Item | Value |
---|---|
geneid | 9328 |
ensemblid | ENSG00000148308.18 |
hgncid | 4668 |
symbol | GTF3C5 |
name | general transcription factor IIIC subunit 5 |
refseq_nuc | NM_012087.4 |
refseq_prot | NP_036219.2 |
ensembl_nuc | ENST00000372097.10 |
ensembl_prot | ENSP00000361169.5 |
mane_status | MANE Select |
chr | chr9 |
start | 133030997 |
end | 133058503 |
strand | + |
ver | v1.2 |
region | chr9:133030997-133058503 |
region5000 | chr9:133025997-133063503 |
regionname0 | GTF3C5_chr9_133030997_133058503 |
regionname5000 | GTF3C5_chr9_133025997_133063503 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 519 | 377 | 89 | 74 | 164 | 14 | 34 | 118 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | MAAEA others(514): Show |
chr9 | 133025997 | 133063503 |
a0002 | 0/0 | 519 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | MAAEA others(514): Show |
chr9 | 133025997 | 133063503 |
a0003 | 0/0 | 519 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | MAAEA others(514): Show |
chr9 | 133025997 | 133063503 |
a0004 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | MAAEA others(514): Show |
chr9 | 133025997 | 133063503 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1557 | 362 | 78 | 74 | 160 | 14 | 34 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0001c0002 | 0/0 | 1557 | 6 | 6 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0001c0003 | 0/0 | 1557 | 4 | 4 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0001c0004 | 0/0 | 1557 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0001c0005 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0001c0007 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0001c0010 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0002c0008 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0003c0009 | 0/0 | 1557 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 | ||
a0004c0006 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | ATGGC others(1552): Show |
chr9 | 133025997 | 133063503 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2098 | 283 | 70 | 46 | 129 | 9 | 27 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0001t0002 | 0/0 | 2098 | 74 | 6 | 27 | 31 | 5 | 5 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0001t0003 | 0/0 | 2098 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0001t0004 | 0/0 | 2098 | 2 | 0 | 0 | 0 | 0 | 2 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0001t0005 | 0/0 | 2098 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0002t0001 | 0/0 | 2098 | 6 | 6 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0003t0002 | 0/0 | 2098 | 4 | 4 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0004t0001 | 0/0 | 2098 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0005t0001 | 0/0 | 2098 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0007t0001 | 0/0 | 2098 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0001c0010t0001 | 0/0 | 2098 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0002c0008t0001 | 0/0 | 2098 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0003c0009t0001 | 0/0 | 2098 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
a0004c0006t0001 | 0/0 | 2098 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | GCCAG others(2093): Show |
chr9 | 133025997 | 133063503 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 63 | 10 | 14 | 26 | 6 | 7 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0002 | 0/0 | 39 | 0 | 10 | 26 | 0 | 3 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0004 | 0/0 | 15 | 4 | 2 | 7 | 0 | 2 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0005 | 0/0 | 13 | 1 | 0 | 10 | 1 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0006 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0008 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0031 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0003 | 0/0 | 29 | 1 | 16 | 7 | 4 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0003t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0004t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0007t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0001c0010t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0002c0008t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0003c0009t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
a0004c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00558 | hp1 | a0001 | c0010 | t0001 | g0140 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01261 | hp1 | a0002 | c0008 | t0001 | g0001 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01433 | hp1 | a0003 | c0009 | t0001 | g0116 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02717 | hp2 | a0001 | c0003 | t0002 | g0023 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02723 | hp1 | a0001 | c0003 | t0002 | g0023 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02886 | hp2 | a0001 | c0003 | t0002 | g0023 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03579 | hp1 | a0001 | c0003 | t0002 | g0047 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0139 | SAS | STU | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18944 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18961 | hp1 | a0001 | c0005 | t0001 | g0135 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19004 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | LWK | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | TSI | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0040 | SAS | GIH | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02109 | hp1 | a0001 | c0007 | t0001 | g0026 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG02559 | hp2 | a0004 | c0006 | t0001 | g0014 | AFR | ACB | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0042 | REF | REF | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0031 | REF | REF | GTF3C5_chr9_133025997_133063503 | GTF3C5 | chr9 | 133025997 | 133063503 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:133042195 | A | G | 1 | a0003 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.262A>G | p.Ile88Val | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/11 | 277/2098 | 262/1560 | 88/519 | chr9 | 133042195 | |||
chr9:133043811 | C | T | 1 | a0002 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.457C>T | p.Arg153Trp | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/11 | 472/2098 | 457/1560 | 153/519 | chr9 | 133043811 | |||
chr9:133043838 | C | A | 1 | a0004 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.484C>A | p.Gln162Lys | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/11 | 499/2098 | 484/1560 | 162/519 | chr9 | 133043838 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:133031047 | C | T | 1 | a0001c0010 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.36C>T | p.Ala12Ala | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/11 | 51/2098 | 36/1560 | 12/519 | chr9 | 133031047 | |||
chr9:133031119 | G | A | 1 | a0001c0005 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.108G>A | p.Val36Val | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/11 | 123/2098 | 108/1560 | 36/519 | chr9 | 133031119 | |||
chr9:133043891 | G | T | 1 | a0001c0002 | 6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
synonymous_variant | LOW | c.537G>T | p.Pro179Pro | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/11 | 552/2098 | 537/1560 | 179/519 | chr9 | 133043891 | |||
chr9:133054460 | C | T | 1 | a0001c0004 | 2 | NA18944.hp1 NA19004.hp2 |
synonymous_variant | LOW | c.1041C>T | p.Tyr347Tyr | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 7/11 | 1056/2098 | 1041/1560 | 347/519 | chr9 | 133054460 | |||
chr9:133054797 | G | A | 1 | a0001c0003 | 4 | HG02717.hp2 HG02723.hp1 HG02886.hp2 others(1): Show |
synonymous_variant | LOW | c.1155G>A | p.Lys385Lys | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/11 | 1170/2098 | 1155/1560 | 385/519 | chr9 | 133054797 | |||
chr9:133057968 | G | A | 1 | a0001c0007 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1548G>A | p.Leu516Leu | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 11/11 | 1563/2098 | 1548/1560 | 516/519 | chr9 | 133057968 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:133057993 | C | A | 1 | a0001c0001t0005 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 11/11 | 13 | chr9 | 133057993 | ||||||
chr9:133058150 | A | G | 1 | a0001c0001t0004 | 2 | HG04115.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*170A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 11/11 | 170 | chr9 | 133058150 | ||||||
