Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 121643 |
|---|---|
| ensemblid | ENSG00000139445.18 |
| hgncid | 21399 |
| symbol | FOXN4 |
| name | forkhead box N4 |
| refseq_nuc | NM_213596.3 |
| refseq_prot | NP_998761.2 |
| ensembl_nuc | ENST00000299162.10 |
| ensembl_prot | ENSP00000299162.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 109277978 |
| end | 109309284 |
| strand | - |
| ver | v1.2 |
| region | chr12:109277978-109309284 |
| region5000 | chr12:109272978-109314284 |
| regionname0 | FOXN4_chr12_109277978_109309284 |
| regionname5000 | FOXN4_chr12_109272978_109314284 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 517 | 354 | 90 | 65 | 142 | 15 | 41 | 104 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0002 | 0/1 | 517 | 4 | 1 | 1 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0003 | 0/0 | 517 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0004 | 0/0 | 517 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0005 | 0/0 | 517 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0006 | 0/0 | 517 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0007 | 0/0 | 517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0008 | 0/0 | 517 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1554 | 215 | 66 | 31 | 82 | 6 | 29 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0002 | 0/0 | 1554 | 92 | 9 | 23 | 52 | 5 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0003 | 0/0 | 1554 | 18 | 4 | 8 | 0 | 3 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0004 | 0/0 | 1554 | 17 | 7 | 2 | 4 | 1 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0005 | 0/0 | 1554 | 7 | 3 | 1 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0006 | 0/1 | 1554 | 4 | 1 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0007 | 0/0 | 1554 | 3 | 0 | 0 | 0 | 0 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0008 | 0/0 | 1554 | 3 | 0 | 1 | 0 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0009 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0010 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0011 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0012 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0013 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0014 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0015 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| c0016 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1863 | 183 | 58 | 35 | 53 | 7 | 28 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0002 | 0/0 | 1863 | 116 | 11 | 32 | 53 | 11 | 9 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0003 | 0/0 | 1863 | 19 | 4 | 0 | 13 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0004 | 0/0 | 1863 | 17 | 3 | 0 | 12 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0005 | 0/0 | 1863 | 6 | 2 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0006 | 0/0 | 1863 | 5 | 0 | 0 | 5 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0007 | 0/0 | 1863 | 4 | 4 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0008 | 0/0 | 1863 | 3 | 3 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0009 | 0/0 | 1863 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0010 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0011 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0012 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0013 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0014 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0015 | 0/0 | 1863 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0016 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0017 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0018 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0019 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0020 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0021 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| t0022 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 0 | 4 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0002 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0004 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0005 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0010 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0012 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0021 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1554 | 215 | 66 | 31 | 82 | 6 | 29 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0002 | 0/0 | 1554 | 92 | 9 | 23 | 52 | 5 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0003 | 0/0 | 1554 | 18 | 4 | 8 | 0 | 3 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0004 | 0/0 | 1554 | 17 | 7 | 2 | 4 | 1 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0005 | 0/0 | 1554 | 7 | 3 | 1 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0007 | 0/0 | 1554 | 3 | 0 | 0 | 0 | 0 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0012 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0015 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0002c0006 | 0/1 | 1554 | 4 | 1 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0003c0008 | 0/0 | 1554 | 3 | 0 | 1 | 0 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0004c0013 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0004c0016 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0005c0009 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0006c0014 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0007c0011 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0008c0010 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3416 | 153 | 47 | 30 | 45 | 6 | 24 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0003 | 0/0 | 3416 | 19 | 4 | 0 | 13 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0004 | 0/0 | 3416 | 17 | 3 | 0 | 12 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0005 | 0/0 | 3416 | 6 | 2 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0006 | 0/0 | 3416 | 5 | 0 | 0 | 5 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0007 | 0/0 | 3416 | 4 | 4 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0009 | 0/0 | 3416 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0010 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0012 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0014 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0015 | 0/0 | 3416 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0017 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0018 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0019 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0020 | 0/0 | 3416 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0001t0021 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0002t0002 | 0/0 | 3416 | 88 | 6 | 23 | 51 | 5 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0002t0008 | 0/0 | 3416 | 3 | 3 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0002t0016 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0003t0002 | 0/0 | 3416 | 18 | 4 | 8 | 0 | 3 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0004t0001 | 0/0 | 3416 | 16 | 6 | 2 | 4 | 1 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0004t0011 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0005t0001 | 0/0 | 3416 | 6 | 3 | 1 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0005t0013 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0007t0002 | 0/0 | 3416 | 3 | 0 | 0 | 0 | 0 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0012t0001 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0001c0015t0002 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0002c0006t0001 | 0/1 | 3416 | 4 | 1 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0003c0008t0002 | 0/0 | 3416 | 3 | 0 | 1 | 0 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0004c0013t0001 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0004c0016t0002 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0005c0009t0002 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0005c0009t0022 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0006c0014t0001 | 0/0 | 3416 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0007c0011t0001 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| a0008c0010t0002 | 0/0 | 3416 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | copy fasta | chr12 | 109272978 | 109314284 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0004 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0005 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0009g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0015g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0017g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0018g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0019g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0020g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0021g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0001 | 0/0 | 6 | 0 | 0 | 4 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0016g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0007t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0007t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0012t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0015t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0002c0006t0001g0021 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0002c0006t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0002c0006t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0003c0008t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0003c0008t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0003c0008t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0004c0013t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0004c0016t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0005c0009t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0005c0009t0022g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0006c0014t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0007c0011t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0008c0010t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0180 | EUR | GBR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0245 | EUR | GBR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0076 | EUR | GBR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0036 | EUR | FIN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0182 | EUR | FIN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0036 | EUR | FIN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00408 | hp1 | a0004 | c0013 | t0001 | g0224 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00544 | hp2 | a0004 | c0016 | t0002 | g0133 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0189 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0116 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0195 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0098 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0272 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0203 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0239 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0037 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0037 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0259 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0240 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01099 | hp2 | a0002 | c0006 | t0001 | g0021 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0168 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0129 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01175 | hp1 | a0003 | c0008 | t0002 | g0150 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0237 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0190 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01261 | hp2 | a0006 | c0014 | t0001 | g0135 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0265 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01433 | hp1 | a0001 | c0001 | t0015 | g0254 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0118 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01516 | hp2 | a0003 | c0008 | t0002 | g0145 