Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MIESD others(512): Show |
chr12 | 109272978 | 109314284 |
| a0002 | 0/1 | 517 | 4 | 1 | 1 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | MIESD others(512): Show |
chr12 | 109272978 | 109314284 |
| a0003 | 0/0 | 517 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | MIESD others(512): Show |
chr12 | 109272978 | 109314284 |
| a0004 | 0/0 | 517 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | MIESD others(512): Show |
chr12 | 109272978 | 109314284 |
| a0005 | 0/0 | 517 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | MIESD others(512): Show |
chr12 | 109272978 | 109314284 |
| a0006 | 0/0 | 517 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | MIESD others(512): Show |
chr12 | 109272978 | 109314284 |
| a0007 | 0/0 | 517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | MIESD others(512): Show |
chr12 | 109272978 | 109314284 |
| a0008 | 0/0 | 517 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | MIESD others(512): Show |
chr12 | 109272978 | 109314284 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1551 | 215 | 66 | 31 | 82 | 6 | 29 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0001c0002 | 0/0 | 1551 | 92 | 9 | 23 | 52 | 5 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0001c0003 | 0/0 | 1551 | 18 | 4 | 8 | 0 | 3 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0001c0004 | 0/0 | 1551 | 17 | 7 | 2 | 4 | 1 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0001c0005 | 0/0 | 1551 | 7 | 3 | 1 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0001c0007 | 0/0 | 1551 | 3 | 0 | 0 | 0 | 0 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0001c0012 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0001c0015 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0002c0006 | 0/1 | 1551 | 4 | 1 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0003c0008 | 0/0 | 1551 | 3 | 0 | 1 | 0 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0004c0013 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0004c0016 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0005c0009 | 0/0 | 1551 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0006c0014 | 0/0 | 1551 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0007c0011 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
chr12 | 109272978 | 109314284 | ||
| a0008c0010 | 0/0 | 1551 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGAT others(1546): Show |
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 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0003 | 0/0 | 3416 | 19 | 4 | 0 | 13 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0004 | 0/0 | 3416 | 17 | 3 | 0 | 12 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0005 | 0/0 | 3416 | 6 | 2 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0006 | 0/0 | 3416 | 5 | 0 | 0 | 5 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0007 | 0/0 | 3416 | 4 | 4 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0009 | 0/0 | 3416 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0010 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0012 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0014 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0015 | 0/0 | 3416 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0017 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0018 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0019 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0020 | 0/0 | 3416 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0001t0021 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0002t0002 | 0/0 | 3416 | 88 | 6 | 23 | 51 | 5 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0002t0008 | 0/0 | 3416 | 3 | 3 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0002t0016 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0003t0002 | 0/0 | 3416 | 18 | 4 | 8 | 0 | 3 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0004t0001 | 0/0 | 3416 | 16 | 6 | 2 | 4 | 1 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0004t0011 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0005t0001 | 0/0 | 3416 | 6 | 3 | 1 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0005t0013 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0007t0002 | 0/0 | 3416 | 3 | 0 | 0 | 0 | 0 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0012t0001 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0001c0015t0002 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0002c0006t0001 | 0/1 | 3416 | 4 | 1 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0003c0008t0002 | 0/0 | 3416 | 3 | 0 | 1 | 0 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0004c0013t0001 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0004c0016t0002 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0005c0009t0002 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0005c0009t0022 | 0/0 | 3416 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0006c0014t0001 | 0/0 | 3416 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0007c0011t0001 | 0/0 | 3416 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| a0008c0010t0002 | 0/0 | 3416 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | ATGCT others(3411): Show |
chr12 | 109272978 | 109314284 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 6 | 1 | 9 | 2 | 4 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0003 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0011 | 0/0 | 5 | 1 | 0 | 1 | 0 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0095 | 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 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0180 | 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 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0006g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0009g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0014g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0015g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0017g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0020g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0001t0021g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0002 | 0/0 | 13 | 0 | 0 | 11 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0013 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0053 | 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 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0008g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0002t0016g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0016 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0202 | 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 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0004t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0005t0013g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0007t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0007t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0012t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0001c0015t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0002c0006t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0002c0006t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0002c0006t0001g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0003c0008t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0003c0008t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0004c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0004c0016t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0005c0009t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0005c0009t0022g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0006c0014t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0007c0011t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| a0008c0010t0002g0167 | 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 | g0149 | EUR | GBR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0191 | EUR | GBR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0062 | EUR | GBR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0042 | EUR | FIN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0151 | EUR | FIN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0042 | EUR | FIN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00408 | hp1 | a0004 | c0013 | t0001 | g0143 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00544 | hp2 | a0004 | c0016 | t0002 | g0107 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0123 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0098 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0141 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0202 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0124 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0045 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0045 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0206 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01099 | hp2 | a0002 | c0006 | t0001 | g0071 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0114 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01175 | hp1 | a0003 | c0008 | t0002 | g0036 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0125 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01261 | hp2 | a0006 | c0014 | t0001 | g0113 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0203 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0019 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01433 | hp1 | a0001 | c0001 | t0015 | g0192 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0105 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01516 | hp2 | a0003 | c0008 | t0002 | g0153 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01517 | hp2 | a0003 | c0008 | t0002 | g0036 | EUR | IBS | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01934 | hp2 | a0001 | c0005 | t0001 | g0201 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0073 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02027 | hp2 | a0001 | c0002 | t0016 | g0096 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0020 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02056 | hp1 | a0001 | c0005 | t0013 | g0199 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02080 | hp1 | a0001 | c0005 | t0001 | g0205 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0018 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02145 | hp1 | a0002 | c0006 | t0001 | g0031 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0020 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02257 | hp1 | a0001 | c0015 | t0002 | g0101 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0087 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0016 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0207 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02602 | hp1 | a0001 | c0001 | t0020 | g0170 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0016 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02615 | hp1 | a0001 | c0002 | t0008 | g0017 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0060 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02630 | hp1 | a0001 | c0002 | t0008 | g0017 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0016 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0039 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0195 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0188 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0184 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0118 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02976 | hp2 | a0001 | c0004 | t0011 | g0103 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03017 | hp2 | a0001 | c0004 | t0001 | g0100 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0111 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03195 | hp1 | a0001 | c0001 | t0021 | g0214 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03209 | hp2 | a0001 | c0002 | t0008 | g0017 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03225 | hp1 | a0001 | c0001 | t0019 | g0208 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | 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 | g0044 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0108 | 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 | g0044 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0183 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0115 | AFR | GWD | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03579 | hp2 | a0007 | c0011 | t0001 | g0157 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03654 | hp2 | a0002 | c0006 | t0001 | g0031 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03704 | hp2 | a0001 | c0007 | t0002 | g0200 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0219 | SAS | PJL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0130 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0099 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0016 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | CHB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | CHB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18747 | hp1 | a0001 | c0001 | t0009 | g0033 | EAS | CHB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | CHB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18906 | hp1 | a0001 | c0001 | t0018 | g0210 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18965 | hp2 | a0001 | c0001 | t0017 | g0097 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18966 | hp2 | a0001 | c0004 | t0001 | g0104 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0033 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0106 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18969 | hp1 | a0001 | c0012 | t0001 | g0068 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18984 | hp1 | a0005 | c0009 | t0022 | g0215 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19000 | hp1 | a0001 | c0005 | t0001 | g0204 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19011 | hp2 | a0005 | c0009 | t0002 | g0146 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0198 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0094 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19089 | hp2 | a0001 | c0004 | t0001 | g0051 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0193 | AFR | YRI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ASW | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0197 | AFR | ASW | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20752 | hp2 | a0008 | c0010 | t0002 | g0167 | EUR | TSI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0156 | SAS | GIH | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | GIH | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | CLM | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0102 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0043 | AFR | ACB | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0116 | AFR | MSL | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| HG06807 | hp2 | a0001 | c0005 | t0001 | g0043 | AFR | USA | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | USA | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| homoSapiens | chm13v2 | a0002 | c0006 | t0001 | g0090 | REF | REF | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0163 | REF | REF | FOXN4_chr12_109272978_109314284 | FOXN4 | chr12 | 109272978 | 109314284 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 3 | HG01099.hp2 HG02145.hp1 HG03654.hp2 |
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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0002 a0001c0003 a0001c0007 others(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 | a0001c0003 a0001c0005 a0001c0007 |
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 | a0001c0004 a0001c0015 a0004c0016 others(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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0019 others(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 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0016 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0019 others(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 | a0001c0001t0007 a0001c0001t0021 |
