Item | Value |
---|---|
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 | 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 | MHWGV others(404): Show |
chr6 | 99266168 | 99354674 |
a0002 | 0/0 | 409 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | MHWGV others(404): Show |
chr6 | 99266168 | 99354674 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1227 | 374 | 81 | 62 | 171 | 16 | 43 | FAXC_chr6_99266168_99354674 | FAXC | ATGCA others(1222): Show |
chr6 | 99266168 | 99354674 | ||
a0001c0002 | 1/0 | 1227 | 21 | 1 | 15 | 0 | 2 | 2 | FAXC_chr6_99266168_99354674 | FAXC | ATGCA others(1222): Show |
chr6 | 99266168 | 99354674 | ||
a0001c0003 | 0/0 | 1227 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | ATGCA others(1222): Show |
chr6 | 99266168 | 99354674 | ||
a0001c0004 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | ATGCA others(1222): Show |
chr6 | 99266168 | 99354674 | ||
a0002c0005 | 0/0 | 1227 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | ATGCA others(1222): Show |
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 | GGCCT others(11503): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0002 | 0/0 | 11531 | 26 | 0 | 6 | 18 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0003 | 0/0 | 11528 | 4 | 0 | 3 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11523): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0004 | 0/0 | 11508 | 12 | 0 | 9 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11503): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0005 | 0/0 | 11521 | 11 | 3 | 2 | 2 | 3 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0006 | 0/0 | 11533 | 11 | 0 | 4 | 7 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11528): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0007 | 0/0 | 11538 | 10 | 0 | 0 | 10 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11533): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0008 | 0/0 | 11537 | 8 | 0 | 0 | 8 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11532): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0009 | 0/0 | 11535 | 8 | 0 | 1 | 4 | 0 | 3 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0010 | 0/0 | 11535 | 7 | 0 | 0 | 7 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0011 | 0/0 | 11545 | 7 | 0 | 0 | 5 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11540): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0012 | 0/0 | 11522 | 7 | 4 | 3 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11517): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0013 | 0/0 | 11513 | 7 | 7 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11508): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0014 | 0/0 | 11527 | 6 | 1 | 0 | 4 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11522): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0015 | 0/0 | 11536 | 6 | 0 | 0 | 5 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11531): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0016 | 0/0 | 11533 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11528): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0017 | 0/0 | 11508 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11503): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0018 | 0/0 | 11538 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11533): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0019 | 0/1 | 11522 | 5 | 0 | 2 | 0 | 1 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11517): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0020 | 0/0 | 11539 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11534): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0021 | 0/0 | 11517 | 5 | 1 | 2 | 0 | 2 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11512): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0022 | 0/0 | 11540 | 5 | 1 | 0 | 3 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11535): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0023 | 0/0 | 11534 | 5 | 0 | 0 | 5 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11529): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0024 | 0/0 | 11523 | 4 | 2 | 1 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11518): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0025 | 0/0 | 11524 | 4 | 0 | 0 | 1 | 0 | 3 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11519): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0026 | 0/0 | 11519 | 4 | 0 | 1 | 0 | 2 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11514): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0027 | 0/0 | 11529 | 4 | 0 | 1 | 1 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11524): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0028 | 0/0 | 11524 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11519): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0029 | 0/0 | 11520 | 3 | 1 | 1 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11515): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0030 | 0/0 | 11522 | 3 | 0 | 0 | 1 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11517): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0031 | 0/0 | 11547 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11542): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0032 | 0/0 | 11541 | 3 | 1 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11536): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0033 | 0/0 | 11535 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0034 | 0/0 | 11518 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11513): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0035 | 0/0 | 11529 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11524): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0036 | 0/0 | 11525 | 3 | 0 | 0 | 2 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11520): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0037 | 0/0 | 11521 | 3 | 3 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0038 | 0/0 | 11519 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11514): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0039 | 0/0 | 11542 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11537): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0040 | 0/0 | 11540 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11535): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0041 | 0/0 | 11521 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0042 | 0/0 | 11534 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11529): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0043 | 0/0 | 11528 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11523): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0044 | 0/0 | 11526 | 2 | 1 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11521): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0045 | 0/0 | 11511 | 2 | 0 | 1 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11506): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0046 | 0/0 | 11535 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0047 | 0/0 | 11543 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11538): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0048 | 0/0 | 11533 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11528): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0049 | 0/0 | 11540 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11535): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0050 | 0/0 | 11529 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11524): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0051 | 0/0 | 11521 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0052 | 0/0 | 11518 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11513): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0053 | 0/0 | 11516 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11511): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0054 | 0/0 | 11517 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11512): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0055 | 0/0 | 11537 | 2 | 0 | 0 | 1 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11532): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0056 | 0/0 | 11533 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11528): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0057 | 0/0 | 11531 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0058 | 0/0 | 11542 | 2 | 1 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11537): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0059 | 0/0 | 11537 | 2 | 1 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11532): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0060 | 0/0 | 11541 | 2 | 1 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11536): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0061 | 0/0 | 11535 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0062 | 0/0 | 11533 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11528): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0063 | 0/0 | 11516 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11511): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0064 | 0/0 | 11539 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11534): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0065 | 0/0 | 11508 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11503): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0066 | 0/0 | 11508 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11503): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0067 | 0/0 | 11544 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11539): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0068 | 0/0 | 11540 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11535): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0069 | 0/0 | 11534 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11529): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0071 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0072 | 0/0 | 11538 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11533): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0073 | 0/0 | 11525 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11520): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0074 | 0/0 | 11519 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11514): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0075 | 0/0 | 11523 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11518): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0076 | 0/0 | 11526 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11521): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0077 | 0/0 | 11524 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11519): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0078 | 0/0 | 11538 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11533): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0079 | 0/0 | 11536 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11531): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0080 | 0/0 | 11534 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11529): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0081 | 0/0 | 11534 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11529): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0082 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11527): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0083 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0084 | 0/0 | 11537 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11532): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0085 | 0/0 | 11541 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11536): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0086 | 0/0 | 11535 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0087 | 0/0 | 11539 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11534): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0088 | 0/0 | 11537 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11532): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0089 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0090 | 0/0 | 11537 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11532): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0091 | 0/0 | 11527 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11522): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0092 | 0/0 | 11537 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11532): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0093 | 0/0 | 11533 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11528): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0094 | 0/0 | 11529 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11524): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0095 | 0/0 | 11527 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11522): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0096 | 0/0 | 11544 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11539): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0097 | 0/0 | 11544 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11539): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0098 | 0/0 | 11539 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11534): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0099 | 0/0 | 11542 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11537): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0100 | 0/0 | 11535 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0101 | 0/0 | 11543 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11538): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0102 | 0/0 | 11538 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11533): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0103 | 0/0 | 11531 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0104 | 0/0 | 11534 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11529): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0105 | 0/0 | 11532 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11527): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0106 | 0/0 | 11522 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11517): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0107 | 0/0 | 11501 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11496): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0108 | 0/0 | 11531 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0109 | 0/0 | 11527 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11522): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0110 | 0/0 | 11543 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11538): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0111 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11508): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0112 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0113 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0114 | 0/0 | 11517 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11512): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0115 | 0/0 | 11517 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11512): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0116 | 0/0 | 11529 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11524): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0117 | 0/0 | 11521 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0118 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11515): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0119 | 0/0 | 11517 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11512): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0120 | 0/0 | 11521 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11516): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0122 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0123 | 0/0 | 11536 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11531): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0124 | 0/0 | 11534 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11529): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0125 | 0/0 | 11539 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11534): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0126 | 0/0 | 11531 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0127 | 0/0 | 11531 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0128 | 0/0 | 11527 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11522): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0129 | 0/0 | 11523 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11518): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0130 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0131 | 0/0 | 11525 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11520): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0132 | 0/0 | 11533 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11528): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0133 | 0/0 | 11526 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11521): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0134 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11508): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0135 | 0/0 | 11523 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11518): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0136 | 0/0 | 11508 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11503): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0137 | 0/0 | 11519 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11514): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0138 | 0/0 | 11536 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11531): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0139 | 0/0 | 11531 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0140 | 0/0 | 11544 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11539): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0141 | 0/0 | 11542 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11537): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0143 | 0/0 | 11530 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11525): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0145 | 0/0 | 11534 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11529): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0146 | 0/0 | 11529 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11524): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0147 | 0/0 | 11526 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11521): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0148 | 0/0 | 11538 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11533): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0149 | 0/0 | 11540 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11535): Show |
chr6 | 99266168 | 99354674 |
a0001c0001t0151 | 0/0 | 11544 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11539): Show |