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01517 | hp2 | a0003 | c0008 | t0002 | g0146 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01934 | hp2 | a0001 | c0005 | t0001 | g0258 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02027 | hp2 | a0001 | c0002 | t0016 | g0115 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0022 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02056 | hp1 | a0001 | c0005 | t0013 | g0267 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02080 | hp1 | a0001 | c0005 | t0001 | g0262 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02145 | hp1 | a0002 | c0006 | t0001 | g0081 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0022 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02257 | hp1 | a0001 | c0015 | t0002 | g0124 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0086 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0253 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0270 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02602 | hp1 | a0001 | c0001 | t0020 | g0213 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0257 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02615 | hp1 | a0001 | c0002 | t0008 | g0016 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0073 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0131 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02630 | hp1 | a0001 | c0002 | t0008 | g0041 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0264 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0090 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0238 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0260 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0300 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0235 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0139 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0186 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02976 | hp2 | a0001 | c0004 | t0011 | g0125 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0301 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03017 | hp2 | a0001 | c0004 | t0001 | g0113 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0087 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03195 | hp1 | a0001 | c0001 | t0021 | g0281 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03209 | hp2 | a0001 | c0002 | t0008 | g0016 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03225 | hp1 | a0001 | c0001 | t0019 | g0271 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0056 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03491 | hp1 | a0001 | c0007 | t0002 | g0038 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0114 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03492 | hp2 | a0001 | c0007 | t0002 | g0038 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0234 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0122 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0055 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03579 | hp2 | a0007 | c0011 | t0001 | g0199 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03654 | hp2 | a0002 | c0006 | t0001 | g0067 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0285 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03704 | hp2 | a0001 | c0007 | t0002 | g0256 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0289 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0226 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0117 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0249 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | CHB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CHB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18747 | hp1 | a0001 | c0001 | t0009 | g0171 | EAS | CHB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | CHB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18906 | hp1 | a0001 | c0001 | t0018 | g0274 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18965 | hp2 | a0001 | c0001 | t0017 | g0130 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18966 | hp2 | a0001 | c0004 | t0001 | g0120 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0207 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0132 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18969 | hp1 | a0001 | c0012 | t0001 | g0088 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0099 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18984 | hp1 | a0005 | c0009 | t0022 | g0283 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19000 | hp1 | a0001 | c0005 | t0001 | g0269 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19011 | hp2 | a0005 | c0009 | t0002 | g0178 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0266 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0123 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19089 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0246 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0255 | AFR | ASW | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20752 | hp2 | a0008 | c0010 | t0002 | g0218 | EUR | TSI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0147 | SAS | GIH | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | GIH | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0252 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0137 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0268 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0138 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG06807 | hp2 | a0001 | c0005 | t0001 | g0261 | AFR | USA | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | USA | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0006 | t0001 | g0021 | REF | REF | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0201 | REF | REF | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109279780
|
G | T | 1 | a0008 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1445C>A | p.Thr482Lys | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1614/3416 | 1445/1554 | 482/517 | chr12 | 109279780 | ||
| chr12:109281506
|
C | T | 1 | a0005 | 2 | NA18984.hp1 NA19011.hp2 |
missense_variant | MODERATE | c.1195G>A | p.Ala399Thr | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/10 | 1364/3416 | 1195/1554 | 399/517 | chr12 | 109281506 | ||
| chr12:109281520
|
G | A | 1 | a0007 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1181C>T | p.Pro394Leu | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/10 | 1350/3416 | 1181/1554 | 394/517 | chr12 | 109281520 | ||
| chr12:109281754
|
C | T | 1 | a0006 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.947G>A | p.Arg316His | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/10 | 1116/3416 | 947/1554 | 316/517 | chr12 | 109281754 | ||
| chr12:109281778
|
G | A | 1 | a0004 | 2 | HG00408.hp1 HG00544.hp2 |
missense_variant | MODERATE | c.923C>T | p.Ser308Phe | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/10 | 1092/3416 | 923/1554 | 308/517 | chr12 | 109281778 | ||
| chr12:109287858
|
G | A | 1 | a0003 | 3 | HG01175.hp1 HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.454C>T | p.Pro152Ser | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 5/10 | 623/3416 | 454/1554 | 152/517 | chr12 | 109287858 | ||
| chr12:109287902
|
G | A | 1 | a0002 | 4 | HG01099.hp2 HG02145.hp1 HG03654.hp2 others(1): Show |
missense_variant | MODERATE | c.410C>T | p.Pro137Leu | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 5/10 | 579/3416 | 410/1554 | 137/517 | chr12 | 109287902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109279860
|
C | T | 1 | a0001c0007 | 3 | HG03491.hp1 HG03492.hp2 HG03704.hp2 |
synonymous_variant | LOW | c.1365G>A | p.Pro455Pro | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1534/3416 | 1365/1554 | 455/517 | chr12 | 109279860 | ||
| chr12:109279892
|
A | G | 8 | a0001c0002a0001c0003a0001c0007others(5): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
synonymous_variant | LOW | c.1333T>C | p.Leu445Leu | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1502/3416 | 1333/1554 | 445/517 | chr12 | 109279892 | ||
| chr12:109281558
|
G | A | 1 | a0001c0012 | 1 | NA18969.hp1 | synonymous_variant | LOW | c.1143C>T | p.Thr381Thr | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/10 | 1312/3416 | 1143/1554 | 381/517 | chr12 | 109281558 | ||
| chr12:109285428
|
G | A | 3 | a0001c0003a0001c0005a0001c0007 | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(25): Show |
synonymous_variant | LOW | c.777C>T | p.Ser259Ser | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/10 | 946/3416 | 777/1554 | 259/517 | chr12 | 109285428 | ||
| chr12:109287883
|
G | A | 4 | a0001c0004a0001c0015a0004c0016others(1): Show | 20 | HG00544.hp2 HG00733.hp2 HG01168.hp2 others(17): Show |
synonymous_variant | LOW | c.429C>T | p.Ala143Ala | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 5/10 | 598/3416 | 429/1554 | 143/517 | chr12 | 109287883 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109278063
|
A | G | 1 | a0001c0001t0006 | 5 | HG02132.hp1 NA18955.hp1 NA18969.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1608T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1608 | chr12 | 109278063 | |||||
| chr12:109278127
|
C | A | 1 | a0001c0001t0012 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1544G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1544 | chr12 | 109278127 | |||||
| chr12:109278250
|
G | A | 1 | a0001c0005t0013 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1421 | chr12 | 109278250 | |||||
| chr12:109278487
|
A | G | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0019others(1): Show | 25 | HG00673.hp1 HG02040.hp1 HG02109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1184T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1184 | chr12 | 109278487 | |||||
| chr12:109278526
|
G | A | 11 | a0001c0002t0002a0001c0002t0008a0001c0002t0016others(8): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1145C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1145 | chr12 | 109278526 | |||||
| chr12:109278585
|
G | A | 1 | a0001c0001t0014 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1086C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 1086 | chr12 | 109278585 | |||||
| chr12:109278675
|
A | G | 1 | a0001c0001t0020 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 996 | chr12 | 109278675 | |||||
| chr12:109278987
|
T | C | 1 | a0001c0001t0009 | 2 | NA18747.hp1 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*684A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 684 | chr12 | 109278987 | |||||
| chr12:109278988
|
G | A | 1 | a0001c0001t0015 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*683C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 683 | chr12 | 109278988 | |||||
| chr12:109279095
|
G | A | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0019others(1): Show | 25 | HG00673.hp1 HG02040.hp1 HG02109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*576C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 576 | chr12 | 109279095 | |||||
| chr12:109279252
|
G | A | 2 | a0001c0001t0007a0001c0001t0021 | 5 | HG02965.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*419C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 419 | chr12 | 109279252 | |||||
| chr12:109279262
|
C | T | 1 | a0001c0004t0011 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 409 | chr12 | 109279262 | |||||
| chr12:109279405
|
G | A | 11 | a0001c0002t0002a0001c0002t0008a0001c0002t0016others(8): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*266C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 266 | chr12 | 109279405 | |||||
| chr12:109279495
|
C | T | 1 | a0001c0001t0010 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 176 | chr12 | 109279495 | |||||
| chr12:109279573
|
G | A | 1 | a0001c0002t0016 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 98 | chr12 | 109279573 | |||||
| chr12:109279578
|
C | A | 1 | a0001c0001t0017 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 93 | chr12 | 109279578 | |||||
| chr12:109279642
|
