| geneid | 84553 |
|---|---|
| ensemblid | ENSG00000146267.12 |
| hgncid | 20742 |
| symbol | FAXC |
| name | failed axon connections homolog, metaxin like GST domain containing |
| refseq_nuc | NM_032511.4 |
| refseq_prot | NP_115900.1 |
| ensembl_nuc | ENST00000389677.6 |
| ensembl_prot | ENSP00000374328.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 99271168 |
| end | 99349674 |
| strand | - |
| ver | v1.2 |
| region | chr6:99271168-99349674 |
| region5000 | chr6:99266168-99354674 |
| regionname0 | FAXC_chr6_99271168_99349674 |
| regionname5000 | FAXC_chr6_99266168_99354674 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 409 | 397 | 82 | 78 | 172 | 18 | 45 | 140 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0002 | 0/0 | 409 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1230 | 374 | 81 | 62 | 171 | 16 | 43 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| c0002 | 1/0 | 1230 | 21 | 1 | 15 | 0 | 2 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| c0003 | 0/0 | 1230 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| c0004 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| c0005 | 0/0 | 1230 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 10279 | 27 | 0 | 10 | 14 | 1 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0002 | 0/0 | 10302 | 26 | 0 | 6 | 18 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0003 | 1/0 | 10299 | 20 | 1 | 15 | 0 | 1 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0004 | 0/0 | 10279 | 14 | 0 | 11 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0005 | 0/0 | 10292 | 11 | 3 | 2 | 2 | 3 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0006 | 0/0 | 10304 | 11 | 0 | 4 | 7 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0007 | 0/0 | 10309 | 10 | 0 | 0 | 10 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0008 | 0/0 | 10308 | 8 | 0 | 0 | 8 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0009 | 0/0 | 10306 | 8 | 0 | 1 | 4 | 0 | 3 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0010 | 0/0 | 10306 | 7 | 0 | 0 | 7 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0011 | 0/0 | 10316 | 7 | 0 | 0 | 5 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0012 | 0/0 | 10293 | 7 | 4 | 3 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0013 | 0/0 | 10284 | 7 | 7 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0014 | 0/0 | 10298 | 6 | 1 | 0 | 4 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0015 | 0/0 | 10307 | 6 | 0 | 0 | 5 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0016 | 0/0 | 10304 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0017 | 0/0 | 10279 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0018 | 0/0 | 10309 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0019 | 0/1 | 10293 | 5 | 0 | 2 | 0 | 1 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0020 | 0/0 | 10310 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0021 | 0/0 | 10288 | 5 | 1 | 2 | 0 | 2 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0022 | 0/0 | 10311 | 5 | 1 | 0 | 3 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0023 | 0/0 | 10305 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0024 | 0/0 | 10294 | 4 | 2 | 1 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0025 | 0/0 | 10295 | 4 | 0 | 0 | 1 | 0 | 3 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0026 | 0/0 | 10290 | 4 | 0 | 1 | 0 | 2 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0027 | 0/0 | 10300 | 4 | 0 | 1 | 1 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0028 | 0/0 | 10295 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0029 | 0/0 | 10291 | 3 | 1 | 1 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0030 | 0/0 | 10293 | 3 | 0 | 0 | 1 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0031 | 0/0 | 10318 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0032 | 0/0 | 10312 | 3 | 1 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0033 | 0/0 | 10306 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0034 | 0/0 | 10289 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0035 | 0/0 | 10300 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0036 | 0/0 | 10296 | 3 | 0 | 0 | 2 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0037 | 0/0 | 10292 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0038 | 0/0 | 10290 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0039 | 0/0 | 10313 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0040 | 0/0 | 10311 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0041 | 0/0 | 10292 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0042 | 0/0 | 10305 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0043 | 0/0 | 10299 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0044 | 0/0 | 10297 | 2 | 1 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0045 | 0/0 | 10282 | 2 | 0 | 1 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0046 | 0/0 | 10306 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0047 | 0/0 | 10314 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0048 | 0/0 | 10304 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0049 | 0/0 | 10311 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0050 | 0/0 | 10300 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0051 | 0/0 | 10292 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0052 | 0/0 | 10289 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0053 | 0/0 | 10287 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0054 | 0/0 | 10288 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0055 | 0/0 | 10308 | 2 | 0 | 0 | 1 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0056 | 0/0 | 10304 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0057 | 0/0 | 10302 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0058 | 0/0 | 10313 | 2 | 1 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0059 | 0/0 | 10308 | 2 | 1 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0060 | 0/0 | 10312 | 2 | 1 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0061 | 0/0 | 10306 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0062 | 0/0 | 10304 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0063 | 0/0 | 10287 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0064 | 0/0 | 10310 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0065 | 0/0 | 10279 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0066 | 0/0 | 10279 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0067 | 0/0 | 10315 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0068 | 0/0 | 10311 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0069 | 0/0 | 10305 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0070 | 0/0 | 10306 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0071 | 0/0 | 10292 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0072 | 0/0 | 10309 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0073 | 0/0 | 10296 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0074 | 0/0 | 10290 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0075 | 0/0 | 10294 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0076 | 0/0 | 10297 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0077 | 0/0 | 10295 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0078 | 0/0 | 10309 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0079 | 0/0 | 10307 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0080 | 0/0 | 10305 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0081 | 0/0 | 10305 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0082 | 0/0 | 10303 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0083 | 0/0 | 10292 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0084 | 0/0 | 10308 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0085 | 0/0 | 10312 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0086 | 0/0 | 10306 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0087 | 0/0 | 10310 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0088 | 0/0 | 10308 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0089 | 0/0 | 10302 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0090 | 0/0 | 10308 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0091 | 0/0 | 10298 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0092 | 0/0 | 10308 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0093 | 0/0 | 10304 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0094 | 0/0 | 10300 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0095 | 0/0 | 10298 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0096 | 0/0 | 10315 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0097 | 0/0 | 10315 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0098 | 0/0 | 10310 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0099 | 0/0 | 10313 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0100 | 0/0 | 10306 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0101 | 0/0 | 10314 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0102 | 0/0 | 10309 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0103 | 0/0 | 10302 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0104 | 0/0 | 10305 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0105 | 0/0 | 10303 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0106 | 0/0 | 10293 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0107 | 0/0 | 10272 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0108 | 0/0 | 10302 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0109 | 0/0 | 10298 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0110 | 0/0 | 10314 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0111 | 0/0 | 10284 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0112 | 0/0 | 10292 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0113 | 0/0 | 10292 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0114 | 0/0 | 10288 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0115 | 0/0 | 10288 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0116 | 0/0 | 10300 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0117 | 0/0 | 10292 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0118 | 0/0 | 10291 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0119 | 0/0 | 10288 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0120 | 0/0 | 10292 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0121 | 0/0 | 10279 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0122 | 0/0 | 10302 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0123 | 0/0 | 10307 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0124 | 0/0 | 10305 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0125 | 0/0 | 10310 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0126 | 0/0 | 10302 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0127 | 0/0 | 10302 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0128 | 0/0 | 10298 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0129 | 0/0 | 10294 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0130 | 0/0 | 10302 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0131 | 0/0 | 10296 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0132 | 0/0 | 10304 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0133 | 0/0 | 10297 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0134 | 0/0 | 10284 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0135 | 0/0 | 10294 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0136 | 0/0 | 10279 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0137 | 0/0 | 10290 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0138 | 0/0 | 10307 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0139 | 0/0 | 10302 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0140 | 0/0 | 10315 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0141 | 0/0 | 10313 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0142 | 0/0 | 10303 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0143 | 0/0 | 10301 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0144 | 0/0 | 10297 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0145 | 0/0 | 10305 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0146 | 0/0 | 10300 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0147 | 0/0 | 10297 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0148 | 0/0 | 10309 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0149 | 0/0 | 10311 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0150 | 0/0 | 10306 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| t0151 | 0/0 | 10315 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1230 | 374 | 81 | 62 | 171 | 16 | 43 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0002 | 1/0 | 1230 | 21 | 1 | 15 | 0 | 2 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0003 | 0/0 | 1230 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0004 | 0/0 | 1230 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0002c0005 | 0/0 | 1230 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11508 | 27 | 0 | 10 | 14 | 1 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0002 | 0/0 | 11531 | 26 | 0 | 6 | 18 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0003 | 0/0 | 11528 | 4 | 0 | 3 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0004 | 0/0 | 11508 | 12 | 0 | 9 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0005 | 0/0 | 11521 | 11 | 3 | 2 | 2 | 3 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0006 | 0/0 | 11533 | 11 | 0 | 4 | 7 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0007 | 0/0 | 11538 | 10 | 0 | 0 | 10 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0008 | 0/0 | 11537 | 8 | 0 | 0 | 8 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0009 | 0/0 | 11535 | 8 | 0 | 1 | 4 | 0 | 3 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0010 | 0/0 | 11535 | 7 | 0 | 0 | 7 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0011 | 0/0 | 11545 | 7 | 0 | 0 | 5 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0012 | 0/0 | 11522 | 7 | 4 | 3 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0013 | 0/0 | 11513 | 7 | 7 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0014 | 0/0 | 11527 | 6 | 1 | 0 | 4 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0015 | 0/0 | 11536 | 6 | 0 | 0 | 5 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0016 | 0/0 | 11533 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0017 | 0/0 | 11508 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0018 | 0/0 | 11538 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0019 | 0/1 | 11522 | 5 | 0 | 2 | 0 | 1 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0020 | 0/0 | 11539 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0021 | 0/0 | 11517 | 5 | 1 | 2 | 0 | 2 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0022 | 0/0 | 11540 | 5 | 1 | 0 | 3 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0023 | 0/0 | 11534 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0024 | 0/0 | 11523 | 4 | 2 | 1 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0025 | 0/0 | 11524 | 4 | 0 | 0 | 1 | 0 | 3 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0026 | 0/0 | 11519 | 4 | 0 | 1 | 0 | 2 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0027 | 0/0 | 11529 | 4 | 0 | 1 | 1 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0028 | 0/0 | 11524 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0029 | 0/0 | 11520 | 3 | 1 | 1 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0030 | 0/0 | 11522 | 3 | 0 | 0 | 1 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0031 | 0/0 | 11547 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0032 | 0/0 | 11541 | 3 | 1 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0033 | 0/0 | 11535 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0034 | 0/0 | 11518 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0035 | 0/0 | 11529 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0036 | 0/0 | 11525 | 3 | 0 | 0 | 2 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0037 | 0/0 | 11521 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0038 | 0/0 | 11519 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0039 | 0/0 | 11542 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0040 | 0/0 | 11540 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0041 | 0/0 | 11521 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0042 | 0/0 | 11534 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0043 | 0/0 | 11528 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0044 | 0/0 | 11526 | 2 | 1 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0045 | 0/0 | 11511 | 2 | 0 | 1 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0046 | 0/0 | 11535 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0047 | 0/0 | 11543 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0048 | 0/0 | 11533 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0049 | 0/0 | 11540 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0050 | 0/0 | 11529 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0051 | 0/0 | 11521 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0052 | 0/0 | 11518 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0053 | 0/0 | 11516 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0054 | 0/0 | 11517 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0055 | 0/0 | 11537 | 2 | 0 | 0 | 1 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0056 | 0/0 | 11533 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0057 | 0/0 | 11531 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0058 | 0/0 | 11542 | 2 | 1 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0059 | 0/0 | 11537 | 2 | 1 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0060 | 0/0 | 11541 | 2 | 1 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0061 | 0/0 | 11535 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0062 | 0/0 | 11533 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0063 | 0/0 | 11516 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0064 | 0/0 | 11539 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0065 | 0/0 | 11508 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0066 | 0/0 | 11508 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0067 | 0/0 | 11544 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0068 | 0/0 | 11540 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0069 | 0/0 | 11534 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0071 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0072 | 0/0 | 11538 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0073 | 0/0 | 11525 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0074 | 0/0 | 11519 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0075 | 0/0 | 11523 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0076 | 0/0 | 11526 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0077 | 0/0 | 11524 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0078 | 0/0 | 11538 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0079 | 0/0 | 11536 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0080 | 0/0 | 11534 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0081 | 0/0 | 11534 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0082 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0083 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0084 | 0/0 | 11537 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0085 | 0/0 | 11541 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0086 | 0/0 | 11535 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0087 | 0/0 | 11539 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0088 | 0/0 | 11537 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0089 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0090 | 0/0 | 11537 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0091 | 0/0 | 11527 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0092 | 0/0 | 11537 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0093 | 0/0 | 11533 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0094 | 0/0 | 11529 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0095 | 0/0 | 11527 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0096 | 0/0 | 11544 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0097 | 0/0 | 11544 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0098 | 0/0 | 11539 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0099 | 0/0 | 11542 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0100 | 0/0 | 11535 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0101 | 0/0 | 11543 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0102 | 0/0 | 11538 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0103 | 0/0 | 11531 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0104 | 0/0 | 11534 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0105 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0106 | 0/0 | 11522 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0107 | 0/0 | 11501 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0108 | 0/0 | 11531 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0109 | 0/0 | 11527 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0110 | 0/0 | 11543 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0111 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0112 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0113 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0114 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0115 | 0/0 | 11517 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0116 | 0/0 | 11529 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0117 | 0/0 | 11521 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0118 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0119 | 0/0 | 11517 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0120 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0122 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0123 | 0/0 | 11536 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0124 | 0/0 | 11534 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0125 | 0/0 | 11539 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0126 | 0/0 | 11531 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0127 | 0/0 | 11531 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0128 | 0/0 | 11527 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0129 | 0/0 | 11523 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0130 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0131 | 0/0 | 11525 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0132 | 0/0 | 11533 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0133 | 0/0 | 11526 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0134 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0135 | 0/0 | 11523 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0136 | 0/0 | 11508 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0137 | 0/0 | 11519 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0138 | 0/0 | 11536 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0139 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0140 | 0/0 | 11544 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0141 | 0/0 | 11542 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0143 | 0/0 | 11530 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0145 | 0/0 | 11534 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0146 | 0/0 | 11529 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0147 | 0/0 | 11526 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0148 | 0/0 | 11538 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0149 | 0/0 | 11540 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0001t0151 | 0/0 | 11544 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0002t0003 | 1/0 | 11528 | 16 | 1 | 12 | 0 | 1 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0002t0004 | 0/0 | 11508 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0002t0121 | 0/0 | 11508 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0002t0142 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0002t0144 | 0/0 | 11526 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0003t0057 | 0/0 | 11531 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0001c0004t0150 | 0/0 | 11535 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| a0002c0005t0070 | 0/0 | 11535 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | copy fasta | chr6 | 99266168 | 99354674 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0003g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0004g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0006g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0007g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0008g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0009g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0009g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0009g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0009g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0009g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0009g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0009g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0010g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0010g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0011g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0011g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0011g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0012g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0012g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0012g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0012g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0013g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0013g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0013g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0013g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0013g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0014g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0014g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0014g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0014g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0014g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0014g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0015g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0015g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0015g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0015g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0015g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0015g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0016g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0016g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0016g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0017g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0017g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0017g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0017g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0017g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0018g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0018g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0018g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0018g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0018g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0019g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0019g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0019g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0019g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0019g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0020g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0020g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0020g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0020g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0020g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0021g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0021g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0021g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0021g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0021g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0022g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0022g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0022g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0022g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0022g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0023g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0023g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0023g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0023g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0023g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0024g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0024g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0024g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0024g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0025g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0025g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0025g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0025g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0026g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0026g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0026g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0027g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0027g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0027g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0027g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0028g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0028g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0028g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0029g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0029g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0029g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0030g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0030g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0030g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0031g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0031g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0031g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0032g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0032g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0032g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0033g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0033g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0033g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0034g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0034g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0034g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0035g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0035g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0035g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0036g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0036g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0036g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0037g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0037g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0037g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0038g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0038g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0039g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0039g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0040g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0040g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0041g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0041g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0042g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0042g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0043g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0043g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0044g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0044g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0045g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0045g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0046g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0046g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0047g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0048g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0048g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0049g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0049g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0050g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0051g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0051g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0052g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0052g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0053g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0053g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0054g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0054g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0055g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0055g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0056g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0056g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0057g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0058g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0058g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0059g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0059g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0060g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0060g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0061g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0062g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0063g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0064g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0065g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0066g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0067g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0068g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0069g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0071g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0072g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0073g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0074g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0075g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0076g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0077g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0078g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0079g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0080g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0081g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0082g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0083g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0084g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0085g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0086g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0087g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0088g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0089g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0090g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0091g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0092g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0093g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0094g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0095g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0096g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0097g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0098g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0099g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0100g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0101g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0102g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0103g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0104g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0105g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0106g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0107g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0108g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0109g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0110g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0111g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0112g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0113g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0114g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0115g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0116g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0117g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0118g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0119g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0120g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0122g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0123g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0124g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0125g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0126g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0127g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0128g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0129g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0130g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0131g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0132g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0133g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0134g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0135g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0136g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0137g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0138g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0139g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0140g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0141g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0143g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0145g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0146g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0147g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0148g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0149g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0001t0151g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0121g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0142g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0002t0144g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0003t0057g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0001c0004t0150g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| a0002c0005t0070g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0141 | g0288 | EUR | GBR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0180 | EUR | GBR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00140 | hp1 | a0001 | c0001 | t0117 | g0249 | EUR | GBR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0007 | EUR | GBR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0196 | EUR | FIN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00280 | hp2 | a0001 | c0001 | t0073 | g0168 | EUR | FIN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00323 | hp1 | a0001 | c0001 | t0061 | g0015 | EUR | FIN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00323 | hp2 | a0001 | c0001 | t0019 | g0156 | EUR | FIN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00408 | hp1 | a0001 | c0001 | t0020 | g0116 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00408 | hp2 | a0001 | c0001 | t0122 | g0354 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00544 | hp1 | a0001 | c0001 | t0023 | g0232 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00558 | hp1 | a0001 | c0001 | t0092 | g0120 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00558 | hp2 | a0001 | c0001 | t0010 | g0151 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0152 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00609 | hp2 | a0001 | c0001 | t0015 | g0248 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00621 | hp1 | a0001 | c0001 | t0023 | g0251 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00621 | hp2 | a0001 | c0001 | t0018 | g0071 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0333 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0200 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00673 | hp1 | a0001 | c0001 | t0102 | g0111 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00673 | hp2 | a0001 | c0001 | t0049 | g0103 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0378 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00735 | hp2 | a0001 | c0001 | t0116 | g0264 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0358 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0192 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG00741 | hp2 | a0001 | c0001 | t0021 | g0252 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01069 | hp2 | a0001 | c0001 | t0046 | g0118 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01074 | hp1 | a0001 | c0001 | t0046 | g0106 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0193 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0190 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0334 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0318 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01099 | hp2 | a0001 | c0001 | t0012 | g0275 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01106 | hp1 | a0001 | c0001 | t0019 | g0158 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01106 | hp2 | a0001 | c0001 | t0143 | g0360 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01109 | hp1 | a0001 | c0001 | t0145 | g0293 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01109 | hp2 | a0001 | c0001 | t0101 | g0076 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01167 | hp1 | a0001 | c0001 | t0012 | g0010 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0205 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01168 | hp1 | a0001 | c0001 | t0029 | g0181 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0009 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01169 | hp1 | a0001 | c0001 | t0012 | g0010 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0009 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0204 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01192 | hp2 | a0001 | c0001 | t0106 | g0164 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01243 | hp1 | a0001 | c0001 | t0057 | g0352 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01243 | hp2 | a0001 | c0001 | t0081 | g0169 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0367 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01256 | hp1 | a0001 | c0001 | t0054 | g0231 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01258 | hp1 | a0001 | c0001 | t0054 | g0238 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0194 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0370 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01358 | hp1 | a0001 | c0001 | t0060 | g0280 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0346 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01361 | hp2 | a0001 | c0001 | t0021 | g0226 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01433 | hp1 | a0001 | c0001 | t0128 | g0297 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01433 | hp2 | a0001 | c0001 | t0084 | g0130 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0198 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01496 | hp2 | a0001 | c0001 | t0045 | g0092 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01515 | hp1 | a0001 | c0001 | t0026 | g0011 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01515 | hp2 | a0001 | c0001 | t0024 | g0182 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01516 | hp1 | a0001 | c0001 | t0029 | g0185 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01516 | hp2 | a0001 | c0001 | t0021 | g0256 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01517 | hp1 | a0001 | c0001 | t0026 | g0011 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0177 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01891 | hp1 | a0001 | c0001 | t0135 | g0362 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01891 | hp2 | a0001 | c0001 | t0013 | g0214 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0206 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0361 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0304 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0366 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01952 | hp2 | a0001 | c0001 | t0024 | g0091 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01975 | hp2 | a0001 | c0003 | t0057 | g0307 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0368 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0338 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01981 | hp2 | a0001 | c0001 | t0019 | g0172 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01993 | hp2 | a0001 | c0001 | t0009 | g0332 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0369 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02004 | hp2 | a0001 | c0001 | t0132 | g0341 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0119 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02015 | hp2 | a0001 | c0001 | t0014 | g0302 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02055 | hp1 | a0001 | c0001 | t0037 | g0276 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02055 | hp2 | a0001 | c0001 | t0029 | g0095 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02074 | hp1 | a0001 | c0001 | t0015 | g0247 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02074 | hp2 | a0001 | c0001 | t0048 | g0146 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02080 | hp1 | a0001 | c0001 | t0017 | g0051 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02080 | hp2 | a0001 | c0001 | t0098 | g0112 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0128 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02083 | hp2 | a0001 | c0001 | t0069 | g0038 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02129 | hp1 | a0001 | c0001 | t0008 | g0127 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02135 | hp1 | a0001 | c0001 | t0022 | g0284 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02145 | hp1 | a0001 | c0001 | t0037 | g0337 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02145 | hp2 | a0001 | c0001 | t0059 | g0290 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02165 | hp1 | a0001 | c0001 | t0041 | g0090 | EAS | CDX | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0343 | EAS | CDX | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02257 | hp1 | a0001 | c0001 | t0013 | g0213 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02257 | hp2 | a0001 | c0001 | t0042 | g0075 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02258 | hp1 | a0001 | c0001 | t0111 | g0261 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02258 | hp2 | a0001 | c0001 | t0082 | g0084 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0335 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0191 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02280 | hp1 | a0001 | c0001 | t0147 | g0211 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0218 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02293 | hp2 | a0001 | c0002 | t0121 | g0199 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0359 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02451 | hp1 | a0001 | c0001 | t0056 | g0258 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02451 | hp2 | a0001 | c0001 | t0035 | g0296 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0308 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02523 | hp2 | a0001 | c0001 | t0087 | g0150 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0217 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02572 | hp2 | a0001 | c0001 | t0037 | g0286 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02602 | hp1 | a0001 | c0001 | t0074 | g0073 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02615 | hp1 | a0001 | c0001 | t0146 | g0223 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02615 | hp2 | a0001 | c0001 | t0024 | g0183 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02622 | hp1 | a0001 | c0001 | t0062 | g0048 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02622 | hp2 | a0001 | c0001 | t0109 | g0188 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02630 | hp1 | a0001 | c0001 | t0035 | g0299 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02630 | hp2 | a0001 | c0001 | t0083 | g0100 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02647 | hp1 | a0001 | c0001 | t0104 | g0093 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02647 | hp2 | a0001 | c0001 | t0079 | g0094 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02683 | hp1 | a0001 | c0001 | t0019 | g0159 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02683 | hp2 | a0001 | c0001 | t0055 | g0328 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02698 | hp1 | a0001 | c0001 | t0126 | g0325 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02698 | hp2 | a0001 | c0001 | t0068 | g0042 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0379 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02723 | hp2 | a0001 | c0001 | t0050 | g0004 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02735 | hp1 | a0001 | c0001 | t0009 | g0300 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02735 | hp2 | a0001 | c0001 | t0148 | g0375 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02738 | hp1 | a0001 | c0001 | t0025 | g0162 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02809 | hp1 | a0001 | c0001 | t0028 | g0099 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02809 | hp2 | a0001 | c0001 | t0056 | g0259 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0216 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02886 | hp2 | a0001 | c0001 | t0118 | g0263 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02895 | hp1 | a0001 | c0001 | t0047 | g0003 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02895 | hp2 | a0001 | c0001 | t0034 | g0274 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02896 | hp1 | a0001 | c0001 | t0052 | g0257 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0215 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02922 | hp1 | a0001 | c0001 | t0103 | g0083 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0271 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02965 | hp1 | a0001 | c0001 | t0028 | g0097 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02965 | hp2 | a0001 | c0001 | t0051 | g0268 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0170 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02976 | hp2 | a0001 | c0001 | t0075 | g0072 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03017 | hp1 | a0001 | c0001 | t0015 | g0295 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03017 | hp2 | a0001 | c0001 | t0027 | g0372 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0272 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03041 | hp2 | a0001 | c0001 | t0113 | g0267 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03098 | hp1 | a0001 | c0001 | t0032 | g0078 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03098 | hp2 | a0001 | c0001 | t0120 | g0373 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03130 | hp1 | a0001 | c0001 | t0058 | g0219 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03130 | hp2 | a0001 | c0001 | t0052 | g0355 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0096 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03209 | hp2 | a0001 | c0001 | t0028 | g0102 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03225 | hp1 | a0001 | c0001 | t0105 | g0079 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03225 | hp2 | a0001 | c0001 | t0014 | g0374 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0197 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03239 | hp2 | a0001 | c0001 | t0149 | g0381 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0273 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03453 | hp2 | a0001 | c0001 | t0100 | g0082 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03486 | hp1 | a0001 | c0001 | t0044 | g0098 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03486 | hp2 | a0001 | c0001 | t0077 | g0074 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03490 | hp1 | a0001 | c0001 | t0066 | g0056 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03490 | hp2 | a0001 | c0001 | t0011 | g0005 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0179 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0012 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0012 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0005 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03516 | hp1 | a0001 | c0001 | t0114 | g0283 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03516 | hp2 | a0001 | c0001 | t0012 | g0270 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03540 | hp1 | a0001 | c0001 | t0050 | g0004 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03540 | hp2 | a0001 | c0001 | t0072 | g0167 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03579 | hp1 | a0001 | c0001 | t0034 | g0313 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03579 | hp2 | a0001 | c0001 | t0042 | g0101 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03654 | hp1 | a0001 | c0001 | t0014 | g0344 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03654 | hp2 | a0001 | c0001 | t0030 | g0165 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03669 | hp1 | a0001 | c0001 | t0115 | g0246 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03669 | hp2 | a0001 | c0001 | t0125 | g0324 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03688 | hp1 | a0001 | c0001 | t0080 | g0160 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03688 | hp2 | a0001 | c0001 | t0110 | g0294 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03710 | hp1 | a0001 | c0002 | t0144 | g0203 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03710 | hp2 | a0001 | c0001 | t0067 | g0047 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03831 | hp1 | a0001 | c0001 | t0039 | g0041 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03831 | hp2 | a0001 | c0001 | t0025 | g0154 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03834 | hp1 | a0001 | c0001 | t0025 | g0163 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03834 | hp2 | a0001 | c0001 | t0136 | g0320 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03927 | hp2 | a0001 | c0001 | t0063 | g0055 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03942 | hp1 | a0001 | c0001 | t0039 | g0023 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0349 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG04115 | hp1 | a0001 | c0001 | t0093 | g0085 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG04115 | hp2 | a0001 | c0001 | t0030 | g0166 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG04199 | hp1 | a0001 | c0001 | t0022 | g0285 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG04199 | hp2 | a0001 | c0001 | t0036 | g0376 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG04204 | hp2 | a0001 | c0001 | t0058 | g0287 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG04228 | hp1 | a0001 | c0001 | t0044 | g0153 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG04228 | hp2 | a0001 | c0001 | t0027 | g0339 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18522 | hp1 | a0001 | c0001 | t0134 | g0212 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18522 | hp2 | a0001 | c0001 | t0047 | g0003 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18612 | hp1 | a0001 | c0001 | t0023 | g0292 | EAS | CHB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18612 | hp2 | a0001 | c0001 | t0008 | g0126 | EAS | CHB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18747 | hp1 | a0001 | c0001 | t0064 | g0018 | EAS | CHB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18747 | hp2 | a0001 | c0001 | t0041 | g0087 | EAS | CHB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18906 | hp1 | a0001 | c0001 | t0060 | g0289 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18906 | hp2 | a0001 | c0001 | t0076 | g0077 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18939 | hp2 | a0001 | c0001 | t0091 | g0115 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18940 | hp1 | a0001 | c0001 | t0011 | g0144 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18940 | hp2 | a0001 | c0001 | t0130 | g0316 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18941 | hp1 | a0001 | c0001 | t0027 | g0326 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18941 | hp2 | a0001 | c0001 | t0010 | g0114 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18942 | hp1 | a0001 | c0001 | t0022 | g0243 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18942 | hp2 | a0001 | c0001 | t0043 | g0132 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18943 | hp1 | a0001 | c0001 | t0017 | g0052 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0353 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18944 | hp1 | a0001 | c0001 | t0133 | g0342 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18946 | hp1 | a0001 | c0001 | t0015 | g0245 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18948 | hp2 | a0001 | c0001 | t0015 | g0235 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18949 | hp1 | a0001 | c0001 | t0018 | g0068 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18950 | hp2 | a0001 | c0001 | t0032 | g0176 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18951 | hp1 | a0001 | c0001 | t0017 | g0025 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0345 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18952 | hp2 | a0001 | c0001 | t0017 | g0050 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18956 | hp1 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18956 | hp2 | a0001 | c0001 | t0129 | g0347 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18957 | hp2 | a0001 | c0001 | t0033 | g0173 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0220 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18959 | hp2 | a0001 | c0001 | t0016 | g0026 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18961 | hp1 | a0001 | c0001 | t0016 | g0034 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18961 | hp2 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18962 | hp1 | a0001 | c0001 | t0065 | g0049 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18964 | hp1 | a0001 | c0001 | t0016 | g0037 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18964 | hp2 | a0001 | c0001 | t0010 | g0086 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18966 | hp1 | a0001 | c0001 | t0033 | g0081 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0250 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18967 | hp2 | a0001 | c0001 | t0014 | g0357 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18969 | hp1 | a0001 | c0001 | t0036 | g0340 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0147 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18970 | hp2 | a0001 | c0001 | t0030 | g0129 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18971 | hp1 | a0001 | c0001 | t0094 | g0142 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18974 | hp1 | a0001 | c0001 | t0032 | g0105 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18974 | hp2 | a0001 | c0001 | t0015 | g0236 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18975 | hp2 | a0001 | c0001 | t0023 | g0227 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0230 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18977 | hp2 | a0001 | c0001 | t0055 | g0351 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18978 | hp1 | a0001 | c0001 | t0010 | g0140 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18978 | hp2 | a0001 | c0001 | t0040 | g0065 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18979 | hp1 | a0001 | c0004 | t0150 | g0382 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18979 | hp2 | a0001 | c0001 | t0022 | g0229 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18981 | hp2 | a0001 | c0001 | t0099 | g0107 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18982 | hp2 | a0001 | c0001 | t0011 | g0110 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18983 | hp2 | a0001 | c0001 | t0009 | g0319 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18984 | hp1 | a0001 | c0001 | t0014 | g0327 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18986 | hp2 | a0001 | c0001 | t0048 | g0080 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18988 | hp1 | a0001 | c0001 | t0095 | g0124 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18988 | hp2 | a0001 | c0001 | t0124 | g0278 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18989 | hp1 | a0001 | c0001 | t0138 | g0380 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18993 | hp1 | a0001 | c0001 | t0040 | g0067 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18993 | hp2 | a0001 | c0001 | t0017 | g0021 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18998 | hp1 | a0001 | c0001 | t0018 | g0066 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18999 | hp1 | a0001 | c0001 | t0008 | g0148 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA18999 | hp2 | a0001 | c0001 | t0036 | g0310 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19001 | hp1 | a0001 | c0001 | t0088 | g0171 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0317 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19002 | hp2 | a0001 | c0001 | t0018 | g0069 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19003 | hp1 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19003 | hp2 | a0001 | c0001 | t0038 | g0029 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19004 | hp2 | a0001 | c0001 | t0031 | g0134 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19005 | hp1 | a0001 | c0001 | t0010 | g0006 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0291 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19006 | hp1 | a0001 | c0001 | t0014 | g0322 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19006 | hp2 | a0001 | c0001 | t0008 | g0149 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19007 | hp2 | a0001 | c0001 | t0031 | g0104 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19009 | hp1 | a0001 | c0001 | t0018 | g0070 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19009 | hp2 | a0001 | c0001 | t0097 | g0136 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19010 | hp1 | a0001 | c0001 | t0023 | g0237 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19010 | hp2 | a0001 | c0001 | t0025 | g0157 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19030 | hp1 | a0001 | c0001 | t0140 | g0265 | AFR | LWK | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0260 | AFR | LWK | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19043 | hp1 | a0001 | c0001 | t0151 | g0383 | AFR | LWK | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | LWK | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19054 | hp1 | a0001 | c0001 | t0006 | g0330 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19054 | hp2 | a0001 | c0001 | t0078 | g0138 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0364 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19055 | hp2 | a0001 | c0001 | t0139 | g0254 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19060 | hp1 | a0001 | c0001 | t0085 | g0108 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0350 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19062 | hp1 | a0001 | c0001 | t0043 | g0131 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0241 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19063 | hp1 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0311 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19065 | hp1 | a0001 | c0001 | t0011 | g0113 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0356 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19068 | hp1 | a0001 | c0001 | t0020 | g0125 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19070 | hp1 | a0001 | c0001 | t0020 | g0121 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19070 | hp2 | a0001 | c0001 | t0038 | g0019 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19078 | hp1 | a0001 | c0001 | t0123 | g0323 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19078 | hp2 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19079 | hp1 | a0001 | c0001 | t0033 | g0175 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19080 | hp2 | a0001 | c0001 | t0010 | g0006 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19081 | hp1 | a0001 | c0001 | t0086 | g0145 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19081 | hp2 | a0001 | c0001 | t0016 | g0030 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19082 | hp1 | a0001 | c0001 | t0016 | g0022 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19082 | hp2 | a0001 | c0001 | t0090 | g0141 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19083 | hp2 | a0001 | c0001 | t0020 | g0135 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19084 | hp1 | a0001 | c0001 | t0009 | g0329 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19084 | hp2 | a0001 | c0001 | t0020 | g0122 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19085 | hp2 | a0001 | c0001 | t0011 | g0123 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19086 | hp1 | a0001 | c0001 | t0089 | g0139 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19086 | hp2 | a0001 | c0001 | t0131 | g0309 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19088 | hp1 | a0001 | c0001 | t0011 | g0137 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19088 | hp2 | a0001 | c0001 | t0045 | g0109 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19089 | hp2 | a0001 | c0001 | t0096 | g0133 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19090 | hp1 | a0001 | c0001 | t0009 | g0348 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19090 | hp2 | a0001 | c0001 | t0031 | g0117 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19091 | hp1 | a0001 | c0001 | t0049 | g0174 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19091 | hp2 | a0001 | c0001 | t0059 | g0242 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19240 | hp1 | a0001 | c0001 | t0112 | g0266 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA19240 | hp2 | a0001 | c0001 | t0022 | g0371 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20129 | hp1 | a0001 | c0001 | t0053 | g0240 | AFR | ASW | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20129 | hp2 | a0001 | c0001 | t0053 | g0269 | AFR | ASW | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20752 | hp1 | a0001 | c0001 | t0021 | g0255 | EUR | TSI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20752 | hp2 | a0001 | c0002 | t0142 | g0202 | EUR | TSI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20805 | hp1 | a0001 | c0001 | t0119 | g0233 | EUR | TSI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20905 | hp1 | a0002 | c0005 | t0070 | g0063 | SAS | GIH | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20905 | hp2 | a0001 | c0001 | t0026 | g0253 | SAS | GIH | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01123 | hp1 | a0001 | c0001 | t0026 | g0239 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG01123 | hp2 | a0001 | c0001 | t0027 | g0377 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02109 | hp1 | a0001 | c0001 | t0035 | g0281 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02109 | hp2 | a0001 | c0001 | t0034 | g0277 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02486 | hp1 | a0001 | c0001 | t0024 | g0184 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02486 | hp2 | a0001 | c0001 | t0137 | g0222 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02559 | hp1 | a0001 | c0001 | t0051 | g0262 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG02559 | hp2 | a0001 | c0001 | t0071 | g0064 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0195 | AFR | USA | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| HG06807 | hp2 | a0001 | c0001 | t0127 | g0298 | AFR | USA | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20300 | hp1 | a0001 | c0001 | t0107 | g0186 | AFR | USA | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| NA20300 | hp2 | a0001 | c0001 | t0108 | g0187 | AFR | USA | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0019 | g0155 | REF | REF | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0201 | REF | REF | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:99349261