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 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0016 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0019 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0019 others(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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0021 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109280015 | G | A | 18 | a0001c0001t0003g0226 a0001c0001t0015g0192 a0001c0004t0001g0020 others(15): 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 | a0001c0001t0007g0058 a0001c0001t0007g0059 a0001c0001t0007g0066 others(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 | 14 | a0001c0001t0001g0009 a0001c0001t0001g0072 a0001c0001t0001g0082 others(11): 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 | 103 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0050 others(100): 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 | 7 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0002t0002g0034 others(4): 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 | 3 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0095 |
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 | a0001c0001t0007g0066 | 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 | a0001c0001t0007g0058 a0001c0001t0007g0059 a0001c0001t0007g0118 others(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 | a0001c0001t0001g0028 | 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 | 5 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0061 others(2): 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 | 65 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0010 others(62): 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0065 | 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 | a0001c0004t0001g0114 | 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 | 44 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): 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 | a0001c0001t0001g0159 | 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 | 20 | a0001c0001t0004g0008 a0001c0001t0004g0212 a0001c0001t0004g0213 others(17): 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 | a0001c0001t0004g0222 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0005g0063 | 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 | a0001c0001t0004g0217 a0001c0001t0004g0230 |
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 | a0001c0002t0002g0148 | 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 | a0001c0001t0003g0227 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
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 | a0001c0002t0002g0129 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
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 | a0001c0001t0007g0058 a0001c0001t0007g0059 |
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 | a0001c0001t0001g0092 | 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 | a0001c0004t0001g0105 | 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 | 173 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(170): 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 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
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 | a0001c0001t0001g0069 | 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 | 21 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0093 others(18): 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 | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(96): 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 | 30 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0189 others(27): 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 | 29 | a0001c0001t0001g0092 a0001c0001t0001g0189 a0001c0002t0002g0013 others(26): 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 | 69 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): 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 | 12 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0091 others(9): 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 | a0001c0001t0001g0122 a0001c0001t0001g0173 a0001c0001t0001g0174 others(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 | a0001c0002t0002g0053 a0001c0002t0002g0176 a0001c0002t0002g0177 |
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 | a0001c0001t0004g0221 | 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 | a0001c0001t0003g0226 | 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 | 31 | a0001c0001t0001g0092 a0001c0001t0001g0189 a0001c0002t0002g0013 others(28): 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 | 3 | a0001c0001t0001g0014 a0001c0001t0003g0226 a0001c0002t0002g0177 |
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 |
52 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0093 others(49): 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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0211 others(4): 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 | a0001c0001t0001g0194 | 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 | 84 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(81): 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 | a0001c0002t0002g0149 a0001c0002t0002g0151 |
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 | a0001c0001t0012g0193 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0015g0192 | 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 | 6 | a0001c0001t0001g0014 a0001c0001t0003g0226 a0001c0002t0002g0019 others(3): 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 | a0001c0001t0001g0112 | 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 | 52 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0093 others(49): 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 | 171 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(168): 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 | 52 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0093 others(49): 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 | a0001c0001t0001g0159 | 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 | a0001c0004t0001g0115 | 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 | a0004c0016t0002g0107 | 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 | a0001c0001t0001g0083 | 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 | 26 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0162 others(23): 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 | a0001c0001t0001g0189 a0001c0001t0003g0228 a0001c0001t0004g0217 others(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 | 15 | a0001c0001t0001g0092 a0001c0002t0002g0188 a0001c0003t0002g0016 others(12): 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 |
7 | a0001c0001t0004g0220 a0001c0002t0002g0013 a0001c0002t0002g0039 others(4): 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 | 9 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0161 others(6): 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 | a0001c0001t0001g0161 | 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 | 52 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(49): 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 | 19 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0127 others(16): 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 | 82 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): 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 | 2 | a0001c0001t0001g0014 a0001c0001t0003g0226 |