G | A | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0019others(1): Show | 25 | HG00673.hp1 HG02040.hp1 HG02109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*29C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 29 | chr12 | 109279642 | |||||
| chr12:109279645
|
G | A | 1 | a0001c0001t0018 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 26 | chr12 | 109279645 | |||||
| chr12:109279668
|
A | G | 1 | a0001c0001t0019 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 3 | chr12 | 109279668 | |||||
| chr12:109279669
|
G | C | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0019others(1): Show | 25 | HG00673.hp1 HG02040.hp1 HG02109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 10/10 | 2 | chr12 | 109279669 | |||||
| chr12:109309186
|
G | A | 4 | a0001c0001t0003a0001c0001t0004a0001c0001t0021others(1): Show | 38 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-71C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 1/10 | 865 | chr12 | 109309186 | |||||
| chr12:109309199
|
C | T | 1 | a0001c0002t0008 | 3 | HG02615.hp1 HG02630.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-84G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 1/10 | 878 | chr12 | 109309199 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109280015
|
G | A | 20 | a0001c0001t0003g0295a0001c0001t0015g0254a0001c0004t0001g0022others(17): Show | 21 | HG00733.hp2 HG01168.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1295-85C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280015 | ||||||
| chr12:109280296
|
T | C | 5 | a0001c0001t0007g0055a0001c0001t0007g0056a0001c0001t0007g0087others(2): Show | 5 | HG02965.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-366A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280296 | ||||||
| chr12:109280342
|
C | CA | 15 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0068others(12): Show | 18 | HG00423.hp1 HG00423.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1295-413dupT | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280342 | ||||||
| chr12:109280342
|
CA | C | 127 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0035others(124): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1295-413delT | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280342 | ||||||
| chr12:109280342
|
CAA | C | 11 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0282others(8): Show | 15 | HG00609.hp1 HG01256.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1295-414_1295-413d others(4): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280342 | ||||||
| chr12:109280342
|
CAAA | C | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-415_1295-413d others(5): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280342 | ||||||
| chr12:109280347
|
A | G | 1 | a0001c0001t0007g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1295-417T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280347 | ||||||
| chr12:109280348
|
A | G | 4 | a0001c0001t0007g0055a0001c0001t0007g0056a0001c0001t0007g0139others(1): Show | 4 | HG02965.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1295-418T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280348 | ||||||
| chr12:109280385
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1295-455G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280385 | ||||||
| chr12:109280407
|
C | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0074others(6): Show | 13 | HG02258.hp1 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1295-477G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280407 | ||||||
| chr12:109280514
|
G | C | 84 | a0001c0002t0002g0001a0001c0002t0002g0003a0001c0002t0002g0013others(81): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1295-584C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280514 | ||||||
| chr12:109280755
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1294+652G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280755 | ||||||
| chr12:109280832
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1294+575G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280832 | ||||||
| chr12:109280854
|
C | T | 1 | a0001c0004t0001g0129 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1294+553G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109280854 | ||||||
| chr12:109281088
|
C | T | 59 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0025others(56): Show | 69 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1294+319G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109281088 | ||||||
| chr12:109281155
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1294+252G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109281155 | ||||||
| chr12:109281213
|
G | A | 23 | a0001c0001t0004g0009a0001c0001t0004g0276a0001c0001t0004g0277others(20): Show | 26 | HG00673.hp1 HG02040.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1294+194C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109281213 | ||||||
| chr12:109281275
|
G | A | 1 | a0001c0001t0004g0277 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1294+132C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 9/9 | chr12 | 109281275 | ||||||
| chr12:109281923
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.902-124T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109281923 | ||||||
| chr12:109281932
|
C | T | 1 | a0001c0001t0005g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.902-133G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109281932 | ||||||
| chr12:109282163
|
G | C | 2 | a0001c0001t0004g0280a0001c0001t0004g0293 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.902-364C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109282163 | ||||||
| chr12:109282562
|
T | C | 1 | a0001c0002t0002g0165 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.902-763A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109282562 | ||||||
| chr12:109282563
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.902-764C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109282563 | ||||||
| chr12:109282583
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0136 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.902-784G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109282583 | ||||||
| chr12:109282709
|
T | C | 1 | a0001c0002t0002g0173 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.902-910A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109282709 | ||||||
| chr12:109282817
|
G | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0136 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.902-1018C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109282817 | ||||||
| chr12:109282940
|
C | T | 2 | a0001c0001t0007g0055a0001c0001t0007g0056 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.902-1141G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109282940 | ||||||
| chr12:109282953
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.902-1154C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109282953 | ||||||
| chr12:109283123
|
G | A | 1 | a0001c0004t0001g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.902-1324C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283123 | ||||||
| chr12:109283175
|
AT | A | 219 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0023others(216): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.902-1377delA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283175 | ||||||
| chr12:109283284
|
A | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0136 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.902-1485T>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283284 | ||||||
| chr12:109283440
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.902-1641A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283440 | ||||||
| chr12:109283475
|
C | CT | 24 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0112others(21): Show | 30 | HG00558.hp1 HG00673.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.902-1677dupA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283475 | ||||||
| chr12:109283475
|
CT | C | 135 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0024others(132): Show | 160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.902-1677delA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283475 | ||||||
| chr12:109283720
|
C | A | 36 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0241others(33): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.901+1584G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283720 | ||||||
| chr12:109283766
|
G | A | 35 | a0001c0001t0001g0108a0001c0001t0001g0241a0001c0002t0002g0007others(32): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.901+1538C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283766 | ||||||
| chr12:109283862
|
C | A | 97 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0025others(94): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.901+1442G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283862 | ||||||
| chr12:109283862
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0106a0001c0001t0001g0155others(10): Show | 14 | HG00735.hp1 HG02129.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.901+1442G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283862 | ||||||
| chr12:109283958
|
T | C | 4 | a0001c0001t0001g0154a0001c0001t0001g0185a0001c0001t0001g0227others(1): Show | 4 | HG01167.hp1 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+1346A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283958 | ||||||
| chr12:109283977
|
T | C | 3 | a0001c0002t0002g0047a0001c0002t0002g0170a0001c0002t0002g0187 | 3 | NA18948.hp2 NA18985.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.901+1327A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109283977 | ||||||
| chr12:109284114
|
C | T | 1 | a0001c0001t0004g0284 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.901+1190G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284114 | ||||||
| chr12:109284229
|
G | C | 1 | a0001c0001t0003g0295 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.901+1075C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284229 | ||||||
| chr12:109284308
|
A | G | 37 | a0001c0001t0001g0108a0001c0001t0001g0241a0001c0002t0002g0007others(34): Show | 44 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.901+996T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284308 | ||||||
| chr12:109284426
|
G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.901+878C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284426 | ||||||
| chr12:109284446
|
T | TATGTGTG others(5): Show |
59 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0112others(56): Show | 70 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.901+846_901+857dup others(12): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284446 | ||||||
| chr12:109284558
|
C | CGTGT | 11 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0247others(8): Show | 15 | HG01081.hp2 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.901+742_901+745dup others(4): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284558 | ||||||
| chr12:109284568
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.901+736G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284568 | ||||||
| chr12:109284573
|
G | A | 113 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0025others(110): Show | 133 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.901+731C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284573 | ||||||
| chr12:109284582
|
T | C | 2 | a0001c0002t0002g0180a0001c0002t0002g0182 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.901+722A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284582 | ||||||
| chr12:109284659
|
C | T | 1 | a0001c0001t0012g0246 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.901+645G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284659 | ||||||
| chr12:109284709
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.901+595C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284709 | ||||||
| chr12:109284718
|
C | T | 1 | a0001c0001t0015g0254 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.901+586G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284718 | ||||||
| chr12:109284747
|