chr9:133058293 | G | A | 1 | a0001c0001t0003 | 2 | HG02717.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*313G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 11/11 | 313 | chr9 | 133058293 | ||||||
chr9:133058374 | C | T | 2 | a0001c0001t0002 a0001c0003t0002 |
78 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*394C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 11/11 | 394 | chr9 | 133058374 | ||||||
chr9:133058400 | C | T | 1 | a0001c0001t0004 | 2 | HG04115.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*420C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 11/11 | 420 | chr9 | 133058400 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:133031252 | T | G | 1 | a0001c0001t0004g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.153+88T>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133031252 | |||||||
chr9:133031340 | T | G | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+176T>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133031340 | |||||||
chr9:133031464 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.153+300G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133031464 | |||||||
chr9:133031641 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0002t0001g0141 |
11 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.153+477C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133031641 | |||||||
chr9:133032043 | C | T | 3 | a0001c0001t0004g0040 a0001c0001t0004g0139 a0001c0010t0001g0140 |
3 | HG00558.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.153+879C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133032043 | |||||||
chr9:133032172 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.153+1008C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133032172 | |||||||
chr9:133032236 | G | T | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+1072G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133032236 | |||||||
chr9:133032488 | CAAGGGAG others(5691): Show |
C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.153+1353_154-3873d others(2): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133032488 | ||||||
chr9:133032646 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.153+1482G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133032646 | |||||||
chr9:133032770 | A | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(8): Show |
24 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.153+1606A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133032770 | |||||||
chr9:133032804 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(9): Show |
25 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.153+1640A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133032804 | |||||||
chr9:133032812 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.153+1648G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133032812 | |||||||
chr9:133032913 | A | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(13): Show |
30 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.153+1749A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133032913 | |||||||
chr9:133033238 | C | G | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.153+2074C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033238 | |||||||
chr9:133033239 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0091 others(1): Show |
9 | HG01081.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+2075G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033239 | |||||||
chr9:133033496 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.153+2332A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033496 | |||||||
chr9:133033624 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0041 |
6 | HG02015.hp2 NA18941.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+2460G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033624 | |||||||
chr9:133033666 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0087 |
4 | HG02257.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+2502C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033666 | |||||||
chr9:133033715 | G | C | 4 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(1): Show |
5 | HG02258.hp2 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+2551G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033715 | |||||||
chr9:133033730 | T | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.153+2566T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033730 | |||||||
chr9:133033741 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0024 |
10 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+2577T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033741 | |||||||
chr9:133033902 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.153+2738C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133033902 | |||||||
chr9:133034066 | C | T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0095 others(3): Show |
13 | HG00558.hp2 HG00738.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+2902C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034066 | |||||||
chr9:133034067 | G | A | 5 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+2903G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034067 | |||||||
chr9:133034180 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0067 |
4 | HG02145.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+3016G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034180 | |||||||
chr9:133034217 | A | T | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+3053A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034217 | |||||||
chr9:133034236 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.153+3072C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034236 | |||||||
chr9:133034246 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.153+3082A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034246 | |||||||
chr9:133034403 | T | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(20): Show |
38 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.153+3239T>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034403 | |||||||
chr9:133034463 | A | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(20): Show |
38 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.153+3299A>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034463 | |||||||
chr9:133034538 | C | G | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+3374C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034538 | |||||||
chr9:133034589 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.153+3425G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034589 | |||||||
chr9:133034792 | A | C | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+3628A>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034792 | |||||||
chr9:133034824 | A | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+3660A>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034824 | |||||||
chr9:133034941 | T | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(20): Show |
37 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.153+3777T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133034941 | |||||||
chr9:133035085 | A | G | 5 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+3921A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035085 | |||||||
chr9:133035151 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.153+3987A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035151 | |||||||
chr9:133035184 | A | T | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+4020A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035184 | |||||||
chr9:133035185 | T | A | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+4021T>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035185 | |||||||
chr9:133035216 | A | G | 5 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+4052A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035216 | |||||||
chr9:133035296 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.153+4132C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035296 | |||||||
chr9:133035344 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+4180T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035344 | |||||||
chr9:133035346 | A | T | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+4182A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035346 | |||||||