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 | a0001c0002t0002g0183 a0001c0003t0002g0045 a0001c0003t0002g0202 others(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 | 16 | a0001c0004t0001g0020 a0001c0004t0001g0094 a0001c0004t0001g0098 others(13): 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 | 36 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0093 others(33): 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 | a0001c0001t0015g0192 | 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 | 4 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0216 others(1): 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 | 90 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): 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 | 33 | a0001c0001t0001g0092 a0001c0001t0001g0185 a0001c0001t0001g0189 others(30): Show |
46 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.694-357delA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 7/9 | chr12 | 109285867 | |||||||
| chr12:109286092 | A | G | 1 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0050 | 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 | a0001c0002t0002g0052 a0001c0002t0002g0129 |
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 | a0001c0001t0001g0078 a0001c0001t0005g0079 |
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 | 3 | a0001c0001t0001g0014 a0001c0001t0003g0226 a0001c0001t0007g0118 |
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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0194 others(5): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0181 | 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 | 10 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0093 others(7): 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 | 24 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0047 others(21): 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 | 29 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0002t0002g0013 others(26): 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0132 a0001c0002t0002g0138 |
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 | a0001c0002t0002g0154 | 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 | 4 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0216 others(1): 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 | a0006c0014t0001g0113 | 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 | 2 | a0001c0002t0002g0015 a0001c0002t0002g0137 |
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 | a0001c0001t0001g0092 | 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 | a0001c0001t0004g0230 | 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 | 55 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0092 others(52): 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 | a0001c0001t0004g0230 | 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 | 2 | a0001c0001t0001g0014 a0001c0001t0003g0226 |
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 | 4 | a0001c0001t0001g0021 a0001c0001t0001g0093 a0001c0001t0001g0112 others(1): 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 | a0001c0002t0002g0040 | 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 | 4 | a0001c0001t0001g0189 a0001c0002t0002g0013 a0001c0002t0002g0040 others(1): 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 | 86 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): 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 | a0001c0002t0002g0136 | 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 | 85 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): 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 | a0001c0001t0019g0208 | 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 | a0001c0001t0020g0170 | 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 | 30 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0002t0002g0013 others(27): 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 | a0001c0001t0003g0223 a0001c0001t0004g0219 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0084 |
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 | a0001c0001t0007g0058 | 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 | 28 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0093 others(25): 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 | a0001c0001t0001g0126 | 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 | 4 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0216 others(1): 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 | 5 | a0001c0004t0001g0020 a0001c0004t0001g0102 a0001c0004t0001g0115 others(2): 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0004g0231 | 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 | a0004c0016t0002g0107 | 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 | 18 | a0001c0004t0001g0020 a0001c0004t0001g0051 a0001c0004t0001g0094 others(15): 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 | 34 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0185 others(31): 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 | 1 | a0001c0001t0001g0025 | 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 | a0001c0003t0002g0156 | 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 | 8 | a0001c0001t0001g0189 a0001c0002t0002g0013 a0001c0002t0002g0039 others(5): 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 | a0007c0011t0001g0157 | 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 | a0001c0015t0002g0101 | 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 | a0001c0001t0004g0224 a0001c0005t0001g0204 a0001c0005t0001g0205 |
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 | 70 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(67): 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 | a0001c0001t0004g0219 | 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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0194 others(5): 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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0194 others(5): 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0017g0097 | 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 | 3 | a0001c0002t0002g0048 a0001c0002t0002g0073 a0001c0002t0008g0017 |
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 | a0001c0001t0001g0011 | 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 | 5 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0216 others(2): 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 | a0001c0002t0002g0074 | 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 | a0001c0004t0001g0099 a0001c0004t0001g0100 a0001c0004t0001g0108 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
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 | a0001c0001t0007g0118 | 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 | a0001c0004t0001g0108 | 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 | a0001c0001t0005g0179 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
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 | 28 | a0001c0001t0001g0133 a0001c0001t0003g0007 a0001c0001t0003g0026 others(25): 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 | a0008c0010t0002g0167 | 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 | a0001c0001t0001g0109 | 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(44): Show |
92 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(89): 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 | a0001c0004t0001g0114 a0006c0014t0001g0113 |
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 | a0001c0001t0001g0075 | 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 | 31 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0004g0218 others(28): 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 | a0001c0001t0001g0095 | 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 | 1 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0092 | 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(44): Show |
92 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(89): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0003g0225 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0076 | 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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.87-4179T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294465 | |||||||