chr6 | 99266168 | 99354674 |
a0001c0002t0003 | 1/0 | 11528 | 16 | 1 | 12 | 0 | 1 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11523): Show |
chr6 | 99266168 | 99354674 |
a0001c0002t0004 | 0/0 | 11508 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11503): Show |
chr6 | 99266168 | 99354674 |
a0001c0002t0121 | 0/0 | 11508 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11503): Show |
chr6 | 99266168 | 99354674 |
a0001c0002t0142 | 0/0 | 11532 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11527): Show |
chr6 | 99266168 | 99354674 |
a0001c0002t0144 | 0/0 | 11526 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11521): Show |
chr6 | 99266168 | 99354674 |
a0001c0003t0057 | 0/0 | 11531 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11526): Show |
chr6 | 99266168 | 99354674 |
a0001c0004t0150 | 0/0 | 11535 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
a0002c0005t0070 | 0/0 | 11535 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | GGCCT others(11530): Show |
chr6 | 99266168 | 99354674 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 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 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0001g0056 | 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 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0299 | 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 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 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 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0004g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0005g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0006g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0006g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0006g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0006g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0006g0341 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0006g0344 | 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 |
a0001c0001t0006g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0006g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0007g0239 | 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 |
a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0008g0125 | 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 |
a0001c0001t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0008g0142 | 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 |
a0001c0001t0009g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0009g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0009g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0009g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0009g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0009g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0010g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0010g0118 | 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 |
a0001c0001t0011g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0011g0112 | 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 |
a0001c0001t0012g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0012g0269 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0001t0012g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0013g0212 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0001t0013g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0014g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0014g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0014g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0014g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0014g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0014g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0015g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0015g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0015g0243 | 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 |
a0001c0001t0015g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0015g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0016g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0016g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0016g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0016g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0017g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0017g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0017g0049 | 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 |
a0001c0001t0018g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0018g0067 | 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 |
a0001c0001t0019g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0019g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0019g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0019g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0020g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0020g0120 | 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 |
a0001c0001t0020g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0020g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0021g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0021g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0021g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0021g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0021g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0022g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0022g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0022g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0022g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0022g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0023g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0023g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0023g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0023g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0023g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0024g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0024g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0024g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0024g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0025g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0025g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0025g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0026g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0026g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0026g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0027g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0027g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0027g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0027g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0028g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0028g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0028g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0029g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0029g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0029g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0030g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0030g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0031g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0031g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0031g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0032g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0032g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0032g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0033g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0033g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0033g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0034g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0034g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0034g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0035g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0035g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0035g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0036g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0036g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0036g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0037g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0037g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0037g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0038g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0038g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0039g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0039g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0040g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0040g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0041g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0041g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0042g0074 | 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 |
a0001c0001t0043g0130 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0044g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0044g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0045g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0045g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0046g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0046g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0047g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0048g0079 | 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 |
a0001c0001t0049g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0049g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0050g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0051g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0051g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0052g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0052g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0053g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0053g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0054g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0054g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0055g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0055g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0056g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0056g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0057g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0058g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0058g0285 | 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 |
a0001c0001t0060g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0060g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0061g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0062g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0063g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0064g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0065g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0066g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0067g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0068g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0069g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0071g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0072g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0073g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0074g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0075g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0076g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0077g0073 | 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 |
a0001c0001t0079g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0080g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0081g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0082g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0083g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0084g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0085g0107 | 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 |
a0001c0001t0088g0170 | 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 |
a0001c0001t0091g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0092g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0093g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0094g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0095g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0096g0132 | 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 |
a0001c0001t0098g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0099g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0100g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0101g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0102g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0103g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0104g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0105g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0106g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0107g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0108g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0109g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0110g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0111g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0112g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0113g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0114g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0115g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0116g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0117g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0118g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0119g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0120g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0122g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0123g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0124g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0125g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0126g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0127g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0128g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0129g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0130g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0131g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0132g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0133g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0134g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0135g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0136g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0137g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0138g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0139g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0140g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0141g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0143g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0145g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0146g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0147g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0148g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0149g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0001t0151g0381 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0002t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0003g0189 | 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 |
a0001c0002t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
a0001c0002t0003g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0003g0202 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0002t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0121g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0142g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0002t0144g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0003t0057g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0001c0004t0150g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
