Item | Value |
---|---|
geneid | 1660 |
ensemblid | ENSG00000135829.17 |
hgncid | 2750 |
symbol | DHX9 |
name | DExH-box helicase 9 |
refseq_nuc | NM_001357.5 |
refseq_prot | NP_001348.2 |
ensembl_nuc | ENST00000367549.4 |
ensembl_prot | ENSP00000356520.3 |
mane_status | MANE Select |
chr | chr1 |
start | 182839347 |
end | 182887982 |
strand | + |
ver | v1.2 |
region | chr1:182839347-182887982 |
region5000 | chr1:182834347-182892982 |
regionname0 | DHX9_chr1_182839347_182887982 |
regionname5000 | DHX9_chr1_182834347_182892982 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3810 | 166 | 40 | 45 | 55 | 6 | 19 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0002 | 0/0 | 3810 | 71 | 28 | 4 | 34 | 1 | 4 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0003 | 0/0 | 3810 | 10 | 1 | 8 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0004 | 0/0 | 3810 | 9 | 9 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0005 | 1/0 | 3810 | 8 | 5 | 2 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0006 | 0/0 | 3810 | 5 | 0 | 0 | 5 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0007 | 0/0 | 3810 | 2 | 1 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0008 | 0/0 | 3810 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0009 | 0/0 | 3810 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0010 | 0/0 | 3810 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0011 | 0/0 | 3810 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 | ||
a0001c0012 | 0/0 | 3810 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | ATGGG others(3805): Show |
chr1 | 182834347 | 182892982 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4493 | 162 | 36 | 45 | 55 | 6 | 19 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0001t0002 | 0/0 | 4493 | 4 | 4 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0002t0001 | 0/0 | 4493 | 69 | 26 | 4 | 34 | 1 | 4 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0002t0003 | 0/0 | 4493 | 2 | 2 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0003t0001 | 0/0 | 4493 | 10 | 1 | 8 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0004t0001 | 0/0 | 4493 | 9 | 9 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0005t0001 | 1/0 | 4493 | 8 | 5 | 2 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0006t0001 | 0/0 | 4493 | 5 | 0 | 0 | 5 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0007t0001 | 0/0 | 4493 | 2 | 1 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0008t0001 | 0/0 | 4493 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0009t0001 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0010t0004 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0011t0001 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
a0001c0012t0001 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | GCCAT others(4488): Show |
chr1 | 182834347 | 182892982 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 1 | 2 | 3 | 1 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0004 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0003t0001g0007 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0005t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0005t0001g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0005t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0005t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0006t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0006t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0007t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0008t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0009t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0010t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0011t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
a0001c0012t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0138 | EUR | GBR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | CHS | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0046 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0175 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01109 | hp1 | a0001 | c0005 | t0001 | g0125 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01243 | hp2 | a0001 | c0005 | t0001 | g0053 | AMR | PUR | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0174 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01496 | hp2 | a0001 | c0007 | t0001 | g0084 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | IBS | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0176 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0177 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0200 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02056 | hp2 | a0001 | c0006 | t0001 | g0156 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02074 | hp2 | a0001 | c0006 | t0001 | g0112 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | CDX | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02165 | hp2 | a0001 | c0006 | t0001 | g0074 | EAS | CDX | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0057 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02622 | hp1 | a0001 | c0012 | t0001 | g0133 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02723 | hp1 | a0001 | c0004 | t0001 | g0222 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0210 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02965 | hp1 | a0001 | c0010 | t0004 | g0221 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0216 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02976 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03041 | hp1 | a0001 | c0005 | t0001 | g0003 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0212 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03209 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0211 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03486 | hp2 | a0001 | c0005 | t0001 | g0054 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0043 | AFR | ESN | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03579 | hp2 | a0001 | c0011 | t0001 | g0055 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | BEB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | BEB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG04228 | hp1 | a0001 | c0008 | t0001 | g0063 | SAS | STU | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18522 | hp1 | a0001 | c0002 | t0003 | g0131 | AFR | YRI | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0215 | AFR | YRI | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | YRI | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19000 | hp2 | a0001 | c0006 | t0001 | g0035 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | LWK | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19074 | hp1 | a0001 | c0006 | t0001 | g0071 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19240 | hp1 | a0001 | c0007 | t0001 | g0096 | AFR | YRI | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0217 | AFR | YRI | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | GIH | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02109 | hp2 | a0001 | c0009 | t0001 | g0152 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0213 | AFR | MSL | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | USA | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | USA | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0164 | REF | REF | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
homoSapiens | grch38p0 | a0001 | c0005 | t0001 | g0052 | REF | REF | DHX9_chr1_182834347_182892982 | DHX9 | chr1 | 182834347 | 182892982 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182843296 | T | A | 1 | a0001c0008 | 1 | HG04228.hp1 | splice_region_variant&synonymous_variant | LOW | c.114T>A | p.Val38Val | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/28 | 246/4493 | 114/3813 | 38/1270 | chr1 | 182843296 | |||
chr1:182843431 | T | C | 1 | a0001c0009 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.249T>C | p.Phe83Phe | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/28 | 381/4493 | 249/3813 | 83/1270 | chr1 | 182843431 | |||
chr1:182854035 | A | G | 1 | a0001c0012 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.483A>G | p.Leu161Leu | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/28 | 615/4493 | 483/3813 | 161/1270 | chr1 | 182854035 | |||
chr1:182858162 | G | A | 2 | a0001c0004 a0001c0012 |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
synonymous_variant | LOW | c.732G>A | p.Leu244Leu | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 8/28 | 864/4493 | 732/3813 | 244/1270 | chr1 | 182858162 | |||
chr1:182858625 | T | A | 1 | a0001c0012 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.885T>A | p.Leu295Leu | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 9/28 | 1017/4493 | 885/3813 | 295/1270 | chr1 | 182858625 | |||
chr1:182858747 | T | G | 1 | a0001c0007 | 2 | HG01496.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.915T>G | p.Ser305Ser | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 10/28 | 1047/4493 | 915/3813 | 305/1270 | chr1 | 182858747 | |||
chr1:182866527 | C | T | 1 | a0001c0006 | 5 | HG02056.hp2 HG02074.hp2 HG02165.hp2 others(2): Show |
synonymous_variant | LOW | c.1416C>T | p.Ser472Ser | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 13/28 | 1548/4493 | 1416/3813 | 472/1270 | chr1 | 182866527 | |||
chr1:182874885 | C | T | 3 | a0001c0002 a0001c0003 a0001c0009 |
82 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(79): Show |
synonymous_variant | LOW | c.1746C>T | p.Thr582Thr | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/28 | 1878/4493 | 1746/3813 | 582/1270 | chr1 | 182874885 | |||
chr1:182876211 | C | T | 1 | a0001c0003 | 10 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(7): Show |
synonymous_variant | LOW | c.1977C>T | p.Gly659Gly | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 17/28 | 2109/4493 | 1977/3813 | 659/1270 | chr1 | 182876211 | |||
chr1:182878072 | C | T | 1 | a0001c0011 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.2250C>T | p.Thr750Thr | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/28 | 2382/4493 | 2250/3813 | 750/1270 | chr1 | 182878072 | |||
chr1:182881264 | C | T | 1 | a0001c0010 | 1 | HG02965.hp1 | splice_region_variant&synonymous_variant | LOW | c.2625C>T | p.Tyr875Tyr | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 23/28 | 2757/4493 | 2625/3813 | 875/1270 | chr1 | 182881264 | |||
chr1:182881592 | T | C | 10 | a0001c0001 a0001c0002 a0001c0003 others(7): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
synonymous_variant | LOW | c.2859T>C | p.Thr953Thr | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/28 | 2991/4493 | 2859/3813 | 953/1270 | chr1 | 182881592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182839432 | G | A | 1 | a0001c0010t0004 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/28 | 3135 | chr1 | 182839432 | ||||||
chr1:182887522 | C | T | 1 | a0001c0002t0003 | 2 | HG03516.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*88C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 28/28 | 88 | chr1 | 182887522 | ||||||
chr1:182887642 | A | T | 1 | a0001c0001t0002 | 4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*208A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 28/28 | 208 | chr1 | 182887642 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182839474 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0223 |
3 | HG03239.hp2 HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-23+18C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839474 | |||||||
chr1:182839493 | C | CG | 22 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(19): Show |
22 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+41dupG | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 182839493 | ||||||
chr1:182839504 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-23+48G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839504 | |||||||
chr1:182839511 | C | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-23+55C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839511 | |||||||
