 | HG01515.hp1 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.277+2613G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674802 | |||||||
| chr13:21674909 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.277+2720A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674909 | |||||||
| chr13:21674914 | A | G | 1 | a0001c0001t0004g0179 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.277+2725A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674914 | |||||||
| chr13:21674940 | G | A | 2 | a0001c0001t0004g0064 a0001c0001t0004g0065 |
2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.277+2751G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21674940 | |||||||
| chr13:21675005 | C | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(216): Show |
303 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.277+2816C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675005 | |||||||
| chr13:21675046 | A | T | 2 | a0001c0001t0004g0064 a0001c0001t0004g0065 |
2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.277+2857A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675046 | |||||||
| chr13:21675115 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.277+2926G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675115 | |||||||
| chr13:21675145 | C | A | 1 | a0001c0001t0002g0199 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.277+2956C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675145 | |||||||
| chr13:21675239 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.277+3050A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675239 | |||||||
| chr13:21675410 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
6 | NA18956.hp2 NA18998.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+3221C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675410 | |||||||
| chr13:21675451 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0030g0094 |
6 | HG00438.hp1 HG02523.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+3262G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675451 | |||||||
| chr13:21675648 | A | G | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG01517.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.277+3459A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675648 | |||||||
| chr13:21675836 | A | G | 120 | a0001c0001t0001g0034 a0001c0001t0001g0168 a0001c0001t0002g0002 others(117): Show |
155 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.277+3647A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675836 | |||||||
| chr13:21675924 | C | CT | 10 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0156 others(7): Show |
11 | HG00558.hp2 HG01167.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.277+3750dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21675924 | ||||||
| chr13:21675924 | CT | C | 21 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0061 others(18): Show |
24 | HG01074.hp2 HG01243.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.277+3750delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21675924 | ||||||
| chr13:21675939 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0095 a0001c0001t0001g0096 others(11): Show |
22 | HG01256.hp2 HG01361.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.277+3750T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675939 | |||||||
| chr13:21675970 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.277+3781T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21675970 | |||||||
| chr13:21676050 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0105 a0001c0001t0001g0151 others(4): Show |
10 | HG00423.hp2 HG02083.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+3861A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676050 | |||||||
| chr13:21676177 | G | C | 1 | a0001c0001t0002g0204 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.277+3988G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676177 | |||||||
| chr13:21676524 | T | G | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.277+4335T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676524 | |||||||
| chr13:21676645 | C | G | 1 | a0001c0001t0002g0245 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.278-4397C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676645 | |||||||
| chr13:21676659 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.278-4383G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21676659 | |||||||
| chr13:21677244 | A | C | 81 | a0001c0001t0001g0168 a0001c0001t0002g0002 a0001c0001t0002g0011 others(78): Show |
107 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.278-3798A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21677244 | |||||||
| chr13:21677664 | A | G | 1 | a0001c0001t0032g0167 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.278-3378A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21677664 | |||||||
| chr13:21677668 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.278-3374C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21677668 | |||||||
| chr13:21678023 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.278-3019C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678023 | |||||||
| chr13:21678116 | A | G | 2 | a0001c0001t0002g0045 a0001c0001t0043g0045 |
2 | NA18944.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.278-2926A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678116 | |||||||
| chr13:21678170 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.278-2872A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678170 | |||||||
| chr13:21678339 | C | T | 1 | a0001c0001t0019g0164 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.278-2703C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678339 | |||||||
| chr13:21678565 | G | C | 6 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(3): Show |
6 | HG00438.hp2 HG02683.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-2477G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678565 | |||||||
| chr13:21678572 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.278-2470T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678572 | |||||||
| chr13:21678846 | A | C | 4 | a0001c0001t0004g0163 a0001c0002t0006g0173 a0001c0002t0006g0174 others(1): Show |
4 | HG02976.hp2 HG03130.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2196A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678846 | |||||||
| chr13:21678980 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.278-2062G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678980 | |||||||
| chr13:21678991 | C | G | 19 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0161 others(16): Show |
22 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.278-2051C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21678991 | |||||||
| chr13:21679016 | G | T | 7 | a0001c0001t0002g0011 a0001c0001t0002g0038 a0001c0001t0002g0205 others(4): Show |