chr9:133035358 | C | G | 1 | a0001c0001t0001g0041 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.153+4194C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035358 | |||||||
chr9:133035544 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.153+4380G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035544 | |||||||
chr9:133035639 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.153+4475T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035639 | |||||||
chr9:133035683 | GT | G | 5 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+4521delT | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133035683 | ||||||
chr9:133035841 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.153+4677G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035841 | |||||||
chr9:133035863 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.153+4699G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035863 | |||||||
chr9:133035864 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.153+4700G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035864 | |||||||
chr9:133035865 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.153+4701T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035865 | |||||||
chr9:133035916 | G | A | 1 | a0001c0003t0002g0023 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.153+4752G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035916 | |||||||
chr9:133035936 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0080 |
2 | HG01106.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.153+4772G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133035936 | |||||||
chr9:133036013 | A | G | 1 | a0001c0001t0002g0003 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.153+4849A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036013 | |||||||
chr9:133036092 | A | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(15): Show |
32 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.153+4928A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036092 | |||||||
chr9:133036172 | A | G | 1 | a0001c0001t0004g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.153+5008A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036172 | |||||||
chr9:133036175 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0041 |
2 | NA19060.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.153+5011G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036175 | |||||||
chr9:133036233 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0054 |
2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.153+5069G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036233 | |||||||
chr9:133036384 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.153+5220A>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036384 | |||||||
chr9:133036437 | G | C | 1 | a0001c0001t0001g0005 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.153+5273G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036437 | |||||||
chr9:133036437 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.153+5273G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036437 | |||||||
chr9:133036496 | G | C | 1 | a0001c0001t0001g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.153+5332G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036496 | |||||||
chr9:133036660 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.154-5427T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036660 | |||||||
chr9:133036716 | A | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0017 others(74): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.154-5371A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036716 | |||||||
chr9:133036745 | C | T | 1 | a0001c0007t0001g0026 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.154-5342C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036745 | |||||||
chr9:133036777 | T | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(15): Show |
32 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.154-5310T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036777 | |||||||
chr9:133036821 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0101 |
5 | NA18612.hp2 NA18941.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-5266C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036821 | |||||||
chr9:133036843 | T | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(20): Show |
38 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.154-5244T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133036843 | |||||||
chr9:133037009 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.154-5078G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037009 | |||||||
chr9:133037072 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.154-5015C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037072 | |||||||
chr9:133037096 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.154-4991A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037096 | |||||||
chr9:133037116 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.154-4971C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037116 | |||||||
chr9:133037159 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0004 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.154-4928C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037159 | |||||||
chr9:133037177 | G | A | 2 | a0001c0001t0003g0001 a0001c0001t0003g0004 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.154-4910G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037177 | |||||||
chr9:133037189 | A | G | 66 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0036 others(63): Show |
129 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.154-4898A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037189 | |||||||
chr9:133037247 | A | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154-4840A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037247 | |||||||
chr9:133037403 | A | G | 1 | a0001c0001t0005g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.154-4684A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037403 | |||||||
chr9:133037487 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.154-4600A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037487 | |||||||
chr9:133037496 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0044 |
4 | NA18974.hp1 NA18977.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-4591C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037496 | |||||||
chr9:133037522 | TG | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(13): Show |
30 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.154-4558delG | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133037522 | ||||||
chr9:133037523 | G | C | 1 | a0001c0001t0001g0004 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.154-4564G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037523 | |||||||
chr9:133037602 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.154-4485G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037602 | |||||||
chr9:133037712 | T | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-4375T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037712 | |||||||
chr9:133037818 | C | T | 1 | a0003c0009t0001g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.154-4269C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037818 | |||||||
chr9:133037854 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.154-4233C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133037854 | |||||||
chr9:133038096 | C | T | 50 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0043 others(47): Show |
98 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.154-3991C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038096 | |||||||
chr9:133038121 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.154-3966G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038121 | |||||||
chr9:133038142 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0002g0014 a0004c0006t0001g0014 |
5 | HG01069.hp2 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-3945G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038142 | |||||||
chr9:133038186 | G | C | 1 | a0001c0001t0001g0024 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.154-3901G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038186 | |||||||
chr9:133038235 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.154-3852G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038235 | |||||||