chr1:182839532 | C | T | 1 | a0001c0004t0001g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+76C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839532 | |||||||
chr1:182839636 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-23+180G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839636 | |||||||
chr1:182839660 | C | G | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+204C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839660 | |||||||
chr1:182839670 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-23+214C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839670 | |||||||
chr1:182839724 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0218 |
3 | HG02630.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-23+268C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839724 | |||||||
chr1:182839725 | GCT | G | 3 | a0001c0004t0001g0215 a0001c0004t0001g0216 a0001c0004t0001g0217 |
3 | HG02970.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-23+270_-23+271del others(2): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182839725 | |||||||
chr1:182840024 | G | A | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+568G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840024 | |||||||
chr1:182840299 | C | CT | 68 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0023 others(65): Show |
83 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-23+864dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 182840299 | ||||||
chr1:182840299 | C | CTT | 33 | a0001c0001t0001g0011 a0001c0001t0001g0180 a0001c0001t0001g0181 others(30): Show |
42 | HG00642.hp2 HG00738.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.-23+863_-23+864dup others(2): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 182840299 | ||||||
chr1:182840299 | C | CTTT | 15 | a0001c0001t0001g0047 a0001c0001t0001g0201 a0001c0001t0001g0202 others(12): Show |
15 | HG00735.hp2 HG01261.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-23+862_-23+864dup others(3): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 182840299 | ||||||
chr1:182840299 | C | CTTTT | 7 | a0001c0001t0001g0048 a0001c0002t0001g0214 a0001c0004t0001g0210 others(4): Show |
7 | HG02602.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+861_-23+864dup others(4): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 182840299 | ||||||
chr1:182840420 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+964C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840420 | |||||||
chr1:182840598 | G | C | 1 | a0001c0002t0001g0127 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-23+1142G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840598 | |||||||
chr1:182840700 | G | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.-23+1244G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840700 | |||||||
chr1:182840702 | T | A | 1 | a0001c0008t0001g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-23+1246T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840702 | |||||||
chr1:182840741 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-23+1285A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840741 | |||||||
chr1:182840741 | AT | A | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+1287delT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 182840741 | ||||||
chr1:182840828 | C | G | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+1372C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840828 | |||||||
chr1:182840961 | T | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
17 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-23+1505T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840961 | |||||||
chr1:182840968 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
17 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-23+1512C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840968 | |||||||
chr1:182840981 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-23+1525A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182840981 | |||||||
chr1:182841290 | C | CA | 28 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0047 others(25): Show |
32 | HG01069.hp1 HG01123.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-22-1244dupA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 182841290 | ||||||
chr1:182841451 | T | A | 1 | a0001c0001t0001g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-22-1094T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182841451 | |||||||
chr1:182841461 | A | G | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-22-1084A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182841461 | |||||||
chr1:182841748 | A | C | 15 | a0001c0001t0001g0048 a0001c0001t0002g0026 a0001c0001t0002g0049 others(12): Show |
16 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-22-797A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182841748 | |||||||
chr1:182841775 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-22-770A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182841775 | |||||||
chr1:182841993 | A | G | 2 | a0001c0002t0003g0043 a0001c0002t0003g0131 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-22-552A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182841993 | |||||||
chr1:182842089 | C | T | 2 | a0001c0004t0001g0212 a0001c0004t0001g0213 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-22-456C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182842089 | |||||||
chr1:182842091 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-22-454G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182842091 | |||||||
chr1:182842361 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-22-184G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182842361 | |||||||
chr1:182842384 | CAT | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(10): Show |
16 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-157_-22-156del others(2): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | 182842384 | ||||||
chr1:182842487 | G | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0180 others(3): Show |
7 | HG01069.hp1 HG01884.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22-58G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 1/27 | chr1 | 182842487 | |||||||
chr1:182842777 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.111+100T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 2/27 | chr1 | 182842777 | |||||||
chr1:182842904 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0208 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.111+227A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 2/27 | chr1 | 182842904 | |||||||
chr1:182843077 | G | GA | 6 | a0001c0003t0001g0007 a0001c0003t0001g0046 a0001c0003t0001g0174 others(3): Show |
9 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.112-208dupA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 182843077 | ||||||
chr1:182843082 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
9 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.112-212A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 2/27 | chr1 | 182843082 | |||||||
chr1:182843275 | C | CT | 23 | a0001c0001t0001g0048 a0001c0002t0001g0037 a0001c0002t0001g0129 others(20): Show |
26 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.112-5dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr1 | 182843275 | ||||||
chr1:182843443 | C | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
6 | NA18963.hp2 NA18982.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+9C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182843443 | |||||||
chr1:182843449 | C | T | 66 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(63): Show |
82 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.252+15C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182843449 | |||||||
chr1:182843495 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.252+61C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182843495 | |||||||
chr1:182843658 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0208 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.252+224C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182843658 | |||||||
chr1:182843744 | T | G | 1 | a0001c0002t0001g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.252+310T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182843744 | |||||||
chr1:182843792 | A | G | 5 | a0001c0003t0001g0007 a0001c0003t0001g0046 a0001c0003t0001g0175 others(2): Show |
8 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+358A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182843792 | |||||||
chr1:182843818 | G | A | 3 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 |
4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+384G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182843818 | |||||||
chr1:182843821 | G | A | 66 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(63): Show |
82 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.252+387G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182843821 | |||||||
chr1:182844049 | A | G | 1 | a0001c0003t0001g0174 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.252+615A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844049 | |||||||
chr1:182844178 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.252+744C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844178 | |||||||
chr1:182844496 | G | A | 6 | a0001c0004t0001g0211 a0001c0004t0001g0212 a0001c0004t0001g0213 others(3): Show |
6 | HG02970.hp1 HG03195.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+1062G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844496 | |||||||
chr1:182844505 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0067 others(3): Show |
8 | NA18940.hp1 NA18959.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+1071G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844505 | |||||||
chr1:182844540 | G | T | 14 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(11): Show |
17 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.252+1106G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844540 | |||||||
chr1:182844591 | G | A | 1 | a0001c0006t0001g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.252+1157G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844591 | |||||||
chr1:182844723 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(10): Show |
16 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.252+1289G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844723 | |||||||
chr1:182844756 | A | T | 1 | a0001c0001t0002g0220 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.252+1322A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844756 | |||||||
chr1:182844859 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.252+1425C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844859 | |||||||
chr1:182844905 | C | T | 2 | a0001c0004t0001g0212 a0001c0004t0001g0213 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.252+1471C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844905 | |||||||
chr1:182844916 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0208 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.252+1482G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844916 | |||||||
chr1:182844920 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.252+1486C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844920 | |||||||
chr1:182844937 | A | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 |
4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1503A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182844937 | |||||||
chr1:182845148 | T | C | 94 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(91): Show |
114 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.252+1714T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182845148 | |||||||
chr1:182845287 | A | G | 11 | a0001c0001t0001g0048 a0001c0004t0001g0057 a0001c0004t0001g0210 others(8): Show |
11 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+1853A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182845287 | |||||||