11 | HG00544.hp2 HG01346.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-2026G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679016 | |||||||
| chr13:21679278 | C | T | 5 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0006g0178 others(2): Show |
6 | HG02559.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-1764C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679278 | |||||||
| chr13:21679533 | A | C | 3 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0002t0005g0054 |
3 | HG02630.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.278-1509A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679533 | |||||||
| chr13:21679600 | T | C | 2 | a0001c0001t0004g0064 a0001c0001t0004g0065 |
2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.278-1442T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679600 | |||||||
| chr13:21679674 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.278-1368C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679674 | |||||||
| chr13:21679721 | G | T | 18 | a0001c0001t0001g0168 a0001c0001t0002g0020 a0001c0001t0002g0043 others(15): Show |
23 | HG00408.hp2 HG00558.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.278-1321G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679721 | |||||||
| chr13:21679742 | T | C | 77 | a0001c0001t0001g0168 a0001c0001t0002g0002 a0001c0001t0002g0011 others(74): Show |
103 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.278-1300T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679742 | |||||||
| chr13:21679754 | C | T | 1 | a0001c0002t0003g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.278-1288C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679754 | |||||||
| chr13:21679755 | A | G | 1 | a0001c0002t0003g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.278-1287A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679755 | |||||||
| chr13:21679782 | C | CA | 21 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0024 others(18): Show |
25 | HG00280.hp2 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.278-1239dupA | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21679782 | ||||||
| chr13:21679782 | CA | C | 25 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(22): Show |
33 | HG01074.hp1 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.278-1239delA | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21679782 | ||||||
| chr13:21679804 | T | A | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.278-1238T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679804 | |||||||
| chr13:21679813 | G | A | 2 | a0001c0001t0017g0112 a0001c0002t0033g0113 |
2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.278-1229G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679813 | |||||||
| chr13:21679818 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278-1224G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679818 | |||||||
| chr13:21679853 | A | T | 1 | a0001c0002t0022g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.278-1189A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21679853 | |||||||
| chr13:21679956 | C | CA | 35 | a0001c0001t0001g0071 a0001c0001t0001g0114 a0001c0001t0001g0115 others(32): Show |
43 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.278-1064dupA | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21679956 | ||||||
| chr13:21679956 | CA | C | 20 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0048 others(17): Show |
22 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.278-1064delA | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21679956 | ||||||
| chr13:21680151 | C | T | 26 | a0001c0001t0001g0049 a0001c0001t0001g0089 a0001c0001t0004g0036 others(23): Show |
30 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.278-891C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680151 | |||||||
| chr13:21680447 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0171 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.278-595G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680447 | |||||||
| chr13:21680452 | C | CT | 17 | a0001c0001t0001g0107 a0001c0001t0002g0205 a0001c0001t0002g0250 others(14): Show |
21 | HG00280.hp2 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.278-576dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr13 | 21680452 | ||||||
| chr13:21680458 | T | C | 1 | a0001c0001t0002g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.278-584T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680458 | |||||||
| chr13:21680469 | T | C | 1 | a0001c0002t0006g0173 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.278-573T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680469 | |||||||
| chr13:21680526 | A | C | 1 | a0001c0001t0002g0221 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.278-516A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680526 | |||||||
| chr13:21680766 | A | G | 80 | a0001c0001t0001g0168 a0001c0001t0002g0002 a0001c0001t0002g0011 others(77): Show |
106 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.278-276A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680766 | |||||||
| chr13:21680873 | A | G | 1 | a0001c0001t0002g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.278-169A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21680873 | |||||||
| chr13:21681014 | T | C | 20 | a0001c0001t0001g0089 a0001c0001t0004g0036 a0001c0001t0004g0052 others(17): Show |
24 | HG01074.hp2 HG01099.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.278-28T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21681014 | |||||||
| chr13:21681028 | C | T | 75 | a0001c0001t0001g0168 a0001c0001t0002g0002 a0001c0001t0002g0011 others(72): Show |
101 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.278-14C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 1/2 | chr13 | 21681028 | |||||||
| chr13:21681162 | C | T | 79 | a0001c0001t0001g0168 a0001c0001t0002g0002 a0001c0001t0002g0011 others(76): Show |
105 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.381+17C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21681162 | |||||||
| chr13:21681261 | T | C | 20 | a0001c0001t0001g0089 a0001c0001t0004g0036 a0001c0001t0004g0052 others(17): Show |
24 | HG01074.hp2 HG01099.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.381+116T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21681261 | |||||||
| chr13:21681284 | G | A | 1 | a0001c0002t0005g0057 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.381+139G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21681284 | |||||||
| chr13:21681811 | G | A | 14 | a0001c0001t0001g0089 a0001c0001t0004g0161 a0001c0001t0004g0179 others(11): Show |
17 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.381+666G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21681811 | |||||||
| chr13:21682029 | G | C | 1 | a0001c0001t0042g0228 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.381+884G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682029 | |||||||