a0002c0005t0070g0062 | 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 | g0286 | EUR | GBR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0178 | EUR | GBR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00140 | hp1 | a0001 | c0001 | t0117 | g0247 | EUR | GBR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0001 | EUR | GBR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00280 | hp1 | a0001 | c0002 | t0003 | g0194 | EUR | FIN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00280 | hp2 | a0001 | c0001 | t0073 | g0167 | EUR | FIN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00323 | hp1 | a0001 | c0001 | t0061 | g0016 | EUR | FIN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00323 | hp2 | a0001 | c0001 | t0019 | g0155 | EUR | FIN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00408 | hp1 | a0001 | c0001 | t0020 | g0115 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00408 | hp2 | a0001 | c0001 | t0122 | g0352 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00544 | hp1 | a0001 | c0001 | t0023 | g0230 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00558 | hp1 | a0001 | c0001 | t0092 | g0119 | 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 | g0135 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00609 | hp2 | a0001 | c0001 | t0015 | g0245 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00621 | hp1 | a0001 | c0001 | t0023 | g0249 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00621 | hp2 | a0001 | c0001 | t0018 | g0070 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0331 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00642 | hp2 | a0001 | c0002 | t0003 | g0198 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00673 | hp1 | a0001 | c0001 | t0102 | g0110 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00673 | hp2 | a0001 | c0001 | t0049 | g0102 | EAS | CHS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0376 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00735 | hp2 | a0001 | c0001 | t0116 | g0262 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0356 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0190 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG00741 | hp2 | a0001 | c0001 | t0021 | g0250 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01069 | hp2 | a0001 | c0001 | t0046 | g0117 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0009 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01074 | hp1 | a0001 | c0001 | t0046 | g0105 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0191 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0188 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0316 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01099 | hp2 | a0001 | c0001 | t0012 | g0273 | 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 | g0358 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01109 | hp1 | a0001 | c0001 | t0145 | g0291 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01109 | hp2 | a0001 | c0001 | t0101 | g0075 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01167 | hp1 | a0001 | c0001 | t0012 | g0011 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01167 | hp2 | a0001 | c0002 | t0004 | g0203 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01168 | hp1 | a0001 | c0001 | t0029 | g0179 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01168 | hp2 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01169 | hp1 | a0001 | c0001 | t0012 | g0011 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01169 | hp2 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0202 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01192 | hp2 | a0001 | c0001 | t0106 | g0163 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01243 | hp1 | a0001 | c0001 | t0057 | g0349 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01243 | hp2 | a0001 | c0001 | t0081 | g0168 | AMR | PUR | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0365 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01255 | hp2 | a0001 | c0002 | t0003 | g0009 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01256 | hp1 | a0001 | c0001 | t0054 | g0229 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01258 | hp1 | a0001 | c0001 | t0054 | g0236 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0192 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0368 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01358 | hp1 | a0001 | c0001 | t0060 | g0278 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0344 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01361 | hp2 | a0001 | c0001 | t0021 | g0224 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01433 | hp1 | a0001 | c0001 | t0128 | g0294 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01433 | hp2 | a0001 | c0001 | t0084 | g0129 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0196 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01496 | hp2 | a0001 | c0001 | t0045 | g0091 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01515 | hp1 | a0001 | c0001 | t0026 | g0012 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01515 | hp2 | a0001 | c0001 | t0024 | g0180 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01516 | hp1 | a0001 | c0001 | t0029 | g0183 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01516 | hp2 | a0001 | c0001 | t0021 | g0254 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01517 | hp1 | a0001 | c0001 | t0026 | g0012 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0176 | EUR | IBS | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01891 | hp1 | a0001 | c0001 | t0135 | g0360 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01891 | hp2 | a0001 | c0001 | t0013 | g0212 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01934 | hp1 | a0001 | c0002 | t0003 | g0204 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0359 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0302 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0364 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01952 | hp2 | a0001 | c0001 | t0024 | g0090 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01975 | hp2 | a0001 | c0003 | t0057 | g0305 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0333 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0366 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0337 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01981 | hp2 | a0001 | c0001 | t0019 | g0171 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01993 | hp2 | a0001 | c0001 | t0009 | g0330 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0367 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02004 | hp2 | a0001 | c0001 | t0132 | g0339 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02015 | hp1 | a0001 | c0001 | t0010 | g0118 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02015 | hp2 | a0001 | c0001 | t0014 | g0300 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02055 | hp1 | a0001 | c0001 | t0037 | g0274 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02055 | hp2 | a0001 | c0001 | t0029 | g0094 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02074 | hp1 | a0001 | c0001 | t0015 | g0246 | 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 | g0111 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0127 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02083 | hp2 | a0001 | c0001 | t0069 | g0033 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02129 | hp1 | a0001 | c0001 | t0008 | g0126 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02135 | hp1 | a0001 | c0001 | t0022 | g0282 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02145 | hp1 | a0001 | c0001 | t0037 | g0336 | 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 | g0089 | EAS | CDX | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02165 | hp2 | a0001 | c0001 | t0006 | g0341 | EAS | CDX | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02257 | hp1 | a0001 | c0001 | t0013 | g0211 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02257 | hp2 | a0001 | c0001 | t0042 | g0074 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02258 | hp1 | a0001 | c0001 | t0111 | g0259 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02258 | hp2 | a0001 | c0001 | t0082 | g0082 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0334 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0189 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02280 | hp1 | a0001 | c0001 | t0147 | g0209 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02280 | hp2 | a0001 | c0001 | t0013 | g0216 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02293 | hp2 | a0001 | c0002 | t0121 | g0197 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0357 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0205 | AMR | PEL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02451 | hp1 | a0001 | c0001 | t0056 | g0256 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02451 | hp2 | a0001 | c0001 | t0035 | g0295 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0306 | 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 | g0215 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02572 | hp2 | a0001 | c0001 | t0037 | g0284 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02602 | hp1 | a0001 | c0001 | t0074 | g0072 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02615 | hp1 | a0001 | c0001 | t0146 | g0221 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02615 | hp2 | a0001 | c0001 | t0024 | g0181 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02622 | hp1 | a0001 | c0001 | t0062 | g0047 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02622 | hp2 | a0001 | c0001 | t0109 | g0186 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02630 | hp1 | a0001 | c0001 | t0035 | g0297 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02630 | hp2 | a0001 | c0001 | t0083 | g0099 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02647 | hp1 | a0001 | c0001 | t0104 | g0092 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02647 | hp2 | a0001 | c0001 | t0079 | g0093 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02683 | hp1 | a0001 | c0001 | t0019 | g0157 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02683 | hp2 | a0001 | c0001 | t0055 | g0327 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02698 | hp1 | a0001 | c0001 | t0126 | g0323 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02698 | hp2 | a0001 | c0001 | t0068 | g0041 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02723 | hp1 | a0001 | c0001 | t0021 | g0377 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02723 | hp2 | a0001 | c0001 | t0050 | g0006 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02735 | hp1 | a0001 | c0001 | t0009 | g0298 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02735 | hp2 | a0001 | c0001 | t0148 | g0373 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02738 | hp1 | a0001 | c0001 | t0025 | g0161 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0280 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02809 | hp1 | a0001 | c0001 | t0028 | g0098 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02809 | hp2 | a0001 | c0001 | t0056 | g0257 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02886 | hp1 | a0001 | c0001 | t0013 | g0214 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02886 | hp2 | a0001 | c0001 | t0118 | g0261 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02895 | hp1 | a0001 | c0001 | t0047 | g0005 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02895 | hp2 | a0001 | c0001 | t0034 | g0272 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02896 | hp1 | a0001 | c0001 | t0052 | g0255 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02896 | hp2 | a0001 | c0001 | t0013 | g0213 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02922 | hp1 | a0001 | c0001 | t0103 | g0081 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0269 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02965 | hp1 | a0001 | c0001 | t0028 | g0096 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02965 | hp2 | a0001 | c0001 | t0051 | g0266 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0169 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02976 | hp2 | a0001 | c0001 | t0075 | g0071 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03017 | hp1 | a0001 | c0001 | t0015 | g0293 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03017 | hp2 | a0001 | c0001 | t0027 | g0370 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0270 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03041 | hp2 | a0001 | c0001 | t0113 | g0265 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03098 | hp1 | a0001 | c0001 | t0032 | g0077 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03098 | hp2 | a0001 | c0001 | t0120 | g0371 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03130 | hp1 | a0001 | c0001 | t0058 | g0217 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03130 | hp2 | a0001 | c0001 | t0052 | g0353 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03209 | hp2 | a0001 | c0001 | t0028 | g0100 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03225 | hp1 | a0001 | c0001 | t0105 | g0078 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0372 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0195 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03239 | hp2 | a0001 | c0001 | t0149 | g0379 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0271 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03453 | hp2 | a0001 | c0001 | t0100 | g0083 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03486 | hp1 | a0001 | c0001 | t0044 | g0097 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03486 | hp2 | a0001 | c0001 | t0077 | g0073 | AFR | MSL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03490 | hp1 | a0001 | c0001 | t0066 | g0055 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03490 | hp2 | a0001 | c0001 | t0011 | g0007 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0177 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03491 | hp2 | a0001 | c0001 | t0009 | g0013 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03492 | hp1 | a0001 | c0001 | t0009 | g0013 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03492 | hp2 | a0001 | c0001 | t0011 | g0007 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03516 | hp1 | a0001 | c0001 | t0114 | g0281 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0268 | AFR | ESN | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03540 | hp1 | a0001 | c0001 | t0050 | g0006 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03540 | hp2 | a0001 | c0001 | t0072 | g0166 | AFR | GWD | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03579 | hp1 | a0001 | c0001 | t0034 | g0311 | 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 | g0342 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03654 | hp2 | a0001 | c0001 | t0030 | g0164 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03669 | hp1 | a0001 | c0001 | t0115 | g0244 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03669 | hp2 | a0001 | c0001 | t0125 | g0322 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03688 | hp1 | a0001 | c0001 | t0080 | g0159 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03688 | hp2 | a0001 | c0001 | t0110 | g0292 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03710 | hp1 | a0001 | c0002 | t0144 | g0201 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03710 | hp2 | a0001 | c0001 | t0067 | g0046 | SAS | PJL | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03831 | hp1 | a0001 | c0001 | t0039 | g0040 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03831 | hp2 | a0001 | c0001 | t0025 | g0153 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03834 | hp1 | a0001 | c0001 | t0025 | g0162 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03834 | hp2 | a0001 | c0001 | t0136 | g0318 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03927 | hp2 | a0001 | c0001 | t0063 | g0054 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03942 | hp1 | a0001 | c0001 | t0039 | g0024 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0348 | SAS | BEB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG04115 | hp1 | a0001 | c0001 | t0093 | g0084 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG04115 | hp2 | a0001 | c0001 | t0030 | g0165 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG04199 | hp1 | a0001 | c0001 | t0022 | g0283 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG04199 | hp2 | a0001 | c0001 | t0036 | g0374 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG04204 | hp2 | a0001 | c0001 | t0058 | g0285 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG04228 | hp1 | a0001 | c0001 | t0044 | g0152 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG04228 | hp2 | a0001 | c0001 | t0027 | g0338 | SAS | STU | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18522 | hp1 | a0001 | c0001 | t0134 | g0210 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18522 | hp2 | a0001 | c0001 | t0047 | g0005 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18612 | hp1 | a0001 | c0001 | t0023 | g0289 | EAS | CHB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18612 | hp2 | a0001 | c0001 | t0008 | g0125 | EAS | CHB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18747 | hp1 | a0001 | c0001 | t0064 | g0019 | EAS | CHB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18747 | hp2 | a0001 | c0001 | t0041 | g0086 | EAS | CHB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18906 | hp1 | a0001 | c0001 | t0060 | g0287 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18906 | hp2 | a0001 | c0001 | t0076 | g0076 | 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 | g0114 | 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 | g0314 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18941 | hp1 | a0001 | c0001 | t0027 | g0324 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18941 | hp2 | a0001 | c0001 | t0010 | g0113 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18942 | hp1 | a0001 | c0001 | t0022 | g0240 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18942 | hp2 | a0001 | c0001 | t0043 | g0131 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18943 | hp1 | a0001 | c0001 | t0017 | g0050 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18943 | hp2 | a0001 | c0001 | t0006 | g0351 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18944 | hp1 | a0001 | c0001 | t0133 | g0340 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18944 | hp2 | a0001 | c0001 | t0007 | g0232 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18946 | hp1 | a0001 | c0001 | t0015 | g0243 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18948 | hp2 | a0001 | c0001 | t0015 | g0233 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18949 | hp1 | a0001 | c0001 | t0018 | g0067 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18950 | hp2 | a0001 | c0001 | t0032 | g0175 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18951 | hp1 | a0001 | c0001 | t0017 | g0026 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0343 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18952 | hp2 | a0001 | c0001 | t0017 | g0049 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18956 | hp1 | a0001 | c0001 | t0007 | g0241 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18956 | hp2 | a0001 | c0001 | t0129 | g0345 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18957 | hp2 | a0001 | c0001 | t0033 | g0172 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0218 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18959 | hp2 | a0001 | c0001 | t0016 | g0027 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18961 | hp1 | a0001 | c0001 | t0016 | g0032 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18961 | hp2 | a0001 | c0001 | t0007 | g0223 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18962 | hp1 | a0001 | c0001 | t0065 | g0048 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18964 | hp1 | a0001 | c0001 | t0016 | g0031 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18964 | hp2 | a0001 | c0001 | t0010 | g0085 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18966 | hp1 | a0001 | c0001 | t0033 | g0080 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18967 | hp1 | a0001 | c0001 | t0007 | g0248 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18967 | hp2 | a0001 | c0001 | t0014 | g0355 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18969 | hp1 | a0001 | c0001 | t0036 | g0335 | 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 | g0310 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18970 | hp2 | a0001 | c0001 | t0030 | g0128 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18971 | hp1 | a0001 | c0001 | t0094 | g0143 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18974 | hp1 | a0001 | c0001 | t0032 | g0104 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18974 | hp2 | a0001 | c0001 | t0015 | g0234 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18975 | hp2 | a0001 | c0001 | t0023 | g0225 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0228 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18977 | hp2 | a0001 | c0001 | t0055 | g0346 | 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 | g0064 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18979 | hp1 | a0001 | c0004 | t0150 | g0380 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18979 | hp2 | a0001 | c0001 | t0022 | g0227 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18981 | hp2 | a0001 | c0001 | t0099 | g0106 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18982 | hp2 | a0001 | c0001 | t0011 | g0109 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18983 | hp2 | a0001 | c0001 | t0009 | g0317 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18984 | hp1 | a0001 | c0001 | t0014 | g0325 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18986 | hp2 | a0001 | c0001 | t0048 | g0079 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18988 | hp1 | a0001 | c0001 | t0095 | g0122 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18988 | hp2 | a0001 | c0001 | t0124 | g0276 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18989 | hp1 | a0001 | c0001 | t0138 | g0378 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18993 | hp1 | a0001 | c0001 | t0040 | g0066 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18993 | hp2 | a0001 | c0001 | t0017 | g0022 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18998 | hp1 | a0001 | c0001 | t0018 | g0065 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0313 | 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 | g0308 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19001 | hp1 | a0001 | c0001 | t0088 | g0170 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19002 | hp1 | a0001 | c0001 | t0009 | g0315 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19002 | hp2 | a0001 | c0001 | t0018 | g0068 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19003 | hp1 | a0001 | c0001 | t0007 | g0219 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19003 | hp2 | a0001 | c0001 | t0038 | g0035 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19004 | hp2 | a0001 | c0001 | t0031 | g0133 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19005 | hp1 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19005 | hp2 | a0001 | c0001 | t0007 | g0288 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19006 | hp1 | a0001 | c0001 | t0014 | g0321 | 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 | g0088 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19007 | hp2 | a0001 | c0001 | t0031 | g0103 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19009 | hp1 | a0001 | c0001 | t0018 | g0069 | 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 | g0235 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19010 | hp2 | a0001 | c0001 | t0025 | g0156 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19030 | hp1 | a0001 | c0001 | t0140 | g0263 | AFR | LWK | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0258 | AFR | LWK | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19043 | hp1 | a0001 | c0001 | t0151 | g0381 | AFR | LWK | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | LWK | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19054 | hp1 | a0001 | c0001 | t0006 | g0326 | 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 | g0362 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19055 | hp2 | a0001 | c0001 | t0139 | g0252 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19060 | hp1 | a0001 | c0001 | t0085 | g0107 | 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 | g0130 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19062 | hp2 | a0001 | c0001 | t0007 | g0239 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19063 | hp1 | a0001 | c0001 | t0008 | g0142 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19063 | hp2 | a0001 | c0001 | t0006 | g0309 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19065 | hp1 | a0001 | c0001 | t0011 | g0112 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0354 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19068 | hp1 | a0001 | c0001 | t0020 | g0124 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19070 | hp1 | a0001 | c0001 | t0020 | g0120 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19070 | hp2 | a0001 | c0001 | t0038 | g0020 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19078 | hp1 | a0001 | c0001 | t0123 | g0320 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19078 | hp2 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19079 | hp1 | a0001 | c0001 | t0033 | g0174 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19080 | hp2 | a0001 | c0001 | t0010 | g0008 | 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 | g0036 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19082 | hp1 | a0001 | c0001 | t0016 | g0023 | 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 | g0312 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19083 | hp2 | a0001 | c0001 | t0020 | g0134 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19084 | hp1 | a0001 | c0001 | t0009 | g0328 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19084 | hp2 | a0001 | c0001 | t0020 | g0121 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0319 | 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 | g0307 | 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 | g0108 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19089 | hp2 | a0001 | c0001 | t0096 | g0132 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19090 | hp1 | a0001 | c0001 | t0009 | g0347 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19090 | hp2 | a0001 | c0001 | t0031 | g0116 | EAS | JPT | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19091 | hp1 | a0001 | c0001 | t0049 | g0173 | 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 | g0264 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA19240 | hp2 | a0001 | c0001 | t0022 | g0369 | AFR | YRI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20129 | hp1 | a0001 | c0001 | t0053 | g0238 | AFR | ASW | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20129 | hp2 | a0001 | c0001 | t0053 | g0267 | AFR | ASW | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20752 | hp1 | a0001 | c0001 | t0021 | g0253 | EUR | TSI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20752 | hp2 | a0001 | c0002 | t0142 | g0200 | EUR | TSI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20805 | hp1 | a0001 | c0001 | t0119 | g0231 | EUR | TSI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20905 | hp1 | a0002 | c0005 | t0070 | g0062 | SAS | GIH | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20905 | hp2 | a0001 | c0001 | t0026 | g0251 | SAS | GIH | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01123 | hp1 | a0001 | c0001 | t0026 | g0237 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG01123 | hp2 | a0001 | c0001 | t0027 | g0375 | AMR | CLM | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02109 | hp1 | a0001 | c0001 | t0035 | g0279 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02109 | hp2 | a0001 | c0001 | t0034 | g0275 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02486 | hp1 | a0001 | c0001 | t0024 | g0182 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02486 | hp2 | a0001 | c0001 | t0137 | g0220 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02559 | hp1 | a0001 | c0001 | t0051 | g0260 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG02559 | hp2 | a0001 | c0001 | t0071 | g0063 | AFR | ACB | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0193 | AFR | USA | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
HG06807 | hp2 | a0001 | c0001 | t0127 | g0296 | AFR | USA | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20300 | hp1 | a0001 | c0001 | t0107 | g0184 | AFR | USA | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
NA20300 | hp2 | a0001 | c0001 | t0108 | g0185 | AFR | USA | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
homoSapiens | chm13v2 | a0001 | c0001 | t0019 | g0154 | REF | REF | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0199 | REF | REF | FAXC_chr6_99266168_99354674 | FAXC | chr6 | 99266168 | 99354674 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0001c0001 a0001c0003 a0001c0004 others(1): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): 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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0001c0001t0066 a0001c0001t0136 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(95): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): 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 | a0001c0001t0056 a0001c0001t0079 |
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 | a0001c0001t0035 a0001c0001t0081 a0001c0001t0082 others(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 | a0001c0001t0027 a0001c0001t0035 a0001c0001t0082 others(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 | a0001c0001t0002 a0001c0001t0042 a0001c0001t0057 others(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 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0056 others(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 | a0001c0001t0009 a0001c0001t0061 a0001c0001t0072 others(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 | a0001c0001t0055 a0001c0001t0148 |
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 | a0001c0001t0060 a0001c0001t0064 a0001c0001t0125 |
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 | a0001c0001t0010 a0001c0001t0033 a0001c0001t0046 others(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 | a0001c0001t0008 a0001c0001t0018 a0001c0001t0023 others(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 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0040 others(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 | a0001c0001t0007 a0001c0001t0032 a0001c0001t0078 others(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 | a0001c0001t0022 a0001c0001t0047 a0001c0001t0068 others(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 | a0001c0001t0011 a0001c0001t0039 a0001c0001t0058 others(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 | a0001c0001t0031 a0001c0001t0067 a0001c0001t0140 others(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 | a0001c0001t0036 a0001c0001t0043 a0001c0001t0050 others(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 | a0001c0001t0044 a0001c0001t0094 a0001c0001t0129 others(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 | a0001c0001t0012 a0001c0001t0025 a0001c0001t0028 others(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 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0026 others(12): Show |
28 | HG00323.hp2 HG01106.hp1 HG01123.hp1 others(25): 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 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0029 others(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 | a0001c0001t0063 a0001c0001t0074 |
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 | a0001c0001t0013 a0001c0001t0111 a0001c0001t0134 |
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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0017 others(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 | a0001c0001t0014 a0001c0001t0105 a0001c0001t0109 others(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 | a0001c0001t0036 a0001c0001t0043 a0001c0001t0131 others(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 | a0001c0001t0044 a0001c0001t0129 a0001c0001t0135 |
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 | a0001c0001t0012 a0001c0001t0025 a0001c0001t0028 others(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 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0026 others(12): Show |
28 | HG00323.hp2 HG01106.hp1 HG01123.hp1 others(25): 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 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0029 others(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 | a0001c0001t0063 a0001c0001t0074 |
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 | a0001c0001t0013 a0001c0001t0111 a0001c0001t0134 |
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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0017 others(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 | a0001c0001t0049 a0001c0001t0059 |
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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0017 others(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 | 4 | HG00323.hp2 HG01106.hp1 HG01981.hp2 others(1): 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 | a0001c0001t0050 a0001c0001t0147 |
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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(52): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): 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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(52): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): 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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(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 | a0001c0001t0100 a0001c0001t0101 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(90): Show |
253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): 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 | a0001c0001t0060 a0001c0001t0104 a0001c0001t0146 others(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 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0021 others(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 | a0001c0001t0017 a0001c0001t0065 |
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 | a0001c0001t0130 a0001c0001t0131 |
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 | a0001c0001t0051 a0001c0001t0075 a0001c0001t0113 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(141): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(141): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): 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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(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 | a0001c0001t0060 a0001c0001t0076 a0001c0001t0077 others(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 | a0001c0001t0013 a0001c0001t0019 a0001c0001t0021 others(25): Show |
60 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(57): 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(136): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): 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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0017 others(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 | a0001c0001t0100 a0001c0001t0101 |
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 | a0001c0001t0019 a0001c0001t0025 a0001c0001t0030 others(6): Show |
21 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(18): 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 | a0001c0001t0057 a0001c0003t0057 |
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 | a0001c0001t0060 a0001c0001t0104 a0001c0001t0105 others(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 | a0001c0001t0060 a0001c0001t0104 a0001c0001t0105 others(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 | a0001c0001t0100 a0001c0001t0101 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(95): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): 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 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0021 others(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 | a0001c0001t0019 a0001c0001t0025 a0001c0001t0030 others(5): Show |
20 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(17): 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 | a0001c0001t0100 a0001c0001t0101 |
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 | a0001c0001t0060 a0001c0001t0104 a0001c0001t0105 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(96): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): 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 | a0001c0001t0050 a0001c0001t0103 a0001c0001t0147 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(146): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0010 a0001c0001t0086 a0001c0001t0087 others(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 | a0001c0001t0060 a0001c0001t0104 a0001c0001t0105 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(96): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): 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 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(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 | a0001c0001t0060 a0001c0001t0104 a0001c0001t0105 others(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 | a0001c0001t0051 a0001c0001t0099 a0001c0001t0112 others(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 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(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 | a0001c0001t0046 a0001c0001t0084 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(91): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): 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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(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 | a0001c0001t0050 a0001c0001t0103 a0001c0001t0147 |
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 | a0001c0001t0060 a0001c0001t0104 a0001c0001t0105 others(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 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0018 others(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 | a0001c0001t0108 a0001c0001t0109 |
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 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(57): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): 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 | a0001c0001t0018 a0001c0001t0040 |
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 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0017 others(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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99281595 | G | GGTTC | 73 | a0001c0001t0005g0001 a0001c0001t0005g0087 a0001c0001t0005g0088 others(70): 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 | a0001c0001t0113g0265 | 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 | a0001c0001t0025g0156 | 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 | a0001c0001t0071g0063 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0024g0090 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(151): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.941-572C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99282025 | |||||||
chr6:99282079 | C | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(157): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): 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 | a0001c0001t0056g0256 a0001c0001t0056g0257 a0001c0001t0079g0093 |
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 | a0001c0001t0002g0303 a0001c0001t0027g0338 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0042g0074 a0001c0001t0042g0101 |
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 | a0001c0001t0022g0282 | 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 | a0001c0001t0021g0377 | 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 | 9 | a0001c0001t0005g0001 a0001c0001t0005g0176 a0001c0001t0005g0177 others(6): 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 | a0001c0001t0029g0094 a0001c0001t0114g0281 |