CTGTG | C | 9 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(6): Show | 11 | HG00140.hp1 HG00738.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.901+553_901+556del others(4): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284747 | ||||||
| chr12:109284823
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.901+481C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284823 | ||||||
| chr12:109284869
|
CGT | C | 59 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0112others(56): Show | 70 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.901+433_901+434del others(2): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284869 | ||||||
| chr12:109284887
|
T | C | 216 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(213): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.901+417A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284887 | ||||||
| chr12:109284898
|
G | A | 59 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0112others(56): Show | 70 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.901+406C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109284898 | ||||||
| chr12:109285109
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.901+195G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285109 | ||||||
| chr12:109285144
|
TTGTGTGT others(17): Show |
T | 1 | a0001c0004t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.901+136_901+159del others(24): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285144 | ||||||
| chr12:109285153
|
T | TGCGCATA others(13): Show |
1 | a0004c0016t0002g0133 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.901+131_901+150dup others(20): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285153 | ||||||
| chr12:109285174
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.901+130C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285174 | ||||||
| chr12:109285244
|
C | CGT | 32 | a0001c0001t0001g0091a0001c0001t0001g0103a0001c0001t0001g0126others(29): Show | 40 | HG00558.hp1 HG00673.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.901+58_901+59dupAC | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285244 | ||||||
| chr12:109285244
|
C | CGTGT | 5 | a0001c0001t0001g0241a0001c0001t0003g0299a0001c0001t0004g0280others(2): Show | 5 | HG00323.hp2 HG01891.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.901+56_901+59dupAC others(2): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285244 | ||||||
| chr12:109285244
|
C | CGTGTGT | 19 | a0001c0001t0001g0108a0001c0002t0002g0242a0001c0003t0002g0036others(16): Show | 20 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.901+54_901+59dupAC others(4): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285244 | ||||||
| chr12:109285244
|
C | CGTGTGTG others(1): Show |
9 | a0001c0001t0004g0290a0001c0002t0002g0007a0001c0002t0002g0034others(6): Show | 13 | HG00099.hp2 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.901+52_901+59dupAC others(6): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285244 | ||||||
| chr12:109285244
|
CGT | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0160others(10): Show | 17 | HG00280.hp2 HG01081.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.901+58_901+59delAC | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285244 | ||||||
| chr12:109285270
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.901+34A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285270 | ||||||
| chr12:109285272
|
T | C | 71 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(68): Show | 86 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.901+32A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285272 | ||||||
| chr12:109285272
|
T | TGC | 29 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0001g0149others(26): Show | 34 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.901+31_901+32insGC | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285272 | ||||||
| chr12:109285274
|
T | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0025others(108): Show | 131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.901+30A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285274 | ||||||
| chr12:109285274
|
T | TGTGC | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.901+29_901+30insGC others(2): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285274 | ||||||
| chr12:109285274
|
T | TGTGTGC | 6 | a0001c0002t0002g0234a0001c0003t0002g0037a0001c0003t0002g0265others(3): Show | 7 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.901+29_901+30insGC others(4): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285274 | ||||||
| chr12:109285274
|
TGC | T | 17 | a0001c0004t0001g0022a0001c0004t0001g0113a0001c0004t0001g0114others(14): Show | 18 | HG00544.hp2 HG00733.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.901+28_901+29delGC | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285274 | ||||||
| chr12:109285276
|
C | T | 42 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0112others(39): Show | 52 | HG00558.hp1 HG00673.hp1 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.901+28G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 8/9 | chr12 | 109285276 | ||||||
| chr12:109285553
|
C | T | 1 | a0001c0001t0015g0254 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.694-42G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109285553 | ||||||
| chr12:109285606
|
G | A | 7 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0282others(4): Show | 11 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.694-95C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109285606 | ||||||
| chr12:109285867
|
C | CT | 122 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0025others(119): Show | 146 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.694-357dupA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109285867 | ||||||
| chr12:109285867
|
CT | C | 39 | a0001c0001t0001g0108a0001c0001t0001g0236a0001c0001t0001g0241others(36): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.694-357delA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109285867 | ||||||
| chr12:109286092
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0212 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.693+556T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109286092 | ||||||
| chr12:109286200
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.693+448T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109286200 | ||||||
| chr12:109286233
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.693+415C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109286233 | ||||||
| chr12:109286441
|
C | A | 2 | a0001c0002t0002g0046a0001c0002t0002g0173 | 2 | NA18974.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.693+207G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109286441 | ||||||
| chr12:109286495
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0005g0096 | 2 | NA18962.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.693+153A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109286495 | ||||||
| chr12:109286760
|
GGGGCA | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-21_597-17delTG others(3): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 6/9 | chr12 | 109286760 | ||||||
| chr12:109286760
|
GGGGCAGG others(3): Show |
G | 12 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0247others(9): Show | 16 | HG01081.hp2 HG01433.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.597-26_597-17delTG others(8): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 6/9 | chr12 | 109286760 | ||||||
| chr12:109286767
|
G | GGCGGGGC others(15): Show |
1 | a0001c0001t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.597-24_597-23insAC others(20): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 6/9 | chr12 | 109286767 | ||||||
| chr12:109286793
|
C | A | 1 | a0001c0001t0001g0230 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.597-49G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 6/9 | chr12 | 109286793 | ||||||
| chr12:109287587
|
C | T | 11 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0112others(8): Show | 13 | HG01168.hp1 HG01169.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.469-63G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 5/9 | chr12 | 109287587 | ||||||
| chr12:109287795
|
AG | A | 29 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0040others(26): Show | 37 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.468+48delC | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 5/9 | chr12 | 109287795 | ||||||
| chr12:109287796
|
G | T | 35 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0002t0002g0007others(32): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.468+48C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 5/9 | chr12 | 109287796 | ||||||
| chr12:109287991
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.358-37C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 4/9 | chr12 | 109287991 | ||||||
| chr12:109288026
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.357+30C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 4/9 | chr12 | 109288026 | ||||||
| chr12:109288042
|
G | T | 2 | a0001c0001t0001g0155a0001c0002t0002g0209 | 2 | NA18980.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.357+14C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 4/9 | chr12 | 109288042 | ||||||
| chr12:109288274
|
G | A | 1 | a0001c0002t0002g0159 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.233-94C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109288274 | ||||||
| chr12:109288323
|
C | T | 7 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0282others(4): Show | 11 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.233-143G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109288323 | ||||||
| chr12:109288354
|
T | G | 1 | a0006c0014t0001g0135 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.233-174A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109288354 | ||||||
| chr12:109288417
|
C | T | 5 | a0001c0002t0002g0163a0001c0002t0002g0175a0001c0002t0002g0204others(2): Show | 5 | HG02040.hp2 HG02056.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-237G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109288417 | ||||||
| chr12:109288557
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233-377T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109288557 | ||||||
| chr12:109288600
|
C | T | 1 | a0001c0001t0004g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.233-420G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109288600 | ||||||
| chr12:109288755
|
T | C | 62 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0108others(59): Show | 73 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.233-575A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109288755 | ||||||
| chr12:109288930
|
G | C | 1 | a0001c0001t0004g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.233-750C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109288930 | ||||||
| chr12:109289022
|
C | T | 5 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-842G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289022 | ||||||
| chr12:109289083
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0112a0001c0001t0001g0127others(2): Show | 6 | HG02976.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-903C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289083 | ||||||
| chr12:109289214
|
G | A | 1 | a0001c0002t0002g0034 | 2 | HG00738.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.232+927C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289214 | ||||||
| chr12:109289216
|
G | A | 5 | a0001c0001t0001g0241a0001c0002t0002g0007a0001c0002t0002g0034others(2): Show | 9 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+925C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289216 | ||||||
| chr12:109289231
|
T | C | 115 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0025others(112): Show | 135 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.232+910A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289231 | ||||||
| chr12:109289250
|