chr9:133038235 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.154-3852G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038235 | |||||||
chr9:133038256 | T | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154-3831T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038256 | |||||||
chr9:133038305 | C | T | 1 | a0001c0003t0002g0023 | 3 | HG02717.hp2 HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.154-3782C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038305 | |||||||
chr9:133038353 | C | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(22): Show |
40 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.154-3734C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038353 | |||||||
chr9:133038450 | C | CT | 10 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(7): Show |
10 | HG01433.hp1 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-3619dupT | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133038450 | ||||||
chr9:133038450 | CT | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0121 others(3): Show |
6 | HG02451.hp2 HG03098.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-3619delT | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133038450 | ||||||
chr9:133038490 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.154-3597G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038490 | |||||||
chr9:133038623 | G | GTT | 14 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(11): Show |
28 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.154-3452_154-3451d others(4): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133038623 | ||||||
chr9:133038623 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154-3464G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038623 | |||||||
chr9:133038654 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.154-3433A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038654 | |||||||
chr9:133038701 | C | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154-3386C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038701 | |||||||
chr9:133038914 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.154-3173A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038914 | |||||||
chr9:133038965 | G | T | 28 | a0001c0001t0001g0109 a0001c0001t0002g0003 a0001c0001t0002g0007 others(25): Show |
73 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.154-3122G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038965 | |||||||
chr9:133038988 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-3099C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133038988 | |||||||
chr9:133039003 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.154-3084G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039003 | |||||||
chr9:133039069 | G | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0091 others(1): Show |
9 | HG01081.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-3018G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039069 | |||||||
chr9:133039086 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0137 others(1): Show |
4 | HG02451.hp2 HG02698.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-3001C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039086 | |||||||
chr9:133039123 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.154-2964A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039123 | |||||||
chr9:133039290 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-2797A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039290 | |||||||
chr9:133039447 | A | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154-2640A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039447 | |||||||
chr9:133039527 | C | A | 32 | a0001c0001t0001g0109 a0001c0001t0001g0125 a0001c0001t0002g0003 others(29): Show |
79 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.154-2560C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039527 | |||||||
chr9:133039611 | T | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0036 others(30): Show |
49 | HG00558.hp1 HG01106.hp1 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.154-2476T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039611 | |||||||
chr9:133039770 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.154-2317G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039770 | |||||||
chr9:133039884 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154-2203A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039884 | |||||||
chr9:133039891 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154-2196A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133039891 | |||||||
chr9:133040019 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.154-2068G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040019 | |||||||
chr9:133040027 | C | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154-2060C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040027 | |||||||
chr9:133040040 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154-2047C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040040 | |||||||
chr9:133040159 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154-1928C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040159 | |||||||
chr9:133040190 | A | G | 5 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-1897A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040190 | |||||||
chr9:133040196 | G | A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154-1891G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040196 | |||||||
chr9:133040266 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0087 |
4 | HG02257.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-1821C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040266 | |||||||
chr9:133040339 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.154-1748C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040339 | |||||||
chr9:133040463 | A | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(12): Show |
29 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-1624A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040463 | |||||||
chr9:133040552 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG02015.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.154-1535G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040552 | |||||||
chr9:133040750 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.154-1337C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040750 | |||||||
chr9:133040775 | G | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0086 |
4 | HG01361.hp2 HG01891.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-1312G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040775 | |||||||
chr9:133040838 | A | T | 29 | a0001c0001t0001g0085 a0001c0001t0001g0109 a0001c0001t0002g0003 others(26): Show |
74 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.154-1249A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133040838 | |||||||
chr9:133041015 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0027 |
5 | HG02015.hp2 NA18941.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-1072G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041015 | |||||||
chr9:133041088 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(12): Show |
29 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-999C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041088 | |||||||
chr9:133041115 | T | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-972T>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041115 | |||||||
chr9:133041137 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(12): Show |
29 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-950C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041137 | |||||||
chr9:133041179 | C | T | 1 | a0001c0001t0001g0024 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.154-908C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041179 | |||||||
chr9:133041299 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.154-788G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041299 | |||||||
chr9:133041334 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.154-753G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041334 | |||||||
chr9:133041428 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(12): Show |
29 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.154-659T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041428 | |||||||