|
A | G | 1 | a0002 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.112T>C | p.Phe38Leu | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 414/11528 | 112/1230 | 38/409 | chr6 | 99349261 | ||
| chr6:99349351
|
C | A | 1 | a0002 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.22G>T | p.Ala8Ser | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 324/11528 | 22/1230 | 8/409 | chr6 | 99349351 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:99291714
|
C | T | 1 | a0001c0004 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.930G>A | p.Arg310Arg | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/6 | 1232/11528 | 930/1230 | 310/409 | chr6 | 99291714 | ||
| chr6:99323664
|
T | C | 4 | a0001c0001a0001c0003a0001c0004others(1): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
synonymous_variant | LOW | c.603A>G | p.Thr201Thr | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/6 | 905/11528 | 603/1230 | 201/409 | chr6 | 99323664 | ||
| chr6:99333383
|
C | T | 1 | a0001c0003 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.567G>A | p.Ala189Ala | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/6 | 869/11528 | 567/1230 | 189/409 | chr6 | 99333383 | ||
| chr6:99349262
|
G | C | 1 | a0002c0005 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.111C>G | p.Ser37Ser | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 413/11528 | 111/1230 | 37/409 | chr6 | 99349262 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:99271296
|
C | A | 1 | a0001c0001t0126 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9868G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9868 | chr6 | 99271296 | |||||
| chr6:99271378
|
C | T | 2 | a0001c0001t0066a0001c0001t0136 | 2 | HG03490.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9786G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9786 | chr6 | 99271378 | |||||
| chr6:99271498
|
A | G | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(95): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*9666T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9666 | chr6 | 99271498 | |||||
| chr6:99271696
|
C | G | 2 | a0001c0001t0056a0001c0001t0079 | 3 | HG02451.hp1 HG02647.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9468G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9468 | chr6 | 99271696 | |||||
| chr6:99272018
|
C | G | 1 | a0001c0001t0149 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9146G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9146 | chr6 | 99272018 | |||||
| chr6:99272075
|
G | A | 5 | a0001c0001t0035a0001c0001t0081a0001c0001t0082others(2): Show | 7 | HG01243.hp2 HG01433.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9089C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9089 | chr6 | 99272075 | |||||
| chr6:99272142
|
C | CTA | 5 | a0001c0001t0027a0001c0001t0035a0001c0001t0082others(2): Show | 10 | HG00735.hp2 HG01123.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*9020_*9021dupTA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9021 | chr6 | 99272142 | |||||
| chr6:99272146
|
A | ATATG | 12 | a0001c0001t0002a0001c0001t0042a0001c0001t0057others(9): Show | 38 | HG00408.hp2 HG00544.hp2 HG01081.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*9017_*9018insCATA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATATGTG | 8 | a0001c0001t0006a0001c0001t0016a0001c0001t0056others(5): Show | 23 | HG00642.hp1 HG01099.hp1 HG01361.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*9017_*9018insCACA others(2): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATATGTGT others(1): Show |
6 | a0001c0001t0009a0001c0001t0061a0001c0001t0072others(3): Show | 13 | HG00323.hp1 HG01993.hp2 HG02735.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*9017_*9018insCACA others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATATGTGT others(3): Show |
2 | a0001c0001t0055a0001c0001t0148 | 3 | HG02683.hp2 HG02735.hp2 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9017_*9018insCACA others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATATGTGT others(5): Show |
3 | a0001c0001t0060a0001c0001t0064a0001c0001t0125 | 4 | HG01358.hp1 HG03669.hp2 NA18747.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9017_*9018insCACA others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATG | 6 | a0001c0001t0010a0001c0001t0033a0001c0001t0046others(3): Show | 15 | HG00558.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*9016_*9017dupCA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATGTG | 9 | a0001c0001t0008a0001c0001t0018a0001c0001t0023others(6): Show | 24 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*9014_*9017dupCACA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATGTGTG | 6 | a0001c0001t0015a0001c0001t0020a0001c0001t0040others(3): Show | 16 | HG00408.hp1 HG00609.hp2 HG01109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*9012_*9017dupCACA others(2): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0007a0001c0001t0032a0001c0001t0078others(2): Show | 16 | HG00673.hp1 HG03098.hp1 NA18944.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*9010_*9017dupCACA others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATGTGTGT others(3): Show |
5 | a0001c0001t0022a0001c0001t0047a0001c0001t0068others(2): Show | 10 | HG02135.hp1 HG02698.hp2 HG02895.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*9008_*9017dupCACA others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATGTGTGT others(5): Show |
5 | a0001c0001t0011a0001c0001t0039a0001c0001t0058others(2): Show | 13 | HG00099.hp1 HG01109.hp2 HG03130.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*9006_*9017dupCACA others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | ATGTGTGT others(7): Show |
4 | a0001c0001t0031a0001c0001t0067a0001c0001t0140others(1): Show | 6 | HG03710.hp2 NA19004.hp2 NA19007.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9004_*9017dupCACA others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9017 | chr6 | 99272146 | |||||
| chr6:99272146
|
A | G | 1 | a0001c0001t0093 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9018T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9018 | chr6 | 99272146 | |||||
| chr6:99272146
|
ATG | A | 8 | a0001c0001t0036a0001c0001t0043a0001c0001t0050others(5): Show | 12 | HG02280.hp1 HG02723.hp2 HG03540.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*9016_*9017delCA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9016 | chr6 | 99272146 | |||||
| chr6:99272146
|
ATGTG | A | 4 | a0001c0001t0044a0001c0001t0094a0001c0001t0129others(1): Show | 5 | HG01891.hp1 HG03486.hp1 HG04228.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9014_*9017delCACA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9014 | chr6 | 99272146 | |||||
| chr6:99272146
|
ATGTGTG | A | 9 | a0001c0001t0012a0001c0001t0025a0001c0001t0028others(6): Show | 22 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*9012_*9017delCACA others(2): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9012 | chr6 | 99272146 | |||||
| chr6:99272146
|
ATGTGTGT others(1): Show |
A | 15 | a0001c0001t0019a0001c0001t0024a0001c0001t0026others(12): Show | 29 | HG00323.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*9010_*9017delCACA others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9010 | chr6 | 99272146 | |||||
| chr6:99272146
|
ATGTGTGT others(3): Show |
A | 13 | a0001c0001t0005a0001c0001t0021a0001c0001t0029others(10): Show | 35 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*9008_*9017delCACA others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9008 | chr6 | 99272146 | |||||
| chr6:99272146
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0063a0001c0001t0074 | 2 | HG02602.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9006_*9017delCACA others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9006 | chr6 | 99272146 | |||||
| chr6:99272146
|
ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0013a0001c0001t0111a0001c0001t0134 | 9 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9004_*9017delCACA others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9004 | chr6 | 99272146 | |||||
| chr6:99272146
|
ATGTGTGT others(13): Show |
A | 9 | a0001c0001t0001a0001c0001t0004a0001c0001t0017others(6): Show | 52 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*8998_*9017delCACA others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8998 | chr6 | 99272146 | |||||
| chr6:99272148
|
G | A | 5 | a0001c0001t0014a0001c0001t0105a0001c0001t0109others(2): Show | 10 | HG01433.hp1 HG02015.hp2 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*9016C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9016 | chr6 | 99272148 | |||||
| chr6:99272150
|
G | A | 4 | a0001c0001t0036a0001c0001t0043a0001c0001t0131others(1): Show | 7 | HG04199.hp2 NA18942.hp2 NA18944.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9014C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9014 | chr6 | 99272150 | |||||
| chr6:99272152
|
G | A | 3 | a0001c0001t0044a0001c0001t0129a0001c0001t0135 | 4 | HG01891.hp1 HG03486.hp1 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9012C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9012 | chr6 | 99272152 | |||||
| chr6:99272154
|
G | A | 7 | a0001c0001t0012a0001c0001t0025a0001c0001t0028others(4): Show | 20 | HG00140.hp1 HG00280.hp2 HG01099.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*9010C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9010 | chr6 | 99272154 | |||||
| chr6:99272156
|
G | A | 15 | a0001c0001t0019a0001c0001t0024a0001c0001t0026others(12): Show | 29 | HG00323.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*9008C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9008 | chr6 | 99272156 | |||||
| chr6:99272158
|
G | A | 13 | a0001c0001t0005a0001c0001t0021a0001c0001t0029others(10): Show | 35 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*9006C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9006 | chr6 | 99272158 | |||||
| chr6:99272160
|
G | A | 2 | a0001c0001t0063a0001c0001t0074 | 2 | HG02602.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9004C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9004 | chr6 | 99272160 | |||||
| chr6:99272162
|
G | A | 3 | a0001c0001t0013a0001c0001t0111a0001c0001t0134 | 9 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9002C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 9002 | chr6 | 99272162 | |||||
| chr6:99272168
|
G | A | 9 | a0001c0001t0001a0001c0001t0004a0001c0001t0017others(6): Show | 52 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*8996C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8996 | chr6 | 99272168 | |||||
| chr6:99272169
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0096 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8984_*8994dupCACA others(7): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8994 | chr6 | 99272169 | |||||
| chr6:99272172
|
G | T | 1 | a0001c0001t0130 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8992C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8992 | chr6 | 99272172 | |||||
| chr6:99272191
|
T | TGTGTGTG | 2 | a0001c0001t0049a0001c0001t0059 | 4 | HG00673.hp2 HG02145.hp2 NA19091.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8972_*8973insCACA others(3): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8972 | chr6 | 99272191 | |||||
| chr6:99272191
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0097 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8972_*8973insCACA others(7): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8972 | chr6 | 99272191 | |||||
| chr6:99272191
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0110 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8972_*8973insCACA others(9): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8972 | chr6 | 99272191 | |||||
| chr6:99272336
|
C | T | 10 | a0001c0001t0001a0001c0001t0004a0001c0001t0017others(7): Show | 53 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*8828G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8828 | chr6 | 99272336 | |||||
| chr6:99272571
|
C | G | 1 | a0001c0001t0019 | 5 | HG00323.hp2 HG01106.hp1 HG01981.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8593G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8593 | chr6 | 99272571 | |||||
| chr6:99272605
|
G | A | 2 | a0001c0001t0050a0001c0001t0147 | 3 | HG02280.hp1 HG02723.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8559C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8559 | chr6 | 99272605 | |||||
| chr6:99272962
|
C | T | 38 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(35): Show | 99 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*8202G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8202 | chr6 | 99272962 | |||||
| chr6:99273127
|
C | T | 55 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(52): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*8037G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 8037 | chr6 | 99273127 | |||||
| chr6:99273173
|
G | A | 55 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(52): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*7991C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7991 | chr6 | 99273173 | |||||
| chr6:99273231
|
G | A | 1 | a0001c0001t0038 | 2 | NA19003.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7933C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7933 | chr6 | 99273231 | |||||
| chr6:99273732
|
C | T | 38 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(35): Show | 99 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*7432G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7432 | chr6 | 99273732 | |||||
| chr6:99273770
|
A | G | 1 | a0001c0001t0092 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7394T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7394 | chr6 | 99273770 | |||||
| chr6:99273808
|
T | C | 2 | a0001c0001t0100a0001c0001t0101 | 2 | HG01109.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7356A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7356 | chr6 | 99273808 | |||||
| chr6:99273893
|
A | G | 1 | a0001c0001t0113 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7271T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7271 | chr6 | 99273893 | |||||
| chr6:99273923
|
T | C | 1 | a0001c0001t0101 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7241A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7241 | chr6 | 99273923 | |||||
| chr6:99273930
|
A | G | 93 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(90): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*7234T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7234 | chr6 | 99273930 | |||||
| chr6:99274057
|
C | T | 1 | a0001c0001t0034 | 3 | HG02109.hp2 HG02895.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7107G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 7107 | chr6 | 99274057 | |||||
| chr6:99274628
|
C | T | 4 | a0001c0001t0060a0001c0001t0104a0001c0001t0146others(1): Show | 5 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6536G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 6536 | chr6 | 99274628 | |||||
| chr6:99274874
|
A | G | 28 | a0001c0001t0005a0001c0001t0012a0001c0001t0021others(25): Show | 65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*6290T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 6290 | chr6 | 99274874 | |||||
| chr6:99275065
|
C | T | 2 | a0001c0001t0017a0001c0001t0065 | 6 | HG02080.hp1 NA18943.hp1 NA18951.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6099G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 6099 | chr6 | 99275065 | |||||
| chr6:99275248
|
A | G | 1 | a0001c0001t0041 | 2 | HG02165.hp1 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5916T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5916 | chr6 | 99275248 | |||||
| chr6:99275415
|
G | C | 2 | a0001c0001t0130a0001c0001t0131 | 2 | NA18940.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5749C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5749 | chr6 | 99275415 | |||||
| chr6:99275423
|
G | A | 3 | a0001c0001t0051a0001c0001t0075a0001c0001t0113 | 4 | HG02559.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5741C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5741 | chr6 | 99275423 | |||||
| chr6:99275573
|
T | C | 1 | a0001c0001t0132 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5591A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5591 | chr6 | 99275573 | |||||
| chr6:99275611
|
G | T | 1 | a0001c0001t0091 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5553C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5553 | chr6 | 99275611 | |||||
| chr6:99275678
|
T | A | 144 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(141): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
3_prime_UTR_variant | MODIFIER | c.*5486A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5486 | chr6 | 99275678 | |||||
| chr6:99275886
|
A | C | 144 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(141): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
3_prime_UTR_variant | MODIFIER | c.*5278T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5278 | chr6 | 99275886 | |||||
| chr6:99276053
|
T | C | 38 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(35): Show | 99 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*5111A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5111 | chr6 | 99276053 | |||||
| chr6:99276147
|
T | TA | 7 | a0001c0001t0060a0001c0001t0076a0001c0001t0077others(4): Show | 8 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5016dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5016 | chr6 | 99276147 | |||||
| chr6:99276147
|
TA | T | 28 | a0001c0001t0013a0001c0001t0019a0001c0001t0021others(25): Show | 61 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*5016delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5016 | chr6 | 99276147 | |||||
| chr6:99276162
|
C | T | 139 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(136): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*5002G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 5002 | chr6 | 99276162 | |||||
| chr6:99276220
|
C | T | 10 | a0001c0001t0001a0001c0001t0004a0001c0001t0017others(7): Show | 53 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4944G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4944 | chr6 | 99276220 | |||||
| chr6:99276232
|
A | C | 2 | a0001c0001t0100a0001c0001t0101 | 2 | HG01109.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4932T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4932 | chr6 | 99276232 | |||||
| chr6:99276339
|
C | T | 9 | a0001c0001t0019a0001c0001t0025a0001c0001t0030others(6): Show | 22 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4825G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4825 | chr6 | 99276339 | |||||
| chr6:99276456
|
G | C | 2 | a0001c0001t0057a0001c0003t0057 | 2 | HG01243.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4708C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4708 | chr6 | 99276456 | |||||
| chr6:99276487
|
T | C | 5 | a0001c0001t0060a0001c0001t0104a0001c0001t0105others(2): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4677A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4677 | chr6 | 99276487 | |||||
| chr6:99276677
|
A | G | 5 | a0001c0001t0060a0001c0001t0104a0001c0001t0105others(2): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4487T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4487 | chr6 | 99276677 | |||||
| chr6:99276709
|
G | A | 1 | a0001c0001t0134 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4455C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4455 | chr6 | 99276709 | |||||
| chr6:99276741
|
A | G | 1 | a0001c0001t0065 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4423T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4423 | chr6 | 99276741 | |||||
| chr6:99276834
|
G | A | 2 | a0001c0001t0100a0001c0001t0101 | 2 | HG01109.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4330C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4330 | chr6 | 99276834 | |||||
| chr6:99276837
|
G | A | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(95): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*4327C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4327 | chr6 | 99276837 | |||||
| chr6:99277009
|
G | A | 29 | a0001c0001t0005a0001c0001t0012a0001c0001t0021others(26): Show | 66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*4155C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4155 | chr6 | 99277009 | |||||
| chr6:99277028
|
T | C | 1 | a0001c0001t0141 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4136A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4136 | chr6 | 99277028 | |||||
| chr6:99277030
|
G | A | 1 | a0001c0001t0119 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4134C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4134 | chr6 | 99277030 | |||||
| chr6:99277156
|
C | G | 8 | a0001c0001t0019a0001c0001t0025a0001c0001t0030others(5): Show | 21 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4008G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 4008 | chr6 | 99277156 | |||||
| chr6:99277291
|
C | T | 2 | a0001c0001t0100a0001c0001t0101 | 2 | HG01109.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3873G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 3873 | chr6 | 99277291 | |||||
| chr6:99277821
|
T | C | 5 | a0001c0001t0060a0001c0001t0104a0001c0001t0105others(2): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3343A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 3343 | chr6 | 99277821 | |||||
| chr6:99278103
|
G | A | 99 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(96): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*3061C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 3061 | chr6 | 99278103 | |||||
| chr6:99278167
|
G | T | 1 | a0001c0001t0041 | 2 | HG02165.hp1 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2997C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 2997 | chr6 | 99278167 | |||||
| chr6:99278381
|
T | C | 3 | a0001c0001t0050a0001c0001t0103a0001c0001t0147 | 4 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2783A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 2783 | chr6 | 99278381 | |||||
| chr6:99278512
|
C | T | 149 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(146): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*2652G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 2652 | chr6 | 99278512 | |||||
| chr6:99278584
|
A | C | 7 | a0001c0001t0010a0001c0001t0086a0001c0001t0087others(4): Show | 13 | HG00558.hp2 HG02015.hp1 HG02523.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2580T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 2580 | chr6 | 99278584 | |||||
| chr6:99278730
|
T | C | 5 | a0001c0001t0060a0001c0001t0104a0001c0001t0105others(2): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2434A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 2434 | chr6 | 99278730 | |||||
| chr6:99278745
|
T | C | 99 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(96): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*2419A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 2419 | chr6 | 99278745 | |||||
| chr6:99278879
|
A | C | 1 | a0001c0001t0115 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2285T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 2285 | chr6 | 99278879 | |||||
| chr6:99278961
|
T | C | 45 | a0001c0001t0007a0001c0001t0008a0001c0001t0010others(42): Show | 103 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2203A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 2203 | chr6 | 99278961 | |||||
| chr6:99279283
|
T | C | 5 | a0001c0001t0060a0001c0001t0104a0001c0001t0105others(2): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1881A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1881 | chr6 | 99279283 | |||||
| chr6:99279290
|
C | T | 1 | a0001c0001t0114 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1874G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1874 | chr6 | 99279290 | |||||
| chr6:99279301
|
A | G | 1 | a0001c0001t0134 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1863T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1863 | chr6 | 99279301 | |||||
| chr6:99279329
|
C | T | 1 | a0001c0001t0086 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1835G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1835 | chr6 | 99279329 | |||||
| chr6:99279370
|
G | T | 1 | a0001c0001t0107 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1794C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1794 | chr6 | 99279370 | |||||
| chr6:99279414
|
C | T | 1 | a0001c0001t0085 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1750G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1750 | chr6 | 99279414 | |||||
| chr6:99279463
|
G | GT | 5 | a0001c0001t0051a0001c0001t0099a0001c0001t0112others(2): Show | 6 | HG02559.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1700dupA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1700 | chr6 | 99279463 | |||||
| chr6:99279463
|
G | GTT | 43 | a0001c0001t0007a0001c0001t0008a0001c0001t0010others(40): Show | 101 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1699_*1700dupAA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1700 | chr6 | 99279463 | |||||
| chr6:99279463
|
GT | G | 36 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(33): Show | 98 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1700delA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1700 | chr6 | 99279463 | |||||
| chr6:99279629
|
C | T | 2 | a0001c0001t0046a0001c0001t0084 | 3 | HG01069.hp2 HG01074.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1535G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1535 | chr6 | 99279629 | |||||
| chr6:99279631
|
C | G | 94 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(91): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*1533G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1533 | chr6 | 99279631 | |||||
| chr6:99279642
|
C | A | 1 | a0001c0001t0120 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1522G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1522 | chr6 | 99279642 | |||||
| chr6:99279777
|
C | T | 37 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(34): Show | 98 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1387G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1387 | chr6 | 99279777 | |||||
| chr6:99279797
|
C | T | 37 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(34): Show | 98 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1367G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1367 | chr6 | 99279797 | |||||
| chr6:99279850
|
C | T | 1 | a0001c0001t0122 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1314G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1314 | chr6 | 99279850 | |||||
| chr6:99280022
|
C | A | 1 | a0001c0001t0102 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1142 | chr6 | 99280022 | |||||
| chr6:99280084
|
T | C | 3 | a0001c0001t0050a0001c0001t0103a0001c0001t0147 | 4 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1080A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1080 | chr6 | 99280084 | |||||
| chr6:99280087
|
G | C | 1 | a0001c0001t0054 | 2 | HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1077C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1077 | chr6 | 99280087 | |||||
| chr6:99280168
|
G | C | 5 | a0001c0001t0060a0001c0001t0104a0001c0001t0105others(2): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*996C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 996 | chr6 | 99280168 | |||||
| chr6:99280284
|
A | C | 1 | a0001c0002t0121 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 880 | chr6 | 99280284 | |||||
| chr6:99280467
|
A | G | 1 | a0001c0001t0028 | 3 | HG02809.hp1 HG02965.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*697T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 697 | chr6 | 99280467 | |||||
| chr6:99280566
|
A | G | 34 | a0001c0001t0005a0001c0001t0012a0001c0001t0018others(31): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*598T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 598 | chr6 | 99280566 | |||||
| chr6:99280597
|
C | T | 1 | a0001c0001t0111 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 567 | chr6 | 99280597 | |||||
| chr6:99280747
|
T | C | 1 | a0001c0001t0147 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 417 | chr6 | 99280747 | |||||
| chr6:99280857
|
G | C | 1 | a0001c0001t0106 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 307 | chr6 | 99280857 | |||||
| chr6:99281051
|
A | G | 1 | a0001c0001t0110 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 113 | chr6 | 99281051 | |||||
| chr6:99281163
|
G | A | 1 | a0001c0001t0148 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 6/6 | 1 | chr6 | 99281163 | |||||
| chr6:99349386
|
C | T | 2 | a0001c0001t0108a0001c0001t0109 | 2 | HG02622.hp2 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-14G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 14 | chr6 | 99349386 | |||||
| chr6:99349409
|
C | A | 1 | a0001c0001t0149 | 1 | HG03239.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | chr6 | 99349409 | ||||||
| chr6:99349428
|
G | A | 1 | a0002c0005t0070 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 56 | chr6 | 99349428 | |||||
| chr6:99349483
|
G | T | 1 | a0002c0005t0070 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 111 | chr6 | 99349483 | |||||
| chr6:99349483
|
GGGCGGCG others(11): Show |
G | 1 | a0001c0001t0107 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-129_-112delTCCTCA others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 112 | chr6 | 99349483 | |||||
| chr6:99349495
|
C | T | 1 | a0001c0001t0061 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-123G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 123 | chr6 | 99349495 | |||||
| chr6:99349505
|
G | A | 1 | a0001c0004t0150 | 1 | NA18979.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-133C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | chr6 | 99349505 | ||||||
| chr6:99349529
|
A | AGAG | 60 | a0001c0001t0005a0001c0001t0008a0001c0001t0010others(57): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
5_prime_UTR_variant | MODIFIER | c.-160_-158dupCTC | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 158 | chr6 | 99349529 | |||||
| chr6:99349529
|
A | AGAGGAG | 2 | a0001c0001t0018a0001c0001t0040 | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-163_-158dupCTCCTC | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 158 | chr6 | 99349529 | |||||
| chr6:99349566
|
G | A | 1 | a0001c0001t0151 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-194C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 194 | chr6 | 99349566 | |||||
| chr6:99349625
|
C | G | 1 | a0001c0001t0071 | 1 | HG02559.hp2 | 5_prime_UTR_variant | MODIFIER | c.-253G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 253 | chr6 | 99349625 | |||||
| chr6:99349640
|
C | T | 1 | a0002c0005t0070 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-268G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 268 | chr6 | 99349640 | |||||
| chr6:99349644
|
C | T | 1 | a0002c0005t0070 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-272G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 272 | chr6 | 99349644 | |||||
| chr6:99349645
|
C | T | 14 | a0001c0001t0001a0001c0001t0016a0001c0001t0017others(11): Show | 50 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-273G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/6 | 273 | chr6 | 99349645 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:99281595
|
G | GGTTC | 74 | a0001c0001t0005g0007a0001c0001t0005g0088a0001c0001t0005g0089others(71): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.941-146_941-143dup others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99281595 | ||||||
| chr6:99281719
|
A | C | 1 | a0001c0001t0113g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.941-266T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99281719 | ||||||
| chr6:99281782
|
T | C | 1 | a0001c0001t0025g0157 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.941-329A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99281782 | ||||||
| chr6:99281911
|
C | T | 1 | a0001c0001t0071g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.941-458G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99281911 | ||||||
| chr6:99281943
|
C | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.941-490G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99281943 | ||||||
| chr6:99281985
|
G | A | 1 | a0001c0001t0024g0091 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.941-532C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99281985 | ||||||
| chr6:99282021
|
C | T | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(4): Show | 7 | NA18949.hp2 NA18950.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-568G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99282021 | ||||||
| chr6:99282025
|
G | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(154): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.941-572C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99282025 | ||||||
| chr6:99282079
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(160): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.941-626G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99282079 | ||||||
| chr6:99282238
|
G | A | 3 | a0001c0001t0056g0258a0001c0001t0056g0259a0001c0001t0079g0094 | 3 | HG02451.hp1 HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.941-785C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99282238 | ||||||
| chr6:99282696
|
A | C | 2 | a0001c0001t0002g0305a0001c0001t0027g0339 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.941-1243T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99282696 | ||||||
| chr6:99282745
|
TTATA | T | 93 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(90): Show | 97 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.941-1296_941-1293d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99282745 | ||||||