| chr13:21682035 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.381+890G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682035 | |||||||
| chr13:21682082 | C | T | 1 | a0001c0002t0037g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.381+937C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682082 | |||||||
| chr13:21682438 | A | G | 74 | a0001c0001t0001g0168 a0001c0001t0002g0002 a0001c0001t0002g0011 others(71): Show |
100 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.381+1293A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682438 | |||||||
| chr13:21682486 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.381+1341A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682486 | |||||||
| chr13:21682551 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0029g0155 |
2 | NA19066.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.381+1406A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682551 | |||||||
| chr13:21682582 | A | G | 80 | a0001c0001t0001g0168 a0001c0001t0002g0002 a0001c0001t0002g0011 others(77): Show |
106 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.381+1437A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682582 | |||||||
| chr13:21682694 | G | GT | 80 | a0001c0001t0001g0095 a0001c0001t0001g0140 a0001c0001t0001g0141 others(77): Show |
106 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.381+1566dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21682694 | ||||||
| chr13:21682694 | G | GTT | 10 | a0001c0001t0002g0205 a0001c0001t0002g0206 a0001c0001t0002g0207 others(7): Show |
10 | HG00544.hp2 HG01928.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+1565_381+1566d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21682694 | ||||||
| chr13:21682701 | T | G | 17 | a0001c0001t0001g0089 a0001c0001t0004g0052 a0001c0001t0004g0053 others(14): Show |
20 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.381+1556T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682701 | |||||||
| chr13:21682861 | A | G | 1 | a0001c0002t0020g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.381+1716A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21682861 | |||||||
| chr13:21683014 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.381+1869T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683014 | |||||||
| chr13:21683152 | C | T | 1 | a0001c0002t0026g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.381+2007C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683152 | |||||||
| chr13:21683219 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.381+2074A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683219 | |||||||
| chr13:21683287 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.381+2142C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683287 | |||||||
| chr13:21683347 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0009g0021 others(3): Show |
10 | HG00735.hp1 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+2202G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683347 | |||||||
| chr13:21683655 | A | G | 109 | a0001c0001t0001g0008 a0001c0001t0001g0089 a0001c0001t0001g0107 others(106): Show |
142 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.381+2510A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683655 | |||||||
| chr13:21683905 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.381+2760G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21683905 | |||||||
| chr13:21684069 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.381+2924C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684069 | |||||||
| chr13:21684182 | C | A | 1 | a0001c0001t0004g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+3037C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684182 | |||||||
| chr13:21684206 | T | C | 2 | a0001c0001t0017g0112 a0001c0002t0033g0113 |
2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.381+3061T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684206 | |||||||
| chr13:21684295 | T | C | 1 | a0001c0001t0004g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+3150T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684295 | |||||||
| chr13:21684444 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0121 |
2 | HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.381+3299T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684444 | |||||||
| chr13:21684476 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0108 a0001c0001t0001g0122 others(1): Show |
4 | HG02523.hp2 NA18952.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+3331G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684476 | |||||||
| chr13:21684490 | T | G | 1 | a0001c0001t0004g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+3345T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684490 | |||||||
| chr13:21684540 | T | C | 1 | a0001c0001t0004g0064 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.381+3395T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684540 | |||||||
| chr13:21684575 | G | GGT | 3 | a0001c0001t0046g0183 a0001c0002t0022g0184 a0001c0002t0022g0185 |
3 | HG01069.hp2 HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.381+3438_381+3439d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21684575 | ||||||
| chr13:21684636 | G | A | 96 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0168 others(93): Show |
127 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.381+3491G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684636 | |||||||
| chr13:21684820 | T | C | 3 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0191 |
3 | HG00438.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.381+3675T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21684820 | |||||||
| chr13:21685228 | C | T | 18 | a0001c0001t0001g0089 a0001c0001t0004g0036 a0001c0001t0004g0065 others(15): Show |
21 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.381+4083C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685228 | |||||||
| chr13:21685233 | C | T | 15 | a0001c0001t0001g0089 a0001c0001t0004g0036 a0001c0001t0004g0161 others(12): Show |
18 | HG00639.hp1 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.381+4088C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685233 | |||||||
| chr13:21685271 | C | T | 111 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0168 others(108): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.381+4126C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685271 | |||||||
| chr13:21685272 | G | A | 109 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0168 others(106): Show |
144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.381+4127G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685272 | |||||||
| chr13:21685312 | T | C | 1 | a0001c0002t0026g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.381+4167T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685312 | |||||||