chr9:133041432 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.154-655A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041432 | |||||||
chr9:133041468 | CCTCT | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0034 others(4): Show |
12 | HG00140.hp1 HG01070.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-616_154-613del others(4): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133041468 | ||||||
chr9:133041532 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.154-555G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041532 | |||||||
chr9:133041544 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.154-543A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041544 | |||||||
chr9:133041631 | A | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0019 others(19): Show |
67 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.154-456A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041631 | |||||||
chr9:133041643 | A | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0036 others(64): Show |
130 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.154-444A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041643 | |||||||
chr9:133041838 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.154-249G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041838 | |||||||
chr9:133041999 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.154-88C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 1/10 | chr9 | 133041999 | |||||||
chr9:133042357 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(12): Show |
29 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.373+51C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133042357 | |||||||
chr9:133042500 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.373+194T>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133042500 | |||||||
chr9:133042509 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.373+203A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133042509 | |||||||
chr9:133042951 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.373+645C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133042951 | |||||||
chr9:133042960 | A | G | 1 | a0001c0001t0002g0016 | 4 | HG02630.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.373+654A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133042960 | |||||||
chr9:133042980 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.373+674C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133042980 | |||||||
chr9:133043094 | G | T | 28 | a0001c0001t0001g0109 a0001c0001t0002g0003 a0001c0001t0002g0007 others(25): Show |
73 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.374-634G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133043094 | |||||||
chr9:133043251 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.374-477T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133043251 | |||||||
chr9:133043279 | G | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.374-449G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133043279 | |||||||
chr9:133043287 | C | T | 8 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0043 others(5): Show |
9 | HG02109.hp1 HG02897.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.374-441C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133043287 | |||||||
chr9:133043439 | G | T | 7 | a0001c0001t0004g0040 a0001c0001t0004g0139 a0001c0002t0001g0038 others(4): Show |
8 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.374-289G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133043439 | |||||||
chr9:133043498 | T | C | 7 | a0001c0001t0004g0040 a0001c0001t0004g0139 a0001c0002t0001g0038 others(4): Show |
8 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.374-230T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133043498 | |||||||
chr9:133043508 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.374-220C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133043508 | |||||||
chr9:133043697 | A | G | 5 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.374-31A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 2/10 | chr9 | 133043697 | |||||||
chr9:133043991 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(11): Show |
28 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.572+65G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133043991 | |||||||
chr9:133044029 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.572+103C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044029 | |||||||
chr9:133044076 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.572+150C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044076 | |||||||
chr9:133044099 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.572+173C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044099 | |||||||
chr9:133044102 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0087 |
4 | HG02257.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.572+176G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044102 | |||||||
chr9:133044114 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG01070.hp2 HG01081.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.572+188C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044114 | |||||||
chr9:133044118 | C | G | 1 | a0001c0001t0001g0024 | 3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.572+192C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044118 | |||||||
chr9:133044120 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.572+194G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044120 | |||||||
chr9:133044139 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.572+213T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044139 | |||||||
chr9:133044146 | C | CA | 39 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0017 others(36): Show |
99 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.572+243dupA | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 133044146 | ||||||
chr9:133044146 | C | CAA | 7 | a0001c0001t0001g0109 a0001c0001t0002g0007 a0001c0001t0002g0070 others(4): Show |
13 | HG00621.hp2 HG01346.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.572+242_572+243dup others(2): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 133044146 | ||||||
chr9:133044146 | CA | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0043 others(8): Show |
12 | HG02109.hp1 HG02897.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.572+243delA | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 133044146 | ||||||
chr9:133044146 | CAAAA | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(13): Show |
31 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.572+240_572+243del others(4): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 133044146 | ||||||
chr9:133044166 | A | AG | 3 | a0001c0001t0001g0125 a0001c0003t0002g0023 a0001c0003t0002g0047 |
5 | HG02717.hp2 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+240_572+241ins others(1): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044166 | |||||||
chr9:133044424 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.572+498C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044424 | |||||||
chr9:133044568 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+642C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044568 | |||||||
chr9:133044680 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.572+754C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044680 | |||||||
chr9:133044696 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.572+770C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044696 | |||||||
chr9:133044880 | CAT | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+956_572+957del others(2): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 133044880 | ||||||
chr9:133044923 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+997C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133044923 | |||||||
chr9:133045072 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.572+1146T>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045072 | |||||||
chr9:133045219 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(11): Show |
28 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.572+1293G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045219 | |||||||
chr9:133045322 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02109.hp1 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.572+1396C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045322 | |||||||