chr1:182845328 | T | G | 1 | a0001c0002t0001g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.252+1894T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182845328 | |||||||
chr1:182845429 | G | GA | 79 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0116 others(76): Show |
96 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.252+2008dupA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182845429 | ||||||
chr1:182845430 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.252+1996A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182845430 | |||||||
chr1:182845641 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.252+2207C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182845641 | |||||||
chr1:182845644 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.252+2210C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182845644 | |||||||
chr1:182845987 | A | G | 7 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0002t0001g0060 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+2553A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182845987 | |||||||
chr1:182846082 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0171 |
3 | HG01168.hp2 HG01433.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.252+2648C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182846082 | |||||||
chr1:182846215 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.252+2781A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182846215 | |||||||
chr1:182846237 | C | CT | 9 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0002t0001g0060 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+2820dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182846237 | ||||||
chr1:182846237 | CT | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(10): Show |
16 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.252+2820delT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182846237 | ||||||
chr1:182846801 | A | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(10): Show |
16 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.252+3367A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182846801 | |||||||
chr1:182846802 | T | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(10): Show |
16 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.252+3368T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182846802 | |||||||
chr1:182846852 | A | G | 1 | a0001c0005t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.252+3418A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182846852 | |||||||
chr1:182846862 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.252+3428A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182846862 | |||||||
chr1:182846943 | TTTA | T | 3 | a0001c0006t0001g0035 a0001c0006t0001g0071 a0001c0006t0001g0112 |
3 | HG02074.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.252+3512_252+3514d others(5): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182846943 | ||||||
chr1:182847138 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.252+3704A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847138 | |||||||
chr1:182847218 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0182 others(1): Show |
6 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+3784T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847218 | |||||||
chr1:182847375 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0223 |
3 | HG03239.hp2 HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.252+3941T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847375 | |||||||
chr1:182847456 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.252+4022C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847456 | |||||||
chr1:182847459 | A | G | 6 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0002t0001g0060 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+4025A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847459 | |||||||
chr1:182847570 | G | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 |
4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+4136G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847570 | |||||||
chr1:182847619 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(10): Show |
16 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.252+4185C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847619 | |||||||
chr1:182847774 | C | T | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.252+4340C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847774 | |||||||
chr1:182847775 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.252+4341G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847775 | |||||||
chr1:182847969 | T | A | 2 | a0001c0002t0001g0058 a0001c0002t0001g0059 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.253-4264T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182847969 | |||||||
chr1:182848154 | CATT | C | 15 | a0001c0001t0001g0048 a0001c0001t0002g0026 a0001c0001t0002g0049 others(12): Show |
16 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.253-4076_253-4074d others(5): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182848154 | ||||||
chr1:182848541 | A | G | 8 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(5): Show |
8 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-3692A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182848541 | |||||||
chr1:182848563 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.253-3670A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182848563 | |||||||
chr1:182848573 | GTT | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0199 a0001c0001t0001g0208 |
3 | HG01123.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.253-3655_253-3654d others(4): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182848573 | ||||||
chr1:182848590 | G | A | 94 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(91): Show |
114 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.253-3643G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182848590 | |||||||
chr1:182848697 | T | G | 1 | a0001c0002t0001g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.253-3536T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182848697 | |||||||
chr1:182848798 | T | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(25): Show |
32 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.253-3435T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182848798 | |||||||
chr1:182848918 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.253-3315A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182848918 | |||||||
chr1:182849022 | A | C | 2 | a0001c0002t0003g0043 a0001c0002t0003g0131 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.253-3211A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849022 | |||||||
chr1:182849181 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.253-3052C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849181 | |||||||
chr1:182849203 | AT | A | 15 | a0001c0001t0001g0048 a0001c0001t0002g0026 a0001c0001t0002g0049 others(12): Show |
16 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.253-3026delT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182849203 | ||||||
chr1:182849207 | T | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(10): Show |
16 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.253-3026T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849207 | |||||||
chr1:182849212 | T | A | 15 | a0001c0001t0001g0048 a0001c0001t0002g0026 a0001c0001t0002g0049 others(12): Show |
16 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.253-3021T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849212 | |||||||
chr1:182849222 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0154 a0001c0001t0001g0155 |
4 | HG00621.hp2 HG02135.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-3011T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849222 | |||||||
chr1:182849300 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.253-2933A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849300 | |||||||
chr1:182849314 | T | C | 4 | a0001c0001t0001g0132 a0001c0001t0001g0199 a0001c0001t0001g0208 others(1): Show |
4 | HG01123.hp1 HG02145.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-2919T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849314 | |||||||
chr1:182849317 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.253-2916C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849317 | |||||||
chr1:182849405 | T | C | 29 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.253-2828T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849405 | |||||||
chr1:182849452 | T | C | 5 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0002t0001g0060 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-2781T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849452 | |||||||
chr1:182849539 | G | A | 2 | a0001c0006t0001g0074 a0001c0006t0001g0156 |
2 | HG02056.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.253-2694G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849539 | |||||||
chr1:182849579 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.253-2654A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849579 | |||||||
chr1:182849613 | A | C | 1 | a0001c0002t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.253-2620A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849613 | |||||||
chr1:182849811 | T | A | 2 | a0001c0002t0001g0058 a0001c0002t0001g0059 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.253-2422T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849811 | |||||||
chr1:182849908 | C | T | 6 | a0001c0004t0001g0211 a0001c0004t0001g0212 a0001c0004t0001g0213 others(3): Show |
6 | HG02970.hp1 HG03195.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-2325C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182849908 | |||||||
chr1:182849947 | C | CA | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.253-2279dupA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182849947 | ||||||
chr1:182849982 | A | AC | 33 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(30): Show |
39 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.253-2241dupC | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182849982 | ||||||
chr1:182849982 | A | ACC | 10 | a0001c0001t0001g0157 a0001c0001t0001g0209 a0001c0002t0001g0137 others(7): Show |
13 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-2242_253-2241d others(4): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182849982 | ||||||
chr1:182849982 | AC | A | 62 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0015 others(59): Show |
73 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.253-2241delC | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182849982 | ||||||
chr1:182850014 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.253-2219C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182850014 | |||||||
chr1:182850255 | A | G | 43 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(40): Show |
56 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.253-1978A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182850255 | |||||||
chr1:182850320 | C | T | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.253-1913C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182850320 | |||||||
chr1:182850321 | G | A | 14 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(11): Show |
15 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.253-1912G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182850321 | |||||||
chr1:182850352 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.253-1881C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182850352 | |||||||
chr1:182850589 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0092 |
3 | HG01346.hp1 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.253-1644T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182850589 | |||||||