| chr13:21685373 | G | A | 2 | a0001c0001t0017g0143 a0001c0001t0027g0119 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.381+4228G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685373 | |||||||
| chr13:21685502 | A | G | 109 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0168 others(106): Show |
144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.381+4357A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685502 | |||||||
| chr13:21685596 | C | T | 2 | a0001c0001t0002g0219 a0001c0002t0007g0162 |
2 | HG03139.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.381+4451C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685596 | |||||||
| chr13:21685862 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.381+4717C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21685862 | |||||||
| chr13:21686060 | T | C | 11 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(8): Show |
15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+4915T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686060 | |||||||
| chr13:21686345 | A | C | 1 | a0001c0001t0019g0164 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.381+5200A>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686345 | |||||||
| chr13:21686493 | T | C | 2 | a0001c0001t0002g0043 a0001c0001t0002g0237 |
3 | HG01167.hp1 HG01169.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.381+5348T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686493 | |||||||
| chr13:21686518 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.381+5373G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686518 | |||||||
| chr13:21686541 | C | G | 1 | a0001c0001t0002g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.381+5396C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686541 | |||||||
| chr13:21686620 | T | A | 96 | a0001c0001t0001g0014 a0001c0001t0001g0141 a0001c0001t0001g0168 others(93): Show |
129 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.381+5475T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686620 | |||||||
| chr13:21686621 | C | A | 85 | a0001c0001t0001g0014 a0001c0001t0001g0141 a0001c0001t0001g0168 others(82): Show |
114 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.381+5476C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686621 | |||||||
| chr13:21686696 | A | G | 94 | a0001c0001t0001g0014 a0001c0001t0001g0141 a0001c0001t0001g0168 others(91): Show |
126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.381+5551A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686696 | |||||||
| chr13:21686762 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0009g0021 others(4): Show |
11 | HG00735.hp1 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+5617G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21686762 | |||||||
| chr13:21687256 | C | T | 1 | a0001c0001t0004g0036 | 2 | HG01099.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+6111C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687256 | |||||||
| chr13:21687493 | T | C | 1 | a0001c0002t0003g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+6348T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687493 | |||||||
| chr13:21687528 | A | G | 11 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(8): Show |
15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+6383A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687528 | |||||||
| chr13:21687670 | G | C | 2 | a0001c0001t0017g0143 a0001c0001t0027g0119 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.381+6525G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687670 | |||||||
| chr13:21687865 | G | A | 10 | a0001c0001t0001g0089 a0001c0001t0001g0123 a0001c0001t0004g0179 others(7): Show |
11 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+6720G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687865 | |||||||
| chr13:21687904 | A | G | 1 | a0001c0002t0008g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.381+6759A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687904 | |||||||
| chr13:21687979 | A | G | 1 | a0001c0001t0004g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.381+6834A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687979 | |||||||
| chr13:21687988 | C | T | 1 | a0001c0002t0005g0057 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.381+6843C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21687988 | |||||||
| chr13:21688051 | G | A | 2 | a0001c0001t0017g0112 a0001c0002t0033g0113 |
2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.381+6906G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688051 | |||||||
| chr13:21688092 | C | T | 78 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(75): Show |
106 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.381+6947C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688092 | |||||||
| chr13:21688385 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.381+7240G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688385 | |||||||
| chr13:21688448 | C | T | 1 | a0001c0002t0003g0144 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.381+7303C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688448 | |||||||
| chr13:21688451 | T | C | 1 | a0001c0001t0015g0059 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.381+7306T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688451 | |||||||
| chr13:21688554 | T | C | 87 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(84): Show |
115 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.381+7409T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688554 | |||||||
| chr13:21688752 | A | AT | 17 | a0001c0001t0001g0030 a0001c0001t0001g0121 a0001c0001t0002g0011 others(14): Show |
22 | HG01069.hp2 HG01346.hp1 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.381+7623dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21688752 | ||||||
| chr13:21688752 | A | ATT | 69 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(66): Show |
92 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.381+7622_381+7623d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21688752 | ||||||
| chr13:21688752 | AT | A | 11 | a0001c0001t0001g0025 a0001c0001t0004g0053 a0001c0001t0006g0178 others(8): Show |
12 | HG00438.hp2 HG01074.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+7623delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21688752 | ||||||
| chr13:21688872 | G | T | 2 | a0001c0001t0002g0020 a0001c0001t0025g0239 |
4 | HG00408.hp2 NA18956.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+7727G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688872 | |||||||
| chr13:21688894 | A | T | 1 | a0001c0001t0002g0200 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.381+7749A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688894 | |||||||
| chr13:21688964 | G | T | 2 | a0001c0001t0034g0086 a0001c0002t0026g0165 |
2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.381+7819G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21688964 | |||||||