| chr6:99282950
|
C | G | 2 | a0001c0001t0042g0075a0001c0001t0042g0101 | 2 | HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.941-1497G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99282950 | ||||||
| chr6:99283101
|
T | A | 1 | a0001c0001t0022g0284 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.941-1648A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99283101 | ||||||
| chr6:99283153
|
T | C | 1 | a0001c0001t0021g0379 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.941-1700A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99283153 | ||||||
| chr6:99283656
|
T | G | 1 | a0001c0001t0011g0123 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.941-2203A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99283656 | ||||||
| chr6:99283876
|
C | T | 1 | a0001c0001t0019g0158 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.941-2423G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99283876 | ||||||
| chr6:99284419
|
C | T | 10 | a0001c0001t0005g0007a0001c0001t0005g0177a0001c0001t0005g0178others(7): Show | 11 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.941-2966G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284419 | ||||||
| chr6:99284551
|
T | C | 2 | a0001c0001t0029g0095a0001c0001t0114g0283 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.941-3098A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284551 | ||||||
| chr6:99284559
|
C | CTG | 36 | a0001c0001t0007g0225a0001c0001t0008g0126a0001c0001t0008g0127others(33): Show | 36 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.941-3108_941-3107d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284559 | ||||||
| chr6:99284559
|
C | CTGTG | 9 | a0001c0001t0007g0234a0001c0001t0008g0128a0001c0001t0010g0006others(6): Show | 10 | HG00544.hp1 HG02083.hp1 HG03669.hp1 others(7): Show |
intron_variant | MODIFIER | c.941-3110_941-3107d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284559 | ||||||
| chr6:99284559
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0116g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.941-3116_941-3107d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284559 | ||||||
| chr6:99284559
|
C | G | 3 | a0001c0001t0060g0289a0001c0001t0146g0223a0001c0001t0148g0375 | 3 | HG02615.hp1 HG02735.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.941-3106G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284559 | ||||||
| chr6:99284559
|
CTG | C | 28 | a0001c0001t0003g0189a0001c0001t0003g0282a0001c0001t0003g0358others(25): Show | 30 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.941-3108_941-3107d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284559 | ||||||
| chr6:99284559
|
CTGTG | C | 41 | a0001c0001t0002g0279a0001c0001t0002g0334a0001c0001t0002g0336others(38): Show | 43 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.941-3110_941-3107d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284559 | ||||||
| chr6:99284559
|
CTGTGTG | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(82): Show | 90 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.941-3112_941-3107d others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284559 | ||||||
| chr6:99284559
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0013g0214 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.941-3118_941-3107d others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284559 | ||||||
| chr6:99284598
|
T | A | 14 | a0001c0001t0005g0177a0001c0001t0013g0214a0001c0001t0019g0155others(11): Show | 14 | HG01358.hp1 HG01516.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.941-3145A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284598
|
T | TGA | 26 | a0001c0001t0005g0007a0001c0001t0005g0178a0001c0001t0005g0179others(23): Show | 27 | HG00140.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.941-3147_941-3146d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284598
|
T | TGTGA | 38 | a0001c0001t0005g0088a0001c0001t0005g0089a0001c0001t0005g0096others(35): Show | 38 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.941-3146_941-3145i others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284598
|
T | TGTGTGA | 33 | a0001c0001t0005g0161a0001c0001t0005g0170a0001c0001t0012g0270others(30): Show | 34 | HG00140.hp1 HG01099.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.941-3146_941-3145i others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284598
|
T | TGTGTGTG others(1): Show |
16 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0040others(13): Show | 17 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.941-3146_941-3145i others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284598
|
T | TGTGTGTG others(3): Show |
12 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(9): Show | 12 | HG00738.hp2 HG01123.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.941-3146_941-3145i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284598
|
T | TGTGTGTG others(5): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0032others(25): Show | 30 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.941-3146_941-3145i others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284598
|
T | TGTGTGTG others(7): Show |
9 | a0001c0001t0001g0053a0001c0001t0017g0021a0001c0001t0017g0050others(6): Show | 9 | HG02080.hp1 HG02630.hp2 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.941-3146_941-3145i others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284598
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0020 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.941-3146_941-3145i others(18): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | ||||||
| chr6:99284667
|
C | G | 2 | a0001c0001t0042g0075a0001c0001t0042g0101 | 2 | HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.941-3214G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284667 | ||||||
| chr6:99284817
|
C | G | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.941-3364G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284817 | ||||||
| chr6:99284906
|
C | T | 1 | a0001c0001t0021g0252 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.941-3453G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284906 | ||||||
| chr6:99284911
|
T | C | 1 | a0001c0001t0133g0342 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.941-3458A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284911 | ||||||
| chr6:99284914
|
CA | C | 7 | a0001c0001t0029g0181a0001c0001t0060g0280a0001c0001t0060g0289others(4): Show | 7 | HG01168.hp1 HG01358.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-3462delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284914 | ||||||
| chr6:99284927
|
A | G | 2 | a0001c0001t0100g0082a0001c0001t0101g0076 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.941-3474T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284927 | ||||||
| chr6:99284977
|
T | C | 2 | a0001c0001t0100g0082a0001c0001t0101g0076 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.941-3524A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284977 | ||||||
| chr6:99285025
|
T | TA | 352 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(349): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.941-3573dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99285025 | ||||||
| chr6:99285098
|
G | GC | 3 | a0001c0001t0028g0097a0001c0001t0028g0099a0001c0001t0028g0102 | 3 | HG02809.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.941-3646dupG | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99285098 | ||||||
| chr6:99285151
|
T | C | 1 | a0001c0001t0151g0383 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.941-3698A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99285151 | ||||||
| chr6:99285393
|
T | C | 6 | a0001c0001t0021g0379a0001c0001t0028g0097a0001c0001t0028g0099others(3): Show | 6 | HG02055.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.941-3940A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99285393 | ||||||
| chr6:99285786
|
C | A | 13 | a0001c0001t0021g0226a0001c0001t0021g0252a0001c0001t0021g0255others(10): Show | 14 | HG00140.hp1 HG00741.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.941-4333G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99285786 | ||||||
| chr6:99285915
|
A | G | 1 | a0001c0001t0002g0365 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.941-4462T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99285915 | ||||||
| chr6:99286063
|
T | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(79): Show | 84 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.941-4610A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286063 | ||||||
| chr6:99286185
|
C | T | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.941-4732G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286185 | ||||||
| chr6:99286187
|
T | C | 1 | a0001c0001t0118g0263 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.941-4734A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286187 | ||||||
| chr6:99286257
|
C | T | 2 | a0001c0001t0015g0295a0001c0001t0149g0381 | 2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.941-4804G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286257 | ||||||
| chr6:99286299
|
A | T | 1 | a0001c0001t0052g0355 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.941-4846T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286299 | ||||||
| chr6:99286309
|
A | G | 99 | a0001c0001t0007g0220a0001c0001t0007g0221a0001c0001t0007g0224others(96): Show | 102 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.941-4856T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286309 | ||||||
| chr6:99286334
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.941-4881C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286334 | ||||||
| chr6:99286621
|
G | C | 1 | a0001c0001t0055g0351 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.940+5083C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286621 | ||||||
| chr6:99286712
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 54 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.940+4992A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286712 | ||||||
| chr6:99286903
|
C | G | 99 | a0001c0001t0007g0220a0001c0001t0007g0221a0001c0001t0007g0224others(96): Show | 102 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.940+4801G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286903 | ||||||
| chr6:99286993
|
A | G | 22 | a0001c0001t0019g0155a0001c0001t0019g0156a0001c0001t0019g0158others(19): Show | 22 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.940+4711T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286993 | ||||||
| chr6:99287136
|
A | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(155): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.940+4568T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287136 | ||||||
| chr6:99287317
|
C | T | 3 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0147g0211 | 4 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+4387G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287317 | ||||||
| chr6:99287446
|
A | G | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+4258T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287446 | ||||||
| chr6:99287461
|
T | C | 7 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(4): Show | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+4243A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287461 | ||||||
| chr6:99287496
|
C | T | 2 | a0001c0002t0003g0197a0001c0002t0003g0198 | 2 | HG01496.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.940+4208G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287496 | ||||||
| chr6:99287516
|
C | T | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+4188G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287516 | ||||||
| chr6:99287640
|
G | A | 2 | a0001c0001t0040g0067a0001c0001t0071g0064 | 2 | HG02559.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.940+4064C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287640 | ||||||
| chr6:99287674
|
G | A | 1 | a0001c0001t0014g0374 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.940+4030C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287674 | ||||||
| chr6:99287726
|
G | T | 1 | a0001c0001t0118g0263 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.940+3978C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287726 | ||||||
| chr6:99287978
|
C | T | 1 | a0001c0001t0020g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.940+3726G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287978 | ||||||
| chr6:99287988
|
T | C | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+3716A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99287988 | ||||||
| chr6:99288256
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 54 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.940+3448C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288256 | ||||||
| chr6:99288343
|
T | C | 94 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(91): Show | 98 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.940+3361A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288343 | ||||||
| chr6:99288453
|
G | A | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+3251C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288453 | ||||||
| chr6:99288564
|
C | T | 1 | a0001c0001t0117g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.940+3140G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288564 | ||||||
| chr6:99288589
|
A | T | 63 | a0001c0001t0007g0220a0001c0001t0007g0221a0001c0001t0007g0224others(60): Show | 64 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.940+3115T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288589 | ||||||
| chr6:99288647
|
C | G | 1 | a0001c0001t0107g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.940+3057G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288647 | ||||||
| chr6:99288688
|
C | T | 1 | a0001c0001t0078g0138 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.940+3016G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288688 | ||||||
| chr6:99288798
|
G | A | 1 | a0001c0001t0117g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.940+2906C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288798 | ||||||
| chr6:99288846
|
C | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(80): Show | 85 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(82): Show |
intron_variant | MODIFIER | c.940+2858G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288846 | ||||||
| chr6:99288847
|
G | A | 1 | a0001c0001t0027g0339 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.940+2857C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288847 | ||||||
| chr6:99288847
|
G | GACACACA others(1): Show |
4 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0146g0223others(1): Show | 4 | HG01358.hp1 HG02615.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+2849_940+2856d others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288847 | ||||||
| chr6:99288847
|
G | GACACACA others(3): Show |
1 | a0001c0001t0104g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.940+2847_940+2856d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288847 | ||||||
| chr6:99288847
|
G | GACACACA others(7): Show |
1 | a0001c0001t0105g0079 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.940+2856_940+2857i others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288847 | ||||||
| chr6:99288847
|
G | GACACACA others(11): Show |
3 | a0001c0001t0021g0226a0001c0001t0026g0239a0001c0001t0053g0240 | 3 | HG01123.hp1 HG01361.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.940+2856_940+2857i others(20): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288847 | ||||||
| chr6:99288847
|
G | GACACACA others(15): Show |
9 | a0001c0001t0021g0252a0001c0001t0021g0255a0001c0001t0021g0256others(6): Show | 10 | HG00741.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.940+2856_940+2857i others(24): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288847 | ||||||
| chr6:99288847
|
G | GACACACA others(21): Show |
1 | a0001c0001t0117g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.940+2856_940+2857i others(30): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288847 | ||||||
| chr6:99288851
|
C | CACACACA others(3): Show |
1 | a0001c0001t0001g0044 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.940+2852_940+2853i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288851 | ||||||
| chr6:99288859
|
T | C | 21 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0021g0226others(18): Show | 22 | HG00140.hp1 HG00741.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.940+2845A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACAC | 16 | a0001c0001t0003g0282a0001c0001t0003g0358a0001c0001t0003g0378others(13): Show | 17 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.940+2841_940+2844d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACAC | 87 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0004g0308others(84): Show | 91 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.940+2839_940+2844d others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(1): Show |
23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0033others(20): Show | 23 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.940+2837_940+2844d others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(3): Show |
126 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0027others(123): Show | 131 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.940+2835_940+2844d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(5): Show |
22 | a0001c0001t0005g0170a0001c0001t0013g0213a0001c0001t0013g0214others(19): Show | 22 | HG01496.hp2 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.940+2833_940+2844d others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(7): Show |
27 | a0001c0001t0012g0010a0001c0001t0012g0270a0001c0001t0012g0271others(24): Show | 29 | HG00280.hp2 HG01099.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.940+2831_940+2844d others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(9): Show |
35 | a0001c0001t0005g0007a0001c0001t0005g0088a0001c0001t0005g0096others(32): Show | 36 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.940+2829_940+2844d others(18): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(11): Show |
7 | a0001c0001t0005g0089a0001c0001t0019g0172a0001c0001t0042g0101others(4): Show | 7 | HG01891.hp1 HG01981.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+2827_940+2844d others(20): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(13): Show |
3 | a0001c0001t0018g0069a0001c0001t0018g0071a0001c0001t0029g0095 | 3 | HG00621.hp2 HG02055.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.940+2825_940+2844d others(22): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(15): Show |
3 | a0001c0001t0040g0067a0001c0001t0075g0072a0001c0001t0114g0283 | 3 | HG02976.hp2 HG03516.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.940+2823_940+2844d others(24): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(17): Show |
4 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0070others(1): Show | 4 | NA18949.hp1 NA18978.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+2821_940+2844d others(26): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288859
|
T | TACACACA others(11): Show |
1 | a0001c0001t0042g0075 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.940+2844_940+2845i others(20): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288859 | ||||||
| chr6:99288922
|
A | C | 1 | a0001c0001t0118g0263 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.940+2782T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288922 | ||||||
| chr6:99288947
|
C | G | 1 | a0001c0001t0125g0324 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.940+2757G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99288947 | ||||||
| chr6:99289065
|
C | T | 99 | a0001c0001t0007g0220a0001c0001t0007g0221a0001c0001t0007g0224others(96): Show | 102 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.940+2639G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289065 | ||||||
| chr6:99289224
|
G | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(155): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.940+2480C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289224 | ||||||
| chr6:99289242
|
A | G | 2 | a0001c0001t0100g0082a0001c0001t0101g0076 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.940+2462T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289242 | ||||||
| chr6:99289370
|
G | T | 1 | a0001c0001t0002g0306 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.940+2334C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289370 | ||||||
| chr6:99289490
|
A | T | 1 | a0001c0001t0127g0298 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.940+2214T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289490 | ||||||
| chr6:99289498
|
A | T | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+2206T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289498 | ||||||
| chr6:99289551
|
T | C | 2 | a0001c0001t0100g0082a0001c0001t0101g0076 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.940+2153A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289551 | ||||||
| chr6:99289614
|
T | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.940+2090A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289614 | ||||||
| chr6:99289687
|
ATATGTGT others(1): Show |
A | 5 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(2): Show | 5 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.940+2009_940+2016d others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289687 | ||||||
| chr6:99289689
|
ATG | A | 21 | a0001c0001t0010g0151a0001c0001t0015g0247a0001c0001t0019g0155others(18): Show | 21 | HG00323.hp2 HG00558.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.940+2013_940+2014d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289689 | ||||||
| chr6:99289689
|
ATGTG | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(163): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.940+2011_940+2014d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289689 | ||||||
| chr6:99289689
|
ATGTGTG | A | 159 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(156): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.940+2009_940+2014d others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289689 | ||||||
| chr6:99289715
|
G | A | 1 | a0001c0001t0146g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.940+1989C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289715 | ||||||
| chr6:99289715
|
GTGTGTA | G | 4 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0137g0222others(1): Show | 5 | HG02280.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+1983_940+1988d others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289715 | ||||||
| chr6:99289717
|
G | A | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+1987C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289717 | ||||||
| chr6:99289719
|
G | A | 10 | a0001c0001t0021g0379a0001c0001t0028g0097a0001c0001t0028g0099others(7): Show | 10 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.940+1985C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289719 | ||||||
| chr6:99289771
|
T | G | 13 | a0001c0001t0021g0226a0001c0001t0021g0252a0001c0001t0021g0255others(10): Show | 14 | HG00140.hp1 HG00741.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.940+1933A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289771 | ||||||
| chr6:99289866
|
T | C | 1 | a0001c0001t0018g0071 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.940+1838A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289866 | ||||||
| chr6:99289926
|
C | T | 1 | a0001c0001t0116g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.940+1778G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289926 | ||||||
| chr6:99289927
|
TCGGCACC others(6): Show |
T | 1 | a0001c0001t0007g0220 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.940+1764_940+1776d others(15): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289927 | ||||||
| chr6:99289948
|
G | GCA | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+1754_940+1755d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289948 | ||||||
| chr6:99289948
|
G | T | 2 | a0001c0001t0011g0144a0001c0001t0031g0134 | 2 | NA18940.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.940+1756C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289948 | ||||||
| chr6:99289968
|
C | A | 1 | a0001c0001t0002g0303 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.940+1736G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289968 | ||||||
| chr6:99289982
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.940+1722T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99289982 | ||||||
| chr6:99290060
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0004g0335 | 3 | HG01256.hp2 HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.940+1644T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290060 | ||||||
| chr6:99290101
|
C | CCA | 180 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0045others(177): Show | 187 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.940+1601_940+1602d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290101
|
C | CCACA | 78 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(75): Show | 81 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.940+1599_940+1602d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290101
|
C | CCACACA | 58 | a0001c0001t0002g0303a0001c0001t0004g0308a0001c0001t0004g0369others(55): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.940+1597_940+1602d others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290101
|
C | CCACACAC others(1): Show |
8 | a0001c0001t0012g0275a0001c0001t0018g0069a0001c0001t0024g0091others(5): Show | 8 | HG01099.hp2 HG01952.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.940+1595_940+1602d others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290101
|
C | CCACACAC others(3): Show |
1 | a0001c0001t0137g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.940+1593_940+1602d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290101
|
C | CCACACAC others(5): Show |
1 | a0001c0001t0008g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.940+1591_940+1602d others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290101
|
C | CCACACAC others(7): Show |
7 | a0001c0001t0013g0213a0001c0001t0013g0214a0001c0001t0013g0216others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+1589_940+1602d others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290101
|
C | CCACACAC others(9): Show |
1 | a0001c0001t0013g0215 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.940+1587_940+1602d others(18): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290101
|
CCA | C | 12 | a0001c0001t0002g0306a0001c0001t0002g0359a0001c0001t0002g0361others(9): Show | 13 | HG01346.hp1 HG01361.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.940+1601_940+1602d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290101 | ||||||
| chr6:99290138
|
T | C | 1 | a0001c0001t0111g0261 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.940+1566A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290138 | ||||||
| chr6:99290174
|
T | C | 1 | a0001c0001t0104g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.940+1530A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290174 | ||||||
| chr6:99290296
|
C | T | 2 | a0001c0001t0007g0241a0001c0001t0022g0243 | 2 | NA18942.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.940+1408G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290296 | ||||||
| chr6:99290426
|
G | T | 1 | a0001c0001t0122g0354 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.940+1278C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290426 | ||||||
| chr6:99290451
|
T | C | 1 | a0001c0001t0002g0363 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.940+1253A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290451 | ||||||
| chr6:99290515
|
G | A | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+1189C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290515 | ||||||
| chr6:99290562
|
C | T | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+1142G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290562 | ||||||
| chr6:99290675
|
C | G | 2 | a0001c0001t0011g0144a0001c0001t0031g0134 | 2 | NA18940.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.940+1029G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99290675 | ||||||
| chr6:99291043
|
T | C | 8 | a0001c0001t0011g0005a0001c0001t0011g0113a0001c0001t0011g0123others(5): Show | 9 | HG03490.hp2 HG03492.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.940+661A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99291043 | ||||||
| chr6:99291106
|
G | A | 3 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0147g0211 | 4 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+598C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99291106 | ||||||
| chr6:99291421
|
T | C | 7 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(4): Show | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.940+283A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99291421 | ||||||
| chr6:99291488
|
T | A | 1 | a0001c0001t0071g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.940+216A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99291488 | ||||||
| chr6:99291621
|
G | T | 1 | a0001c0001t0031g0117 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.940+83C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99291621 | ||||||
| chr6:99291683
|
G | C | 1 | a0001c0001t0033g0081 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.940+21C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99291683 | ||||||
| chr6:99291863
|
T | TGCCCCAC others(3): Show |
1 | a0001c0001t0016g0030 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.824-53_824-44dupGA others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99291863 | ||||||
| chr6:99291921
|
C | T | 3 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0147g0211 | 4 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-101G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99291921 | ||||||
| chr6:99291928
|
G | C | 2 | a0001c0001t0100g0082a0001c0001t0101g0076 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.824-108C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99291928 | ||||||
| chr6:99291941
|
G | A | 9 | a0001c0001t0013g0213a0001c0001t0013g0214a0001c0001t0013g0215others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-121C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99291941 | ||||||
| chr6:99291965
|
T | TA | 7 | a0001c0001t0015g0295a0001c0001t0060g0280a0001c0001t0060g0289others(4): Show | 7 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-146dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99291965 | ||||||
| chr6:99292066
|
A | G | 361 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(358): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.824-246T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292066 | ||||||
| chr6:99292159
|
A | C | 2 | a0001c0001t0011g0144a0001c0001t0031g0134 | 2 | NA18940.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.824-339T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292159 | ||||||
| chr6:99292244
|
A | G | 5 | a0001c0001t0006g0311a0001c0001t0006g0350a0001c0001t0009g0317others(2): Show | 5 | NA18977.hp2 NA19002.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-424T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292244 | ||||||
| chr6:99292616
|
G | A | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-796C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292616 | ||||||
| chr6:99292644
|
C | T | 2 | a0001c0001t0100g0082a0001c0001t0101g0076 | 2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.824-824G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292644 | ||||||
| chr6:99292893
|
A | G | 6 | a0001c0001t0060g0280a0001c0001t0060g0289a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1073T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292893 | ||||||
| chr6:99292947
|
C | A | 92 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(89): Show | 96 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.824-1127G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292947 | ||||||
| chr6:99292964
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(157): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.824-1144C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292964 | ||||||
| chr6:99292999
|
G | T | 1 | a0001c0001t0019g0158 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.824-1179C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99292999 | ||||||
| chr6:99293068
|
A | C | 6 | a0001c0001t0003g0282a0001c0001t0060g0280a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1248T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293068 | ||||||
| chr6:99293358
|
C | A | 1 | a0001c0001t0016g0030 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.824-1538G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293358 | ||||||
| chr6:99293378
|
C | A | 1 | a0001c0001t0007g0220 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-1558G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293378 | ||||||
| chr6:99293380
|
C | A | 1 | a0001c0001t0007g0220 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-1560G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293380 | ||||||
| chr6:99293383
|
C | A | 1 | a0001c0001t0007g0220 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-1563G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293383 | ||||||
| chr6:99293387
|
C | T | 2 | a0001c0001t0104g0093a0001c0001t0146g0223 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.824-1567G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293387 | ||||||
| chr6:99293398
|
T | G | 1 | a0001c0001t0007g0220 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-1578A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293398 | ||||||
| chr6:99293399
|
A | G | 1 | a0001c0001t0007g0220 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-1579T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293399 | ||||||
| chr6:99293413
|