chr1:182850594 | C | CA | 11 | a0001c0001t0001g0205 a0001c0002t0001g0037 a0001c0002t0001g0128 others(8): Show |
11 | HG01361.hp1 HG01891.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.253-1624dupA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182850594 | ||||||
chr1:182850594 | CA | C | 15 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0105 others(12): Show |
15 | HG00597.hp1 HG01257.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.253-1624delA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr1 | 182850594 | ||||||
chr1:182850876 | G | A | 66 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(63): Show |
82 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.253-1357G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182850876 | |||||||
chr1:182851087 | G | A | 2 | a0001c0004t0001g0210 a0001c0004t0001g0222 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.253-1146G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182851087 | |||||||
chr1:182851113 | T | A | 51 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(48): Show |
64 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.253-1120T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182851113 | |||||||
chr1:182851130 | A | C | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.253-1103A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182851130 | |||||||
chr1:182851160 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.253-1073A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182851160 | |||||||
chr1:182851198 | A | T | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-1035A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182851198 | |||||||
chr1:182851239 | A | G | 1 | a0001c0008t0001g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.253-994A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182851239 | |||||||
chr1:182851561 | G | A | 1 | a0001c0002t0001g0138 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.253-672G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182851561 | |||||||
chr1:182852161 | A | G | 15 | a0001c0001t0001g0048 a0001c0001t0002g0026 a0001c0001t0002g0049 others(12): Show |
16 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.253-72A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 3/27 | chr1 | 182852161 | |||||||
chr1:182852350 | G | T | 10 | a0001c0004t0001g0057 a0001c0004t0001g0210 a0001c0004t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.364+6G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182852350 | |||||||
chr1:182852368 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.364+24G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182852368 | |||||||
chr1:182852417 | G | A | 1 | a0001c0006t0001g0112 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.364+73G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182852417 | |||||||
chr1:182852450 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
17 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.364+106A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182852450 | |||||||
chr1:182852461 | C | T | 9 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0045 others(6): Show |
13 | HG01192.hp1 HG01884.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.364+117C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182852461 | |||||||
chr1:182852563 | C | A | 94 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(91): Show |
114 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.364+219C>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182852563 | |||||||
chr1:182852623 | G | A | 1 | a0001c0004t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.364+279G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182852623 | |||||||
chr1:182852939 | C | CTTTGAGG others(446): Show |
12 | a0001c0002t0001g0128 a0001c0002t0001g0129 a0001c0002t0001g0130 others(9): Show |
15 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.365-364_365-363ins others(453): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182852939 | C | CTTTGAGG others(447): Show |
1 | a0001c0002t0003g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.365-364_365-363ins others(454): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182852939 | C | CTTTGAGG others(446): Show |
2 | a0001c0002t0001g0037 a0001c0002t0001g0179 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.365-364_365-363ins others(453): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182852939 | C | CTTTGAGG others(446): Show |
53 | a0001c0001t0001g0048 a0001c0002t0001g0002 a0001c0002t0001g0009 others(50): Show |
66 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.365-364_365-363ins others(453): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182852939 | C | CTTTGAGG others(447): Show |
8 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(5): Show |
9 | HG02451.hp2 HG02622.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.365-364_365-363ins others(454): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182852939 | C | CTTTGAGG others(447): Show |
2 | a0001c0004t0001g0212 a0001c0004t0001g0213 |
2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.365-364_365-363ins others(454): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182852939 | C | CTTTGAGG others(446): Show |
14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
17 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.365-364_365-363ins others(453): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182852939 | C | CTTTGAGG others(447): Show |
1 | a0001c0002t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.365-364_365-363ins others(454): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182852939 | C | CTTTGAGG others(448): Show |
2 | a0001c0002t0001g0060 a0001c0009t0001g0152 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.365-364_365-363ins others(455): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr1 | 182852939 | ||||||
chr1:182853034 | C | T | 1 | a0001c0011t0001g0055 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.365-272C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182853034 | |||||||
chr1:182853163 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.365-143G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182853163 | |||||||
chr1:182853232 | A | G | 51 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(48): Show |
64 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.365-74A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 4/27 | chr1 | 182853232 | |||||||
chr1:182853516 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.477+98G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 5/27 | chr1 | 182853516 | |||||||
chr1:182853669 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0091 |
6 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.477+251A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 5/27 | chr1 | 182853669 | |||||||
chr1:182853720 | A | G | 1 | a0001c0002t0001g0147 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.477+302A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 5/27 | chr1 | 182853720 | |||||||
chr1:182853726 | A | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.478-304A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 5/27 | chr1 | 182853726 | |||||||
chr1:182853793 | A | AT | 7 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0119 others(4): Show |
7 | HG00621.hp1 HG01175.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-225dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr1 | 182853793 | ||||||
chr1:182853793 | AT | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0020 others(12): Show |
18 | HG01069.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.478-225delT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr1 | 182853793 | ||||||
chr1:182853794 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.478-236T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 5/27 | chr1 | 182853794 | |||||||
chr1:182853983 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.478-47A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 5/27 | chr1 | 182853983 | |||||||
chr1:182854252 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0173 |
2 | HG01168.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.626+74A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182854252 | |||||||
chr1:182854385 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.626+207G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182854385 | |||||||
chr1:182854512 | A | AT | 4 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
5 | NA18982.hp2 NA18998.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+344dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr1 | 182854512 | ||||||
chr1:182854607 | A | G | 1 | a0001c0005t0001g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.626+429A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182854607 | |||||||
chr1:182854919 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+741G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182854919 | |||||||
chr1:182855054 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0088 |
2 | HG00558.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.626+876A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182855054 | |||||||
chr1:182855175 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.626+997G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182855175 | |||||||
chr1:182855811 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.627-721T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182855811 | |||||||
chr1:182856050 | T | C | 2 | a0001c0006t0001g0035 a0001c0006t0001g0071 |
2 | NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.627-482T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182856050 | |||||||
chr1:182856153 | G | A | 3 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 |
4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-379G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182856153 | |||||||
chr1:182856178 | T | C | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.627-354T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182856178 | |||||||
chr1:182856188 | G | T | 6 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.627-344G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182856188 | |||||||
chr1:182856284 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.627-248T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182856284 | |||||||
chr1:182856323 | A | G | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.627-209A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 6/27 | chr1 | 182856323 | |||||||
chr1:182856613 | C | T | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.673+35C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182856613 | |||||||
chr1:182856702 | A | T | 1 | a0001c0002t0001g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.673+124A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182856702 | |||||||
chr1:182856802 | G | A | 2 | a0001c0004t0001g0210 a0001c0004t0001g0222 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.673+224G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182856802 | |||||||
chr1:182856990 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0171 |
3 | HG01168.hp2 HG01433.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.673+412C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182856990 | |||||||
chr1:182856994 | T | A | 14 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(11): Show |
15 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.673+416T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182856994 | |||||||
chr1:182857080 | C | G | 10 | a0001c0004t0001g0057 a0001c0004t0001g0210 a0001c0004t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.673+502C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182857080 | |||||||
chr1:182857531 | C | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.674-573C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182857531 | |||||||