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 | a0001c0001t0007g0223 a0001c0001t0008g0125 a0001c0001t0008g0126 others(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 | a0001c0001t0007g0232 a0001c0001t0008g0127 a0001c0001t0010g0008 others(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 | a0001c0001t0116g0262 | 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 | a0001c0001t0060g0287 a0001c0001t0146g0221 a0001c0001t0148g0373 |
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 | a0001c0001t0003g0187 a0001c0001t0003g0280 a0001c0001t0003g0356 others(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 | a0001c0001t0002g0277 a0001c0001t0002g0332 a0001c0001t0002g0333 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0013g0212 | 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 | 13 | a0001c0001t0005g0176 a0001c0001t0013g0212 a0001c0001t0021g0254 others(10): Show |
13 | HG01358.hp1 HG01516.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.941-3145A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99284598 | |||||||
chr6:99284598 | T | TGA | 25 | a0001c0001t0005g0001 a0001c0001t0005g0177 a0001c0001t0007g0218 others(22): 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 | a0001c0001t0005g0087 a0001c0001t0005g0088 a0001c0001t0005g0095 others(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 | a0001c0001t0005g0160 a0001c0001t0005g0169 a0001c0001t0012g0268 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0039 others(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 |
27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0025 others(24): 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 | a0001c0001t0001g0052 a0001c0001t0017g0022 a0001c0001t0017g0049 others(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 | a0001c0001t0001g0021 | 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 | a0001c0001t0042g0074 a0001c0001t0042g0101 |
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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0021g0250 | 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 | a0001c0001t0133g0340 | 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 | a0001c0001t0029g0179 a0001c0001t0060g0278 a0001c0001t0060g0287 others(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 | a0001c0001t0100g0083 a0001c0001t0101g0075 |
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 | a0001c0001t0100g0083 a0001c0001t0101g0075 |
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 | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(346): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.941-3573dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99285025 | |||||||
chr6:99285098 | G | GC | 3 | a0001c0001t0028g0096 a0001c0001t0028g0098 a0001c0001t0028g0100 |
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 | a0001c0001t0151g0381 | 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 | a0001c0001t0021g0377 a0001c0001t0028g0096 a0001c0001t0028g0098 others(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 | a0001c0001t0021g0224 a0001c0001t0021g0250 a0001c0001t0021g0253 others(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 | a0001c0001t0002g0363 | 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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(77): Show |
83 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(80): 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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0118g0261 | 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 | a0001c0001t0015g0293 a0001c0001t0149g0379 |
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 | a0001c0001t0052g0353 | 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 | a0001c0001t0007g0218 a0001c0001t0007g0219 a0001c0001t0007g0222 others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0055g0346 | 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 | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(48): 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 | a0001c0001t0007g0218 a0001c0001t0007g0219 a0001c0001t0007g0222 others(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 | 21 | a0001c0001t0019g0155 a0001c0001t0019g0157 a0001c0001t0019g0158 others(18): Show |
21 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.940+4711T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 5/5 | chr6 | 99286993 | |||||||
chr6:99287136 | A | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(152): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): 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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0147g0209 |
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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | a0001c0002t0003g0195 a0001c0002t0003g0196 |
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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0040g0066 a0001c0001t0071g0063 |
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 | a0001c0001t0014g0372 | 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 | a0001c0001t0118g0261 | 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 | a0001c0001t0020g0115 | 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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(48): 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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0117g0247 | 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 | a0001c0001t0007g0218 a0001c0001t0007g0219 a0001c0001t0007g0222 others(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 | a0001c0001t0107g0184 | 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 | a0001c0001t0117g0247 | 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 | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(78): Show |
84 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(81): 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 | a0001c0001t0027g0338 | 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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0146g0221 others(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 | a0001c0001t0104g0092 | 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 | a0001c0001t0105g0078 | 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 | a0001c0001t0021g0224 a0001c0001t0026g0237 a0001c0001t0053g0238 |
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 | a0001c0001t0021g0250 a0001c0001t0021g0253 a0001c0001t0021g0254 others(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 | a0001c0001t0117g0247 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0021g0224 others(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 | a0001c0001t0003g0280 a0001c0001t0003g0356 a0001c0001t0003g0376 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0004g0306 others(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 |
22 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(19): 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 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0028 others(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 | a0001c0001t0005g0169 a0001c0001t0013g0211 a0001c0001t0013g0212 others(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 | a0001c0001t0012g0011 a0001c0001t0012g0268 a0001c0001t0012g0269 others(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 |
33 | a0001c0001t0005g0001 a0001c0001t0005g0087 a0001c0001t0005g0095 others(30): Show |
35 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(32): 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 | a0001c0001t0005g0088 a0001c0001t0019g0171 a0001c0001t0042g0101 others(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 | a0001c0001t0018g0068 a0001c0001t0018g0070 a0001c0001t0029g0094 |
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 | a0001c0001t0040g0066 a0001c0001t0075g0071 a0001c0001t0114g0281 |
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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0069 others(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 | a0001c0001t0042g0074 | 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 | a0001c0001t0118g0261 | 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 | a0001c0001t0125g0322 | 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 | a0001c0001t0007g0218 a0001c0001t0007g0219 a0001c0001t0007g0222 others(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 | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(152): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): 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 | a0001c0001t0100g0083 a0001c0001t0101g0075 |
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 | a0001c0001t0002g0304 | 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 | a0001c0001t0127g0296 | 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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0100g0083 a0001c0001t0101g0075 |
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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | 20 | a0001c0001t0010g0151 a0001c0001t0015g0246 a0001c0001t0019g0155 others(17): Show |
20 | HG00323.hp2 HG00558.hp2 HG01106.hp1 others(17): 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 | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(161): 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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0146g0221 | 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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0137g0220 others(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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0021g0377 a0001c0001t0028g0096 a0001c0001t0028g0098 others(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 | a0001c0001t0021g0224 a0001c0001t0021g0250 a0001c0001t0021g0253 others(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 | a0001c0001t0018g0070 | 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 | a0001c0001t0116g0262 | 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 | a0001c0001t0007g0218 | 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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0011g0144 a0001c0001t0031g0133 |
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 | a0001c0001t0002g0301 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0004g0334 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(73): Show |
80 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(77): 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 | 57 | a0001c0001t0002g0301 a0001c0001t0004g0306 a0001c0001t0004g0367 others(54): 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 | a0001c0001t0012g0273 a0001c0001t0018g0068 a0001c0001t0024g0090 others(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 | a0001c0001t0137g0220 | 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 | a0001c0001t0008g0127 | 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 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0013g0214 others(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 | a0001c0001t0013g0213 | 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 | a0001c0001t0002g0304 a0001c0001t0002g0357 a0001c0001t0002g0359 others(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 | a0001c0001t0111g0259 | 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 | a0001c0001t0104g0092 | 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 | a0001c0001t0007g0239 a0001c0001t0022g0240 |
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 | a0001c0001t0122g0352 | 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 | a0001c0001t0002g0361 | 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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0011g0144 a0001c0001t0031g0133 |
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 | a0001c0001t0011g0007 a0001c0001t0011g0112 a0001c0001t0011g0123 others(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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0147g0209 |
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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | a0001c0001t0071g0063 | 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 | a0001c0001t0031g0116 | 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 | a0001c0001t0033g0080 | 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 | a0001c0001t0016g0036 | 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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0147g0209 |
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 | a0001c0001t0100g0083 a0001c0001t0101g0075 |
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 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0013g0213 others(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 | a0001c0001t0015g0293 a0001c0001t0060g0278 a0001c0001t0060g0287 others(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 | 358 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(355): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): 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 | a0001c0001t0011g0144 a0001c0001t0031g0133 |
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 | a0001c0001t0006g0309 a0001c0001t0006g0350 a0001c0001t0009g0315 others(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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0100g0083 a0001c0001t0101g0075 |
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 | a0001c0001t0060g0278 a0001c0001t0060g0287 a0001c0001t0104g0092 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(154): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): 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 | a0001c0001t0003g0280 a0001c0001t0060g0278 a0001c0001t0104g0092 others(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 | a0001c0001t0016g0036 | 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 | a0001c0001t0007g0218 | 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 | a0001c0001t0007g0218 | 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 | a0001c0001t0007g0218 | 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 | a0001c0001t0104g0092 a0001c0001t0146g0221 |
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 | a0001c0001t0007g0218 | 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 | a0001c0001t0007g0218 | 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 | a0001c0001t0141g0286 | 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 | a0001c0001t0136g0318 | 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 | a0001c0001t0105g0078 | 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 | a0001c0001t0002g0002 a0001c0001t0124g0276 |
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 | 17 | a0001c0001t0001g0057 a0001c0001t0005g0001 a0001c0001t0005g0176 others(14): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0017g0022 others(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 | a0001c0001t0005g0177 a0001c0001t0012g0270 a0001c0001t0017g0026 others(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 | a0001c0001t0012g0271 a0001c0001t0021g0224 a0001c0001t0115g0244 others(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 | a0001c0001t0026g0012 a0001c0001t0026g0237 a0001c0001t0107g0184 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0028 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0277 others(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 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0001t0002g0348 others(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 | a0001c0001t0002g0357 a0001c0001t0002g0359 a0001c0001t0006g0344 others(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 | a0001c0001t0086g0145 a0001c0001t0100g0083 |
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 | a0001c0001t0007g0218 a0001c0001t0007g0219 a0001c0001t0007g0222 others(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 | a0001c0001t0151g0381 | 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 | a0001c0001t0003g0280 a0001c0001t0104g0092 a0001c0001t0105g0078 others(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 | a0001c0001t0007g0288 a0001c0001t0015g0293 a0001c0001t0022g0282 others(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 | a0001c0001t0073g0167 | 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 | a0001c0001t0039g0024 a0001c0001t0058g0285 |
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 | a0001c0001t0007g0288 a0001c0001t0015g0293 a0001c0001t0022g0282 others(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 | a0001c0001t0100g0083 a0001c0001t0101g0075 a0001c0001t0137g0220 |
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 | a0001c0001t0003g0280 a0001c0001t0039g0024 a0001c0001t0058g0285 others(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 | a0001c0001t0021g0377 a0001c0001t0042g0074 a0001c0001t0042g0101 others(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 | a0001c0001t0060g0278 a0001c0001t0137g0220 |
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 | a0001c0001t0002g0332 | 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 | 21 | a0001c0001t0012g0011 a0001c0001t0019g0155 a0001c0001t0019g0157 others(18): Show |
22 | HG00323.hp2 HG01106.hp1 HG01167.hp1 others(19): 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 | a0001c0001t0012g0011 a0001c0001t0136g0318 |
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 | a0001c0001t0019g0155 a0001c0001t0025g0153 a0001c0001t0037g0284 others(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 | a0001c0001t0038g0035 a0001c0001t0044g0097 a0001c0001t0135g0360 |
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 | 5 | a0001c0001t0025g0162 a0001c0001t0030g0128 a0001c0001t0030g0164 others(2): Show |
5 | HG01192.hp2 HG03654.hp2 HG03834.hp1 others(2): 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 | a0001c0001t0019g0157 a0001c0001t0037g0336 a0001c0001t0038g0020 |
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 | a0001c0001t0019g0158 a0001c0001t0019g0171 a0001c0001t0025g0156 |
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 | a0001c0001t0025g0161 a0001c0001t0037g0274 |
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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0147g0209 |
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 | a0001c0001t0003g0280 a0001c0001t0060g0278 a0001c0001t0104g0092 others(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 | a0001c0001t0066g0055 | 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 | a0001c0001t0053g0267 | 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 | a0001c0001t0114g0281 | 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 | a0001c0001t0003g0280 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0012g0011 a0001c0001t0073g0167 |
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 | 21 | a0001c0001t0019g0155 a0001c0001t0019g0157 a0001c0001t0019g0158 others(18): Show |