G | T | 1 | a0001c0001t0141g0288 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.824-1593C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293413 | ||||||
| chr6:99293454
|
G | A | 1 | a0001c0001t0136g0320 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.824-1634C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293454 | ||||||
| chr6:99293621
|
C | G | 1 | a0001c0001t0105g0079 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.824-1801G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293621 | ||||||
| chr6:99293660
|
T | C | 2 | a0001c0001t0002g0001a0001c0001t0124g0278 | 4 | NA18946.hp2 NA18957.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1840A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293660 | ||||||
| chr6:99293665
|
A | AGT | 18 | a0001c0001t0001g0058a0001c0001t0005g0007a0001c0001t0005g0177others(15): Show | 19 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.824-1847_824-1846d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
A | AGTGT | 15 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0017g0021others(12): Show | 15 | HG01168.hp1 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.824-1849_824-1846d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
A | AGTGTGT | 9 | a0001c0001t0005g0179a0001c0001t0012g0272a0001c0001t0017g0025others(6): Show | 9 | HG01516.hp2 HG02976.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-1851_824-1846d others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
A | AGTGTGTG others(1): Show |
4 | a0001c0001t0012g0273a0001c0001t0021g0226a0001c0001t0115g0246others(1): Show | 4 | HG01361.hp2 HG03453.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-1853_824-1846d others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0026g0011a0001c0001t0026g0239a0001c0001t0107g0186 | 4 | HG01123.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-1855_824-1846d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
AGT | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0032others(37): Show | 42 | HG00099.hp2 HG00673.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.824-1847_824-1846d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
AGTGT | A | 38 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0027others(35): Show | 38 | HG00323.hp1 HG00738.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.824-1849_824-1846d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
AGTGTGT | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0279others(57): Show | 64 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.824-1851_824-1846d others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
AGTGTGTG others(1): Show |
A | 9 | a0001c0001t0002g0301a0001c0001t0002g0306a0001c0001t0002g0349others(6): Show | 9 | HG00642.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-1853_824-1846d others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
AGTGTGTG others(3): Show |
A | 15 | a0001c0001t0002g0359a0001c0001t0002g0361a0001c0001t0006g0346others(12): Show | 16 | HG00673.hp2 HG00735.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.824-1855_824-1846d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0086g0145a0001c0001t0100g0082 | 2 | HG03453.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.824-1857_824-1846d others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
AGTGTGTG others(7): Show |
A | 74 | a0001c0001t0007g0220a0001c0001t0007g0221a0001c0001t0007g0224others(71): Show | 76 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.824-1859_824-1846d others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293665
|
AGTGTGTG others(15): Show |
A | 1 | a0001c0001t0151g0383 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-1867_824-1846d others(24): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293665 | ||||||
| chr6:99293696
|
G | C | 5 | a0001c0001t0003g0282a0001c0001t0104g0093a0001c0001t0105g0079others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-1876C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293696 | ||||||
| chr6:99293698
|
G | C | 29 | a0001c0001t0007g0291a0001c0001t0015g0295a0001c0001t0022g0284others(26): Show | 30 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.824-1878C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293698 | ||||||
| chr6:99293698
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0073g0168 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.824-1879_824-1878i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293698 | ||||||
| chr6:99293700
|
G | C | 2 | a0001c0001t0039g0023a0001c0001t0058g0287 | 2 | HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.824-1880C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293700 | ||||||
| chr6:99293700
|
GTGTGTGT others(7): Show |
G | 28 | a0001c0001t0007g0291a0001c0001t0015g0295a0001c0001t0022g0284others(25): Show | 29 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.824-1894_824-1881d others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293700 | ||||||
| chr6:99293702
|
G | C | 3 | a0001c0001t0100g0082a0001c0001t0101g0076a0001c0001t0137g0222 | 3 | HG01109.hp2 HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.824-1882C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293702 | ||||||
| chr6:99293702
|
GTGTGTGT others(5): Show |
G | 7 | a0001c0001t0003g0282a0001c0001t0039g0023a0001c0001t0058g0287others(4): Show | 7 | HG02647.hp1 HG02735.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-1894_824-1883d others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293702 | ||||||
| chr6:99293704
|
G | C | 6 | a0001c0001t0021g0379a0001c0001t0042g0075a0001c0001t0042g0101others(3): Show | 6 | HG00735.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1884C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293704 | ||||||
| chr6:99293704
|
GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0060g0280a0001c0001t0137g0222 | 2 | HG01358.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.824-1894_824-1885d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293704 | ||||||
| chr6:99293710
|
G | C | 1 | a0001c0001t0002g0334 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.824-1890C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293710 | ||||||
| chr6:99293714
|
C | G | 22 | a0001c0001t0012g0010a0001c0001t0019g0155a0001c0001t0019g0156others(19): Show | 23 | HG00323.hp2 HG01106.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-1894G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293714 | ||||||
| chr6:99293716
|
G | C | 2 | a0001c0001t0012g0010a0001c0001t0136g0320 | 3 | HG01167.hp1 HG01169.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.824-1896C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293716 | ||||||
| chr6:99293716
|
G | GTC | 4 | a0001c0001t0019g0156a0001c0001t0025g0154a0001c0001t0037g0286others(1): Show | 4 | HG00323.hp2 HG02572.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1897_824-1896i others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293716 | ||||||
| chr6:99293716
|
G | GTGTC | 3 | a0001c0001t0038g0029a0001c0001t0044g0098a0001c0001t0135g0362 | 3 | HG01891.hp1 HG03486.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.824-1897_824-1896i others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293716 | ||||||
| chr6:99293716
|
G | GTGTGTC | 6 | a0001c0001t0019g0155a0001c0001t0025g0163a0001c0001t0030g0129others(3): Show | 6 | HG01192.hp2 HG03654.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1897_824-1896i others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293716 | ||||||
| chr6:99293716
|
G | GTGTGTGT others(1): Show |
3 | a0001c0001t0019g0159a0001c0001t0037g0337a0001c0001t0038g0019 | 3 | HG02145.hp1 HG02683.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.824-1897_824-1896i others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293716 | ||||||
| chr6:99293716
|
G | GTGTGTGT others(3): Show |
3 | a0001c0001t0019g0158a0001c0001t0019g0172a0001c0001t0025g0157 | 3 | HG01106.hp1 HG01981.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.824-1897_824-1896i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293716 | ||||||
| chr6:99293716
|
G | GTGTGTGT others(5): Show |
2 | a0001c0001t0025g0162a0001c0001t0037g0276 | 2 | HG02055.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.824-1897_824-1896i others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293716 | ||||||
| chr6:99293774
|
AG | A | 3 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0147g0211 | 4 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-1955delC | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99293774 | ||||||
| chr6:99294159
|
A | C | 6 | a0001c0001t0003g0282a0001c0001t0060g0280a0001c0001t0104g0093others(3): Show | 6 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-2339T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294159 | ||||||
| chr6:99294284
|
C | T | 1 | a0001c0001t0066g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.824-2464G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294284 | ||||||
| chr6:99294307
|
C | T | 1 | a0001c0001t0053g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.824-2487G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294307 | ||||||
| chr6:99294422
|
G | A | 1 | a0001c0001t0114g0283 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.824-2602C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294422 | ||||||
| chr6:99294619
|
A | G | 113 | a0001c0001t0003g0282a0001c0001t0007g0220a0001c0001t0007g0221others(110): Show | 116 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.824-2799T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294619 | ||||||
| chr6:99294705
|
A | G | 2 | a0001c0001t0012g0010a0001c0001t0073g0168 | 3 | HG00280.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.824-2885T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294705 | ||||||
| chr6:99294846
|
C | CCCA | 22 | a0001c0001t0019g0155a0001c0001t0019g0156a0001c0001t0019g0158others(19): Show | 22 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.824-3027_824-3026i others(5): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294846 | ||||||
| chr6:99294898
|
G | A | 1 | a0001c0001t0071g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.824-3078C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294898 | ||||||
| chr6:99294905
|
TA | T | 4 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0105g0079others(1): Show | 5 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-3086delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99294905 | ||||||
| chr6:99295045
|
A | G | 2 | a0001c0001t0029g0095a0001c0001t0114g0283 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.824-3225T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295045 | ||||||
| chr6:99295181
|
T | A | 1 | a0001c0001t0100g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.824-3361A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295181 | ||||||
| chr6:99295217
|
A | G | 1 | a0001c0002t0003g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.824-3397T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295217 | ||||||
| chr6:99295317
|
T | C | 6 | a0001c0001t0002g0306a0001c0001t0002g0359a0001c0001t0002g0361others(3): Show | 6 | HG01243.hp1 HG01346.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-3497A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295317 | ||||||
| chr6:99295495
|
G | C | 1 | a0001c0001t0136g0320 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.824-3675C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295495 | ||||||
| chr6:99295499
|
A | AC | 5 | a0001c0001t0042g0075a0001c0001t0042g0101a0001c0001t0062g0048others(2): Show | 5 | HG00735.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-3680dupG | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295499 | ||||||
| chr6:99295627
|
A | C | 1 | a0001c0001t0137g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.824-3807T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295627 | ||||||
| chr6:99295666
|
C | T | 2 | a0001c0001t0108g0187a0001c0001t0109g0188 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.824-3846G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295666 | ||||||
| chr6:99295735
|
A | G | 9 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0303others(6): Show | 12 | HG00544.hp2 HG02015.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-3915T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295735 | ||||||
| chr6:99295957
|
T | C | 113 | a0001c0001t0003g0282a0001c0001t0007g0220a0001c0001t0007g0221others(110): Show | 116 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.824-4137A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295957 | ||||||
| chr6:99295989
|
T | C | 5 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(2): Show | 5 | HG01099.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-4169A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99295989 | ||||||
| chr6:99296054
|
T | C | 1 | a0001c0001t0110g0294 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.824-4234A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296054 | ||||||
| chr6:99296225
|
GGCTTCGG others(6): Show |
G | 1 | a0001c0001t0006g0356 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.824-4418_824-4406d others(15): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296225 | ||||||
| chr6:99296231
|
G | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(235): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.824-4411C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296231 | ||||||
| chr6:99296275
|
C | T | 6 | a0001c0001t0042g0075a0001c0001t0042g0101a0001c0001t0045g0109others(3): Show | 6 | HG00735.hp2 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-4455G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296275 | ||||||
| chr6:99296279
|
CA | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(236): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.824-4460delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296279 | ||||||
| chr6:99296336
|
G | A | 2 | a0001c0001t0044g0098a0001c0001t0135g0362 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.824-4516C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296336 | ||||||
| chr6:99296430
|
T | C | 1 | a0001c0001t0006g0318 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.824-4610A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296430 | ||||||
| chr6:99296460
|
G | A | 3 | a0001c0001t0003g0282a0001c0001t0060g0280a0001c0001t0148g0375 | 3 | HG01358.hp1 HG02735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.824-4640C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296460 | ||||||
| chr6:99296525
|
G | T | 1 | a0001c0001t0105g0079 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.824-4705C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296525 | ||||||
| chr6:99296573
|
C | T | 1 | a0001c0001t0068g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.824-4753G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296573 | ||||||
| chr6:99296587
|
C | T | 1 | a0002c0005t0070g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.824-4767G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296587 | ||||||
| chr6:99296595
|
C | A | 1 | a0001c0001t0005g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.824-4775G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296595 | ||||||
| chr6:99296631
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.824-4811G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296631 | ||||||
| chr6:99296667
|
T | G | 13 | a0001c0001t0021g0226a0001c0001t0021g0252a0001c0001t0021g0255others(10): Show | 14 | HG00140.hp1 HG00741.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.824-4847A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296667 | ||||||
| chr6:99296678
|
T | G | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.824-4858A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296678 | ||||||
| chr6:99296682
|
G | A | 4 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0105g0079others(1): Show | 5 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-4862C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296682 | ||||||
| chr6:99296692
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(241): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.824-4872C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296692 | ||||||
| chr6:99296744
|
G | T | 1 | a0001c0001t0071g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.824-4924C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296744 | ||||||
| chr6:99296817
|
G | A | 1 | a0001c0001t0004g0308 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.824-4997C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296817 | ||||||
| chr6:99296854
|
A | G | 357 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(354): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.824-5034T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296854 | ||||||
| chr6:99297005
|
C | A | 1 | a0001c0001t0068g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.824-5185G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297005 | ||||||
| chr6:99297060
|
C | T | 2 | a0001c0001t0026g0011a0001c0001t0026g0253 | 3 | HG01515.hp1 HG01517.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.824-5240G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297060 | ||||||
| chr6:99297133
|
G | T | 1 | a0001c0001t0123g0323 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.824-5313C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297133 | ||||||
| chr6:99297146
|
A | T | 1 | a0001c0001t0123g0323 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.824-5326T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297146 | ||||||
| chr6:99297302
|
A | C | 1 | a0001c0001t0099g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.824-5482T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297302 | ||||||
| chr6:99297354
|
C | T | 1 | a0001c0001t0010g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.824-5534G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297354 | ||||||
| chr6:99297355
|
A | G | 357 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(354): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.824-5535T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297355 | ||||||
| chr6:99297507
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | NA18939.hp1 NA18948.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-5687C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297507 | ||||||
| chr6:99297615
|
C | T | 7 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(4): Show | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-5795G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297615 | ||||||
| chr6:99297627
|
C | G | 1 | a0001c0001t0099g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.824-5807G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297627 | ||||||
| chr6:99297628
|
G | C | 1 | a0001c0001t0099g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.824-5808C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297628 | ||||||
| chr6:99297695
|
C | T | 15 | a0001c0001t0012g0010a0001c0001t0012g0270a0001c0001t0012g0271others(12): Show | 16 | HG00280.hp2 HG00323.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.824-5875G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297695 | ||||||
| chr6:99297711
|
T | G | 1 | a0001c0001t0123g0323 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.824-5891A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297711 | ||||||
| chr6:99297714
|
A | C | 5 | a0001c0001t0042g0075a0001c0001t0042g0101a0001c0001t0062g0048others(2): Show | 5 | HG00735.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-5894T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297714 | ||||||
| chr6:99297794
|
T | C | 1 | a0001c0001t0022g0284 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.824-5974A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297794 | ||||||
| chr6:99297813
|
A | G | 113 | a0001c0001t0003g0282a0001c0001t0007g0220a0001c0001t0007g0221others(110): Show | 116 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.824-5993T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297813 | ||||||
| chr6:99297922
|
G | A | 6 | a0001c0001t0005g0170a0001c0001t0051g0262a0001c0001t0051g0268others(3): Show | 6 | HG02559.hp1 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-6102C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297922 | ||||||
| chr6:99297991
|
A | C | 1 | a0001c0001t0099g0107 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.824-6171T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99297991 | ||||||
| chr6:99298116
|
C | G | 1 | a0001c0002t0003g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.824-6296G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298116 | ||||||
| chr6:99298229
|
C | CT | 5 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0105g0079others(2): Show | 6 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-6410dupA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298229 | ||||||
| chr6:99298229
|
CT | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(239): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.824-6410delA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298229 | ||||||
| chr6:99298229
|
CTT | C | 113 | a0001c0001t0003g0282a0001c0001t0007g0220a0001c0001t0007g0221others(110): Show | 116 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.824-6411_824-6410d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298229 | ||||||
| chr6:99298647
|
C | T | 1 | a0001c0001t0129g0347 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.824-6827G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298647 | ||||||
| chr6:99298661
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(236): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.824-6841A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298661 | ||||||
| chr6:99298678
|
A | G | 5 | a0001c0001t0042g0075a0001c0001t0042g0101a0001c0001t0062g0048others(2): Show | 5 | HG00735.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-6858T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298678 | ||||||
| chr6:99298888
|
T | A | 1 | a0001c0001t0032g0105 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.824-7068A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298888 | ||||||
| chr6:99298898
|
C | T | 1 | a0001c0001t0036g0340 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.824-7078G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298898 | ||||||
| chr6:99299058
|
T | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(44): Show | 49 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.824-7238A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99299058 | ||||||
| chr6:99299110
|
A | G | 5 | a0001c0001t0042g0075a0001c0001t0042g0101a0001c0001t0062g0048others(2): Show | 5 | HG00735.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-7290T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99299110 | ||||||
| chr6:99299314
|
A | C | 89 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(86): Show | 93 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.824-7494T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99299314 | ||||||
| chr6:99299660
|
G | A | 1 | a0001c0001t0021g0379 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.824-7840C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99299660 | ||||||
| chr6:99299757
|
C | T | 347 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(344): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.824-7937G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99299757 | ||||||
| chr6:99299845
|
A | C | 4 | a0001c0001t0002g0306a0001c0001t0002g0359a0001c0001t0002g0361others(1): Show | 4 | HG01346.hp1 HG01361.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-8025T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99299845 | ||||||
| chr6:99300007
|
C | T | 1 | a0001c0001t0125g0324 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.824-8187G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99300007 | ||||||
| chr6:99300083
|
G | C | 2 | a0001c0001t0026g0011a0001c0001t0026g0253 | 3 | HG01515.hp1 HG01517.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.824-8263C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99300083 | ||||||
| chr6:99300089
|
T | C | 1 | a0001c0001t0013g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.824-8269A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99300089 | ||||||
| chr6:99300338
|
A | G | 1 | a0001c0001t0103g0083 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.824-8518T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99300338 | ||||||
| chr6:99300461
|
T | C | 1 | a0001c0001t0013g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.824-8641A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99300461 | ||||||
| chr6:99300608
|
G | A | 5 | a0001c0001t0025g0162a0001c0001t0025g0163a0001c0001t0030g0165others(2): Show | 5 | HG01192.hp2 HG02738.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-8788C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99300608 | ||||||
| chr6:99300615
|
T | C | 6 | a0001c0001t0017g0021a0001c0001t0017g0025a0001c0001t0017g0050others(3): Show | 6 | HG02080.hp1 NA18943.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-8795A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99300615 | ||||||
| chr6:99300881
|
C | G | 78 | a0001c0001t0007g0220a0001c0001t0007g0221a0001c0001t0007g0224others(75): Show | 80 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.824-9061G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99300881 | ||||||
| chr6:99301120
|
T | A | 348 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(345): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.824-9300A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99301120 | ||||||
| chr6:99301170
|
C | G | 22 | a0001c0001t0019g0155a0001c0001t0019g0156a0001c0001t0019g0158others(19): Show | 22 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.824-9350G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99301170 | ||||||
| chr6:99301413
|
T | C | 5 | a0001c0001t0042g0075a0001c0001t0042g0101a0001c0001t0062g0048others(2): Show | 5 | HG00735.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-9593A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99301413 | ||||||
| chr6:99301462
|
T | C | 1 | a0001c0001t0004g0367 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.824-9642A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99301462 | ||||||
| chr6:99301656
|
C | A | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.824-9836G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99301656 | ||||||
| chr6:99302286
|
C | A | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-10466G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302286 | ||||||
| chr6:99302321
|
T | C | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-10501A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302321 | ||||||
| chr6:99302379
|
C | T | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.824-10559G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302379 | ||||||
| chr6:99302381
|
C | T | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-10561G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302381 | ||||||
| chr6:99302493
|
C | T | 348 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(345): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.824-10673G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302493 | ||||||
| chr6:99302531
|
C | T | 1 | a0001c0001t0036g0310 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.824-10711G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302531 | ||||||
| chr6:99302557
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(289): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.824-10737C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302557 | ||||||
| chr6:99302862
|
T | C | 1 | a0001c0001t0002g0365 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.824-11042A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302862 | ||||||
| chr6:99302868
|
A | T | 22 | a0001c0001t0019g0155a0001c0001t0019g0156a0001c0001t0019g0158others(19): Show | 22 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.824-11048T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302868 | ||||||
| chr6:99303234
|
C | T | 348 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(345): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.824-11414G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303234 | ||||||
| chr6:99303377
|
C | A | 1 | a0001c0001t0151g0383 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-11557G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303377 | ||||||
| chr6:99303442
|
G | T | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-11622C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303442 | ||||||
| chr6:99303584
|
A | T | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-11764T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303584 | ||||||
| chr6:99303635
|
T | C | 1 | a0001c0001t0101g0076 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.824-11815A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303635 | ||||||
| chr6:99303653
|
T | A | 2 | a0001c0001t0006g0330a0001c0001t0009g0319 | 2 | NA18983.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.824-11833A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303653 | ||||||
| chr6:99303674
|
G | A | 1 | a0001c0001t0100g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.824-11854C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303674 | ||||||
| chr6:99303805
|
C | T | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-11985G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303805 | ||||||
| chr6:99303954
|
T | C | 1 | a0001c0001t0067g0047 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.824-12134A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99303954 | ||||||
| chr6:99304147
|
G | A | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-12327C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99304147 | ||||||
| chr6:99304185
|
C | T | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-12365G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99304185 | ||||||
| chr6:99304283
|
C | T | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-12463G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99304283 | ||||||
| chr6:99304313
|
T | TA | 4 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(1): Show | 4 | HG02083.hp1 HG02129.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-12494_824-1249 others(5): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99304313 | ||||||
| chr6:99304314
|
T | A | 55 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(52): Show | 56 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.824-12494A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99304314 | ||||||
| chr6:99304392
|
G | A | 1 | a0001c0001t0002g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.824-12572C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99304392 | ||||||
| chr6:99304733
|
A | T | 1 | a0001c0001t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.824-12913T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99304733 | ||||||
| chr6:99304907
|
G | A | 1 | a0001c0001t0007g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.824-13087C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99304907 | ||||||
| chr6:99305006
|
T | C | 3 | a0001c0001t0012g0271a0001c0001t0012g0272a0001c0001t0012g0275 | 3 | HG01099.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.824-13186A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305006 | ||||||
| chr6:99305018
|
C | A | 8 | a0001c0001t0003g0282a0001c0001t0050g0004a0001c0001t0060g0280others(5): Show | 9 | HG01358.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-13198G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305018 | ||||||
| chr6:99305202
|
G | A | 56 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(53): Show | 58 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.824-13382C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305202 | ||||||
| chr6:99305392
|
C | T | 7 | a0001c0001t0042g0075a0001c0001t0042g0101a0001c0001t0062g0048others(4): Show | 7 | HG00735.hp2 HG01109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-13572G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305392 | ||||||
| chr6:99305623
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(289): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.824-13803C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305623 | ||||||
| chr6:99305715
|
C | CAT | 361 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(358): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.824-13897_824-1389 others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305715 | ||||||
| chr6:99305742
|
G | C | 1 | a0001c0001t0137g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.824-13922C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305742 | ||||||
| chr6:99305801
|
C | T | 1 | a0001c0001t0002g0331 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.824-13981G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305801 | ||||||
| chr6:99305833
|
T | C | 7 | a0001c0001t0042g0075a0001c0001t0042g0101a0001c0001t0062g0048others(4): Show | 7 | HG00735.hp2 HG01109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-14013A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305833 | ||||||
| chr6:99305909
|
A | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0035others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-14089T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305909 | ||||||
| chr6:99305930
|
G | A | 1 | a0001c0001t0027g0372 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.824-14110C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305930 | ||||||
| chr6:99305939
|
A | G | 3 | a0001c0001t0046g0106a0001c0001t0046g0118a0001c0001t0084g0130 | 3 | HG01069.hp2 HG01074.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.824-14119T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305939 | ||||||
| chr6:99306005
|
C | T | 3 | a0001c0001t0034g0274a0001c0001t0034g0277a0001c0001t0034g0313 | 3 | HG02109.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.824-14185G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99306005 | ||||||
| chr6:99306035
|
G | T | 1 | a0001c0001t0002g0361 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.824-14215C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99306035 | ||||||