chr1:182857546 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.674-558A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182857546 | |||||||
chr1:182857628 | A | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 |
4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-476A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182857628 | |||||||
chr1:182857655 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(8): Show |
14 | HG01069.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.674-449A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182857655 | |||||||
chr1:182858069 | T | C | 1 | a0001c0002t0001g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.674-35T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 7/27 | chr1 | 182858069 | |||||||
chr1:182858258 | A | C | 10 | a0001c0004t0001g0057 a0001c0004t0001g0210 a0001c0004t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.810+18A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 8/27 | chr1 | 182858258 | |||||||
chr1:182858292 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.810+52C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 8/27 | chr1 | 182858292 | |||||||
chr1:182858331 | A | C | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.810+91A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 8/27 | chr1 | 182858331 | |||||||
chr1:182858487 | A | G | 1 | a0001c0002t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.811-64A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 8/27 | chr1 | 182858487 | |||||||
chr1:182858662 | T | G | 3 | a0001c0006t0001g0035 a0001c0006t0001g0071 a0001c0006t0001g0112 |
3 | HG02074.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.900+22T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 9/27 | chr1 | 182858662 | |||||||
chr1:182858722 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.901-11T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 9/27 | chr1 | 182858722 | |||||||
chr1:182859204 | C | G | 15 | a0001c0001t0001g0048 a0001c0001t0002g0026 a0001c0001t0002g0049 others(12): Show |
16 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.1140+87C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 11/27 | chr1 | 182859204 | |||||||
chr1:182859373 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
17 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1140+256G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 11/27 | chr1 | 182859373 | |||||||
chr1:182859467 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1140+350A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 11/27 | chr1 | 182859467 | |||||||
chr1:182859482 | C | A | 6 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1140+365C>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 11/27 | chr1 | 182859482 | |||||||
chr1:182859532 | A | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0163 a0001c0001t0001g0198 |
5 | NA18952.hp1 NA18965.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+415A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 11/27 | chr1 | 182859532 | |||||||
chr1:182859789 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1141-204T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 11/27 | chr1 | 182859789 | |||||||
chr1:182860379 | C | T | 11 | a0001c0001t0001g0048 a0001c0004t0001g0057 a0001c0004t0001g0210 others(8): Show |
11 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1332+195C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182860379 | |||||||
chr1:182860592 | C | G | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1332+408C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182860592 | |||||||
chr1:182860636 | A | G | 66 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(63): Show |
82 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1332+452A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182860636 | |||||||
chr1:182860734 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0073 others(3): Show |
7 | HG00280.hp2 HG02165.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.1332+550C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182860734 | |||||||
chr1:182860938 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0092 |
3 | HG01346.hp1 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1332+754G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182860938 | |||||||
chr1:182861091 | T | C | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1332+907T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182861091 | |||||||
chr1:182861386 | C | T | 7 | a0001c0003t0001g0007 a0001c0003t0001g0046 a0001c0003t0001g0174 others(4): Show |
10 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1332+1202C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182861386 | |||||||
chr1:182861432 | C | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0180 others(3): Show |
7 | HG01069.hp1 HG01884.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1332+1248C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182861432 | |||||||
chr1:182861468 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1332+1284A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182861468 | |||||||
chr1:182861736 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1332+1552T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182861736 | |||||||
chr1:182861797 | G | A | 1 | a0001c0003t0001g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1332+1613G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182861797 | |||||||
chr1:182861874 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0182 others(1): Show |
6 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1332+1690A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182861874 | |||||||
chr1:182862072 | ACTT | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1332+1892_1332+189 others(7): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr1 | 182862072 | ||||||
chr1:182862245 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1332+2061C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862245 | |||||||
chr1:182862303 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1332+2119A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862303 | |||||||
chr1:182862350 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1332+2166A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862350 | |||||||
chr1:182862549 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
17 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1332+2365C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862549 | |||||||
chr1:182862600 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1332+2416G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862600 | |||||||
chr1:182862684 | T | C | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.1332+2500T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862684 | |||||||
chr1:182862761 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0073 others(3): Show |
7 | HG00280.hp2 HG02165.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.1332+2577A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862761 | |||||||
chr1:182862777 | A | T | 1 | a0001c0002t0001g0045 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1332+2593A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862777 | |||||||
chr1:182862842 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0132 others(9): Show |
14 | HG01123.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1332+2658T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182862842 | |||||||
chr1:182863162 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
17 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1332+2978C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863162 | |||||||
chr1:182863163 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1332+2979G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863163 | |||||||
chr1:182863415 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(8): Show |
14 | HG01069.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1333-3029A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863415 | |||||||
chr1:182863456 | G | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.1333-2988G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863456 | |||||||
chr1:182863515 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1333-2929C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863515 | |||||||
chr1:182863662 | C | T | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1333-2782C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863662 | |||||||
chr1:182863722 | G | C | 2 | a0001c0002t0001g0141 a0001c0002t0001g0186 |
2 | NA18942.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1333-2722G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863722 | |||||||
chr1:182863793 | A | AT | 77 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0048 others(74): Show |
94 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.1333-2639dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr1 | 182863793 | ||||||
chr1:182863793 | A | ATT | 18 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0182 others(15): Show |
21 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.1333-2640_1333-263 others(6): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr1 | 182863793 | ||||||
chr1:182863911 | G | A | 1 | a0001c0002t0003g0131 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1333-2533G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863911 | |||||||
chr1:182863922 | C | G | 2 | a0001c0004t0001g0210 a0001c0004t0001g0222 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1333-2522C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182863922 | |||||||
chr1:182864029 | T | C | 34 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0021 others(31): Show |
43 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1333-2415T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864029 | |||||||
chr1:182864058 | G | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(12): Show |
18 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1333-2386G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864058 | |||||||
chr1:182864377 | C | T | 1 | a0001c0012t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1333-2067C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864377 | |||||||
chr1:182864447 | C | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333-1997C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864447 | |||||||
chr1:182864549 | T | C | 1 | a0001c0002t0001g0189 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1333-1895T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864549 | |||||||
chr1:182864552 | T | C | 2 | a0001c0002t0001g0141 a0001c0002t0001g0186 |
2 | NA18942.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1333-1892T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864552 | |||||||
chr1:182864617 | A | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 |
4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333-1827A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864617 | |||||||
chr1:182864677 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1333-1767G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864677 | |||||||
chr1:182864980 | T | G | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1333-1464T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182864980 | |||||||
chr1:182865079 | GAAAA | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
6 | NA18963.hp2 NA18982.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333-1361_1333-135 others(8): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr1 | 182865079 | ||||||
chr1:182865109 | A | G | 1 | a0001c0002t0001g0204 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1333-1335A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865109 | |||||||
chr1:182865272 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1333-1172C>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865272 | |||||||
chr1:182865381 | T | C | 1 | a0001c0002t0001g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1333-1063T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865381 | |||||||