A | T | 1 | a0001c0002t0002g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.232+891T>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289250 | ||||||
| chr12:109289400
|
C | G | 114 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0025others(111): Show | 134 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.232+741G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289400 | ||||||
| chr12:109289547
|
T | C | 1 | a0001c0001t0019g0271 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.232+594A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289547 | ||||||
| chr12:109289756
|
C | A | 1 | a0001c0001t0020g0213 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.232+385G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289756 | ||||||
| chr12:109289835
|
T | C | 36 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0002t0002g0007others(33): Show | 43 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.232+306A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109289835 | ||||||
| chr12:109290118
|
G | A | 2 | a0001c0001t0003g0285a0001c0001t0004g0289 | 2 | HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.232+23C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 3/9 | chr12 | 109290118 | ||||||
| chr12:109290348
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0102 | 2 | HG01978.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.87-62C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290348 | ||||||
| chr12:109290369
|
C | T | 1 | a0001c0001t0007g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.87-83G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290369 | ||||||
| chr12:109290370
|
G | A | 30 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0112others(27): Show | 33 | HG00544.hp2 HG00733.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.87-84C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290370 | ||||||
| chr12:109290399
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.87-113C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290399 | ||||||
| chr12:109290425
|
A | C | 7 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0282others(4): Show | 11 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.87-139T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290425 | ||||||
| chr12:109290434
|
C | T | 6 | a0001c0004t0001g0022a0001c0004t0001g0122a0001c0004t0001g0131others(3): Show | 7 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.87-148G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290434 | ||||||
| chr12:109290462
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.87-176C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290462 | ||||||
| chr12:109290547
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.87-261G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290547 | ||||||
| chr12:109290548
|
G | A | 1 | a0001c0001t0004g0296 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.87-262C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290548 | ||||||
| chr12:109290826
|
G | A | 1 | a0004c0016t0002g0133 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.87-540C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290826 | ||||||
| chr12:109290882
|
G | A | 19 | a0001c0004t0001g0022a0001c0004t0001g0045a0001c0004t0001g0113others(16): Show | 20 | HG00544.hp2 HG00733.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.87-596C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290882 | ||||||
| chr12:109290967
|
A | G | 43 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(40): Show | 50 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.87-681T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290967 | ||||||
| chr12:109290969
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0143 | 3 | HG02698.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.87-683C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290969 | ||||||
| chr12:109290993
|
G | A | 1 | a0001c0003t0002g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.87-707C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109290993 | ||||||
| chr12:109291056
|
C | T | 10 | a0001c0001t0001g0241a0001c0002t0002g0007a0001c0002t0002g0034others(7): Show | 14 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.87-770G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291056 | ||||||
| chr12:109291202
|
G | A | 1 | a0007c0011t0001g0199 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.87-916C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291202 | ||||||
| chr12:109291241
|
A | G | 1 | a0001c0015t0002g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.87-955T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291241 | ||||||
| chr12:109291336
|
G | A | 3 | a0001c0001t0004g0278a0001c0005t0001g0262a0001c0005t0001g0269 | 3 | HG02080.hp1 NA18947.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.87-1050C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291336 | ||||||
| chr12:109291336
|
G | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0026others(92): Show | 114 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.87-1050C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291336 | ||||||
| chr12:109291460
|
C | T | 1 | a0001c0001t0004g0289 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.87-1174G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291460 | ||||||
| chr12:109291519
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0247others(9): Show | 16 | HG01081.hp2 HG01433.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.87-1233G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291519 | ||||||
| chr12:109291563
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0247others(9): Show | 16 | HG01081.hp2 HG01433.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.87-1277C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291563 | ||||||
| chr12:109291626
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.87-1340C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291626 | ||||||
| chr12:109291681
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.87-1395G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291681 | ||||||
| chr12:109291797
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.87-1511A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291797 | ||||||
| chr12:109291831
|
G | A | 1 | a0001c0001t0017g0130 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.87-1545C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291831 | ||||||
| chr12:109291920
|
CCCGGCTG others(23): Show |
C | 4 | a0001c0002t0002g0042a0001c0002t0002g0069a0001c0002t0008g0016others(1): Show | 5 | HG01943.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.87-1664_87-1635del others(30): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291920 | ||||||
| chr12:109291944
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.87-1658G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109291944 | ||||||
| chr12:109292055
|
C | T | 8 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0282others(5): Show | 12 | HG02083.hp1 HG03195.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.87-1769G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292055 | ||||||
| chr12:109292456
|
T | G | 1 | a0001c0002t0002g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.87-2170A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292456 | ||||||
| chr12:109292482
|
C | T | 3 | a0001c0004t0001g0113a0001c0004t0001g0114a0001c0004t0001g0117 | 3 | HG03017.hp2 HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.87-2196G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292482 | ||||||
| chr12:109292537
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0184 | 2 | HG01109.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.87-2251C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292537 | ||||||
| chr12:109292673
|
G | A | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.87-2387C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292673 | ||||||
| chr12:109292688
|
G | A | 1 | a0001c0004t0001g0114 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.87-2402C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292688 | ||||||
| chr12:109292838
|
C | T | 1 | a0001c0001t0005g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.87-2552G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292838 | ||||||
| chr12:109292881
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0194 | 2 | HG00558.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.87-2595G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292881 | ||||||
| chr12:109292985
|
C | G | 33 | a0001c0001t0001g0156a0001c0001t0003g0014a0001c0001t0003g0015others(30): Show | 41 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.87-2699G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109292985 | ||||||
| chr12:109293374
|
T | G | 1 | a0008c0010t0002g0218 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.87-3088A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293374 | ||||||
| chr12:109293441
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.87-3155C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293441 | ||||||
| chr12:109293560
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.87-3274G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293560 | ||||||
| chr12:109293584
|
G | A | 2 | a0001c0004t0001g0129a0006c0014t0001g0135 | 2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.87-3298C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293584 | ||||||
| chr12:109293647
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.87-3361C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293647 | ||||||
| chr12:109293663
|
A | G | 37 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0001t0004g0300others(34): Show | 44 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.87-3377T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293663 | ||||||
| chr12:109293818
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.87-3532G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293818 | ||||||
| chr12:109293905
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0083 | 2 | NA18946.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.87-3619C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293905 | ||||||
| chr12:109293914
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.87-3628G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293914 | ||||||
| chr12:109293979
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.87-3693T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109293979 | ||||||
| chr12:109294005
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.87-3719C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294005 | ||||||
| chr12:109294028
|
T | C | 1 | a0001c0001t0003g0291 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.87-3742A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294028 | ||||||
| chr12:109294168
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87-3882C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294168 | ||||||
| chr12:109294187
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87-3901G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294187 | ||||||
| chr12:109294216
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87-3930G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294216 | ||||||
| chr12:109294251
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87-3965G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294251 | ||||||
| chr12:109294465
|
A | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.87-4179T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294465 | ||||||
| chr12:109294466
|
G | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.87-4180C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294466 | ||||||
| chr12:109294478
|
C | A | 1 | a0001c0001t0021g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.87-4192G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294478 | ||||||
| chr12:109294561
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.87-4275C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294561 | ||||||