chr9:133045540 | G | C | 1 | a0001c0001t0004g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.572+1614G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045540 | |||||||
chr9:133045693 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0059 |
7 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.572+1767G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045693 | |||||||
chr9:133045783 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(11): Show |
28 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.572+1857C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045783 | |||||||
chr9:133045843 | G | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02109.hp1 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.572+1917G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045843 | |||||||
chr9:133045880 | G | A | 1 | a0001c0001t0004g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.572+1954G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045880 | |||||||
chr9:133045885 | C | T | 7 | a0001c0001t0004g0040 a0001c0001t0004g0139 a0001c0002t0001g0038 others(4): Show |
8 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+1959C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045885 | |||||||
chr9:133045928 | T | C | 7 | a0001c0001t0004g0040 a0001c0001t0004g0139 a0001c0002t0001g0038 others(4): Show |
8 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+2002T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133045928 | |||||||
chr9:133046156 | T | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0044 |
14 | NA18946.hp1 NA18947.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.572+2230T>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133046156 | |||||||
chr9:133046198 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.572+2272G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133046198 | |||||||
chr9:133046252 | G | A | 28 | a0001c0001t0001g0109 a0001c0001t0002g0003 a0001c0001t0002g0007 others(25): Show |
73 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.572+2326G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133046252 | |||||||
chr9:133046365 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(11): Show |
28 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.572+2439G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133046365 | |||||||
chr9:133046454 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.572+2528A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133046454 | |||||||
chr9:133046662 | G | T | 1 | a0001c0001t0002g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.572+2736G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133046662 | |||||||
chr9:133046934 | C | G | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.572+3008C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133046934 | |||||||
chr9:133047029 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.572+3103C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047029 | |||||||
chr9:133047114 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+3188C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047114 | |||||||
chr9:133047115 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.572+3189G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047115 | |||||||
chr9:133047115 | G | T | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.572+3189G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047115 | |||||||
chr9:133047171 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.572+3245C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047171 | |||||||
chr9:133047193 | C | G | 1 | a0001c0001t0001g0032 | 2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.572+3267C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047193 | |||||||
chr9:133047317 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.572+3391A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047317 | |||||||
chr9:133047459 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.573-3324A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047459 | |||||||
chr9:133047524 | C | CT | 8 | a0001c0001t0004g0040 a0001c0001t0004g0139 a0001c0001t0005g0048 others(5): Show |
9 | HG01106.hp1 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.573-3246dupT | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 133047524 | ||||||
chr9:133047668 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.573-3115C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047668 | |||||||
chr9:133047764 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0121 others(12): Show |
29 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.573-3019C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047764 | |||||||
chr9:133047938 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0099 |
2 | NA18997.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.573-2845G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047938 | |||||||
chr9:133047997 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.573-2786C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133047997 | |||||||
chr9:133048128 | T | TA | 21 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0115 others(18): Show |
36 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(33): Show |
intron_variant | MODIFIER | c.573-2644dupA | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 133048128 | ||||||
chr9:133048129 | A | T | 1 | a0001c0003t0002g0023 | 3 | HG02717.hp2 HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.573-2654A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133048129 | |||||||
chr9:133048475 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.573-2308C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133048475 | |||||||
chr9:133048483 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.573-2300T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133048483 | |||||||
chr9:133048529 | C | T | 5 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.573-2254C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133048529 | |||||||
chr9:133048537 | C | T | 1 | a0001c0001t0005g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.573-2246C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133048537 | |||||||
chr9:133048544 | T | C | 7 | a0001c0001t0004g0040 a0001c0001t0004g0139 a0001c0002t0001g0038 others(4): Show |
8 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.573-2239T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133048544 | |||||||
chr9:133048748 | C | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.573-2035C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133048748 | |||||||
chr9:133049044 | G | A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.573-1739G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049044 | |||||||
chr9:133049050 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.573-1733G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049050 | |||||||
chr9:133049067 | G | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0034 others(4): Show |
12 | HG00140.hp1 HG01070.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.573-1716G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049067 | |||||||
chr9:133049071 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.573-1712G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049071 | |||||||
chr9:133049234 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.573-1549C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049234 | |||||||
chr9:133049305 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.573-1478A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049305 | |||||||
chr9:133049340 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0044 |
14 | NA18946.hp1 NA18947.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.573-1443G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049340 | |||||||
chr9:133049383 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.573-1400C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049383 | |||||||
chr9:133049384 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.573-1399G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049384 | |||||||
chr9:133049577 | T | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.573-1206T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049577 | |||||||
chr9:133049673 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.573-1110G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049673 | |||||||