chr1:182865484 | A | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0162 a0001c0001t0001g0169 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-960A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865484 | |||||||
chr1:182865502 | C | T | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333-942C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865502 | |||||||
chr1:182865545 | G | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
6 | NA18963.hp2 NA18982.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333-899G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865545 | |||||||
chr1:182865626 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0088 |
2 | HG00558.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1333-818A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865626 | |||||||
chr1:182865629 | A | G | 37 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(34): Show |
45 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1333-815A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865629 | |||||||
chr1:182865682 | A | G | 43 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(40): Show |
56 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1333-762A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865682 | |||||||
chr1:182865689 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1333-755T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865689 | |||||||
chr1:182865691 | T | C | 1 | a0001c0004t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1333-753T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865691 | |||||||
chr1:182865742 | C | T | 1 | a0001c0002t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1333-702C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865742 | |||||||
chr1:182865828 | C | A | 1 | a0001c0004t0001g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1333-616C>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865828 | |||||||
chr1:182865922 | T | TAC | 29 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1333-516_1333-515d others(4): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr1 | 182865922 | ||||||
chr1:182865985 | G | A | 1 | a0001c0003t0001g0176 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1333-459G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182865985 | |||||||
chr1:182866145 | G | A | 10 | a0001c0004t0001g0057 a0001c0004t0001g0210 a0001c0004t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1333-299G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182866145 | |||||||
chr1:182866174 | C | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0201 others(1): Show |
4 | HG03688.hp1 HG03710.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333-270C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 12/27 | chr1 | 182866174 | |||||||
chr1:182866625 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1474+40T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 13/27 | chr1 | 182866625 | |||||||
chr1:182866640 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(8): Show |
14 | HG01069.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1474+55A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 13/27 | chr1 | 182866640 | |||||||
chr1:182866734 | G | C | 1 | a0001c0012t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1474+149G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 13/27 | chr1 | 182866734 | |||||||
chr1:182866905 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0223 |
3 | HG03239.hp2 HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1475-56C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 13/27 | chr1 | 182866905 | |||||||
chr1:182867062 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0039 |
3 | HG01069.hp1 HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1557+19A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867062 | |||||||
chr1:182867095 | G | T | 43 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(40): Show |
56 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1557+52G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867095 | |||||||
chr1:182867198 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1557+155T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867198 | |||||||
chr1:182867218 | T | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(12): Show |
18 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1557+175T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867218 | |||||||
chr1:182867380 | T | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(8): Show |
14 | HG01069.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1557+337T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867380 | |||||||
chr1:182867397 | A | G | 1 | a0001c0002t0001g0192 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1557+354A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867397 | |||||||
chr1:182867539 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0172 |
2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1557+496A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867539 | |||||||
chr1:182867564 | G | A | 10 | a0001c0004t0001g0057 a0001c0004t0001g0210 a0001c0004t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1557+521G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867564 | |||||||
chr1:182867703 | TATA | T | 9 | a0001c0004t0001g0210 a0001c0004t0001g0211 a0001c0004t0001g0212 others(6): Show |
9 | HG02622.hp1 HG02723.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+663_1557+665d others(5): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182867703 | ||||||
chr1:182867758 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1557+715A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867758 | |||||||
chr1:182867796 | A | G | 1 | a0001c0001t0001g0023 | 2 | NA19056.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1557+753A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867796 | |||||||
chr1:182867857 | T | C | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1557+814T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867857 | |||||||
chr1:182867993 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1557+950C>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182867993 | |||||||
chr1:182868301 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1557+1258T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182868301 | |||||||
chr1:182868361 | A | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(12): Show |
18 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1557+1318A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182868361 | |||||||
chr1:182868375 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1557+1332A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182868375 | |||||||
chr1:182868520 | C | CTTTTT | 6 | a0001c0003t0001g0007 a0001c0003t0001g0046 a0001c0003t0001g0174 others(3): Show |
9 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+1487_1557+149 others(9): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0048 a0001c0001t0001g0132 a0001c0001t0001g0180 others(3): Show |
6 | HG01123.hp1 HG03130.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1557+1483_1557+149 others(13): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0047 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+1482_1557+149 others(14): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0209 a0001c0010t0004g0221 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1557+1481_1557+149 others(15): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 |
4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1557+1480_1557+149 others(16): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(6): Show |
8 | a0001c0002t0001g0045 a0001c0002t0001g0058 a0001c0002t0001g0059 others(5): Show |
8 | HG01192.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1557+1479_1557+149 others(17): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(24): Show |
1 | a0001c0002t0003g0131 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1557+1490_1557+149 others(35): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(25): Show |
1 | a0001c0002t0003g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1557+1490_1557+149 others(36): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(7): Show |
12 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0061 others(9): Show |
16 | HG01884.hp2 HG02155.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1557+1478_1557+149 others(18): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(8): Show |
22 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0037 others(19): Show |
29 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1557+1491_1557+149 others(19): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(9): Show |
14 | a0001c0002t0001g0021 a0001c0002t0001g0130 a0001c0002t0001g0135 others(11): Show |
15 | HG02132.hp2 HG02602.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.1557+1491_1557+149 others(20): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(10): Show |
2 | a0001c0002t0001g0022 a0001c0002t0001g0146 |
3 | HG03942.hp2 NA18952.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1557+1491_1557+149 others(21): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(11): Show |
1 | a0001c0004t0001g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1557+1491_1557+149 others(22): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(15): Show |
3 | a0001c0004t0001g0215 a0001c0004t0001g0216 a0001c0004t0001g0217 |
3 | HG02970.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1557+1491_1557+149 others(26): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(16): Show |
1 | a0001c0012t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1557+1491_1557+149 others(27): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(17): Show |
1 | a0001c0004t0001g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1557+1491_1557+149 others(28): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(18): Show |
2 | a0001c0004t0001g0211 a0001c0004t0001g0213 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1557+1491_1557+149 others(29): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868520 | C | CTTTTTTT others(20): Show |
1 | a0001c0004t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1557+1491_1557+149 others(31): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182868520 | ||||||
chr1:182868578 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0073 others(3): Show |
7 | HG00280.hp2 HG02165.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.1557+1535G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182868578 | |||||||
chr1:182868587 | T | C | 1 | a0001c0002t0001g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1557+1544T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182868587 | |||||||
chr1:182868896 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1557+1853A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182868896 | |||||||
chr1:182868944 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1557+1901T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182868944 | |||||||
chr1:182868979 | A | G | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1557+1936A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182868979 | |||||||
chr1:182869052 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1557+2009C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869052 | |||||||
chr1:182869161 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0086 a0001c0001t0001g0099 |
3 | HG01070.hp2 HG01358.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1557+2118C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869161 | |||||||
chr1:182869287 | C | T | 10 | a0001c0004t0001g0057 a0001c0004t0001g0210 a0001c0004t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1557+2244C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869287 | |||||||
chr1:182869337 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(12): Show |