| chr6:99306384
|
C | T | 55 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(52): Show | 57 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.824-14564G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99306384 | ||||||
| chr6:99306489
|
T | G | 1 | a0001c0001t0012g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.824-14669A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99306489 | ||||||
| chr6:99306547
|
C | T | 2 | a0001c0001t0005g0088a0001c0001t0005g0089 | 2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.824-14727G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99306547 | ||||||
| chr6:99306844
|
A | C | 1 | a0001c0001t0001g0043 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-15024T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99306844 | ||||||
| chr6:99306875
|
A | G | 1 | a0001c0001t0044g0098 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.824-15055T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99306875 | ||||||
| chr6:99306986
|
C | G | 61 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(58): Show | 63 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.824-15166G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99306986 | ||||||
| chr6:99307217
|
G | T | 61 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(58): Show | 63 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.824-15397C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307217 | ||||||
| chr6:99307238
|
A | G | 61 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(58): Show | 63 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.824-15418T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307238 | ||||||
| chr6:99307262
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.824-15442G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307262 | ||||||
| chr6:99307362
|
T | C | 1 | a0001c0002t0003g0198 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.824-15542A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307362 | ||||||
| chr6:99307400
|
G | A | 1 | a0001c0001t0102g0111 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.824-15580C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307400 | ||||||
| chr6:99307463
|
C | T | 5 | a0001c0001t0003g0282a0001c0001t0060g0280a0001c0001t0104g0093others(2): Show | 5 | HG01358.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-15643G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307463 | ||||||
| chr6:99307547
|
A | G | 13 | a0001c0001t0003g0282a0001c0001t0042g0075a0001c0001t0042g0101others(10): Show | 13 | HG00735.hp2 HG01109.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.824-15727T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307547 | ||||||
| chr6:99307570
|
G | A | 1 | a0001c0001t0151g0383 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-15750C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307570 | ||||||
| chr6:99307664
|
T | A | 4 | a0001c0001t0039g0023a0001c0001t0039g0041a0001c0001t0067g0047others(1): Show | 4 | HG02698.hp2 HG03710.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+15780A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307664 | ||||||
| chr6:99307755
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0046 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.823+15689G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307755 | ||||||
| chr6:99307803
|
C | T | 1 | a0001c0001t0066g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.823+15641G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307803 | ||||||
| chr6:99307904
|
G | C | 3 | a0001c0001t0050g0004a0001c0001t0103g0083a0001c0001t0147g0211 | 4 | HG02280.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+15540C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307904 | ||||||
| chr6:99307933
|
A | G | 295 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(292): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.823+15511T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307933 | ||||||
| chr6:99307963
|
A | G | 2 | a0001c0001t0104g0093a0001c0001t0146g0223 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.823+15481T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99307963 | ||||||
| chr6:99308035
|
A | G | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.823+15409T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308035 | ||||||
| chr6:99308084
|
A | C | 1 | a0001c0001t0018g0069 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.823+15360T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308084 | ||||||
| chr6:99308160
|
G | A | 3 | a0001c0001t0003g0282a0001c0001t0060g0280a0001c0001t0148g0375 | 3 | HG01358.hp1 HG02735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.823+15284C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308160 | ||||||
| chr6:99308200
|
G | A | 2 | a0001c0001t0021g0255a0001c0001t0021g0256 | 2 | HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.823+15244C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308200 | ||||||
| chr6:99308207
|
G | A | 37 | a0001c0001t0005g0007a0001c0001t0005g0088a0001c0001t0005g0089others(34): Show | 39 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.823+15237C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308207 | ||||||
| chr6:99308229
|
G | A | 9 | a0001c0001t0013g0213a0001c0001t0013g0214a0001c0001t0013g0215others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+15215C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308229 | ||||||
| chr6:99308579
|
G | A | 1 | a0001c0001t0101g0076 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+14865C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308579 | ||||||
| chr6:99308610
|
C | CA | 6 | a0001c0001t0005g0170a0001c0001t0014g0322a0001c0001t0017g0021others(3): Show | 6 | HG02080.hp1 HG02976.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+14833dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308610 | ||||||
| chr6:99308610
|
CA | C | 8 | a0001c0001t0007g0224a0001c0001t0012g0270a0001c0001t0012g0271others(5): Show | 8 | HG01099.hp2 HG02922.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+14833delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308610 | ||||||
| chr6:99308715
|
C | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+14729G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308715 | ||||||
| chr6:99308880
|
T | A | 35 | a0001c0001t0007g0220a0001c0001t0007g0221a0001c0001t0007g0224others(32): Show | 36 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.823+14564A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308880 | ||||||
| chr6:99308881
|
T | A | 356 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(353): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.823+14563A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308881 | ||||||
| chr6:99308891
|
G | A | 3 | a0001c0001t0071g0064a0001c0001t0076g0077a0001c0001t0077g0074 | 3 | HG02559.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.823+14553C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308891 | ||||||
| chr6:99308938
|
A | G | 7 | a0001c0001t0013g0213a0001c0001t0013g0214a0001c0001t0013g0215others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+14506T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99308938 | ||||||
| chr6:99309014
|
T | C | 1 | a0001c0001t0023g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.823+14430A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309014 | ||||||
| chr6:99309125
|
C | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+14319G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309125 | ||||||
| chr6:99309174
|
T | G | 3 | a0001c0001t0042g0075a0001c0001t0072g0167a0001c0001t0137g0222 | 3 | HG02257.hp2 HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.823+14270A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309174 | ||||||
| chr6:99309200
|
T | A | 1 | a0001c0002t0003g0204 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.823+14244A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309200 | ||||||
| chr6:99309210
|
GT | G | 6 | a0001c0001t0035g0281a0001c0001t0035g0296a0001c0001t0035g0299others(3): Show | 6 | HG01433.hp1 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+14233delA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309210 | ||||||
| chr6:99309217
|
T | C | 1 | a0001c0001t0137g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.823+14227A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309217 | ||||||
| chr6:99309320
|
A | G | 1 | a0001c0001t0009g0012 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.823+14124T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309320 | ||||||
| chr6:99309371
|
G | A | 1 | a0001c0001t0100g0082 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823+14073C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309371 | ||||||
| chr6:99309379
|
C | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+14065G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309379 | ||||||
| chr6:99309626
|
G | A | 1 | a0001c0001t0136g0320 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.823+13818C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309626 | ||||||
| chr6:99309739
|
T | C | 2 | a0001c0001t0013g0260a0001c0001t0111g0261 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.823+13705A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309739 | ||||||
| chr6:99309755
|
G | A | 1 | a0001c0001t0107g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+13689C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309755 | ||||||
| chr6:99309756
|
A | T | 1 | a0001c0001t0107g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+13688T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309756 | ||||||
| chr6:99309802
|
T | C | 1 | a0001c0001t0053g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.823+13642A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309802 | ||||||
| chr6:99309856
|
G | T | 1 | a0001c0001t0019g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.823+13588C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99309856 | ||||||
| chr6:99310027
|
G | A | 1 | a0001c0002t0003g0191 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.823+13417C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310027 | ||||||
| chr6:99310048
|
C | G | 1 | a0001c0001t0116g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.823+13396G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310048 | ||||||
| chr6:99310077
|
C | T | 22 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(19): Show | 22 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.823+13367G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310077 | ||||||
| chr6:99310204
|
G | C | 278 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(275): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.823+13240C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310204 | ||||||
| chr6:99310315
|
A | G | 361 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(358): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.823+13129T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310315 | ||||||
| chr6:99310384
|
C | T | 1 | a0001c0001t0009g0012 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.823+13060G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310384 | ||||||
| chr6:99310410
|
C | T | 103 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0004g0228others(100): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.823+13034G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310410 | ||||||
| chr6:99310770
|
G | A | 21 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(18): Show | 21 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.823+12674C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310770 | ||||||
| chr6:99310792
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(86): Show | 92 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.823+12652A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310792 | ||||||
| chr6:99310847
|
C | T | 1 | a0001c0002t0003g0191 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.823+12597G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310847 | ||||||
| chr6:99311071
|
C | G | 1 | a0001c0001t0015g0295 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.823+12373G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311071 | ||||||
| chr6:99311150
|
G | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+12294C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311150 | ||||||
| chr6:99311151
|
G | A | 17 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(14): Show | 17 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+12293C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311151 | ||||||
| chr6:99311342
|
C | T | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.823+12102G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311342 | ||||||
| chr6:99311404
|
A | G | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+12040T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311404 | ||||||
| chr6:99311468
|
G | A | 5 | a0001c0001t0021g0379a0001c0001t0029g0095a0001c0001t0052g0257others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+11976C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311468 | ||||||
| chr6:99311516
|
A | C | 2 | a0001c0001t0002g0314a0001c0001t0006g0345 | 2 | NA18951.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.823+11928T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311516 | ||||||
| chr6:99311528
|
T | C | 6 | a0001c0001t0042g0075a0001c0001t0071g0064a0001c0001t0076g0077others(3): Show | 6 | HG01109.hp2 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+11916A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311528 | ||||||
| chr6:99311556
|
T | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+11888A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311556 | ||||||
| chr6:99311569
|
C | T | 1 | a0001c0001t0060g0280 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.823+11875G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311569 | ||||||
| chr6:99311610
|
A | C | 12 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(9): Show | 12 | HG00544.hp1 HG00621.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.823+11834T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311610 | ||||||
| chr6:99311718
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.823+11726G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311718 | ||||||
| chr6:99311872
|
C | T | 1 | a0001c0001t0119g0233 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.823+11572G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311872 | ||||||
| chr6:99311951
|
C | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+11493G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311951 | ||||||
| chr6:99312010
|
C | T | 276 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(273): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.823+11434G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99312010 | ||||||
| chr6:99312044
|
A | C | 10 | a0001c0001t0013g0260a0001c0001t0014g0374a0001c0001t0034g0313others(7): Show | 10 | HG02258.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+11400T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99312044 | ||||||
| chr6:99312169
|
G | A | 15 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(12): Show | 15 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.823+11275C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99312169 | ||||||
| chr6:99312361
|
A | G | 1 | a0001c0001t0029g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.823+11083T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99312361 | ||||||
| chr6:99312613
|
C | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+10831G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99312613 | ||||||
| chr6:99312641
|
C | G | 2 | a0001c0001t0020g0135a0001c0001t0043g0132 | 2 | NA18942.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.823+10803G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99312641 | ||||||
| chr6:99312777
|
T | A | 1 | a0001c0001t0006g0350 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.823+10667A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99312777 | ||||||
| chr6:99312900
|
A | T | 1 | a0001c0001t0010g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.823+10544T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99312900 | ||||||
| chr6:99313125
|
G | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+10319C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99313125 | ||||||
| chr6:99313271
|
C | A | 3 | a0001c0001t0082g0084a0001c0001t0100g0082a0001c0001t0103g0083 | 3 | HG02258.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.823+10173G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99313271 | ||||||
| chr6:99313400
|
C | T | 3 | a0001c0001t0034g0274a0001c0001t0034g0277a0001c0001t0118g0263 | 3 | HG02109.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.823+10044G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99313400 | ||||||
| chr6:99313551
|
C | G | 1 | a0001c0001t0002g0279 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.823+9893G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99313551 | ||||||
| chr6:99313685
|
T | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+9759A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99313685 | ||||||
| chr6:99313686
|
G | A | 9 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0303others(6): Show | 12 | HG00544.hp2 HG02015.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.823+9758C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99313686 | ||||||
| chr6:99313788
|
G | A | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+9656C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99313788 | ||||||
| chr6:99313792
|
C | T | 5 | a0001c0001t0021g0379a0001c0001t0029g0095a0001c0001t0052g0257others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+9652G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99313792 | ||||||
| chr6:99314043
|
G | A | 1 | a0001c0001t0002g0279 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.823+9401C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314043 | ||||||
| chr6:99314325
|
T | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+9119A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314325 | ||||||
| chr6:99314417
|
T | C | 36 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(33): Show | 37 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.823+9027A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314417 | ||||||
| chr6:99314625
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 91 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.823+8819G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314625 | ||||||
| chr6:99314626
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(181): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.823+8818T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314626 | ||||||
| chr6:99314796
|
A | G | 361 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(358): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.823+8648T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314796 | ||||||
| chr6:99314864
|
A | G | 96 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.823+8580T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314864 | ||||||
| chr6:99314918
|
A | C | 1 | a0001c0001t0104g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.823+8526T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314918 | ||||||
| chr6:99315025
|
G | C | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.823+8419C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315025 | ||||||
| chr6:99315102
|
C | T | 1 | a0001c0001t0034g0274 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.823+8342G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315102 | ||||||
| chr6:99315136
|
G | A | 1 | a0001c0001t0146g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823+8308C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315136 | ||||||
| chr6:99315232
|
T | TAAA | 36 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(33): Show | 38 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.823+8209_823+8211d others(5): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315232 | ||||||
| chr6:99315232
|
T | TAAAA | 20 | a0001c0001t0008g0147a0001c0001t0008g0149a0001c0001t0010g0140others(17): Show | 20 | HG01433.hp2 HG02080.hp2 HG02965.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+8208_823+8211d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315232 | ||||||
| chr6:99315232
|
T | TAAAAA | 8 | a0001c0001t0034g0277a0001c0001t0043g0131a0001c0001t0051g0262others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+8207_823+8211d others(7): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315232 | ||||||
| chr6:99315232
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0034g0274 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.823+8202_823+8211d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315232 | ||||||
| chr6:99315252
|
AAAAAAAA others(4): Show |
A | 6 | a0001c0001t0021g0379a0001c0001t0052g0257a0001c0001t0094g0142others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+8181_823+8191d others(13): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315252 | ||||||
| chr6:99315253
|
AAAAAAAA others(3): Show |
A | 4 | a0001c0001t0029g0095a0001c0001t0048g0080a0001c0001t0082g0084others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+8181_823+8190d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315253 | ||||||
| chr6:99315259
|
AAAAC | A | 84 | a0001c0001t0002g0331a0001c0001t0005g0007a0001c0001t0005g0088others(81): Show | 88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.823+8181_823+8184d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315259 | ||||||
| chr6:99315260
|
AAAC | A | 88 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0033others(85): Show | 92 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.823+8181_823+8183d others(5): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315260 | ||||||
| chr6:99315261
|
AAC | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0020others(85): Show | 91 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.823+8181_823+8182d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315261 | ||||||
| chr6:99315262
|
AC | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0046others(4): Show | 7 | HG00741.hp1 HG01346.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+8181delG | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315262 | ||||||
| chr6:99315263
|
C | A | 81 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(78): Show | 83 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.823+8181G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315263 | ||||||
| chr6:99315390
|
A | G | 278 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(275): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.823+8054T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315390 | ||||||
| chr6:99315649
|
G | C | 1 | a0001c0001t0107g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+7795C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315649 | ||||||
| chr6:99315893
|
CCTCTATA others(9): Show |
C | 1 | a0001c0001t0027g0377 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.823+7535_823+7550d others(18): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315893 | ||||||
| chr6:99315955
|
T | C | 3 | a0001c0001t0002g0334a0001c0001t0002g0336a0001c0001t0004g0335 | 3 | HG01081.hp2 HG01978.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.823+7489A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99315955 | ||||||
| chr6:99316019
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.823+7425C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316019 | ||||||
| chr6:99316089
|
C | A | 1 | a0001c0001t0015g0295 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.823+7355G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316089 | ||||||
| chr6:99316157
|
G | GC | 62 | a0001c0001t0001g0058a0001c0001t0002g0363a0001c0001t0003g0282others(59): Show | 64 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.823+7286dupG | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316157 | ||||||
| chr6:99316157
|
GC | G | 95 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(92): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.823+7286delG | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316157 | ||||||
| chr6:99316182
|
C | T | 17 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(14): Show | 17 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+7262G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316182 | ||||||
| chr6:99316268
|
G | A | 97 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(94): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.823+7176C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316268 | ||||||
| chr6:99316274
|
G | A | 3 | a0001c0001t0082g0084a0001c0001t0100g0082a0001c0001t0103g0083 | 3 | HG02258.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.823+7170C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316274 | ||||||
| chr6:99316409
|
A | AGT | 3 | a0001c0001t0042g0075a0001c0001t0076g0077a0001c0001t0101g0076 | 3 | HG01109.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.823+7033_823+7034d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316409 | ||||||
| chr6:99316415
|
G | GCCTTGTC others(7): Show |
5 | a0001c0001t0051g0262a0001c0001t0051g0268a0001c0001t0112g0266others(2): Show | 5 | HG02559.hp1 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+7015_823+7028d others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316415 | ||||||
| chr6:99316440
|
C | G | 97 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(94): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.823+7004G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316440 | ||||||
| chr6:99316772
|
C | T | 1 | a0001c0001t0002g0363 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.823+6672G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316772 | ||||||
| chr6:99316867
|
C | G | 96 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.823+6577G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316867 | ||||||
| chr6:99316955
|
T | C | 97 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(94): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.823+6489A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316955 | ||||||
| chr6:99317101
|
TA | T | 17 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(14): Show | 17 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+6342delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317101 | ||||||
| chr6:99317177
|
AT | A | 321 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(318): Show | 331 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.823+6266delA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317177 | ||||||
| chr6:99317299
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 91 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.823+6145C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317299 | ||||||
| chr6:99317383
|
CA | C | 20 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(17): Show | 20 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.823+6060delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317383 | ||||||
| chr6:99317453
|
G | A | 3 | a0001c0001t0024g0091a0001c0001t0045g0092a0001c0001t0147g0211 | 3 | HG01496.hp2 HG01952.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.823+5991C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317453 | ||||||
| chr6:99317526
|
T | TAAGAAAC others(340): Show |
1 | a0001c0001t0120g0373 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.823+5917_823+5918i others(349): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317526 | ||||||
| chr6:99317526
|
T | TAAGAAAC others(343): Show |
1 | a0001c0001t0112g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.823+5917_823+5918i others(352): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317526 | ||||||
| chr6:99317656
|
C | T | 1 | a0001c0001t0025g0157 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.823+5788G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317656 | ||||||
| chr6:99317908
|
T | G | 74 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(71): Show | 78 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.823+5536A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317908 | ||||||
| chr6:99317954
|
TGGTATAG others(15): Show |
T | 97 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(94): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.823+5468_823+5489d others(24): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317954 | ||||||
| chr6:99317996
|
C | T | 2 | a0001c0001t0010g0140a0001c0001t0090g0141 | 2 | NA18978.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.823+5448G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317996 | ||||||
| chr6:99318024
|
C | A | 97 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(94): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.823+5420G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318024 | ||||||
| chr6:99318083
|
C | T | 6 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(3): Show | 6 | HG01099.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+5361G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318083 | ||||||
| chr6:99318191
|
G | A | 1 | a0001c0001t0044g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.823+5253C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318191 | ||||||
| chr6:99318213
|
G | A | 17 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(14): Show | 17 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.823+5231C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318213 | ||||||
| chr6:99318222
|
G | A | 2 | a0001c0001t0053g0269a0001c0001t0140g0265 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.823+5222C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318222 | ||||||
| chr6:99318236
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.823+5208C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318236 | ||||||
| chr6:99318258
|
C | CAA | 28 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0032others(25): Show | 29 | HG01256.hp2 HG01891.hp2 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.823+5184_823+5185d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318258 | ||||||
| chr6:99318260
|
A | AAAAC | 26 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0027others(23): Show | 27 | HG00642.hp1 HG01081.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.823+5183_823+5184i others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AAAACAC | 24 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0349others(21): Show | 24 | HG01123.hp2 HG01243.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.823+5183_823+5184i others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AAAACACA others(1): Show |
24 | a0001c0001t0002g0001a0001c0001t0002g0208a0001c0001t0002g0303others(21): Show | 26 | HG00738.hp1 HG01099.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.823+5183_823+5184i others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AAAACACA others(3): Show |
13 | a0001c0001t0002g0013a0001c0001t0002g0279a0001c0001t0002g0301others(10): Show | 14 | HG00544.hp2 HG02015.hp2 HG03225.hp2 others(11): Show |
intron_variant | MODIFIER | c.823+5183_823+5184i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AAAACACA others(5): Show |
2 | a0001c0001t0109g0188a0001c0004t0150g0382 | 2 | HG02622.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.823+5183_823+5184i others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AAAACACA others(7): Show |
2 | a0001c0001t0004g0308a0001c0001t0108g0187 | 2 | HG02523.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.823+5183_823+5184i others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AAAACACA others(9): Show |
1 | a0001c0001t0021g0252 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.823+5183_823+5184i others(18): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AAACACAC others(4): Show |
1 | a0001c0001t0131g0309 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.823+5183_823+5184i others(13): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AAC | 8 | a0001c0001t0003g0189a0001c0002t0003g0190a0001c0002t0003g0196others(5): Show | 8 | HG00280.hp1 HG00642.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+5182_823+5183d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AACAC | 6 | a0001c0001t0003g0378a0001c0002t0003g0191a0001c0002t0003g0193others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+5180_823+5183d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
A | AACACACA others(5): Show |
1 | a0001c0001t0023g0232 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.823+5172_823+5183d others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
AAC | A | 65 | a0001c0001t0001g0043a0001c0001t0007g0291a0001c0001t0008g0126others(62): Show | 68 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.823+5182_823+5183d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
AACAC | A | 9 | a0001c0001t0003g0282a0001c0001t0029g0095a0001c0001t0043g0132others(6): Show | 9 | HG01358.hp1 HG02055.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+5180_823+5183d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
AACACAC | A | 19 | a0001c0001t0008g0143a0001c0001t0008g0147a0001c0001t0008g0148others(16): Show | 19 | HG00558.hp2 HG02074.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.823+5178_823+5183d others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
AACACACA others(1): Show |
A | 8 | a0001c0001t0012g0271a0001c0001t0012g0272a0001c0001t0012g0273others(5): Show | 8 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+5176_823+5183d others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318260
|
AACACACA others(3): Show |
A | 9 | a0001c0001t0051g0262a0001c0001t0051g0268a0001c0001t0082g0084others(6): Show | 9 | HG01975.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+5174_823+5183d others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318260 | ||||||
| chr6:99318262
|
C | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(126): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.823+5182G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318262 | ||||||