| chr13:21689016 | A | G | 1 | a0001c0002t0006g0159 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.381+7871A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689016 | |||||||
| chr13:21689060 | G | A | 7 | a0001c0001t0004g0161 a0001c0001t0006g0160 a0001c0001t0034g0086 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+7915G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689060 | |||||||
| chr13:21689076 | A | G | 1 | a0001c0001t0044g0240 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.381+7931A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689076 | |||||||
| chr13:21689083 | G | A | 4 | a0001c0001t0004g0177 a0001c0001t0016g0073 a0001c0001t0038g0176 others(1): Show |
4 | HG02559.hp1 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+7938G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689083 | |||||||
| chr13:21689158 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.381+8013T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689158 | |||||||
| chr13:21689315 | G | A | 2 | a0001c0001t0001g0075 a0001c0002t0003g0076 |
2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.381+8170G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689315 | |||||||
| chr13:21689346 | C | G | 94 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(91): Show |
126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.381+8201C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689346 | |||||||
| chr13:21689372 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.381+8227A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689372 | |||||||
| chr13:21689375 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.381+8230C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689375 | |||||||
| chr13:21689448 | CT | C | 79 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(76): Show |
107 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.381+8315delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21689448 | ||||||
| chr13:21689467 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.381+8322A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689467 | |||||||
| chr13:21689736 | T | C | 79 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(76): Show |
107 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.381+8591T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689736 | |||||||
| chr13:21689811 | T | C | 78 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(75): Show |
106 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.381+8666T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689811 | |||||||
| chr13:21689885 | C | T | 2 | a0001c0001t0034g0086 a0001c0002t0026g0165 |
2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.381+8740C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689885 | |||||||
| chr13:21689886 | G | A | 1 | a0001c0001t0004g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.381+8741G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21689886 | |||||||
| chr13:21690151 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.381+9006A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690151 | |||||||
| chr13:21690223 | C | T | 81 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(78): Show |
109 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.381+9078C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690223 | |||||||
| chr13:21690631 | T | C | 11 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(8): Show |
15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+9486T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690631 | |||||||
| chr13:21690714 | C | T | 17 | a0001c0001t0001g0089 a0001c0001t0001g0123 a0001c0001t0004g0161 others(14): Show |
19 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.381+9569C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690714 | |||||||
| chr13:21690728 | G | A | 1 | a0001c0001t0012g0210 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.381+9583G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690728 | |||||||
| chr13:21690776 | C | T | 2 | a0001c0001t0017g0143 a0001c0001t0027g0119 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.381+9631C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690776 | |||||||
| chr13:21690870 | G | A | 11 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(8): Show |
15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+9725G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690870 | |||||||
| chr13:21690872 | T | C | 2 | a0001c0001t0034g0086 a0001c0002t0026g0165 |
2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.381+9727T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690872 | |||||||
| chr13:21690964 | T | G | 13 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(10): Show |
17 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.381+9819T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690964 | |||||||
| chr13:21690979 | A | G | 11 | a0001c0001t0004g0188 a0001c0001t0010g0187 a0001c0001t0010g0189 others(8): Show |
15 | HG00280.hp2 HG00438.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+9834A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21690979 | |||||||
| chr13:21691382 | A | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0002g0002 others(72): Show |
103 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.382-9808A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691382 | |||||||
| chr13:21691594 | A | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0061 a0001c0001t0002g0062 others(1): Show |
5 | HG00323.hp1 HG01081.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-9596A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691594 | |||||||
| chr13:21691596 | C | A | 1 | a0001c0002t0026g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.382-9594C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691596 | |||||||
| chr13:21691620 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.382-9570C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691620 | |||||||
| chr13:21691710 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.382-9480C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691710 | |||||||
| chr13:21691897 | T | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0123 a0001c0001t0004g0179 others(5): Show |
11 | HG00639.hp1 HG00735.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.382-9293T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691897 | |||||||
| chr13:21691923 | T | A | 1 | a0001c0001t0031g0110 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.382-9267T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21691923 | |||||||
| chr13:21691979 | C | CT | 134 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(131): Show |
181 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.382-9197dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21691979 | ||||||