18 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1557+2294C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869337 | |||||||
chr1:182869373 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1557+2330G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869373 | |||||||
chr1:182869376 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0080 |
2 | HG01358.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1557+2333T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869376 | |||||||
chr1:182869423 | G | A | 3 | a0001c0001t0001g0198 a0001c0002t0001g0128 a0001c0002t0001g0178 |
3 | HG02896.hp2 NA18906.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1557+2380G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869423 | |||||||
chr1:182869440 | T | G | 1 | a0001c0002t0001g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1557+2397T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869440 | |||||||
chr1:182869489 | G | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1557+2446G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869489 | |||||||
chr1:182869539 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1557+2496G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869539 | |||||||
chr1:182869559 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1557+2516A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869559 | |||||||
chr1:182869623 | A | AGTCTT | 29 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1557+2587_1557+259 others(9): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr1 | 182869623 | ||||||
chr1:182869712 | C | T | 1 | a0001c0006t0001g0035 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1558-2625C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182869712 | |||||||
chr1:182870039 | C | T | 43 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(40): Show |
56 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1558-2298C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182870039 | |||||||
chr1:182870093 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(8): Show |
14 | HG01069.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1558-2244A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182870093 | |||||||
chr1:182870468 | CAG | C | 10 | a0001c0004t0001g0057 a0001c0004t0001g0210 a0001c0004t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558-1868_1558-186 others(6): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182870468 | |||||||
chr1:182870522 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1558-1815C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182870522 | |||||||
chr1:182870706 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1558-1631T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182870706 | |||||||
chr1:182870735 | G | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0048 others(4): Show |
8 | HG01069.hp1 HG01884.hp1 HG03540.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-1602G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182870735 | |||||||
chr1:182870891 | G | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(12): Show |
18 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1558-1446G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182870891 | |||||||
chr1:182871406 | C | G | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0201 others(1): Show |
4 | HG03688.hp1 HG03710.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-931C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182871406 | |||||||
chr1:182871471 | C | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0091 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1558-866C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182871471 | |||||||
chr1:182871484 | G | A | 3 | a0001c0002t0001g0021 a0001c0002t0001g0147 a0001c0002t0001g0195 |
4 | NA18965.hp1 NA18970.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-853G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182871484 | |||||||
chr1:182871631 | A | G | 1 | a0001c0002t0001g0142 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1558-706A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182871631 | |||||||
chr1:182871826 | G | A | 1 | a0001c0006t0001g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1558-511G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182871826 | |||||||
chr1:182871897 | C | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0067 others(3): Show |
8 | NA18940.hp1 NA18959.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-440C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182871897 | |||||||
chr1:182872016 | G | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0201 others(1): Show |
4 | HG03688.hp1 HG03710.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-321G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182872016 | |||||||
chr1:182872259 | G | T | 1 | a0001c0009t0001g0152 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1558-78G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182872259 | |||||||
chr1:182872286 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1558-51G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 14/27 | chr1 | 182872286 | |||||||
chr1:182872574 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1714+81A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182872574 | |||||||
chr1:182872646 | T | G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1714+153T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182872646 | |||||||
chr1:182872713 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1714+220T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182872713 | |||||||
chr1:182872725 | G | C | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.1714+232G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182872725 | |||||||
chr1:182872829 | G | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.1714+336G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182872829 | |||||||
chr1:182872952 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
5 | HG00558.hp1 HG00621.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714+459T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182872952 | |||||||
chr1:182872996 | C | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0201 others(1): Show |
4 | HG03688.hp1 HG03710.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714+503C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182872996 | |||||||
chr1:182873058 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1714+565C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873058 | |||||||
chr1:182873080 | T | C | 66 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(63): Show |
82 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1714+587T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873080 | |||||||
chr1:182873261 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1714+768T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873261 | |||||||
chr1:182873303 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1714+810A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873303 | |||||||
chr1:182873314 | G | C | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1714+821G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873314 | |||||||
chr1:182873382 | A | T | 1 | a0001c0001t0001g0024 | 2 | NA19068.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1714+889A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873382 | |||||||
chr1:182873503 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1714+1010G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873503 | |||||||
chr1:182873597 | C | CA | 1 | a0001c0002t0001g0012 | 3 | HG02922.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1714+1107dupA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr1 | 182873597 | ||||||
chr1:182873699 | T | C | 51 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(48): Show |
64 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.1715-1155T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873699 | |||||||
chr1:182873854 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1715-1000C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873854 | |||||||
chr1:182873931 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1715-923G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182873931 | |||||||
chr1:182874312 | A | G | 3 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02145.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1715-542A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182874312 | |||||||
chr1:182874390 | C | G | 1 | a0001c0002t0001g0179 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1715-464C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182874390 | |||||||
chr1:182874497 | A | G | 51 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(48): Show |
64 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.1715-357A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182874497 | |||||||
chr1:182874620 | T | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(17): Show |
22 | HG00280.hp2 HG00621.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1715-234T>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 15/27 | chr1 | 182874620 | |||||||
chr1:182875293 | C | G | 1 | a0001c0007t0001g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1815+339C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | chr1 | 182875293 | |||||||
chr1:182875428 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1815+474C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | chr1 | 182875428 | |||||||
chr1:182875435 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1815+481G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | chr1 | 182875435 | |||||||
chr1:182875610 | GATT | G | 8 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(5): Show |
8 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1816-437_1816-435d others(5): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr1 | 182875610 | ||||||
chr1:182875683 | T | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(12): Show |
18 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1816-367T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | chr1 | 182875683 | |||||||
chr1:182875768 | A | G | 1 | a0001c0002t0001g0141 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1816-282A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | chr1 | 182875768 | |||||||
chr1:182875781 | G | C | 5 | a0001c0002t0001g0140 a0001c0002t0001g0143 a0001c0002t0001g0146 others(2): Show |
5 | NA18940.hp2 NA18969.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1816-269G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | chr1 | 182875781 | |||||||
chr1:182875787 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1816-263T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | chr1 | 182875787 | |||||||
chr1:182875953 | G | A | 3 | a0001c0002t0001g0060 a0001c0002t0001g0062 a0001c0009t0001g0152 |
3 | HG01891.hp1 HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1816-97G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | chr1 | 182875953 | |||||||
chr1:182876039 | G | GT | 4 | a0001c0001t0001g0132 a0001c0001t0001g0199 a0001c0001t0001g0208 others(1): Show |
4 | HG01123.hp1 HG02145.hp1 HG02717.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1816-5dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr1 | 182876039 | ||||||
chr1:182876566 | G | A | 51 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(48): Show |
64 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.2124+25G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 18/27 | chr1 | 182876566 | |||||||
chr1:182876580 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0123 others(1): Show |
5 | HG01168.hp1 HG01243.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.2124+39C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 18/27 | chr1 | 182876580 | |||||||
chr1:182876752 | TTACA | T | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.2125-71_2125-68del others(4): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr1 | 182876752 | ||||||