21 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(18): 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 | a0001c0001t0071g0063 | 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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0105g0078 others(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 | a0001c0001t0029g0094 a0001c0001t0114g0281 |
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 | a0001c0001t0100g0083 | 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 | a0001c0002t0003g0194 | 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 | a0001c0001t0002g0304 a0001c0001t0002g0357 a0001c0001t0002g0359 others(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 | a0001c0001t0136g0318 | 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 | a0001c0001t0042g0074 a0001c0001t0042g0101 a0001c0001t0062g0047 others(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 | a0001c0001t0137g0220 | 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 | a0001c0001t0108g0185 a0001c0001t0109g0186 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0301 others(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 | a0001c0001t0003g0280 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0110g0292 | 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 | a0001c0001t0006g0354 | 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 | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(232): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): 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 | a0001c0001t0042g0074 a0001c0001t0042g0101 a0001c0001t0045g0108 others(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 | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(233): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.824-4460delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99296279 | |||||||
chr6:99296336 | G | A | 2 | a0001c0001t0044g0097 a0001c0001t0135g0360 |
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 | a0001c0001t0006g0316 | 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 | a0001c0001t0003g0280 a0001c0001t0060g0278 a0001c0001t0148g0373 |
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 | a0001c0001t0105g0078 | 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 | a0001c0001t0068g0041 | 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 | a0002c0005t0070g0062 | 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 | a0001c0001t0005g0178 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0021g0224 a0001c0001t0021g0250 a0001c0001t0021g0253 others(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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0105g0078 others(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 | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(238): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): 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 | a0001c0001t0071g0063 | 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 | a0001c0001t0004g0306 | 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 | 354 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(351): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): 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 | a0001c0001t0068g0041 | 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 | a0001c0001t0026g0012 a0001c0001t0026g0251 |
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 | a0001c0001t0123g0320 | 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 | a0001c0001t0123g0320 | 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 | a0001c0001t0099g0106 | 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 | a0001c0001t0010g0118 | 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 | 354 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(351): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): 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 | a0001c0001t0001g0034 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | a0001c0001t0099g0106 | 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 | a0001c0001t0099g0106 | 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 | a0001c0001t0012g0011 a0001c0001t0012g0268 a0001c0001t0012g0269 others(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 | a0001c0001t0123g0320 | 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 | a0001c0001t0042g0074 a0001c0001t0042g0101 a0001c0001t0062g0047 others(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 | a0001c0001t0022g0282 | 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 | a0001c0001t0003g0280 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0005g0169 a0001c0001t0051g0260 a0001c0001t0051g0266 others(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 | a0001c0001t0099g0106 | 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 | a0001c0002t0003g0191 | 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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0105g0078 others(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 | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(236): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.824-6410delA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99298229 | |||||||
chr6:99298229 | CTT | C | 113 | a0001c0001t0003g0280 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0129g0345 | 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 | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(233): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): 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 | a0001c0001t0042g0074 a0001c0001t0042g0101 a0001c0001t0062g0047 others(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 | a0001c0001t0032g0104 | 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 | a0001c0001t0036g0335 | 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 | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(43): 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 | a0001c0001t0042g0074 a0001c0001t0042g0101 a0001c0001t0062g0047 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0021g0377 | 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 | 344 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(341): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): 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 | a0001c0001t0002g0304 a0001c0001t0002g0357 a0001c0001t0002g0359 others(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 | a0001c0001t0125g0322 | 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 | a0001c0001t0026g0012 a0001c0001t0026g0251 |
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 | a0001c0001t0013g0215 | 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 | a0001c0001t0103g0081 | 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 | a0001c0001t0013g0258 | 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 | a0001c0001t0025g0161 a0001c0001t0025g0162 a0001c0001t0030g0164 others(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 | a0001c0001t0017g0022 a0001c0001t0017g0026 a0001c0001t0017g0049 others(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 | a0001c0001t0007g0218 a0001c0001t0007g0219 a0001c0001t0007g0222 others(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 | 345 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(342): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.824-9300A>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99301120 | |||||||
chr6:99301170 | C | G | 21 | a0001c0001t0019g0155 a0001c0001t0019g0157 a0001c0001t0019g0158 others(18): Show |
21 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(18): 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 | a0001c0001t0042g0074 a0001c0001t0042g0101 a0001c0001t0062g0047 others(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 | a0001c0001t0004g0365 | 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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0072g0166 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | 345 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(342): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): 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 | a0001c0001t0036g0308 | 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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(286): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | a0001c0001t0002g0363 | 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 | 21 | a0001c0001t0019g0155 a0001c0001t0019g0157 a0001c0001t0019g0158 others(18): Show |
21 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.824-11048T>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99302868 | |||||||
chr6:99303234 | C | T | 345 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(342): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): 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 | a0001c0001t0151g0381 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0101g0075 | 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 | a0001c0001t0006g0326 a0001c0001t0009g0317 |
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 | a0001c0001t0100g0083 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0067g0046 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0002g0208 | 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 | a0001c0001t0003g0187 | 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 | a0001c0001t0007g0219 | 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 | a0001c0001t0012g0269 a0001c0001t0012g0270 a0001c0001t0012g0273 |
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 | a0001c0001t0003g0280 a0001c0001t0050g0006 a0001c0001t0060g0278 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0042g0074 a0001c0001t0042g0101 a0001c0001t0062g0047 others(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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(286): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.824-13803C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99305623 | |||||||
chr6:99305715 | C | CAT | 358 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(355): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): 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 | a0001c0001t0137g0220 | 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 | a0001c0001t0002g0329 | 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 | a0001c0001t0042g0074 a0001c0001t0042g0101 a0001c0001t0062g0047 others(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 | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0030 |
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 | a0001c0001t0027g0370 | 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 | a0001c0001t0046g0105 a0001c0001t0046g0117 a0001c0001t0084g0129 |
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 | a0001c0001t0034g0272 a0001c0001t0034g0275 a0001c0001t0034g0311 |
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 | a0001c0001t0002g0359 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0012g0270 | 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 | a0001c0001t0005g0087 a0001c0001t0005g0088 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0044g0097 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0001g0052 | 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 | a0001c0002t0003g0196 | 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 | a0001c0001t0102g0110 | 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 | a0001c0001t0003g0280 a0001c0001t0060g0278 a0001c0001t0104g0092 others(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 | a0001c0001t0003g0280 a0001c0001t0042g0074 a0001c0001t0042g0101 others(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 | a0001c0001t0151g0381 | 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 | a0001c0001t0039g0024 a0001c0001t0039g0040 a0001c0001t0067g0046 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0045 |
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 | a0001c0001t0066g0055 | 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 | a0001c0001t0050g0006 a0001c0001t0103g0081 a0001c0001t0147g0209 |
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 | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(289): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0001c0001t0104g0092 a0001c0001t0146g0221 |
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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 | a0001c0001t0018g0068 | 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 | a0001c0001t0003g0280 a0001c0001t0060g0278 a0001c0001t0148g0373 |
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 | a0001c0001t0021g0253 a0001c0001t0021g0254 |
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 | 36 | a0001c0001t0005g0001 a0001c0001t0005g0087 a0001c0001t0005g0088 others(33): 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 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0013g0213 others(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 | a0001c0001t0101g0075 | 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 | a0001c0001t0005g0169 a0001c0001t0014g0321 a0001c0001t0017g0022 others(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 | a0001c0001t0007g0222 a0001c0001t0012g0268 a0001c0001t0012g0269 others(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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0007g0218 a0001c0001t0007g0219 a0001c0001t0007g0222 others(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 | 353 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(350): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): 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 | a0001c0001t0071g0063 a0001c0001t0076g0076 a0001c0001t0077g0073 |
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 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0013g0213 others(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 | a0001c0001t0023g0249 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0042g0074 a0001c0001t0072g0166 a0001c0001t0137g0220 |
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 | a0001c0002t0003g0202 | 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 | a0001c0001t0035g0279 a0001c0001t0035g0295 a0001c0001t0035g0297 others(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 | a0001c0001t0137g0220 | 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 | a0001c0001t0009g0013 | 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 | a0001c0001t0100g0083 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0136g0318 | 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 | a0001c0001t0013g0258 a0001c0001t0111g0259 |
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 | a0001c0001t0107g0184 | 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 | a0001c0001t0107g0184 | 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 | a0001c0001t0053g0267 | 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 | a0001c0001t0019g0157 | 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 | a0001c0002t0003g0189 | 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 | a0001c0001t0116g0262 | 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(272): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.823+13240C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99310204 | |||||||
chr6:99310315 | A | G | 358 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(355): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): 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 | a0001c0001t0009g0013 | 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 | 101 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0004g0226 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(85): 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 | a0001c0002t0003g0189 | 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 | a0001c0001t0015g0293 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0021g0377 a0001c0001t0029g0094 a0001c0001t0052g0255 others(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 | a0001c0001t0002g0312 a0001c0001t0006g0343 |
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 | a0001c0001t0042g0074 a0001c0001t0071g0063 a0001c0001t0076g0076 others(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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0060g0278 | 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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | a0001c0001t0001g0045 | 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 | a0001c0001t0119g0231 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.823+11493G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99311951 | |||||||
chr6:99312010 | C | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(270): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): 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 | a0001c0001t0013g0258 a0001c0001t0014g0372 a0001c0001t0034g0311 others(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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0029g0094 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0020g0134 a0001c0001t0043g0131 |
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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0082g0082 a0001c0001t0100g0083 a0001c0001t0103g0081 |
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 | a0001c0001t0034g0272 a0001c0001t0034g0275 a0001c0001t0118g0261 |
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 | a0001c0001t0002g0277 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0301 others(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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0021g0377 a0001c0001t0029g0094 a0001c0001t0052g0255 others(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 | a0001c0001t0002g0277 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(84): 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 | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(178): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.823+8818T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314626 | |||||||
chr6:99314796 | A | G | 358 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(355): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.823+8648T>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99314796 | |||||||
chr6:99314864 | A | G | 94 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(91): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): 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 | a0001c0001t0104g0092 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0034g0272 | 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 | a0001c0001t0146g0221 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0147 a0001c0001t0008g0149 a0001c0001t0010g0140 others(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 | a0001c0001t0034g0275 a0001c0001t0043g0130 a0001c0001t0051g0260 others(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 | a0001c0001t0034g0272 | 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 | a0001c0001t0021g0377 a0001c0001t0052g0255 a0001c0001t0094g0143 others(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 | a0001c0001t0029g0094 a0001c0001t0048g0079 a0001c0001t0082g0082 others(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 | a0001c0001t0002g0329 a0001c0001t0005g0001 a0001c0001t0005g0087 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0039 others(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 | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(84): Show |