| chr6:99318264
|
C | A | 65 | a0001c0001t0001g0043a0001c0001t0007g0291a0001c0001t0008g0126others(62): Show | 68 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.823+5180G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318264 | ||||||
| chr6:99318266
|
C | A | 9 | a0001c0001t0003g0282a0001c0001t0029g0095a0001c0001t0043g0132others(6): Show | 9 | HG01358.hp1 HG02055.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+5178G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318266 | ||||||
| chr6:99318268
|
C | A | 19 | a0001c0001t0008g0143a0001c0001t0008g0147a0001c0001t0008g0148others(16): Show | 19 | HG00558.hp2 HG02074.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.823+5176G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318268 | ||||||
| chr6:99318270
|
C | A | 8 | a0001c0001t0012g0271a0001c0001t0012g0272a0001c0001t0012g0273others(5): Show | 8 | HG00735.hp2 HG01099.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+5174G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318270 | ||||||
| chr6:99318272
|
C | A | 9 | a0001c0001t0051g0262a0001c0001t0051g0268a0001c0001t0082g0084others(6): Show | 9 | HG01975.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+5172G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318272 | ||||||
| chr6:99318298
|
C | A | 1 | a0001c0001t0045g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.823+5146G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318298 | ||||||
| chr6:99318300
|
C | A | 3 | a0001c0001t0005g0096a0001c0001t0019g0155a0001c0001t0045g0092 | 3 | HG01496.hp2 HG03209.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.823+5144G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318300 | ||||||
| chr6:99318300
|
C | CAAAA | 5 | a0001c0001t0005g0088a0001c0001t0005g0089a0001c0001t0024g0091others(2): Show | 5 | HG00673.hp2 HG01952.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+5143_823+5144i others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318300 | ||||||
| chr6:99318302
|
C | A | 8 | a0001c0001t0005g0088a0001c0001t0005g0089a0001c0001t0005g0096others(5): Show | 8 | HG00673.hp2 HG01496.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+5142G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318302 | ||||||
| chr6:99318302
|
C | CAAAA | 6 | a0001c0001t0019g0158a0001c0001t0019g0159a0001c0001t0019g0172others(3): Show | 6 | HG01106.hp1 HG01981.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+5141_823+5142i others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318302 | ||||||
| chr6:99318304
|
C | A | 15 | a0001c0001t0005g0088a0001c0001t0005g0089a0001c0001t0005g0096others(12): Show | 15 | HG00673.hp2 HG01106.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.823+5140G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318304 | ||||||
| chr6:99318304
|
C | CAAAA | 10 | a0001c0001t0019g0156a0001c0001t0024g0182a0001c0001t0024g0183others(7): Show | 10 | HG00323.hp2 HG01109.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.823+5139_823+5140i others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318304 | ||||||
| chr6:99318304
|
C | CAAAAAA | 6 | a0001c0001t0005g0161a0001c0001t0025g0157a0001c0001t0025g0162others(3): Show | 6 | HG01192.hp2 HG02738.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+5139_823+5140i others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318304 | ||||||
| chr6:99318304
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0018g0069a0001c0001t0018g0071 | 2 | HG00621.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.823+5139_823+5140i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318304 | ||||||
| chr6:99318306
|
C | A | 42 | a0001c0001t0005g0088a0001c0001t0005g0089a0001c0001t0005g0096others(39): Show | 43 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.823+5138G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CAAAAAA | 4 | a0001c0001t0005g0007a0001c0001t0005g0178a0001c0001t0005g0179others(1): Show | 5 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+5137_823+5138i others(8): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CAAAAAAA others(5): Show |
5 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0070others(2): Show | 5 | NA18949.hp1 NA18978.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+5137_823+5138i others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACAAAAA others(1): Show |
5 | a0001c0001t0007g0230a0001c0001t0015g0245a0001c0001t0022g0229others(2): Show | 5 | HG02257.hp2 HG03669.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+5137_823+5138i others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACAAAAA others(3): Show |
3 | a0001c0001t0015g0247a0001c0001t0015g0248a0001c0001t0024g0184 | 3 | HG00609.hp2 HG02074.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.823+5137_823+5138i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACACAAA others(1): Show |
5 | a0001c0001t0007g0220a0001c0001t0021g0226a0001c0001t0026g0239others(2): Show | 5 | HG01123.hp1 HG01361.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+5137_823+5138i others(10): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACACAAA others(3): Show |
13 | a0001c0001t0004g0228a0001c0001t0005g0177a0001c0001t0007g0244others(10): Show | 14 | HG00140.hp1 HG00621.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+5137_823+5138i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACACACA others(2): Show |
6 | a0001c0001t0028g0099a0001c0001t0028g0102a0001c0001t0042g0101others(3): Show | 7 | HG02630.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+5137_823+5138i others(11): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACACACA others(3): Show |
3 | a0001c0001t0021g0256a0001c0001t0054g0231a0001c0001t0054g0238 | 3 | HG01256.hp1 HG01258.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.823+5137_823+5138i others(12): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACACACA others(4): Show |
1 | a0001c0001t0007g0241 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.823+5137_823+5138i others(13): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACACACA others(5): Show |
1 | a0001c0001t0023g0237 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.823+5137_823+5138i others(14): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACACACA others(7): Show |
1 | a0001c0001t0007g0225 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.823+5137_823+5138i others(16): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318306
|
C | CACACACA others(9): Show |
1 | a0001c0001t0021g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.823+5137_823+5138i others(18): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | ||||||
| chr6:99318426
|
AG | A | 5 | a0001c0001t0035g0281a0001c0001t0035g0296a0001c0001t0035g0299others(2): Show | 5 | HG01433.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.823+5017delC | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318426 | ||||||
| chr6:99318663
|
A | C | 1 | a0001c0001t0077g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.823+4781T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318663 | ||||||
| chr6:99318870
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.823+4574G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318870 | ||||||
| chr6:99319163
|
C | T | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.823+4281G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319163 | ||||||
| chr6:99319190
|
G | A | 97 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(94): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.823+4254C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319190 | ||||||
| chr6:99319316
|
G | A | 3 | a0001c0001t0006g0343a0001c0001t0053g0269a0001c0001t0140g0265 | 3 | HG02165.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.823+4128C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319316 | ||||||
| chr6:99319323
|
C | T | 1 | a0001c0001t0014g0344 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.823+4121G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319323 | ||||||
| chr6:99319331
|
G | A | 2 | a0001c0001t0053g0269a0001c0001t0140g0265 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.823+4113C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319331 | ||||||
| chr6:99319341
|
G | C | 1 | a0001c0001t0102g0111 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.823+4103C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319341 | ||||||
| chr6:99319374
|
G | A | 5 | a0001c0001t0005g0170a0001c0001t0012g0010a0001c0001t0073g0168others(2): Show | 6 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+4070C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319374 | ||||||
| chr6:99319374
|
G | T | 2 | a0001c0001t0053g0269a0001c0001t0140g0265 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.823+4070C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319374 | ||||||
| chr6:99319377
|
C | T | 4 | a0001c0001t0021g0379a0001c0001t0029g0095a0001c0001t0052g0257others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+4067G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319377 | ||||||
| chr6:99319378
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(199): Show | 209 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.823+4066C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319378 | ||||||
| chr6:99319398
|
C | CA | 43 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0058others(40): Show | 44 | HG00280.hp2 HG00609.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.823+4045dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319398 | ||||||
| chr6:99319398
|
CA | C | 18 | a0001c0001t0010g0114a0001c0001t0012g0270a0001c0001t0012g0271others(15): Show | 18 | HG01099.hp2 HG01256.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.823+4045delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319398 | ||||||
| chr6:99319398
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0021g0379a0001c0001t0029g0095a0001c0001t0052g0257 | 3 | HG02055.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.823+4035_823+4045d others(13): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319398 | ||||||
| chr6:99319508
|
T | C | 1 | a0001c0001t0008g0148 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.823+3936A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319508 | ||||||
| chr6:99319525
|
A | G | 1 | a0001c0001t0029g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.823+3919T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319525 | ||||||
| chr6:99319529
|
C | T | 2 | a0001c0001t0108g0187a0001c0001t0109g0188 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.823+3915G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319529 | ||||||
| chr6:99319599
|
G | A | 96 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(93): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.823+3845C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319599 | ||||||
| chr6:99319650
|
G | C | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+3794C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99319650 | ||||||
| chr6:99320357
|
G | T | 7 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(4): Show | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+3087C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99320357 | ||||||
| chr6:99320394
|
C | A | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.823+3050G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99320394 | ||||||
| chr6:99320396
|
TTTTG | T | 4 | a0001c0001t0082g0084a0001c0001t0100g0082a0001c0001t0103g0083others(1): Show | 4 | HG01081.hp1 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+3044_823+3047d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99320396 | ||||||
| chr6:99320558
|
G | A | 1 | a0001c0001t0021g0252 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.823+2886C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99320558 | ||||||
| chr6:99320644
|
T | A | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+2800A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99320644 | ||||||
| chr6:99321018
|
T | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(259): Show | 271 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.823+2426A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321018 | ||||||
| chr6:99321056
|
G | C | 1 | a0001c0001t0052g0257 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.823+2388C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321056 | ||||||
| chr6:99321129
|
C | G | 1 | a0001c0001t0009g0012 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.823+2315G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321129 | ||||||
| chr6:99321160
|
G | A | 97 | a0001c0001t0003g0189a0001c0001t0004g0228a0001c0001t0005g0007others(94): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.823+2284C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321160 | ||||||
| chr6:99321743
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.823+1701C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321743 | ||||||
| chr6:99321860
|
A | T | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+1584T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321860 | ||||||
| chr6:99321865
|
T | C | 2 | a0001c0001t0053g0269a0001c0001t0140g0265 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.823+1579A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321865 | ||||||
| chr6:99321944
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.823+1500C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321944 | ||||||
| chr6:99321946
|
C | T | 4 | a0001c0001t0021g0379a0001c0001t0029g0095a0001c0001t0052g0257others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1498G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99321946 | ||||||
| chr6:99322052
|
A | G | 1 | a0001c0001t0016g0026 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.823+1392T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322052 | ||||||
| chr6:99322213
|
A | G | 36 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(33): Show | 37 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.823+1231T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322213 | ||||||
| chr6:99322384
|
C | T | 2 | a0001c0001t0053g0269a0001c0001t0140g0265 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.823+1060G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322384 | ||||||
| chr6:99322421
|
C | T | 6 | a0001c0001t0017g0021a0001c0001t0017g0025a0001c0001t0017g0050others(3): Show | 6 | HG02080.hp1 NA18943.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+1023G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322421 | ||||||
| chr6:99322443
|
A | C | 101 | a0001c0001t0003g0189a0001c0001t0004g0228a0001c0001t0005g0007others(98): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.823+1001T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322443 | ||||||
| chr6:99322484
|
G | A | 1 | a0001c0001t0075g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.823+960C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322484 | ||||||
| chr6:99322646
|
C | G | 1 | a0001c0001t0146g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.823+798G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322646 | ||||||
| chr6:99322818
|
C | T | 1 | a0001c0001t0014g0374 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.823+626G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322818 | ||||||
| chr6:99322944
|
C | G | 1 | a0001c0001t0011g0113 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.823+500G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99322944 | ||||||
| chr6:99323216
|
C | G | 1 | a0001c0001t0021g0379 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.823+228G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99323216 | ||||||
| chr6:99323224
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.823+220C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99323224 | ||||||
| chr6:99323321
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(88): Show | 94 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.823+123A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99323321 | ||||||
| chr6:99323705
|
G | T | 2 | a0001c0001t0056g0258a0001c0001t0056g0259 | 2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.600-38C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99323705 | ||||||
| chr6:99323727
|
T | C | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.600-60A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99323727 | ||||||
| chr6:99323947
|
C | T | 1 | a0001c0001t0019g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.600-280G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99323947 | ||||||
| chr6:99324019
|
G | A | 4 | a0001c0001t0022g0371a0001c0001t0032g0078a0001c0001t0047g0003others(1): Show | 5 | HG02895.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.600-352C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324019 | ||||||
| chr6:99324181
|
C | A | 1 | a0001c0002t0003g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.600-514G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324181 | ||||||
| chr6:99324197
|
T | TA | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.600-531dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324197 | ||||||
| chr6:99324324
|
T | C | 364 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(361): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.600-657A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324324 | ||||||
| chr6:99324464
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.600-797A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324464 | ||||||
| chr6:99324498
|
T | C | 56 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(53): Show | 57 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.600-831A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324498 | ||||||
| chr6:99324545
|
G | A | 6 | a0001c0001t0005g0170a0001c0001t0012g0010a0001c0001t0073g0168others(3): Show | 7 | HG00140.hp1 HG00280.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.600-878C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324545 | ||||||
| chr6:99324720
|
G | A | 6 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(3): Show | 6 | HG01099.hp2 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.600-1053C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324720 | ||||||
| chr6:99324778
|
G | A | 1 | a0001c0001t0066g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.600-1111C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324778 | ||||||
| chr6:99324940
|
G | A | 8 | a0001c0001t0028g0097a0001c0001t0028g0099a0001c0001t0028g0102others(5): Show | 9 | HG02630.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.600-1273C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324940 | ||||||
| chr6:99324983
|
G | A | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.600-1316C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324983 | ||||||
| chr6:99325104
|
G | GT | 338 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(335): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.600-1438dupA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325104 | ||||||
| chr6:99325229
|
T | C | 1 | a0001c0001t0104g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.600-1562A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325229 | ||||||
| chr6:99325305
|
G | A | 1 | a0001c0001t0122g0354 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.600-1638C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325305 | ||||||
| chr6:99325541
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(54): Show | 59 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.600-1874G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325541 | ||||||
| chr6:99325546
|
C | A | 4 | a0001c0001t0021g0379a0001c0001t0034g0277a0001c0001t0052g0257others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-1879G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325546 | ||||||
| chr6:99325561
|
C | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(281): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.600-1894G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325561 | ||||||
| chr6:99325565
|
T | C | 1 | a0001c0001t0014g0357 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.600-1898A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325565 | ||||||
| chr6:99325676
|
G | A | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.600-2009C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325676 | ||||||
| chr6:99325944
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.600-2277G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325944 | ||||||
| chr6:99325953
|
C | A | 3 | a0001c0001t0082g0084a0001c0001t0100g0082a0001c0001t0103g0083 | 3 | HG02258.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.600-2286G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325953 | ||||||
| chr6:99325953
|
C | T | 4 | a0001c0001t0021g0379a0001c0001t0034g0277a0001c0001t0052g0257others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-2286G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325953 | ||||||
| chr6:99326032
|
C | T | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.600-2365G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326032 | ||||||
| chr6:99326033
|
G | A | 1 | a0001c0001t0023g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.600-2366C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326033 | ||||||
| chr6:99326086
|
G | A | 1 | a0001c0001t0051g0268 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.600-2419C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326086 | ||||||
| chr6:99326150
|
T | G | 3 | a0001c0001t0024g0091a0001c0001t0045g0092a0001c0001t0147g0211 | 3 | HG01496.hp2 HG01952.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.600-2483A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326150 | ||||||
| chr6:99326154
|
G | A | 1 | a0001c0001t0021g0252 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.600-2487C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326154 | ||||||
| chr6:99326365
|
G | C | 80 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(77): Show | 82 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.600-2698C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326365 | ||||||
| chr6:99326393
|
C | G | 1 | a0001c0001t0098g0112 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.600-2726G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326393 | ||||||
| chr6:99326520
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 93 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(90): Show |
intron_variant | MODIFIER | c.600-2853A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326520 | ||||||
| chr6:99326551
|
T | C | 1 | a0001c0001t0052g0355 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.600-2884A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326551 | ||||||
| chr6:99326566
|
C | T | 364 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(361): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.600-2899G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326566 | ||||||
| chr6:99326658
|
C | T | 364 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(361): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.600-2991G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326658 | ||||||
| chr6:99326716
|
C | T | 80 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(77): Show | 82 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.600-3049G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326716 | ||||||
| chr6:99326811
|
G | C | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.600-3144C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326811 | ||||||
| chr6:99326841
|
C | T | 2 | a0001c0001t0007g0230a0001c0001t0022g0229 | 2 | NA18977.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.600-3174G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326841 | ||||||
| chr6:99326845
|
G | C | 1 | a0001c0001t0075g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.600-3178C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326845 | ||||||
| chr6:99326865
|
C | T | 3 | a0001c0001t0114g0283a0001c0001t0137g0222a0001c0001t0146g0223 | 3 | HG02486.hp2 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.600-3198G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326865 | ||||||
| chr6:99327088
|
C | T | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.600-3421G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99327088 | ||||||
| chr6:99327112
|
C | T | 1 | a0001c0001t0052g0257 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.600-3445G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99327112 | ||||||
| chr6:99327319
|
T | C | 4 | a0001c0001t0021g0379a0001c0001t0034g0277a0001c0001t0052g0257others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-3652A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99327319 | ||||||
| chr6:99328049
|
T | C | 5 | a0001c0001t0002g0306a0001c0001t0002g0359a0001c0001t0002g0361others(2): Show | 5 | HG00738.hp1 HG01106.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.600-4382A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328049 | ||||||
| chr6:99328107
|
A | G | 2 | a0001c0001t0012g0010a0001c0001t0073g0168 | 3 | HG00280.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.600-4440T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328107 | ||||||
| chr6:99328158
|
C | G | 10 | a0001c0001t0005g0007a0001c0001t0005g0177a0001c0001t0005g0178others(7): Show | 11 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.600-4491G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328158 | ||||||
| chr6:99328508
|
A | G | 181 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(178): Show | 187 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.600-4841T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328508 | ||||||
| chr6:99328683
|
C | T | 102 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(99): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.599+4668G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328683 | ||||||
| chr6:99328714
|
C | T | 98 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(95): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.599+4637G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328714 | ||||||
| chr6:99328768
|
C | A | 1 | a0001c0001t0147g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.599+4583G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328768 | ||||||
| chr6:99328796
|
A | T | 7 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(4): Show | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.599+4555T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328796 | ||||||
| chr6:99328809
|
G | C | 3 | a0001c0001t0034g0274a0001c0001t0116g0264a0001c0001t0118g0263 | 3 | HG00735.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.599+4542C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328809 | ||||||
| chr6:99328859
|
C | G | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.599+4492G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328859 | ||||||
| chr6:99328876
|
C | T | 3 | a0001c0001t0051g0262a0001c0001t0051g0268a0001c0001t0113g0267 | 3 | HG02559.hp1 HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.599+4475G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328876 | ||||||
| chr6:99329007
|
C | T | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.599+4344G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329007 | ||||||
| chr6:99329018
|
G | A | 2 | a0001c0001t0006g0356a0001c0001t0014g0357 | 2 | NA18967.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.599+4333C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329018 | ||||||
| chr6:99329024
|
G | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(258): Show | 269 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.599+4327C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329024 | ||||||
| chr6:99329110
|
A | G | 161 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(158): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.599+4241T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329110 | ||||||
| chr6:99329190
|
T | C | 1 | a0001c0001t0067g0047 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.599+4161A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329190 | ||||||
| chr6:99329287
|
G | T | 1 | a0001c0001t0078g0138 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.599+4064C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329287 | ||||||
| chr6:99329384
|
T | TTAA | 7 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(4): Show | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.599+3964_599+3966d others(5): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329384 | ||||||
| chr6:99329747
|
A | G | 4 | a0001c0001t0021g0379a0001c0001t0034g0277a0001c0001t0052g0257others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+3604T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329747 | ||||||
| chr6:99329749
|
T | G | 1 | a0001c0001t0146g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.599+3602A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329749 | ||||||
| chr6:99329750
|
T | G | 1 | a0001c0001t0146g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.599+3601A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329750 | ||||||
| chr6:99329752
|
T | A | 1 | a0001c0001t0146g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.599+3599A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99329752 | ||||||
| chr6:99330010
|
C | T | 5 | a0001c0001t0005g0170a0001c0001t0012g0010a0001c0001t0073g0168others(2): Show | 6 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.599+3341G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330010 | ||||||
| chr6:99330029
|
C | T | 1 | a0001c0001t0007g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.599+3322G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330029 | ||||||
| chr6:99330041
|
G | A | 1 | a0001c0001t0078g0138 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.599+3310C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330041 | ||||||
| chr6:99330071
|
G | T | 2 | a0001c0001t0008g0149a0001c0001t0085g0108 | 2 | NA19006.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.599+3280C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330071 | ||||||
| chr6:99330169
|
A | G | 1 | a0001c0001t0022g0285 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.599+3182T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330169 | ||||||
| chr6:99330342
|
G | A | 4 | a0001c0001t0021g0379a0001c0001t0034g0277a0001c0001t0052g0257others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+3009C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330342 | ||||||
| chr6:99330417
|
C | G | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.599+2934G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330417 | ||||||
| chr6:99330529
|
C | T | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.599+2822G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330529 | ||||||
| chr6:99330623
|
G | T | 1 | a0001c0001t0032g0105 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.599+2728C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330623 | ||||||
| chr6:99330689
|
C | T | 102 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(99): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.599+2662G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330689 | ||||||
| chr6:99330814
|
G | T | 2 | a0001c0001t0034g0277a0001c0001t0052g0257 | 2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.599+2537C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99330814 | ||||||
| chr6:99331065
|
C | T | 2 | a0001c0001t0004g0228a0001c0001t0139g0254 | 2 | NA18984.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.599+2286G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99331065 | ||||||
| chr6:99331130
|
C | T | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.599+2221G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99331130 | ||||||
| chr6:99331348
|
A | T | 1 | a0001c0001t0102g0111 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.599+2003T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99331348 | ||||||
| chr6:99331635
|
A | C | 1 | a0001c0001t0147g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.599+1716T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99331635 | ||||||
| chr6:99331639
|
G | A | 5 | a0001c0001t0002g0306a0001c0001t0002g0359a0001c0001t0002g0361others(2): Show | 5 | HG00738.hp1 HG01106.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.599+1712C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99331639 | ||||||
| chr6:99331968
|
T | C | 1 | a0002c0005t0070g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.599+1383A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99331968 | ||||||
| chr6:99332062
|
C | G | 1 | a0001c0001t0039g0023 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.599+1289G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99332062 | ||||||
| chr6:99332387
|
C | T | 1 | a0001c0001t0022g0284 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.599+964G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99332387 | ||||||
| chr6:99332565
|
C | T | 59 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(56): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.599+786G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99332565 | ||||||
| chr6:99332616
|
G | A | 89 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(86): Show | 93 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.599+735C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99332616 | ||||||
| chr6:99332646
|
C | G | 17 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(14): Show | 17 | HG00735.hp2 HG01099.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.599+705G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99332646 | ||||||
| chr6:99332710
|
T | C | 63 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(60): Show | 65 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.599+641A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99332710 | ||||||
| chr6:99332757
|
C | A | 1 | a0001c0001t0005g0161 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.599+594G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99332757 | ||||||
| chr6:99333154
|