chr9:133049702 | C | T | 1 | a0001c0001t0004g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.573-1081C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049702 | |||||||
chr9:133049728 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0036 others(32): Show |
51 | HG00558.hp1 HG01106.hp1 HG01257.hp2 others(48): Show |
intron_variant | MODIFIER | c.573-1055T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049728 | |||||||
chr9:133049846 | CCCCAGCC others(7): Show |
C | 5 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.573-935_573-922del others(14): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 133049846 | ||||||
chr9:133049856 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.573-927C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049856 | |||||||
chr9:133049874 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0058 |
6 | HG01891.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.573-909G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133049874 | |||||||
chr9:133050160 | C | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.573-623C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133050160 | |||||||
chr9:133050166 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG02109.hp1 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.573-617C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133050166 | |||||||
chr9:133050536 | G | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.573-247G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133050536 | |||||||
chr9:133050593 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.573-190G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133050593 | |||||||
chr9:133050630 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0036 others(31): Show |
50 | HG00558.hp1 HG01106.hp1 HG01257.hp2 others(47): Show |
intron_variant | MODIFIER | c.573-153A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 3/10 | chr9 | 133050630 | |||||||
chr9:133051213 | C | T | 7 | a0001c0001t0002g0015 a0001c0001t0002g0094 a0001c0001t0002g0098 others(4): Show |
10 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.768+235C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051213 | |||||||
chr9:133051214 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG02015.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.768+236G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051214 | |||||||
chr9:133051224 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.768+246T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051224 | |||||||
chr9:133051333 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.768+355C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051333 | |||||||
chr9:133051348 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.768+370C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051348 | |||||||
chr9:133051374 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.768+396C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051374 | |||||||
chr9:133051472 | G | A | 1 | a0001c0001t0005g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.768+494G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051472 | |||||||
chr9:133051563 | C | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.769-497C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051563 | |||||||
chr9:133051606 | A | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0036 others(33): Show |
52 | HG00558.hp1 HG01106.hp1 HG01257.hp2 others(49): Show |
intron_variant | MODIFIER | c.769-454A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051606 | |||||||
chr9:133051609 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.769-451C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051609 | |||||||
chr9:133051623 | C | T | 1 | a0001c0001t0004g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.769-437C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051623 | |||||||
chr9:133051926 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.769-134C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133051926 | |||||||
chr9:133052042 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.769-18T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 4/10 | chr9 | 133052042 | |||||||
chr9:133052294 | C | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.873+130C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052294 | |||||||
chr9:133052406 | C | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0071 others(13): Show |
30 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.873+242C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052406 | |||||||
chr9:133052512 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.873+348C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052512 | |||||||
chr9:133052560 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.873+396G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052560 | |||||||
chr9:133052603 | A | T | 2 | a0001c0001t0002g0014 a0004c0006t0001g0014 |
4 | HG01069.hp2 HG01071.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.873+439A>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052603 | |||||||
chr9:133052703 | C | T | 4 | a0001c0002t0001g0038 a0001c0002t0001g0122 a0001c0002t0001g0124 others(1): Show |
5 | HG02258.hp2 HG02647.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.873+539C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052703 | |||||||
chr9:133052781 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0053 |
3 | NA18747.hp1 NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.873+617C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052781 | |||||||
chr9:133052866 | T | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.873+702T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052866 | |||||||
chr9:133052867 | CTG | C | 2 | a0001c0003t0002g0023 a0001c0003t0002g0047 |
4 | HG02717.hp2 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.873+705_873+706del others(2): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 133052867 | ||||||
chr9:133052968 | G | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02109.hp1 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.873+804G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052968 | |||||||
chr9:133052992 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.873+828C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133052992 | |||||||
chr9:133053037 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.874-791G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053037 | |||||||
chr9:133053071 | C | A | 1 | a0001c0001t0002g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.874-757C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053071 | |||||||
chr9:133053078 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.874-750G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053078 | |||||||
chr9:133053156 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.874-672A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053156 | |||||||
chr9:133053172 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.874-656A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053172 | |||||||
chr9:133053222 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.874-606T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053222 | |||||||
chr9:133053265 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.874-563G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053265 | |||||||
chr9:133053320 | C | T | 1 | a0001c0002t0001g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.874-508C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053320 | |||||||
chr9:133053342 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.874-486C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053342 | |||||||
chr9:133053387 | C | T | 1 | a0001c0003t0002g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.874-441C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053387 | |||||||
chr9:133053388 | G | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.874-440G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053388 | |||||||
chr9:133053467 | T | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.874-361T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053467 | |||||||
chr9:133053682 | G | C | 1 | a0001c0001t0002g0101 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.874-146G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053682 | |||||||