90 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(87): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 | 275 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(272): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): 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 | a0001c0001t0107g0184 | 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 | a0001c0001t0027g0375 | 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 | a0001c0001t0002g0332 a0001c0001t0002g0333 a0001c0001t0004g0334 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0015g0293 | 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 | a0001c0001t0001g0057 a0001c0001t0002g0361 a0001c0001t0003g0280 others(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 | 93 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(90): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.823+7286delG | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316157 | |||||||
chr6:99316182 | C | T | 17 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | 95 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(92): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): 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 | a0001c0001t0082g0082 a0001c0001t0100g0083 a0001c0001t0103g0081 |
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 | a0001c0001t0042g0074 a0001c0001t0076g0076 a0001c0001t0101g0075 |
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 | a0001c0001t0051g0260 a0001c0001t0051g0266 a0001c0001t0112g0264 others(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 | 95 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(92): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): 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 | a0001c0001t0002g0361 | 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 | 94 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(91): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.823+6577G>C | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99316867 | |||||||
chr6:99316955 | T | C | 95 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(92): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | 319 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(316): Show |
330 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.823+6266delA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99317177 | |||||||
chr6:99317299 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(84): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0024g0090 a0001c0001t0045g0091 a0001c0001t0147g0209 |
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 | a0001c0001t0120g0371 | 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 | a0001c0001t0112g0264 | 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 | a0001c0001t0025g0156 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | 95 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(92): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): 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 | a0001c0001t0010g0140 a0001c0001t0090g0141 |
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 | 95 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(92): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0044g0152 | 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0053g0267 a0001c0001t0140g0263 |
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 | a0001c0001t0003g0280 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0028 others(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 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0348 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0206 a0001c0001t0002g0301 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0277 a0001c0001t0002g0299 others(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 | a0001c0001t0109g0186 a0001c0004t0150g0380 |
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 | a0001c0001t0004g0306 a0001c0001t0108g0185 |
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 | a0001c0001t0021g0250 | 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 | a0001c0001t0131g0307 | 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 | a0001c0001t0003g0187 a0001c0002t0003g0188 a0001c0002t0003g0194 others(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 | a0001c0001t0003g0376 a0001c0002t0003g0189 a0001c0002t0003g0191 others(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 | a0001c0001t0023g0230 | 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 | a0001c0001t0001g0042 a0001c0001t0007g0288 a0001c0001t0008g0125 others(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 | a0001c0001t0003g0280 a0001c0001t0029g0094 a0001c0001t0043g0131 others(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 | a0001c0001t0008g0142 a0001c0001t0008g0147 a0001c0001t0008g0148 others(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 | a0001c0001t0012g0269 a0001c0001t0012g0270 a0001c0001t0012g0271 others(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 | a0001c0001t0051g0260 a0001c0001t0051g0266 a0001c0001t0082g0082 others(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 | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(123): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): 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 | a0001c0001t0001g0042 a0001c0001t0007g0288 a0001c0001t0008g0125 others(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 | a0001c0001t0003g0280 a0001c0001t0029g0094 a0001c0001t0043g0131 others(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 | a0001c0001t0008g0142 a0001c0001t0008g0147 a0001c0001t0008g0148 others(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 | a0001c0001t0012g0269 a0001c0001t0012g0270 a0001c0001t0012g0271 others(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 | a0001c0001t0051g0260 a0001c0001t0051g0266 a0001c0001t0082g0082 others(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 | a0001c0001t0045g0091 | 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 | 2 | a0001c0001t0005g0095 a0001c0001t0045g0091 |
2 | HG01496.hp2 HG03209.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 | a0001c0001t0005g0087 a0001c0001t0005g0088 a0001c0001t0024g0090 others(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 | 7 | a0001c0001t0005g0087 a0001c0001t0005g0088 a0001c0001t0005g0095 others(4): Show |
7 | HG00673.hp2 HG01496.hp2 HG01952.hp2 others(4): 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 | a0001c0001t0019g0157 a0001c0001t0019g0158 a0001c0001t0019g0171 others(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 | 14 | a0001c0001t0005g0087 a0001c0001t0005g0088 a0001c0001t0005g0095 others(11): Show |
14 | HG00673.hp2 HG01106.hp1 HG01496.hp2 others(11): 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 | a0001c0001t0019g0155 a0001c0001t0024g0180 a0001c0001t0024g0181 others(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 | a0001c0001t0005g0160 a0001c0001t0025g0156 a0001c0001t0025g0161 others(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 | a0001c0001t0018g0068 a0001c0001t0018g0070 |
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 | 41 | a0001c0001t0005g0087 a0001c0001t0005g0088 a0001c0001t0005g0095 others(38): Show |
42 | HG00280.hp2 HG00323.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.823+5138G>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 4/5 | chr6 | 99318306 | |||||||
chr6:99318306 | C | CAAAAAA | 3 | a0001c0001t0005g0001 a0001c0001t0005g0177 a0001c0001t0005g0178 |
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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0069 others(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 | a0001c0001t0007g0228 a0001c0001t0015g0243 a0001c0001t0022g0227 others(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 | a0001c0001t0015g0245 a0001c0001t0015g0246 a0001c0001t0024g0182 |
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 | a0001c0001t0007g0218 a0001c0001t0021g0224 a0001c0001t0026g0237 others(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 | a0001c0001t0004g0226 a0001c0001t0005g0176 a0001c0001t0007g0241 others(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 | a0001c0001t0028g0098 a0001c0001t0028g0100 a0001c0001t0042g0101 others(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 | a0001c0001t0021g0254 a0001c0001t0054g0229 a0001c0001t0054g0236 |
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 | a0001c0001t0007g0239 | 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 | a0001c0001t0023g0235 | 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 | a0001c0001t0007g0223 | 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 | a0001c0001t0021g0253 | 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 | a0001c0001t0035g0279 a0001c0001t0035g0295 a0001c0001t0035g0297 others(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 | a0001c0001t0077g0073 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | 95 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(92): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): 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 | a0001c0001t0006g0341 a0001c0001t0053g0267 a0001c0001t0140g0263 |
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 | a0001c0001t0014g0342 | 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 | a0001c0001t0053g0267 a0001c0001t0140g0263 |
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 | a0001c0001t0102g0110 | 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 | a0001c0001t0005g0169 a0001c0001t0012g0011 a0001c0001t0073g0167 others(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 | a0001c0001t0053g0267 a0001c0001t0140g0263 |
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 | a0001c0001t0021g0377 a0001c0001t0029g0094 a0001c0001t0052g0255 others(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 | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(198): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0057 others(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 | a0001c0001t0010g0113 a0001c0001t0012g0268 a0001c0001t0012g0269 others(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 | a0001c0001t0021g0377 a0001c0001t0029g0094 a0001c0001t0052g0255 |
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 | a0001c0001t0029g0094 | 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 | a0001c0001t0108g0185 a0001c0001t0109g0186 |
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 | 94 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(91): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): 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 | a0001c0001t0072g0166 | 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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0082g0082 a0001c0001t0100g0083 a0001c0001t0103g0081 others(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 | a0001c0001t0021g0250 | 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 | a0001c0001t0072g0166 | 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 | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(258): 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 | a0001c0001t0052g0255 | 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 | a0001c0001t0009g0013 | 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 | 95 | a0001c0001t0003g0187 a0001c0001t0004g0226 a0001c0001t0005g0001 others(92): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0072g0166 | 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 | a0001c0001t0053g0267 a0001c0001t0140g0263 |
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 | a0001c0001t0005g0169 | 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 | a0001c0001t0021g0377 a0001c0001t0029g0094 a0001c0001t0052g0255 others(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 | a0001c0001t0016g0027 | 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 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0053g0267 a0001c0001t0140g0263 |
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 | a0001c0001t0017g0022 a0001c0001t0017g0026 a0001c0001t0017g0049 others(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 | 99 | a0001c0001t0003g0187 a0001c0001t0004g0226 a0001c0001t0005g0001 others(96): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): 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 | a0001c0001t0075g0071 | 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 | a0001c0001t0146g0221 | 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 | a0001c0001t0014g0372 | 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 | a0001c0001t0011g0112 | 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 | a0001c0001t0021g0377 | 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 | a0001c0001t0001g0021 | 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 | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(87): 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 | a0001c0001t0056g0256 a0001c0001t0056g0257 |
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 | a0001c0001t0072g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.600-60A>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99323727 | |||||||
chr6:99324019 | G | A | 4 | a0001c0001t0022g0369 a0001c0001t0032g0077 a0001c0001t0047g0005 others(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 | a0001c0002t0003g0204 | 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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.600-531dupT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99324197 | |||||||
chr6:99324324 | T | C | 361 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(358): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): 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 | a0001c0001t0001g0045 | 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 | 55 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(52): Show |
56 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(53): 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 | a0001c0001t0005g0169 a0001c0001t0012g0011 a0001c0001t0073g0167 others(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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0066g0055 | 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 | a0001c0001t0028g0096 a0001c0001t0028g0098 a0001c0001t0028g0100 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | 335 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(332): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.600-1438dupA | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99325104 | |||||||
chr6:99325229 | T | C | 1 | a0001c0001t0104g0092 | 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 | a0001c0001t0122g0352 | 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 | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(53): 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 | a0001c0001t0021g0377 a0001c0001t0034g0275 a0001c0001t0052g0255 others(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 | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(278): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): 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 | a0001c0001t0014g0355 | 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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0082g0082 a0001c0001t0100g0083 a0001c0001t0103g0081 |
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 | a0001c0001t0021g0377 a0001c0001t0034g0275 a0001c0001t0052g0255 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0023g0249 | 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 | a0001c0001t0051g0266 | 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 | a0001c0001t0024g0090 a0001c0001t0045g0091 a0001c0001t0147g0209 |
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 | a0001c0001t0021g0250 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0098g0111 | 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 | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(86): 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 | a0001c0001t0052g0353 | 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 | 361 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(358): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.600-2899G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99326566 | |||||||
chr6:99326658 | C | T | 361 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(358): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0007g0228 a0001c0001t0022g0227 |
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 | a0001c0001t0075g0071 | 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 | a0001c0001t0114g0281 a0001c0001t0137g0220 a0001c0001t0146g0221 |
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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 | a0001c0001t0052g0255 | 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 | a0001c0001t0021g0377 a0001c0001t0034g0275 a0001c0001t0052g0255 others(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 | a0001c0001t0002g0304 a0001c0001t0002g0357 a0001c0001t0002g0359 others(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 | a0001c0001t0012g0011 a0001c0001t0073g0167 |
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 | 9 | a0001c0001t0005g0001 a0001c0001t0005g0176 a0001c0001t0005g0177 others(6): 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 | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(177): 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 | 100 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(97): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.599+4668G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 3/5 | chr6 | 99328683 | |||||||
chr6:99328714 | C | T | 96 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(93): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): 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 | a0001c0001t0147g0209 | 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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | a0001c0001t0034g0272 a0001c0001t0116g0262 a0001c0001t0118g0261 |
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 | a0001c0001t0072g0166 | 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 | a0001c0001t0051g0260 a0001c0001t0051g0266 a0001c0001t0113g0265 |
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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 | a0001c0001t0006g0354 a0001c0001t0014g0355 |