| chr12:109294608
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.87-4322A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294608 | ||||||
| chr12:109294718
|
T | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.87-4432A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294718 | ||||||
| chr12:109294766
|
AC | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.87-4481delG | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294766 | ||||||
| chr12:109294811
|
C | A | 15 | a0001c0001t0003g0040a0001c0001t0003g0285a0001c0001t0003g0291others(12): Show | 19 | HG00558.hp1 HG00673.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.87-4525G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294811 | ||||||
| chr12:109294890
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.87-4604A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294890 | ||||||
| chr12:109294955
|
G | A | 10 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0202others(7): Show | 12 | HG00609.hp2 HG02027.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.87-4669C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294955 | ||||||
| chr12:109295208
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.87-4922A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109295208 | ||||||
| chr12:109295300
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.87-5014T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109295300 | ||||||
| chr12:109295617
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87-5331G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109295617 | ||||||
| chr12:109295651
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.87-5365G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109295651 | ||||||
| chr12:109295765
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.87-5479C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109295765 | ||||||
| chr12:109295767
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.87-5481A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109295767 | ||||||
| chr12:109295818
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.87-5532G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109295818 | ||||||
| chr12:109296082
|
G | A | 11 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0112others(8): Show | 13 | HG01168.hp1 HG01169.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.87-5796C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109296082 | ||||||
| chr12:109296197
|
A | G | 1 | a0001c0004t0001g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.87-5911T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109296197 | ||||||
| chr12:109296612
|
C | T | 2 | a0001c0001t0007g0055a0001c0001t0007g0056 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.87-6326G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109296612 | ||||||
| chr12:109296633
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.87-6347C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109296633 | ||||||
| chr12:109296687
|
C | G | 1 | a0001c0004t0001g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.87-6401G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109296687 | ||||||
| chr12:109296806
|
T | A | 1 | a0001c0004t0001g0045 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.87-6520A>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109296806 | ||||||
| chr12:109297022
|
T | G | 3 | a0001c0001t0001g0089a0001c0001t0005g0096a0001c0001t0005g0099 | 3 | NA18962.hp2 NA18975.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.87-6736A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297022 | ||||||
| chr12:109297081
|
G | C | 2 | a0001c0004t0001g0129a0006c0014t0001g0135 | 2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.87-6795C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297081 | ||||||
| chr12:109297276
|
A | G | 1 | a0001c0003t0002g0036 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.87-6990T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297276 | ||||||
| chr12:109297380
|
G | A | 30 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0040others(27): Show | 38 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.87-7094C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297380 | ||||||
| chr12:109297393
|
T | G | 1 | a0001c0002t0002g0034 | 2 | HG00738.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.87-7107A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297393 | ||||||
| chr12:109297576
|
C | G | 1 | a0001c0002t0002g0076 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.87-7290G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297576 | ||||||
| chr12:109297634
|
A | C | 17 | a0001c0001t0003g0040a0001c0001t0003g0285a0001c0001t0003g0291others(14): Show | 21 | HG00558.hp1 HG00673.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.87-7348T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297634 | ||||||
| chr12:109297839
|
C | A | 38 | a0001c0001t0001g0039a0001c0001t0001g0236a0001c0001t0001g0241others(35): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.87-7553G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297839 | ||||||
| chr12:109297959
|
G | A | 1 | a0001c0004t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.87-7673C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109297959 | ||||||
| chr12:109298008
|
G | A | 1 | a0001c0004t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.87-7722C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298008 | ||||||
| chr12:109298228
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.87-7942G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298228 | ||||||
| chr12:109298331
|
G | GT | 15 | a0001c0001t0001g0031a0001c0001t0001g0140a0001c0001t0001g0162others(12): Show | 20 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.87-8046dupA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298331 | ||||||
| chr12:109298340
|
T | G | 1 | a0001c0001t0001g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.87-8054A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298340 | ||||||
| chr12:109298340
|
T | TG | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-8055_87-8054ins others(1): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298340 | ||||||
| chr12:109298340
|
T | TTG | 27 | a0001c0001t0001g0023a0001c0001t0001g0112a0001c0001t0001g0119others(24): Show | 29 | HG00544.hp2 HG00733.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.87-8055_87-8054ins others(2): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298340 | ||||||
| chr12:109298344
|
G | GT | 13 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0108others(10): Show | 17 | HG01081.hp2 HG01433.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.87-8059dupA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298344 | ||||||
| chr12:109298344
|
G | T | 3 | a0001c0001t0001g0093a0001c0002t0002g0090a0001c0004t0001g0045 | 3 | HG02135.hp1 HG02683.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.87-8058C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298344 | ||||||
| chr12:109298344
|
GT | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 90 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.87-8059delA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298344 | ||||||
| chr12:109298345
|
T | G | 4 | a0001c0001t0001g0093a0001c0002t0002g0054a0001c0002t0002g0090others(1): Show | 4 | HG02135.hp1 HG02683.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.87-8059A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298345 | ||||||
| chr12:109298348
|
T | G | 2 | a0001c0004t0001g0122a0001c0004t0001g0129 | 2 | HG01168.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.87-8062A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298348 | ||||||
| chr12:109298388
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.87-8102A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298388 | ||||||
| chr12:109298454
|
C | G | 1 | a0001c0004t0001g0045 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.87-8168G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298454 | ||||||
| chr12:109298723
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87-8437G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298723 | ||||||
| chr12:109298981
|
A | C | 1 | a0001c0001t0020g0213 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.87-8695T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298981 | ||||||
| chr12:109299274
|
T | C | 30 | a0001c0001t0001g0023a0001c0001t0001g0112a0001c0001t0001g0119others(27): Show | 32 | HG00544.hp2 HG00733.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.86+8962A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299274 | ||||||
| chr12:109299353
|
CAT | C | 12 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0279others(9): Show | 16 | HG01891.hp2 HG02055.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.86+8881_86+8882del others(2): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299353 | ||||||
| chr12:109299392
|
T | C | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+8844A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299392 | ||||||
| chr12:109299507
|
G | A | 38 | a0001c0001t0001g0039a0001c0001t0001g0236a0001c0001t0001g0241others(35): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.86+8729C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299507 | ||||||
| chr12:109299536
|
G | A | 1 | a0001c0002t0002g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.86+8700C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299536 | ||||||
| chr12:109299625
|
G | T | 7 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0282others(4): Show | 11 | HG02083.hp1 NA18612.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.86+8611C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299625 | ||||||
| chr12:109299669
|
G | A | 1 | a0001c0002t0002g0190 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.86+8567C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299669 | ||||||
| chr12:109299705
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0062a0001c0001t0001g0072others(7): Show | 11 | HG01070.hp1 HG01099.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.86+8531C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299705 | ||||||
| chr12:109299808
|
T | C | 1 | a0001c0004t0001g0138 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86+8428A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299808 | ||||||
| chr12:109299820
|
G | A | 1 | a0001c0002t0002g0090 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.86+8416C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299820 | ||||||
| chr12:109299857
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.86+8379G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109299857 | ||||||
| chr12:109300103
|
C | T | 1 | a0001c0002t0002g0190 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.86+8133G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300103 | ||||||
| chr12:109300205
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.86+8031C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300205 | ||||||
| chr12:109300252
|
C | CAGGCACT others(9): Show |
1 | a0001c0004t0001g0045 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.86+7968_86+7983dup others(16): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300252 | ||||||
| chr12:109300265
|
G | A | 30 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0040others(27): Show | 38 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.86+7971C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300265 | ||||||
| chr12:109300271
|
C | T | 30 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0040others(27): Show | 38 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.86+7965G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300271 | ||||||
| chr12:109300685
|
G | A | 2 | a0001c0003t0002g0259a0001c0003t0002g0270 | 2 | HG01074.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.86+7551C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300685 | ||||||
| chr12:109300817
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+7419C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300817 | ||||||