| chr12:109294466 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): 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 | a0001c0001t0021g0214 | 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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.87-4275C>T | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294561 | |||||||
| chr12:109294608 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.87-4322A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294608 | |||||||
| chr12:109294718 | T | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.87-4432A>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294718 | |||||||
| chr12:109294766 | AC | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.87-4481delG | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294766 | |||||||
| chr12:109294811 | C | A | 13 | a0001c0001t0003g0047 a0001c0001t0003g0223 a0001c0001t0003g0225 others(10): 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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.87-4604A>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109294890 | |||||||
| chr12:109294955 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): 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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0092 | 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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): 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 | a0001c0001t0001g0131 | 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 | 10 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0093 others(7): 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 | a0001c0004t0001g0099 | 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 | a0001c0001t0007g0058 a0001c0001t0007g0059 |
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 | a0001c0001t0001g0180 | 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 | a0001c0004t0001g0098 | 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 | a0001c0004t0001g0051 | 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 | a0001c0001t0001g0078 a0001c0001t0005g0077 a0001c0001t0005g0079 |
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 | a0001c0004t0001g0114 a0006c0014t0001g0113 |
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 | a0001c0003t0002g0042 | 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 | 25 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0047 others(22): 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 | a0001c0002t0002g0040 | 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 | a0001c0002t0002g0062 | 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 | 15 | a0001c0001t0003g0047 a0001c0001t0003g0223 a0001c0001t0003g0225 others(12): 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 | 32 | a0001c0001t0001g0046 a0001c0001t0001g0185 a0001c0001t0001g0189 others(29): 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 | a0001c0004t0001g0115 | 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 | a0001c0004t0001g0115 | 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 | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(45): Show |
93 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.87-7942G>A | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298228 | |||||||
| chr12:109298331 | G | GT | 11 | a0001c0001t0001g0022 a0001c0001t0001g0119 a0001c0001t0001g0126 others(8): 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 | a0001c0001t0001g0080 | 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 | 1 | a0001c0001t0001g0014 | 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 | 25 | a0001c0001t0001g0021 a0001c0001t0001g0093 a0001c0001t0001g0095 others(22): 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 | 9 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0092 others(6): 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 | a0001c0001t0001g0081 a0001c0002t0002g0085 a0001c0004t0001g0051 |
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 | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(42): Show |
89 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.87-8059delA | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109298344 | |||||||
| chr12:109298345 | T | G | 4 | a0001c0001t0001g0081 a0001c0002t0002g0057 a0001c0002t0002g0085 others(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 | a0001c0004t0001g0114 a0001c0004t0001g0115 |
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 | a0001c0001t0001g0092 | 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 | a0001c0004t0001g0051 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0020g0170 | 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 | 28 | a0001c0001t0001g0021 a0001c0001t0001g0093 a0001c0001t0001g0095 others(25): 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 | 9 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0216 others(6): 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 | 1 | a0001c0001t0001g0014 | 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 | 32 | a0001c0001t0001g0046 a0001c0001t0001g0185 a0001c0001t0001g0189 others(29): 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 | a0001c0002t0002g0171 | 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 | 4 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0216 others(1): 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 | a0001c0002t0002g0125 | 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 | 5 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): 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 | a0001c0004t0001g0116 | 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 | a0001c0002t0002g0085 | 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 | a0001c0001t0001g0095 | 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 | a0001c0002t0002g0125 | 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 | a0001c0001t0001g0086 | 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 | a0001c0004t0001g0051 | 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 | 25 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0047 others(22): 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 | 25 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0047 others(22): 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 | a0001c0003t0002g0206 a0001c0003t0002g0207 |
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 | 1 | a0001c0001t0001g0014 | 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 | a0001c0003t0002g0191 | 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 | a0001c0001t0021g0214 | 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 | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.86+7030T>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109301206 | |||||||
| chr12:109301246 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0194 others(5): 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 | a0001c0001t0020g0170 | 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 | a0001c0003t0002g0184 a0001c0003t0002g0197 |
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 | a0001c0002t0002g0171 | 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 | a0001c0001t0007g0118 | 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 | a0001c0001t0003g0026 | 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 | 1 | a0001c0001t0001g0014 | 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 | a0001c0001t0010g0087 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0004g0213 | 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 | a0001c0001t0001g0061 a0001c0001t0014g0060 |
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 | a0001c0001t0001g0117 | 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 | a0001c0001t0007g0118 | 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 | a0001c0001t0001g0092 | 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(44): Show |