| chr13:21691979 | CT | C | 18 | a0001c0001t0001g0077 a0001c0001t0004g0052 a0001c0001t0004g0053 others(15): Show |
23 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.382-9197delT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21691979 | ||||||
| chr13:21692095 | A | G | 2 | a0001c0001t0002g0199 a0001c0002t0008g0217 |
2 | HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.382-9095A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692095 | |||||||
| chr13:21692492 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.382-8698C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692492 | |||||||
| chr13:21692577 | A | G | 3 | a0001c0001t0017g0112 a0001c0001t0027g0119 a0001c0002t0006g0175 |
3 | HG01891.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382-8613A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692577 | |||||||
| chr13:21692679 | C | T | 69 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(66): Show |
101 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.382-8511C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692679 | |||||||
| chr13:21692750 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | HG02135.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.382-8440C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692750 | |||||||
| chr13:21692791 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0004g0036 a0001c0001t0004g0179 |
4 | HG01099.hp1 HG02895.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-8399G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692791 | |||||||
| chr13:21692792 | A | T | 1 | a0001c0001t0006g0178 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.382-8398A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692792 | |||||||
| chr13:21692871 | A | T | 1 | a0001c0002t0008g0217 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.382-8319A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692871 | |||||||
| chr13:21692998 | C | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(205): Show |
291 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.382-8192C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21692998 | |||||||
| chr13:21693130 | A | G | 1 | a0001c0001t0002g0253 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.382-8060A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693130 | |||||||
| chr13:21693177 | A | G | 1 | a0001c0002t0037g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.382-8013A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693177 | |||||||
| chr13:21693198 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.382-7992G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693198 | |||||||
| chr13:21693267 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
316 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.382-7923T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693267 | |||||||
| chr13:21693408 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.382-7782C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693408 | |||||||
| chr13:21693519 | C | G | 5 | a0001c0001t0001g0138 a0001c0002t0003g0015 a0001c0002t0003g0131 others(2): Show |
6 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-7671C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693519 | |||||||
| chr13:21693624 | T | C | 5 | a0001c0001t0001g0138 a0001c0002t0003g0015 a0001c0002t0003g0131 others(2): Show |
6 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-7566T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693624 | |||||||
| chr13:21693864 | G | A | 4 | a0001c0002t0018g0074 a0001c0002t0018g0118 a0001c0002t0026g0165 others(1): Show |
4 | HG02055.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-7326G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21693864 | |||||||
| chr13:21694140 | G | A | 3 | a0001c0001t0017g0112 a0001c0001t0017g0143 a0001c0001t0027g0119 |
3 | HG01891.hp2 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382-7050G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21694140 | |||||||
| chr13:21694364 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.382-6826A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21694364 | |||||||
| chr13:21694487 | C | A | 15 | a0001c0001t0017g0112 a0001c0001t0017g0143 a0001c0001t0027g0119 others(12): Show |
17 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.382-6703C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21694487 | |||||||
| chr13:21694507 | C | T | 68 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0014 others(65): Show |
100 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.382-6683C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21694507 | |||||||
| chr13:21695069 | C | CGT | 3 | a0001c0001t0001g0056 a0001c0001t0019g0157 a0001c0001t0019g0164 |
3 | HG01074.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.382-6109_382-6108d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695069 | ||||||
| chr13:21695069 | CGTGTGTG others(11): Show |
C | 3 | a0001c0002t0007g0033 a0001c0002t0007g0092 a0001c0002t0007g0162 |
4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-6107_382-6090d others(20): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695069 | ||||||
| chr13:21695083 | C | CGT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(38): Show |
52 | HG00423.hp1 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.382-6075_382-6074d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | ||||||
| chr13:21695083 | C | CGTGT | 4 | a0001c0001t0001g0077 a0001c0001t0001g0095 a0001c0001t0002g0203 others(1): Show |
4 | HG00099.hp1 HG01884.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-6077_382-6074d others(6): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | ||||||
| chr13:21695083 | C | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0055 others(14): Show |
21 | HG01099.hp1 HG01109.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-6107C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695083 | |||||||
| chr13:21695083 | CGT | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0069 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-6075_382-6074d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | ||||||
| chr13:21695083 | CGTGTGTG others(1): Show |
C | 4 | a0001c0002t0003g0015 a0001c0002t0003g0131 a0001c0002t0003g0137 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-6081_382-6074d others(10): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | ||||||
| chr13:21695083 | CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0170 a0001c0001t0002g0251 |
2 | NA18956.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.382-6087_382-6074d others(16): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21695083 | ||||||
| chr13:21695085 | T | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0055 others(14): Show |
21 | HG01099.hp1 HG01109.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-6105T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695085 | |||||||