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 | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(257): 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 | 159 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(156): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): 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 | a0001c0001t0067g0046 | 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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | a0001c0001t0021g0377 a0001c0001t0034g0275 a0001c0001t0052g0255 others(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 | a0001c0001t0146g0221 | 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 | a0001c0001t0146g0221 | 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 | a0001c0001t0146g0221 | 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 | a0001c0001t0005g0169 a0001c0001t0012g0011 a0001c0001t0073g0167 others(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 | a0001c0001t0007g0219 | 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 | a0001c0001t0008g0149 a0001c0001t0085g0107 |
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 | a0001c0001t0022g0283 | 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 | a0001c0001t0021g0377 a0001c0001t0034g0275 a0001c0001t0052g0255 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0032g0104 | 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 | 100 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(97): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): 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 | a0001c0001t0034g0275 a0001c0001t0052g0255 |
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 | a0001c0001t0004g0226 a0001c0001t0139g0252 |
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 | a0001c0001t0072g0166 | 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 | a0001c0001t0102g0110 | 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 | a0001c0001t0147g0209 | 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 | a0001c0001t0002g0304 a0001c0001t0002g0357 a0001c0001t0002g0359 others(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 | a0002c0005t0070g0062 | 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 | a0001c0001t0039g0024 | 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 | a0001c0001t0022g0282 | 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0005g0160 | 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 | a0001c0001t0021g0377 a0001c0001t0034g0275 a0001c0001t0052g0255 others(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 | a0001c0001t0081g0168 | 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 | a0001c0004t0150g0380 | 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 | a0001c0001t0026g0012 a0001c0001t0026g0251 |
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 | 98 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(95): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): 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 | a0001c0001t0021g0377 a0001c0001t0034g0275 a0001c0001t0052g0255 others(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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.403-251C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99333798 | |||||||
chr6:99333810 | C | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(173): 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 | a0001c0001t0135g0360 | 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 | a0001c0001t0003g0376 | 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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0082g0082 a0001c0001t0100g0083 a0001c0001t0103g0081 |
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 | a0001c0001t0002g0304 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(45): 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 | a0001c0001t0008g0125 a0001c0001t0008g0126 a0001c0001t0008g0127 others(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 | a0001c0001t0072g0166 | 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0053 | 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 | a0001c0002t0003g0188 | 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 | 103 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(100): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): 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 | a0001c0001t0072g0166 | 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 | 103 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(100): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): 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 | a0001c0001t0005g0160 | 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 | a0001c0001t0034g0272 | 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 | a0001c0001t0017g0022 a0001c0001t0017g0049 a0001c0001t0017g0050 others(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 | 167 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(164): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.403-3710delT | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99337256 | |||||||
chr6:99337478 | C | T | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0005g0095 | 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 | a0001c0001t0028g0096 a0001c0001t0028g0098 a0001c0001t0028g0100 others(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 | a0001c0001t0011g0109 | 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 | a0001c0001t0075g0071 | 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 | a0001c0001t0002g0361 | 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 | 179 | a0001c0001t0003g0187 a0001c0001t0004g0226 a0001c0001t0005g0001 others(176): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0114g0281 a0001c0001t0137g0220 a0001c0001t0146g0221 |
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 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 |
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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 | a0001c0001t0001g0052 | 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 | 178 | a0001c0001t0003g0187 a0001c0001t0004g0226 a0001c0001t0005g0001 others(175): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): 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 | a0001c0001t0051g0260 a0001c0001t0051g0266 a0001c0001t0112g0264 others(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 | a0001c0001t0082g0082 a0001c0001t0100g0083 a0001c0001t0103g0081 others(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 | 358 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(355): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): 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 | a0001c0001t0040g0064 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0021g0253 | 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 | a0001c0001t0016g0023 | 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 | a0001c0001t0034g0275 a0001c0001t0037g0274 a0001c0001t0052g0255 |
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 | a0001c0001t0140g0263 | 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 | 182 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(179): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0137g0220 a0001c0001t0146g0221 |
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 | a0001c0001t0025g0153 a0001c0001t0044g0152 |
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 | 182 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(179): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.402+2366dupG | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 2/5 | chr6 | 99340531 | |||||||
chr6:99340597 | G | A | 15 | a0001c0001t0008g0142 a0001c0001t0008g0147 a0001c0001t0008g0148 others(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 | a0001c0001t0007g0223 a0001c0001t0012g0268 a0001c0001t0012g0269 others(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 | 154 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0057 others(151): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): 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 | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0025 others(154): 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0002g0363 others(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 | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(172): 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 | a0001c0001t0002g0301 a0001c0001t0014g0300 |
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 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0004g0015 a0001c0001t0004g0364 a0001c0001t0004g0365 others(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 | a0001c0001t0001g0004 | 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 | 182 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(179): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): 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 | a0001c0001t0031g0103 | 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 | a0001c0001t0007g0222 | 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 | a0001c0001t0137g0220 a0001c0001t0146g0221 |
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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0022g0369 | 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 | a0001c0001t0002g0299 | 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 | 182 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(179): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): 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 | a0001c0001t0036g0374 | 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 | a0001c0001t0003g0187 a0001c0001t0005g0087 a0001c0001t0005g0088 others(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 | a0001c0001t0049g0102 | 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 | a0001c0001t0064g0019 | 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 | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(174): 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 | a0001c0001t0001g0053 a0001c0001t0009g0298 a0001c0001t0012g0273 others(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 | a0001c0001t0008g0135 | 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 | a0001c0001t0082g0082 a0001c0001t0100g0083 a0001c0001t0103g0081 |
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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | 99 | a0001c0001t0004g0226 a0001c0001t0005g0001 a0001c0001t0005g0087 others(96): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | a0001c0001t0074g0072 | 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 | a0001c0001t0019g0171 | 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 | a0001c0001t0060g0278 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0206 others(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 | a0001c0001t0022g0369 | 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 | 183 | a0001c0001t0003g0187 a0001c0001t0004g0226 a0001c0001t0005g0001 others(180): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): 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 | a0001c0001t0105g0078 | 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 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | 183 | a0001c0001t0003g0187 a0001c0001t0004g0226 a0001c0001t0005g0001 others(180): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): 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 | a0001c0001t0003g0187 | 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 | 183 | a0001c0001t0003g0187 a0001c0001t0004g0226 a0001c0001t0005g0001 others(180): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.267-1343C>G | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344376 | |||||||
chr6:99344397 | G | A | 20 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(17): Show |
20 | HG00323.hp2 HG00621.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.267-1364C>T | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99344397 | |||||||
chr6:99344662 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(174): 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 | a0001c0001t0077g0073 | 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 | a0001c0001t0010g0085 | 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 | 360 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(357): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): 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 | a0001c0001t0002g0277 | 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 | 146 | a0001c0001t0003g0187 a0001c0001t0005g0001 a0001c0001t0005g0087 others(143): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): 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 | a0001c0001t0005g0160 | 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 | 146 | a0001c0001t0003g0187 a0001c0001t0005g0001 a0001c0001t0005g0087 others(143): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.267-2318G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99345351 | |||||||
chr6:99345399 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(211): 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 | a0001c0001t0063g0054 | 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 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0109g0186 | 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 | 146 | a0001c0001t0005g0001 a0001c0001t0005g0087 a0001c0001t0005g0088 others(143): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(149): 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 | a0001c0001t0034g0275 a0001c0001t0037g0274 a0001c0001t0052g0255 |
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 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(163): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | 310 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(307): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.266+2544delC | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346562 | |||||||
chr6:99346565 | G | T | 4 | a0001c0001t0005g0169 a0001c0001t0082g0082 a0001c0001t0100g0083 others(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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0005g0169 | 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 | 310 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(307): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.266+2533C>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346574 | |||||||
chr6:99346591 | C | T | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(308): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.266+2516G>A | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346591 | |||||||
chr6:99346612 | A | AG | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.266+2494dupC | FAXC | ENSG00000146267.12 | transcript | ENST00000389677.6 | protein_coding | 1/5 | chr6 | 99346612 | |||||||
chr6:99346647 | G | A | 125 | a0001c0001t0005g0001 a0001c0001t0005g0087 a0001c0001t0005g0088 others(122): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): 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 | a0001c0001t0066g0055 | 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 | a0001c0001t0034g0275 a0001c0001t0037g0274 a0001c0001t0052g0255 |
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 | a0001c0001t0018g0065 a0001c0001t0018g0067 a0001c0001t0018g0068 others(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 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0013g0213 others(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 | a0001c0001t0124g0276 | 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 | a0001c0001t0025g0161 a0001c0001t0025g0162 a0001c0001t0030g0164 others(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 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0137g0220 a0001c0001t0146g0221 |
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 | a0001c0001t0007g0219 | 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 | a0001c0001t0004g0226 a0001c0001t0007g0218 a0001c0001t0007g0219 others(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 | a0001c0001t0005g0169 a0001c0001t0072g0166 a0001c0001t0073g0167 others(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 | a0001c0001t0004g0226 a0001c0001t0007g0219 a0001c0001t0007g0222 others(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 | 282 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(279): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): 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 | a0001c0001t0012g0268 a0001c0001t0012g0269 a0001c0001t0012g0270 others(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 | a0001c0001t0052g0255 | 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 | a0001c0001t0014g0372 a0001c0001t0018g0070 a0001c0001t0036g0374 others(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 | a0001c0001t0013g0211 a0001c0001t0013g0212 a0001c0001t0013g0213 others(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 | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0001t0021g0377 | 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 | a0001c0001t0032g0077 a0001c0001t0042g0074 a0001c0001t0047g0005 others(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 | a0001c0001t0033g0172 a0001c0001t0033g0174 a0001c0001t0049g0173 |
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 | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(308): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): 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 | a0002c0005t0070g0062 | 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 | a0002c0005t0070g0062 | 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 | a0001c0001t0074g0072 | 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 | a0002c0005t0070g0062 | 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 | a0002c0005t0070g0062 | 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 | a0001c0001t0003g0376 | 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 | a0001c0001t0027g0375 | 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 | a0001c0001t0003g0376 | 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 | a0001c0001t0075g0071 | 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 | a0001c0001t0032g0175 | 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 | a0001c0001t0021g0377 | 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 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0208 |
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 | a0002c0005t0070g0062 | 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 | a0001c0001t0138g0378 | 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 | 358 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(355): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): 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 | a0002c0005t0070g0062 | 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 | 9 | a0001c0001t0005g0001 a0001c0001t0005g0176 a0001c0001t0005g0177 others(6): 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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(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 |