92 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(89): 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 | a0001c0001t0001g0122 a0001c0001t0001g0173 a0001c0001t0001g0174 others(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 | 3 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0007g0118 |
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 | 3 | a0001c0001t0001g0180 a0001c0001t0009g0033 a0001c0002t0002g0121 |
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 | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.86+5450G>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109302786 | |||||||
| chr12:109302788 | C | T | 19 | a0001c0002t0002g0196 a0001c0003t0002g0016 a0001c0003t0002g0042 others(16): 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 | a0001c0001t0001g0050 | 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 | a0001c0002t0002g0196 | 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 | 25 | a0001c0001t0003g0007 a0001c0001t0003g0026 a0001c0001t0003g0047 others(22): 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 | a0001c0001t0001g0185 | 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 | a0001c0002t0002g0172 | 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 | a0001c0004t0001g0051 | 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 | a0001c0001t0004g0230 | 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 | a0001c0001t0007g0118 | 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 | a0001c0004t0001g0094 | 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 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0002t0002g0175 |
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 | a0001c0001t0007g0118 | 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 | a0001c0001t0007g0058 a0001c0001t0007g0059 |
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 | 1 | a0001c0001t0001g0014 | 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 | a0001c0002t0002g0053 a0001c0002t0002g0176 a0001c0002t0002g0177 |
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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(44): Show |
92 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.86+4066C>G | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109304170 | |||||||
| chr12:109304188 | C | CA | 33 | a0001c0001t0001g0046 a0001c0001t0001g0178 a0001c0001t0001g0185 others(30): 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 | a0001c0002t0002g0120 | 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 | a0001c0002t0002g0120 | 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 | a0001c0002t0002g0120 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0168 a0001c0001t0006g0018 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0162 a0001c0001t0001g0164 |
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 | a0001c0002t0002g0015 | 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 | a0004c0013t0001g0143 | 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 | a0001c0002t0002g0034 | 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 | a0001c0002t0002g0182 | 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 | a0001c0002t0002g0130 | 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 | a0001c0001t0003g0228 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0109 others(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 | 16 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(13): 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0160 others(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 | a0001c0002t0002g0023 a0001c0003t0002g0156 a0003c0008t0002g0036 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0005g0179 | 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 | a0001c0002t0002g0089 | 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 | a0001c0001t0007g0118 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0007g0059 | 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 | 23 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(20): Show |
29 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(26): 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 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0007g0066 others(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 | a0001c0002t0002g0002 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0014 | 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 | a0001c0001t0007g0058 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0007g0118 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0083 others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0194 a0001c0001t0003g0007 others(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 | a0001c0001t0001g0050 a0001c0001t0004g0008 a0001c0003t0002g0207 others(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 | a0001c0001t0019g0208 | 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 | a0001c0001t0004g0213 a0001c0003t0002g0202 |
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 | a0001c0001t0004g0218 | 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 | a0001c0001t0007g0118 a0001c0003t0002g0191 |
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 | 9 | a0001c0001t0001g0189 a0001c0002t0002g0013 a0001c0002t0002g0039 others(6): 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0005g0179 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0209 |
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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0180 | 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(44): Show |
92 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(89): 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 | a0001c0001t0007g0058 a0001c0001t0007g0059 |
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 | a0001c0001t0007g0118 | 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 | a0001c0002t0002g0057 | 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 | a0001c0001t0001g0181 | 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 | 1 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0093 | 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 | a0001c0002t0002g0182 | 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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): 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 | a0001c0001t0001g0050 | 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 | a0001c0003t0002g0184 | 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 | a0001c0002t0002g0054 | 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 | a0001c0001t0006g0055 | 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 | a0001c0001t0007g0118 | 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 | 39 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0046 others(36): 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 | a0001c0002t0002g0183 | 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 | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): 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 | a0001c0001t0001g0091 | 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(44): Show |
92 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.86+421T>C | FOXN4 | ENSG00000139445.18 | transcript | ENST00000299162.10 | protein_coding | 2/9 | chr12 | 109307815 | |||||||
| chr12:109307869 | A | G | 3 | a0001c0001t0006g0018 a0001c0001t0006g0055 a0001c0001t0006g0056 |
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 | a0001c0001t0001g0050 a0001c0001t0004g0212 a0001c0002t0002g0052 others(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 | 39 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0046 others(36): 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 | a0001c0001t0018g0210 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0003g0232 | 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 | a0001c0002t0002g0048 | 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 | a0001c0001t0001g0211 | 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 |