chr9:133053813 | A | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0039 others(27): Show |
46 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(43): Show |
intron_variant | MODIFIER | c.874-15A>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 5/10 | chr9 | 133053813 | |||||||
chr9:133053983 | C | A | 9 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0004g0040 others(6): Show |
10 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.988+41C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 6/10 | chr9 | 133053983 | |||||||
chr9:133054025 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.988+83C>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 6/10 | chr9 | 133054025 | |||||||
chr9:133054135 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.988+193A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 6/10 | chr9 | 133054135 | |||||||
chr9:133054286 | T | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.989-122T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 6/10 | chr9 | 133054286 | |||||||
chr9:133054375 | C | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.989-33C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 6/10 | chr9 | 133054375 | |||||||
chr9:133054393 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.989-15C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 6/10 | chr9 | 133054393 | |||||||
chr9:133054539 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1069+51G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 7/10 | chr9 | 133054539 | |||||||
chr9:133054541 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1069+53G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 7/10 | chr9 | 133054541 | |||||||
chr9:133054645 | T | G | 1 | a0001c0001t0002g0102 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1070-67T>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 7/10 | chr9 | 133054645 | |||||||
chr9:133054821 | T | TGAGCCCC others(20): Show |
2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1167+13_1167+14ins others(27): Show |
GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 133054821 | ||||||
chr9:133054863 | G | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1167+54G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133054863 | |||||||
chr9:133054934 | T | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1167+125T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133054934 | |||||||
chr9:133054984 | G | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1167+175G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133054984 | |||||||
chr9:133055064 | T | C | 1 | a0001c0003t0002g0023 | 3 | HG02717.hp2 HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1167+255T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055064 | |||||||
chr9:133055079 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0097 a0001c0001t0002g0100 |
5 | HG00621.hp2 NA18998.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167+270C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055079 | |||||||
chr9:133055080 | G | A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1167+271G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055080 | |||||||
chr9:133055104 | C | G | 1 | a0001c0001t0004g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1167+295C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055104 | |||||||
chr9:133055248 | G | T | 1 | a0001c0001t0001g0039 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1167+439G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055248 | |||||||
chr9:133055250 | G | A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1167+441G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055250 | |||||||
chr9:133055284 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1167+475C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055284 | |||||||
chr9:133055288 | C | G | 1 | a0001c0001t0002g0037 | 2 | HG01109.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1167+479C>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055288 | |||||||
chr9:133055348 | T | C | 69 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0026 others(66): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1167+539T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055348 | |||||||
chr9:133055361 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0065 a0001c0001t0001g0087 |
5 | HG02257.hp2 HG02809.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167+552G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055361 | |||||||
chr9:133055402 | T | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0026 others(34): Show |
56 | HG00558.hp1 HG01106.hp1 HG01257.hp2 others(53): Show |
intron_variant | MODIFIER | c.1167+593T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055402 | |||||||
chr9:133055432 | A | G | 8 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(5): Show |
10 | HG02258.hp2 HG02647.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1168-580A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055432 | |||||||
chr9:133055497 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02109.hp1 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168-515G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055497 | |||||||
chr9:133055564 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG02109.hp1 HG02602.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168-448G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055564 | |||||||
chr9:133055742 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1168-270C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055742 | |||||||
chr9:133055875 | G | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1168-137G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 8/10 | chr9 | 133055875 | |||||||
chr9:133056130 | G | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0024 |
10 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+36G>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 9/10 | chr9 | 133056130 | |||||||
chr9:133056340 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1250+246C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 9/10 | chr9 | 133056340 | |||||||
chr9:133056378 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0034 |
2 | HG01074.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1250+284C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 9/10 | chr9 | 133056378 | |||||||
chr9:133056559 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1251-207T>C | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 9/10 | chr9 | 133056559 | |||||||
chr9:133056570 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0092 others(1): Show |
5 | HG02897.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-196C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 9/10 | chr9 | 133056570 | |||||||
chr9:133056572 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0024 |
10 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251-194G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 9/10 | chr9 | 133056572 | |||||||
chr9:133056620 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1251-146G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 9/10 | chr9 | 133056620 | |||||||
chr9:133056654 | G | A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1251-112G>A | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 9/10 | chr9 | 133056654 | |||||||
chr9:133057151 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0139 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1393+243C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 10/10 | chr9 | 133057151 | |||||||
chr9:133057249 | G | T | 1 | a0001c0001t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1393+341G>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 10/10 | chr9 | 133057249 | |||||||
chr9:133057557 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0071 others(14): Show |
31 | HG00558.hp1 HG01257.hp2 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.1394-257A>G | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 10/10 | chr9 | 133057557 | |||||||
chr9:133057709 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1394-105C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 10/10 | chr9 | 133057709 | |||||||
chr9:133057735 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
62 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1394-79C>T | GTF3C5 | ENSG00000148308.18 | transcript | ENST00000372097.10 | protein_coding | 10/10 | chr9 | 133057735 |