| chr12:109300826
|
T | G | 1 | a0001c0003t0002g0245 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.86+7410A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300826 | ||||||
| chr12:109300916
|
A | T | 1 | a0001c0001t0021g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.86+7320T>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109300916 | ||||||
| chr12:109301206
|
A | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.86+7030T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109301206 | ||||||
| chr12:109301246
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0247others(9): Show | 16 | HG01081.hp2 HG01433.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.86+6990C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109301246 | ||||||
| chr12:109301249
|
G | C | 1 | a0001c0001t0020g0213 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.86+6987C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109301249 | ||||||
| chr12:109301574
|
C | T | 2 | a0001c0003t0002g0235a0001c0003t0002g0255 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.86+6662G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109301574 | ||||||
| chr12:109301651
|
T | C | 1 | a0001c0002t0002g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.86+6585A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109301651 | ||||||
| chr12:109301747
|
C | A | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86+6489G>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109301747 | ||||||
| chr12:109301816
|
G | A | 1 | a0001c0001t0003g0014 | 3 | HG02083.hp1 NA18612.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.86+6420C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109301816 | ||||||
| chr12:109302102
|
C | T | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+6134G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302102 | ||||||
| chr12:109302119
|
T | A | 1 | a0001c0001t0010g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.86+6117A>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302119 | ||||||
| chr12:109302167
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.86+6069T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302167 | ||||||
| chr12:109302168
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.86+6068A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302168 | ||||||
| chr12:109302233
|
C | T | 1 | a0001c0001t0004g0298 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.86+6003G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302233 | ||||||
| chr12:109302361
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0014g0073 | 2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.86+5875T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302361 | ||||||
| chr12:109302377
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.86+5859C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302377 | ||||||
| chr12:109302585
|
G | A | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86+5651C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302585 | ||||||
| chr12:109302598
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.86+5638T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302598 | ||||||
| chr12:109302637
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.86+5599C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302637 | ||||||
| chr12:109302679
|
C | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0185a0001c0001t0001g0227others(1): Show | 4 | HG01167.hp1 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+5557G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302679 | ||||||
| chr12:109302728
|
G | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.86+5508C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302728 | ||||||
| chr12:109302748
|
C | T | 4 | a0001c0001t0001g0229a0001c0001t0009g0171a0001c0001t0009g0207others(1): Show | 4 | NA18747.hp1 NA18967.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+5488G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302748 | ||||||
| chr12:109302786
|
C | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.86+5450G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302786 | ||||||
| chr12:109302788
|
C | T | 23 | a0001c0002t0002g0252a0001c0003t0002g0036a0001c0003t0002g0037others(20): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.86+5448G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302788 | ||||||
| chr12:109302843
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.86+5393C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302843 | ||||||
| chr12:109302897
|
C | T | 1 | a0001c0002t0002g0252 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.86+5339G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302897 | ||||||
| chr12:109302931
|
T | C | 30 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0040others(27): Show | 38 | HG00558.hp1 HG00673.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.86+5305A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302931 | ||||||
| chr12:109303039
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.86+5197A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303039 | ||||||
| chr12:109303105
|
G | A | 1 | a0001c0002t0002g0169 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.86+5131C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303105 | ||||||
| chr12:109303120
|
T | G | 1 | a0001c0004t0001g0045 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.86+5116A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303120 | ||||||
| chr12:109303271
|
G | A | 1 | a0001c0001t0004g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.86+4965C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303271 | ||||||
| chr12:109303443
|
G | A | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86+4793C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303443 | ||||||
| chr12:109303539
|
A | G | 1 | a0001c0004t0001g0123 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.86+4697T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303539 | ||||||
| chr12:109303696
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0227a0001c0002t0002g0186 | 3 | HG01167.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.86+4540C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303696 | ||||||
| chr12:109303829
|
G | A | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86+4407C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303829 | ||||||
| chr12:109303929
|
G | A | 2 | a0001c0001t0007g0055a0001c0001t0007g0056 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.86+4307C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109303929 | ||||||
| chr12:109304089
|
G | T | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+4147C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304089 | ||||||
| chr12:109304099
|
G | A | 3 | a0001c0002t0002g0047a0001c0002t0002g0170a0001c0002t0002g0187 | 3 | NA18948.hp2 NA18985.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.86+4137C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304099 | ||||||
| chr12:109304170
|
G | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.86+4066C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304170 | ||||||
| chr12:109304188
|
C | CA | 39 | a0001c0001t0001g0039a0001c0001t0001g0214a0001c0001t0001g0236others(36): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.86+4047dupT | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304188 | ||||||
| chr12:109304209
|
A | G | 1 | a0001c0002t0002g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.86+4027T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304209 | ||||||
| chr12:109304212
|
G | A | 1 | a0001c0002t0002g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.86+4024C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304212 | ||||||
| chr12:109304213
|
A | G | 1 | a0001c0002t0002g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.86+4023T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304213 | ||||||
| chr12:109304221
|
G | GAGAA | 8 | a0001c0001t0001g0031a0001c0001t0001g0136a0001c0001t0001g0205others(5): Show | 9 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.86+4011_86+4014dup others(4): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(1): Show |
11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0214others(8): Show | 11 | HG01257.hp1 HG02040.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.86+4007_86+4014dup others(8): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(5): Show |
5 | a0001c0001t0001g0112a0001c0001t0001g0216a0001c0001t0001g0232others(2): Show | 6 | HG02698.hp2 HG02976.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.86+4003_86+4014dup others(12): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(9): Show |
5 | a0001c0001t0001g0033a0001c0001t0001g0219a0001c0001t0006g0053others(2): Show | 6 | HG00609.hp2 HG02027.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.86+3999_86+4014dup others(16): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(13): Show |
3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222 | 3 | HG01167.hp2 HG01169.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.86+3995_86+4014dup others(20): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(17): Show |
1 | a0001c0002t0002g0223 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.86+3991_86+4014dup others(24): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(21): Show |
1 | a0004c0013t0001g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.86+3987_86+4014dup others(28): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(25): Show |
1 | a0001c0002t0002g0225 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.86+3983_86+4014dup others(32): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(45): Show |
1 | a0001c0002t0002g0233 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.86+3963_86+4014dup others(52): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAAGA others(81): Show |
1 | a0001c0002t0002g0226 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.86+4014_86+4015ins others(88): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
G | GAGAAGAA others(8): Show |
1 | a0001c0001t0003g0299 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.86+4014_86+4015ins others(15): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
GAGAA | G | 29 | a0001c0001t0001g0106a0001c0001t0001g0126a0001c0001t0001g0127others(26): Show | 31 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.86+4011_86+4014del others(4): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
GAGAAAGA others(1): Show |
G | 19 | a0001c0001t0001g0006a0001c0001t0001g0121a0001c0001t0001g0162others(16): Show | 23 | HG00544.hp1 HG00621.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.86+4007_86+4014del others(8): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
GAGAAAGA others(5): Show |
G | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(14): Show | 22 | HG00673.hp2 HG00733.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.86+4003_86+4014del others(12): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
GAGAAAGA others(8): Show |
G | 1 | a0001c0001t0001g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.86+4000_86+4014del others(15): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
GAGAAAGA others(9): Show |
G | 7 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0151others(4): Show | 7 | HG00423.hp2 HG01175.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.86+3999_86+4014del others(16): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
GAGAAAGA others(13): Show |
G | 4 | a0001c0002t0002g0144a0001c0003t0002g0147a0003c0008t0002g0145others(1): Show | 4 | HG01516.hp2 HG01517.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+3995_86+4014del others(20): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
GAGAAAGA others(17): Show |
G | 1 | a0001c0001t0001g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.86+3991_86+4014del others(24): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304221
|
GAGAAAGA others(25): Show |