T | C | 4 | a0001c0001t0021g0379a0001c0001t0034g0277a0001c0001t0052g0257others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+197A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99333154 | ||||||
| chr6:99333198
|
T | A | 1 | a0001c0001t0081g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.599+153A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99333198 | ||||||
| chr6:99333208
|
A | G | 1 | a0001c0004t0150g0382 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.599+143T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99333208 | ||||||
| chr6:99333242
|
G | A | 2 | a0001c0001t0026g0011a0001c0001t0026g0253 | 3 | HG01515.hp1 HG01517.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599+109C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99333242 | ||||||
| chr6:99333342
|
G | A | 100 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(97): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.599+9C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99333342 | ||||||
| chr6:99333774
|
G | A | 4 | a0001c0001t0021g0379a0001c0001t0034g0277a0001c0001t0052g0257others(1): Show | 4 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-227C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99333774 | ||||||
| chr6:99333798
|
G | A | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.403-251C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99333798 | ||||||
| chr6:99333810
|
C | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(174): Show | 183 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.403-263G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99333810 | ||||||
| chr6:99333869
|
T | C | 1 | a0001c0001t0135g0362 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.403-322A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99333869 | ||||||
| chr6:99334069
|
T | C | 1 | a0001c0001t0003g0378 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.403-522A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99334069 | ||||||
| chr6:99334132
|
A | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.403-585T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99334132 | ||||||
| chr6:99334567
|
C | T | 3 | a0001c0001t0082g0084a0001c0001t0100g0082a0001c0001t0103g0083 | 3 | HG02258.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.403-1020G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99334567 | ||||||
| chr6:99334994
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.403-1447G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99334994 | ||||||
| chr6:99335003
|
A | C | 97 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(94): Show | 102 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.403-1456T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335003 | ||||||
| chr6:99335212
|
G | A | 7 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(4): Show | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.403-1665C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335212 | ||||||
| chr6:99335250
|
A | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(46): Show | 50 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.403-1703T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335250 | ||||||
| chr6:99335349
|
A | T | 62 | a0001c0001t0008g0126a0001c0001t0008g0127a0001c0001t0008g0128others(59): Show | 64 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.403-1802T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335349 | ||||||
| chr6:99335462
|
T | A | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.403-1915A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335462 | ||||||
| chr6:99335955
|
A | G | 15 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(12): Show | 15 | HG00735.hp2 HG01099.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.403-2408T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335955 | ||||||
| chr6:99335956
|
C | A | 1 | a0001c0001t0001g0054 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.403-2409G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335956 | ||||||
| chr6:99335957
|
A | C | 1 | a0001c0001t0001g0054 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.403-2410T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335957 | ||||||
| chr6:99335958
|
T | A | 1 | a0001c0001t0001g0054 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.403-2411A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99335958 | ||||||
| chr6:99336145
|
G | T | 1 | a0001c0002t0003g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.403-2598C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99336145 | ||||||
| chr6:99336746
|
G | C | 105 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(102): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.403-3199C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99336746 | ||||||
| chr6:99336820
|
C | T | 1 | a0001c0001t0072g0167 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.403-3273G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99336820 | ||||||
| chr6:99337103
|
T | A | 105 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(102): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.403-3556A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337103 | ||||||
| chr6:99337203
|
T | C | 1 | a0001c0001t0005g0161 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.403-3656A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337203 | ||||||
| chr6:99337239
|
T | C | 1 | a0001c0001t0034g0274 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.403-3692A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337239 | ||||||
| chr6:99337241
|
T | C | 5 | a0001c0001t0017g0021a0001c0001t0017g0050a0001c0001t0017g0051others(2): Show | 5 | HG02080.hp1 NA18943.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.403-3694A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337241 | ||||||
| chr6:99337256
|
GA | G | 169 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(166): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.403-3710delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337256 | ||||||
| chr6:99337478
|
C | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.403-3931G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337478 | ||||||
| chr6:99337574
|
T | C | 1 | a0001c0001t0005g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403-4027A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337574 | ||||||
| chr6:99337798
|
T | A | 10 | a0001c0001t0028g0097a0001c0001t0028g0099a0001c0001t0028g0102others(7): Show | 11 | HG02630.hp2 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.403-4251A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337798 | ||||||
| chr6:99338041
|
A | G | 1 | a0001c0001t0011g0110 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.403-4494T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338041 | ||||||
| chr6:99338112
|
C | T | 1 | a0001c0001t0075g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403-4565G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338112 | ||||||
| chr6:99338236
|
T | A | 1 | a0001c0001t0008g0149 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.402+4662A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338236 | ||||||
| chr6:99338527
|
G | A | 1 | a0001c0001t0002g0363 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.402+4371C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338527 | ||||||
| chr6:99338550
|
A | G | 181 | a0001c0001t0003g0189a0001c0001t0004g0228a0001c0001t0005g0007others(178): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.402+4348T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338550 | ||||||
| chr6:99338677
|
T | A | 15 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(12): Show | 15 | HG00735.hp2 HG01099.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.402+4221A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338677 | ||||||
| chr6:99338681
|
C | G | 3 | a0001c0001t0114g0283a0001c0001t0137g0222a0001c0001t0146g0223 | 3 | HG02486.hp2 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.402+4217G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338681 | ||||||
| chr6:99338708
|
A | C | 3 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210 | 3 | HG02129.hp2 NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.402+4190T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338708 | ||||||
| chr6:99338797
|
T | C | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.402+4101A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338797 | ||||||
| chr6:99338811
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.402+4087A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338811 | ||||||
| chr6:99338960
|
C | A | 180 | a0001c0001t0003g0189a0001c0001t0004g0228a0001c0001t0005g0007others(177): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.402+3938G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99338960 | ||||||
| chr6:99339068
|
C | G | 5 | a0001c0001t0051g0262a0001c0001t0051g0268a0001c0001t0112g0266others(2): Show | 5 | HG02559.hp1 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+3830G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99339068 | ||||||
| chr6:99339636
|
A | G | 4 | a0001c0001t0082g0084a0001c0001t0100g0082a0001c0001t0103g0083others(1): Show | 4 | HG02258.hp2 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+3262T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99339636 | ||||||
| chr6:99339674
|
T | C | 361 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(358): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.402+3224A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99339674 | ||||||
| chr6:99339674
|
T | G | 1 | a0001c0001t0040g0065 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.402+3224A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99339674 | ||||||
| chr6:99339730
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(93): Show | 101 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.402+3168A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99339730 | ||||||
| chr6:99340102
|
A | G | 1 | a0001c0001t0021g0255 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.402+2796T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340102 | ||||||
| chr6:99340116
|
T | C | 1 | a0001c0001t0016g0022 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.402+2782A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340116 | ||||||
| chr6:99340146
|
C | T | 3 | a0001c0001t0034g0277a0001c0001t0037g0276a0001c0001t0052g0257 | 3 | HG02055.hp1 HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.402+2752G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340146 | ||||||
| chr6:99340214
|
C | T | 1 | a0001c0001t0140g0265 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.402+2684G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340214 | ||||||
| chr6:99340224
|
C | T | 184 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(181): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.402+2674G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340224 | ||||||
| chr6:99340288
|
A | C | 16 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(13): Show | 16 | HG00735.hp2 HG01099.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.402+2610T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340288 | ||||||
| chr6:99340309
|
C | A | 2 | a0001c0001t0137g0222a0001c0001t0146g0223 | 2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.402+2589G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340309 | ||||||
| chr6:99340420
|
A | C | 2 | a0001c0001t0025g0154a0001c0001t0044g0153 | 2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.402+2478T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340420 | ||||||
| chr6:99340531
|
T | TC | 184 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(181): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.402+2366dupG | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340531 | ||||||
| chr6:99340597
|
G | A | 15 | a0001c0001t0008g0143a0001c0001t0008g0147a0001c0001t0008g0148others(12): Show | 15 | HG00558.hp2 HG02074.hp2 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.402+2301C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340597 | ||||||
| chr6:99340666
|
CT | C | 33 | a0001c0001t0007g0225a0001c0001t0012g0270a0001c0001t0012g0271others(30): Show | 34 | HG00621.hp2 HG01074.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.402+2231delA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340666 | ||||||
| chr6:99340666
|
CTT | C | 156 | a0001c0001t0001g0020a0001c0001t0001g0057a0001c0001t0001g0058others(153): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.402+2230_402+2231d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340666 | ||||||
| chr6:99340666
|
CTTT | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(155): Show | 163 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.402+2229_402+2231d others(5): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340666 | ||||||
| chr6:99340666
|
CTTTT | C | 12 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0002g0365others(9): Show | 13 | HG01255.hp1 HG01261.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.402+2228_402+2231d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340666 | ||||||
| chr6:99340711
|
C | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(173): Show | 182 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.402+2187G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340711 | ||||||
| chr6:99340964
|
C | T | 2 | a0001c0001t0002g0303a0001c0001t0014g0302 | 2 | HG02015.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.402+1934G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340964 | ||||||
| chr6:99341096
|
C | T | 37 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(34): Show | 39 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.402+1802G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341096 | ||||||
| chr6:99341115
|
T | C | 6 | a0001c0001t0004g0014a0001c0001t0004g0366a0001c0001t0004g0367others(3): Show | 7 | HG01255.hp1 HG01261.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+1783A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341115 | ||||||
| chr6:99341171
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.402+1727A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341171 | ||||||
| chr6:99341204
|
TAGAA | T | 184 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(181): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.402+1690_402+1693d others(6): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341204 | ||||||
| chr6:99341312
|
A | C | 1 | a0001c0001t0031g0104 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.402+1586T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341312 | ||||||
| chr6:99341329
|
C | G | 1 | a0001c0001t0007g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.402+1569G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341329 | ||||||
| chr6:99341387
|
C | T | 2 | a0001c0001t0137g0222a0001c0001t0146g0223 | 2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.402+1511G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341387 | ||||||
| chr6:99341623
|
A | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.402+1275T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341623 | ||||||
| chr6:99341677
|
T | C | 1 | a0001c0001t0022g0371 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.402+1221A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341677 | ||||||
| chr6:99341706
|
A | C | 1 | a0001c0001t0002g0301 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.402+1192T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341706 | ||||||
| chr6:99341898
|
AATG | A | 184 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(181): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.402+997_402+999del others(3): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341898 | ||||||
| chr6:99341933
|
T | C | 1 | a0001c0001t0036g0376 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.402+965A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99341933 | ||||||
| chr6:99342103
|
A | C | 6 | a0001c0001t0003g0189a0001c0001t0005g0088a0001c0001t0005g0089others(3): Show | 6 | HG00673.hp2 HG01257.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+795T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342103 | ||||||
| chr6:99342144
|
T | C | 1 | a0001c0001t0049g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.402+754A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342144 | ||||||
| chr6:99342198
|
A | C | 1 | a0001c0001t0064g0018 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.402+700T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342198 | ||||||
| chr6:99342268
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(175): Show | 184 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.402+630T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342268 | ||||||
| chr6:99342346
|
CT | C | 14 | a0001c0001t0001g0054a0001c0001t0009g0300a0001c0001t0012g0275others(11): Show | 14 | HG01099.hp2 HG01516.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.402+551delA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342346 | ||||||
| chr6:99342478
|
G | A | 1 | a0001c0001t0008g0152 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.402+420C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342478 | ||||||
| chr6:99342583
|
A | G | 3 | a0001c0001t0082g0084a0001c0001t0100g0082a0001c0001t0103g0083 | 3 | HG02258.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.402+315T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342583 | ||||||
| chr6:99342586
|
C | T | 20 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(17): Show | 20 | HG00735.hp2 HG01099.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.402+312G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342586 | ||||||
| chr6:99342663
|
G | T | 101 | a0001c0001t0004g0228a0001c0001t0005g0007a0001c0001t0005g0088others(98): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.402+235C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342663 | ||||||
| chr6:99342677
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | NA18953.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.402+221G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342677 | ||||||
| chr6:99342814
|
G | C | 1 | a0001c0001t0074g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.402+84C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342814 | ||||||
| chr6:99342854
|
T | C | 1 | a0001c0001t0019g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.402+44A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99342854 | ||||||
| chr6:99343067
|
C | T | 1 | a0001c0001t0060g0280 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.267-34G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99343067 | ||||||
| chr6:99343260
|
T | TATTACCA | 95 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0208others(92): Show | 100 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.267-234_267-228dup others(7): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99343260 | ||||||
| chr6:99343379
|
G | A | 1 | a0001c0001t0022g0371 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.267-346C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99343379 | ||||||
| chr6:99343391
|
T | C | 185 | a0001c0001t0003g0189a0001c0001t0004g0228a0001c0001t0005g0007others(182): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.267-358A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99343391 | ||||||
| chr6:99343533
|
T | C | 1 | a0001c0001t0105g0079 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.267-500A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99343533 | ||||||
| chr6:99343554
|
G | A | 37 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(34): Show | 39 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.267-521C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99343554 | ||||||
| chr6:99344065
|
C | T | 185 | a0001c0001t0003g0189a0001c0001t0004g0228a0001c0001t0005g0007others(182): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.267-1032G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344065 | ||||||
| chr6:99344273
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.267-1240G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344273 | ||||||
| chr6:99344376
|
G | C | 185 | a0001c0001t0003g0189a0001c0001t0004g0228a0001c0001t0005g0007others(182): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.267-1343C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344376 | ||||||
| chr6:99344397
|
G | A | 21 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(18): Show | 21 | HG00323.hp2 HG00621.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.267-1364C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344397 | ||||||
| chr6:99344662
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(175): Show | 184 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.267-1629C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344662 | ||||||
| chr6:99344754
|
C | T | 1 | a0001c0001t0077g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.267-1721G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344754 | ||||||
| chr6:99344923
|
C | T | 1 | a0001c0001t0010g0086 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.267-1890G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344923 | ||||||
| chr6:99345002
|
C | T | 363 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(360): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.267-1969G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345002 | ||||||
| chr6:99345183
|
C | T | 1 | a0001c0001t0002g0279 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.267-2150G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345183 | ||||||
| chr6:99345253
|
A | G | 148 | a0001c0001t0003g0189a0001c0001t0005g0007a0001c0001t0005g0088others(145): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.267-2220T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345253 | ||||||
| chr6:99345302
|
T | C | 1 | a0001c0001t0005g0161 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.267-2269A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345302 | ||||||
| chr6:99345351
|
C | T | 148 | a0001c0001t0003g0189a0001c0001t0005g0007a0001c0001t0005g0088others(145): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.267-2318G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345351 | ||||||
| chr6:99345399
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(212): Show | 223 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.267-2366A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345399 | ||||||
| chr6:99345598
|
C | A | 1 | a0001c0001t0063g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.267-2565G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345598 | ||||||
| chr6:99345634
|
A | C | 48 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(45): Show | 50 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.267-2601T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345634 | ||||||
| chr6:99345700
|
T | C | 1 | a0001c0001t0109g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.267-2667A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345700 | ||||||
| chr6:99345739
|
G | A | 148 | a0001c0001t0005g0007a0001c0001t0005g0088a0001c0001t0005g0089others(145): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.267-2706C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345739 | ||||||
| chr6:99345780
|
A | C | 3 | a0001c0001t0034g0277a0001c0001t0037g0276a0001c0001t0052g0257 | 3 | HG02055.hp1 HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.267-2747T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345780 | ||||||
| chr6:99345948
|
T | C | 39 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(36): Show | 41 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.267-2915A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345948 | ||||||
| chr6:99346326
|
T | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(164): Show | 173 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.266+2781A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346326 | ||||||
| chr6:99346534
|
G | A | 20 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(17): Show | 20 | HG00735.hp2 HG01099.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.266+2573C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346534 | ||||||
| chr6:99346562
|
TG | T | 313 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(310): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.266+2544delC | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346562 | ||||||
| chr6:99346565
|
G | T | 4 | a0001c0001t0005g0170a0001c0001t0082g0084a0001c0001t0100g0082others(1): Show | 4 | HG02258.hp2 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.266+2542C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346565 | ||||||
| chr6:99346566
|
G | T | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.266+2541C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346566 | ||||||
| chr6:99346573
|
T | G | 1 | a0001c0001t0005g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.266+2534A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346573 | ||||||
| chr6:99346574
|
G | T | 313 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(310): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.266+2533C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346574 | ||||||
| chr6:99346591
|
C | T | 314 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(311): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.266+2516G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346591 | ||||||
| chr6:99346612
|
A | AG | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.266+2494dupC | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346612 | ||||||
| chr6:99346647
|
G | A | 127 | a0001c0001t0005g0007a0001c0001t0005g0088a0001c0001t0005g0089others(124): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.266+2460C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346647 | ||||||
| chr6:99346669
|
G | A | 1 | a0001c0001t0066g0056 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.266+2438C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346669 | ||||||
| chr6:99346690
|
G | A | 3 | a0001c0001t0034g0277a0001c0001t0037g0276a0001c0001t0052g0257 | 3 | HG02055.hp1 HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.266+2417C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346690 | ||||||
| chr6:99346690
|
G | C | 7 | a0001c0001t0018g0066a0001c0001t0018g0068a0001c0001t0018g0069others(4): Show | 7 | HG00621.hp2 NA18949.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+2417C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346690 | ||||||
| chr6:99346697
|
G | A | 9 | a0001c0001t0013g0213a0001c0001t0013g0214a0001c0001t0013g0215others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.266+2410C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346697 | ||||||
| chr6:99347023
|
A | C | 1 | a0001c0001t0124g0278 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.266+2084T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347023 | ||||||
| chr6:99347079
|
T | C | 5 | a0001c0001t0025g0162a0001c0001t0025g0163a0001c0001t0030g0165others(2): Show | 5 | HG01192.hp2 HG02738.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+2028A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347079 | ||||||
| chr6:99347107
|
T | TA | 37 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(34): Show | 39 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.266+1999dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347107 | ||||||
| chr6:99347108
|
A | T | 2 | a0001c0001t0137g0222a0001c0001t0146g0223 | 2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.266+1999T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347108 | ||||||
| chr6:99347166
|
C | T | 1 | a0001c0001t0007g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.266+1941G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347166 | ||||||
| chr6:99347219
|
C | T | 39 | a0001c0001t0004g0228a0001c0001t0007g0220a0001c0001t0007g0221others(36): Show | 41 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.266+1888G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347219 | ||||||
| chr6:99347331
|
G | C | 5 | a0001c0001t0005g0170a0001c0001t0072g0167a0001c0001t0073g0168others(2): Show | 5 | HG00280.hp2 HG01243.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.266+1776C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347331 | ||||||
| chr6:99347406
|
GA | G | 49 | a0001c0001t0004g0228a0001c0001t0007g0221a0001c0001t0007g0224others(46): Show | 51 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.266+1700delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347406 | ||||||
| chr6:99347406
|
GAA | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(282): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.266+1699_266+1700d others(4): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347406 | ||||||
| chr6:99347406
|
GAAA | G | 28 | a0001c0001t0012g0270a0001c0001t0012g0271a0001c0001t0012g0272others(25): Show | 28 | HG00735.hp2 HG01099.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.266+1698_266+1700d others(5): Show |
FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347406 | ||||||
| chr6:99347423
|
G | T | 1 | a0001c0001t0052g0257 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.266+1684C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347423 | ||||||
| chr6:99347492
|
T | C | 5 | a0001c0001t0014g0374a0001c0001t0018g0071a0001c0001t0036g0376others(2): Show | 5 | HG00621.hp2 HG02735.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+1615A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347492 | ||||||
| chr6:99347502
|
A | G | 9 | a0001c0001t0013g0213a0001c0001t0013g0214a0001c0001t0013g0215others(6): Show | 9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.266+1605T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347502 | ||||||
| chr6:99347552
|
A | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.266+1555T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347552 | ||||||
| chr6:99347682
|
T | C | 1 | a0001c0001t0021g0379 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.266+1425A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347682 | ||||||
| chr6:99347713
|
A | G | 8 | a0001c0001t0032g0078a0001c0001t0042g0075a0001c0001t0047g0003others(5): Show | 9 | HG01109.hp2 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.266+1394T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347713 | ||||||
| chr6:99347766
|
T | A | 3 | a0001c0001t0033g0173a0001c0001t0033g0175a0001c0001t0049g0174 | 3 | NA18957.hp2 NA19079.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.266+1341A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99347766 | ||||||
| chr6:99348147
|
G | A | 314 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(311): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.266+960C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348147 | ||||||
| chr6:99348400
|
C | T | 1 | a0002c0005t0070g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.266+707G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348400 | ||||||
| chr6:99348402
|
A | C | 1 | a0002c0005t0070g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.266+705T>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348402 | ||||||
| chr6:99348479
|
C | T | 1 | a0001c0001t0074g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.266+628G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348479 | ||||||
| chr6:99348572
|
C | A | 1 | a0002c0005t0070g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.266+535G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348572 | ||||||
| chr6:99348573
|
A | T | 1 | a0002c0005t0070g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.266+534T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348573 | ||||||
| chr6:99348596
|
C | T | 1 | a0001c0001t0003g0378 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.266+511G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348596 | ||||||
| chr6:99348703
|
T | C | 1 | a0001c0001t0027g0377 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.266+404A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348703 | ||||||
| chr6:99348802
|
T | C | 1 | a0001c0001t0003g0378 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.266+305A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348802 | ||||||
| chr6:99348859
|
C | G | 1 | a0001c0001t0075g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.266+248G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348859 | ||||||
| chr6:99348881
|
G | C | 1 | a0001c0001t0032g0176 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.266+226C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348881 | ||||||
| chr6:99348909
|
G | A | 1 | a0001c0001t0021g0379 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.266+198C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348909 | ||||||
| chr6:99348918
|
C | G | 3 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210 | 3 | HG02129.hp2 NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.266+189G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348918 | ||||||
| chr6:99348946
|
G | T | 1 | a0002c0005t0070g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.266+161C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348946 | ||||||
| chr6:99348982
|
T | C | 1 | a0001c0001t0138g0380 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.266+125A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99348982 | ||||||
| chr6:99349010
|
T | G | 361 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(358): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.266+97A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99349010 | ||||||
| chr6:99349011
|
T | G | 1 | a0002c0005t0070g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.266+96A>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99349011 | ||||||
| chr6:99349012
|
G | C | 10 | a0001c0001t0005g0007a0001c0001t0005g0177a0001c0001t0005g0178others(7): Show | 11 | HG00099.hp2 HG00140.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.266+95C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99349012 | ||||||
| chr6:99349085
|
C | A | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(3): Show | 6 | NA18949.hp2 NA18950.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.266+22G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99349085 |