| chr13:21695087 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.382-6103T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695087 | |||||||
| chr13:21695113 | T | A | 4 | a0001c0001t0017g0143 a0001c0001t0019g0157 a0001c0001t0019g0164 others(1): Show |
4 | HG01074.hp2 HG01891.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-6077T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695113 | |||||||
| chr13:21695115 | T | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0055 others(20): Show |
27 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.382-6075T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695115 | |||||||
| chr13:21695170 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0075 |
2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.382-6020G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695170 | |||||||
| chr13:21695316 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
296 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.382-5874T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695316 | |||||||
| chr13:21695490 | G | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0055 others(16): Show |
23 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-5700G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695490 | |||||||
| chr13:21695528 | G | C | 8 | a0001c0002t0005g0006 a0001c0002t0020g0194 a0001c0002t0020g0196 others(5): Show |
12 | HG00558.hp1 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.382-5662G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695528 | |||||||
| chr13:21695653 | C | G | 1 | a0001c0002t0022g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.382-5537C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695653 | |||||||
| chr13:21695765 | T | C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0219 |
2 | NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.382-5425T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695765 | |||||||
| chr13:21695850 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0091 |
3 | HG02922.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.382-5340G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695850 | |||||||
| chr13:21695896 | C | T | 1 | a0001c0002t0037g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.382-5294C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695896 | |||||||
| chr13:21695988 | C | T | 4 | a0001c0002t0018g0074 a0001c0002t0018g0118 a0001c0002t0026g0165 others(1): Show |
4 | HG02055.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-5202C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21695988 | |||||||
| chr13:21696000 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0080 a0001c0001t0001g0182 others(3): Show |
7 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-5190C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696000 | |||||||
| chr13:21696329 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
268 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.382-4861C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696329 | |||||||
| chr13:21696333 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(211): Show |
297 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.382-4857A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696333 | |||||||
| chr13:21696547 | C | CAT | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
342 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.382-4643_382-4642i others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696547 | |||||||
| chr13:21696554 | G | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(232): Show |
324 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.382-4636G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696554 | |||||||
| chr13:21696646 | T | G | 1 | a0001c0001t0009g0021 | 3 | HG00735.hp1 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.382-4544T>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696646 | |||||||
| chr13:21696649 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-4541A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696649 | |||||||
| chr13:21696996 | T | C | 1 | a0001c0003t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.382-4194T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21696996 | |||||||
| chr13:21697232 | A | AC | 3 | a0001c0001t0010g0187 a0001c0001t0010g0189 a0001c0001t0010g0191 |
3 | HG00438.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.382-3957dupC | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21697232 | ||||||
| chr13:21697426 | C | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(207): Show |
293 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.382-3764C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697426 | |||||||
| chr13:21697498 | G | A | 1 | a0001c0002t0037g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.382-3692G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697498 | |||||||
| chr13:21697517 | A | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0055 others(18): Show |
25 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.382-3673A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697517 | |||||||
| chr13:21697580 | C | A | 1 | a0001c0002t0022g0184 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.382-3610C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697580 | |||||||
| chr13:21697625 | G | GTATA | 7 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0068 others(4): Show |
8 | HG01099.hp1 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-3564_382-3561d others(6): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21697625 | ||||||
| chr13:21697691 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.382-3499C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697691 | |||||||
| chr13:21697766 | G | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0126 a0001c0001t0031g0110 |
3 | HG00738.hp1 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.382-3424G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697766 | |||||||
| chr13:21697808 | C | CT | 20 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0169 others(17): Show |
22 | HG00639.hp1 HG01069.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.382-3366dupT | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21697808 | ||||||
| chr13:21697869 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
323 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.382-3321C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697869 | |||||||
| chr13:21697933 | G | T | 2 | a0001c0002t0003g0076 a0001c0002t0005g0057 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.382-3257G>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697933 | |||||||
| chr13:21697939 | C | A | 2 | a0001c0002t0003g0076 a0001c0002t0005g0057 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.382-3251C>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697939 | |||||||