G | 1 | a0001c0001t0005g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.86+3983_86+4014del others(32): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304221 | ||||||
| chr12:109304258
|
AGAAAGAA others(30): Show |
A | 1 | a0001c0002t0002g0058 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.86+3941_86+3977del others(37): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304258 | ||||||
| chr12:109304263
|
GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86+3963_86+3972del others(10): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304263 | ||||||
| chr12:109304266
|
AGAAAGAA others(22): Show |
A | 10 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0060others(7): Show | 18 | HG00639.hp2 HG01099.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.86+3941_86+3969del others(29): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304266 | ||||||
| chr12:109304270
|
AGAAAGAA others(18): Show |
A | 17 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(14): Show | 25 | HG00408.hp2 HG00423.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.86+3941_86+3965del others(25): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304270 | ||||||
| chr12:109304273
|
A | G | 1 | a0001c0001t0007g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.86+3963T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304273 | ||||||
| chr12:109304274
|
AGAAAGAA others(14): Show |
A | 24 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0035others(21): Show | 30 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.86+3941_86+3961del others(21): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304274 | ||||||
| chr12:109304278
|
AGAAAGAA others(10): Show |
A | 7 | a0001c0001t0001g0005a0001c0001t0001g0089a0001c0001t0007g0087others(4): Show | 12 | HG00140.hp2 HG01257.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.86+3941_86+3957del others(17): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304278 | ||||||
| chr12:109304281
|
A | G | 1 | a0001c0002t0002g0142 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.86+3955T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304281 | ||||||
| chr12:109304282
|
AGAAAGAA others(6): Show |
A | 15 | a0001c0001t0001g0012a0001c0001t0001g0091a0001c0001t0001g0092others(12): Show | 18 | HG00621.hp1 HG01123.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.86+3941_86+3953del others(13): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304282 | ||||||
| chr12:109304284
|
AAAGAAAG others(5): Show |
A | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86+3940_86+3951del others(12): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304284 | ||||||
| chr12:109304285
|
A | G | 1 | a0001c0001t0007g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.86+3951T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304285 | ||||||
| chr12:109304285
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.86+3941_86+3950del others(10): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304285 | ||||||
| chr12:109304286
|
A | G | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86+3950T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304286 | ||||||
| chr12:109304286
|
AGAAAGAA others(2): Show |
A | 20 | a0001c0001t0001g0008a0001c0001t0001g0093a0001c0001t0001g0094others(17): Show | 29 | HG00673.hp1 HG01081.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.86+3941_86+3949del others(9): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304286 | ||||||
| chr12:109304290
|
AGAAAG | A | 17 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(14): Show | 19 | HG00099.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.86+3941_86+3945del others(5): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304290 | ||||||
| chr12:109304292
|
A | AAAGAAAG others(16): Show |
1 | a0001c0001t0001g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86+3943_86+3944ins others(23): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304292 | ||||||
| chr12:109304294
|
AG | A | 15 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0110others(12): Show | 17 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.86+3941delC | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304294 | ||||||
| chr12:109304295
|
G | GAAA | 11 | a0001c0001t0001g0039a0001c0001t0001g0263a0001c0001t0003g0292others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.86+3940_86+3941ins others(3): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304295 | ||||||
| chr12:109304295
|
G | GAAAGAAA | 8 | a0001c0001t0001g0044a0001c0001t0004g0297a0001c0003t0002g0270others(5): Show | 9 | HG02056.hp1 HG02293.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.86+3940_86+3941ins others(7): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304295 | ||||||
| chr12:109304295
|
G | GAAAGAAA others(4): Show |
1 | a0001c0001t0019g0271 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.86+3940_86+3941ins others(11): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304295 | ||||||
| chr12:109304295
|
G | GAAAGAAA others(8): Show |
2 | a0001c0001t0004g0298a0001c0003t0002g0272 | 2 | HG00741.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.86+3940_86+3941ins others(15): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304295 | ||||||
| chr12:109304295
|
G | GAAAGAAA others(12): Show |
1 | a0001c0001t0004g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.86+3940_86+3941ins others(19): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304295 | ||||||
| chr12:109304297
|
A | G | 2 | a0001c0001t0007g0139a0001c0003t0002g0245 | 2 | HG00099.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.86+3939T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304297 | ||||||
| chr12:109304449
|
C | G | 11 | a0001c0001t0001g0241a0001c0002t0002g0007a0001c0002t0002g0034others(8): Show | 15 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.86+3787G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304449 | ||||||
| chr12:109304651
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.86+3585G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304651 | ||||||
| chr12:109304725
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.86+3511T>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304725 | ||||||
| chr12:109304973
|
G | C | 1 | a0001c0001t0005g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.86+3263C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304973 | ||||||
| chr12:109305107
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0273 | 3 | HG01168.hp1 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.86+3129C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305107 | ||||||
| chr12:109305263
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.86+2973A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305263 | ||||||
| chr12:109305270
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.86+2966C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305270 | ||||||
| chr12:109305279
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.86+2957C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305279 | ||||||
| chr12:109305382
|
G | GTTA | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.86+2851_86+2853dup others(3): Show |
FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305382 | ||||||
| chr12:109305650
|
A | G | 2 | a0001c0001t0007g0055a0001c0001t0007g0056 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.86+2586T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305650 | ||||||
| chr12:109305662
|
G | A | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86+2574C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305662 | ||||||
| chr12:109305780
|
C | G | 1 | a0001c0002t0002g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.86+2456G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305780 | ||||||
| chr12:109305907
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.86+2329C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305907 | ||||||
| chr12:109305988
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.86+2248A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109305988 | ||||||
| chr12:109306117
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86+2119T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109306117 | ||||||
| chr12:109306312
|
T | C | 1 | a0001c0002t0002g0233 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.86+1924A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109306312 | ||||||
| chr12:109306430
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.86+1806G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109306430 | ||||||
| chr12:109306498
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.86+1738G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109306498 | ||||||
| chr12:109306581
|
A | G | 1 | a0001c0003t0002g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.86+1655T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109306581 | ||||||
| chr12:109306680
|
G | A | 1 | a0001c0002t0002g0048 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.86+1556C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109306680 | ||||||
| chr12:109307147
|
G | T | 1 | a0001c0001t0006g0049 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.86+1089C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307147 | ||||||
| chr12:109307191
|
G | A | 1 | a0001c0001t0007g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86+1045C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307191 | ||||||
| chr12:109307233
|
G | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0039others(46): Show | 61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.86+1003C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307233 | ||||||
| chr12:109307485
|
C | G | 1 | a0001c0002t0002g0234 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.86+751G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307485 | ||||||
| chr12:109307492
|
C | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.86+744G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307492 | ||||||
| chr12:109307584
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.86+652C>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307584 | ||||||
| chr12:109307815
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(65): Show | 93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.86+421T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307815 | ||||||
| chr12:109307869
|
A | G | 5 | a0001c0001t0006g0049a0001c0001t0006g0050a0001c0001t0006g0051others(2): Show | 5 | HG02132.hp1 NA18955.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.86+367T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307869 | ||||||
| chr12:109307871
|
G | GT | 6 | a0001c0001t0001g0044a0001c0001t0004g0276a0001c0002t0002g0046others(3): Show | 6 | HG02559.hp1 NA18975.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.86+364dupA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307871 | ||||||
| chr12:109307931
|
G | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0039others(46): Show | 61 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.86+305C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307931 | ||||||
| chr12:109308875
|
G | A | 1 | a0001c0001t0018g0274 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-4+244C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 1/9 | chr12 | 109308875 | ||||||
| chr12:109308933
|
A | C | 1 | a0001c0001t0001g0043 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-4+186T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 1/9 | chr12 | 109308933 | ||||||
| chr12:109309017
|
G | A | 1 | a0001c0001t0003g0301 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-4+102C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 1/9 | chr12 | 109309017 | ||||||
| chr12:109309097
|
A | C | 1 | a0001c0002t0002g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-4+22T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 1/9 | chr12 | 109309097 | ||||||
| chr12:109309114
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG01081.hp2 | splice_region_variant&intron_variant | LOW | c.-4+5C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 1/9 | chr12 | 109309114 |