| chr13:21697958 | C | T | 1 | a0001c0002t0022g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.382-3232C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21697958 | |||||||
| chr13:21698133 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.382-3057C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698133 | |||||||
| chr13:21698228 | A | G | 4 | a0001c0001t0002g0041 a0001c0001t0002g0208 a0001c0001t0002g0213 others(1): Show |
5 | NA18995.hp1 NA19012.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-2962A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698228 | |||||||
| chr13:21698260 | G | A | 1 | a0001c0002t0003g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.382-2930G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698260 | |||||||
| chr13:21698368 | G | A | 1 | a0001c0001t0039g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-2822G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698368 | |||||||
| chr13:21698594 | C | G | 4 | a0001c0002t0003g0015 a0001c0002t0003g0131 a0001c0002t0003g0137 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-2596C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698594 | |||||||
| chr13:21698744 | A | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0142 |
2 | NA18945.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.382-2446A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698744 | |||||||
| chr13:21698768 | G | A | 2 | a0001c0001t0004g0051 a0001c0001t0046g0183 |
2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.382-2422G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698768 | |||||||
| chr13:21698943 | G | A | 3 | a0001c0002t0007g0033 a0001c0002t0007g0092 a0001c0002t0007g0162 |
4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2247G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21698943 | |||||||
| chr13:21699026 | A | G | 4 | a0001c0002t0003g0015 a0001c0002t0003g0131 a0001c0002t0003g0137 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-2164A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699026 | |||||||
| chr13:21699151 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
268 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.382-2039C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699151 | |||||||
| chr13:21699369 | C | T | 4 | a0001c0002t0018g0074 a0001c0002t0018g0118 a0001c0002t0026g0165 others(1): Show |
4 | HG02055.hp2 HG02723.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-1821C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699369 | |||||||
| chr13:21699396 | C | T | 1 | a0001c0002t0003g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382-1794C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699396 | |||||||
| chr13:21699444 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.382-1746A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699444 | |||||||
| chr13:21699765 | C | T | 3 | a0001c0002t0007g0033 a0001c0002t0007g0092 a0001c0002t0007g0162 |
4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-1425C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699765 | |||||||
| chr13:21699933 | T | A | 2 | a0001c0002t0003g0076 a0001c0002t0005g0057 |
2 | HG02257.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.382-1257T>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699933 | |||||||
| chr13:21699993 | C | T | 8 | a0001c0002t0005g0006 a0001c0002t0020g0194 a0001c0002t0020g0196 others(5): Show |
12 | HG00558.hp1 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.382-1197C>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21699993 | |||||||
| chr13:21700015 | G | GGT | 8 | a0001c0002t0001g0084 a0001c0002t0003g0081 a0001c0002t0003g0149 others(5): Show |
12 | HG00558.hp1 HG00642.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-1142_382-1141d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21700015 | ||||||
| chr13:21700015 | G | GGTGTGTG others(1): Show |
3 | a0001c0002t0005g0057 a0001c0002t0023g0190 a0001c0002t0040g0192 |
3 | HG02257.hp1 HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.382-1148_382-1141d others(10): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21700015 | ||||||
| chr13:21700015 | GGT | G | 26 | a0001c0001t0001g0077 a0001c0001t0001g0090 a0001c0001t0001g0099 others(23): Show |
30 | HG00099.hp1 HG00673.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.382-1142_382-1141d others(4): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21700015 | ||||||
| chr13:21700015 | GGTGT | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
277 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.382-1144_382-1141d others(6): Show |
FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr13 | 21700015 | ||||||
| chr13:21700177 | G | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(232): Show |
324 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.382-1013G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700177 | |||||||
| chr13:21700187 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.382-1003C>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700187 | |||||||
| chr13:21700250 | G | C | 1 | a0001c0001t0002g0215 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.382-940G>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700250 | |||||||
| chr13:21700303 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-887T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700303 | |||||||
| chr13:21700623 | A | G | 1 | a0001c0002t0037g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.382-567A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700623 | |||||||
| chr13:21700701 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.382-489A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700701 | |||||||
| chr13:21700836 | T | C | 1 | a0001c0001t0015g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.382-354T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700836 | |||||||
| chr13:21700857 | A | G | 1 | a0001c0001t0039g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-333A>G | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700857 | |||||||
| chr13:21700946 | G | A | 3 | a0001c0002t0007g0033 a0001c0002t0007g0092 a0001c0002t0007g0162 |
4 | HG01243.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-244G>A | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700946 | |||||||
| chr13:21700988 | A | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
325 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.382-202A>T | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21700988 | |||||||
| chr13:21701054 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
325 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.382-136T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21701054 | |||||||
| chr13:21701071 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
325 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.382-119T>C | FGF9 | ENSG00000102678.7 | transcript | ENST00000382353.6 | protein_coding | 2/2 | chr13 | 21701071 |