chr1:182877071 | A | AT | 96 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(93): Show |
116 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(113): Show |
intron_variant | MODIFIER | c.2198+170dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr1 | 182877071 | ||||||
chr1:182877078 | A | G | 15 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(12): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.2198+175A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 19/27 | chr1 | 182877078 | |||||||
chr1:182877295 | G | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(26): Show |
33 | HG01069.hp1 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.2198+392G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 19/27 | chr1 | 182877295 | |||||||
chr1:182877465 | C | T | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2199-556C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 19/27 | chr1 | 182877465 | |||||||
chr1:182877498 | A | G | 4 | a0001c0004t0001g0211 a0001c0004t0001g0215 a0001c0004t0001g0216 others(1): Show |
4 | HG02970.hp1 HG03225.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2199-523A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 19/27 | chr1 | 182877498 | |||||||
chr1:182877670 | C | G | 1 | a0001c0001t0001g0016 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2199-351C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 19/27 | chr1 | 182877670 | |||||||
chr1:182877841 | A | G | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2199-180A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 19/27 | chr1 | 182877841 | |||||||
chr1:182877932 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0070 |
2 | NA18959.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2199-89A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 19/27 | chr1 | 182877932 | |||||||
chr1:182878252 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0078 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2351+79C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | chr1 | 182878252 | |||||||
chr1:182878432 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2351+259C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | chr1 | 182878432 | |||||||
chr1:182878563 | CTT | C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0201 others(1): Show |
4 | HG03688.hp1 HG03710.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2351+392_2351+393d others(4): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr1 | 182878563 | ||||||
chr1:182878617 | A | G | 6 | a0001c0004t0001g0211 a0001c0004t0001g0212 a0001c0004t0001g0213 others(3): Show |
6 | HG02970.hp1 HG03195.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2351+444A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | chr1 | 182878617 | |||||||
chr1:182878663 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2351+490C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | chr1 | 182878663 | |||||||
chr1:182878718 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0201 others(1): Show |
4 | HG03688.hp1 HG03710.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2352-532G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | chr1 | 182878718 | |||||||
chr1:182878928 | T | G | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2352-322T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | chr1 | 182878928 | |||||||
chr1:182879039 | A | T | 1 | a0001c0004t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2352-211A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | chr1 | 182879039 | |||||||
chr1:182879233 | T | C | 3 | a0001c0006t0001g0035 a0001c0006t0001g0071 a0001c0006t0001g0112 |
3 | HG02074.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2352-17T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 20/27 | chr1 | 182879233 | |||||||
chr1:182879575 | A | G | 43 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(40): Show |
56 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.2512+165A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 21/27 | chr1 | 182879575 | |||||||
chr1:182879877 | C | T | 51 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(48): Show |
64 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.2512+467C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 21/27 | chr1 | 182879877 | |||||||
chr1:182879888 | G | A | 14 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(11): Show |
15 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2512+478G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 21/27 | chr1 | 182879888 | |||||||
chr1:182879910 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0039 |
3 | HG01069.hp1 HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2512+500G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 21/27 | chr1 | 182879910 | |||||||
chr1:182879969 | T | C | 51 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(48): Show |
64 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.2513-528T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 21/27 | chr1 | 182879969 | |||||||
chr1:182880051 | T | G | 11 | a0001c0001t0001g0048 a0001c0004t0001g0057 a0001c0004t0001g0210 others(8): Show |
11 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2513-446T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 21/27 | chr1 | 182880051 | |||||||
chr1:182880135 | T | G | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2513-362T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 21/27 | chr1 | 182880135 | |||||||
chr1:182880663 | TCTC | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0154 |
3 | HG02135.hp1 NA19056.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2624+60_2624+62del others(3): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr1 | 182880663 | ||||||
chr1:182880699 | CA | C | 43 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(40): Show |
56 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.2624+101delA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr1 | 182880699 | ||||||
chr1:182880709 | A | AT | 7 | a0001c0003t0001g0007 a0001c0003t0001g0046 a0001c0003t0001g0174 others(4): Show |
10 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2624+102dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr1 | 182880709 | ||||||
chr1:182881192 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2625-72G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 22/27 | chr1 | 182881192 | |||||||
chr1:182881674 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2914+27T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182881674 | |||||||
chr1:182881887 | T | G | 2 | a0001c0004t0001g0210 a0001c0004t0001g0222 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2914+240T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182881887 | |||||||
chr1:182881914 | C | T | 7 | a0001c0003t0001g0007 a0001c0003t0001g0046 a0001c0003t0001g0174 others(4): Show |
10 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2914+267C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182881914 | |||||||
chr1:182882024 | T | C | 8 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(5): Show |
8 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2914+377T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882024 | |||||||
chr1:182882090 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2914+443A>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882090 | |||||||
chr1:182882147 | A | G | 1 | a0001c0002t0001g0145 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2914+500A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882147 | |||||||
chr1:182882158 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2914+511G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882158 | |||||||
chr1:182882234 | G | T | 6 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(3): Show |
6 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2914+587G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882234 | |||||||
chr1:182882575 | T | C | 3 | a0001c0006t0001g0035 a0001c0006t0001g0071 a0001c0006t0001g0112 |
3 | HG02074.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2915-564T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882575 | |||||||
chr1:182882592 | C | T | 2 | a0001c0004t0001g0210 a0001c0004t0001g0222 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2915-547C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882592 | |||||||
chr1:182882632 | C | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(11): Show |
17 | HG01069.hp1 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2915-507C>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882632 | |||||||
chr1:182882682 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0115 |
3 | HG02135.hp2 NA18612.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2915-457C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882682 | |||||||
chr1:182882722 | G | A | 1 | a0001c0012t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2915-417G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882722 | |||||||
chr1:182882728 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2915-411G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882728 | |||||||
chr1:182882738 | G | A | 1 | a0001c0002t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2915-401G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882738 | |||||||
chr1:182882796 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2915-343C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882796 | |||||||
chr1:182882834 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2915-305C>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882834 | |||||||
chr1:182882852 | G | C | 1 | a0001c0002t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2915-287G>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882852 | |||||||
chr1:182882863 | CA | C | 34 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(31): Show |
38 | HG00621.hp1 HG01069.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.2915-259delA | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr1 | 182882863 | ||||||
chr1:182882880 | A | AT | 3 | a0001c0002t0001g0038 a0001c0002t0001g0137 a0001c0002t0001g0191 |
3 | HG00597.hp2 HG01884.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2915-259_2915-258i others(3): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882880 | |||||||
chr1:182882880 | A | T | 48 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(45): Show |
61 | HG00140.hp2 HG01070.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.2915-259A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882880 | |||||||
chr1:182882893 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2915-246A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 24/27 | chr1 | 182882893 | |||||||
chr1:182883412 | C | G | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3144+44C>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 25/27 | chr1 | 182883412 | |||||||
chr1:182883690 | G | A | 1 | a0001c0002t0001g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3260+55G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182883690 | |||||||
chr1:182883844 | AAT | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.3260+210_3260+211d others(4): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182883844 | |||||||
chr1:182883847 | C | T | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.3260+212C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182883847 | |||||||
chr1:182883865 | C | T | 2 | a0001c0002t0003g0043 a0001c0002t0003g0131 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3260+230C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182883865 | |||||||
chr1:182883877 | C | T | 3 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0184 |
3 | HG00140.hp2 HG01070.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3260+242C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182883877 | |||||||
chr1:182883934 | A | G | 15 | a0001c0001t0001g0048 a0001c0001t0002g0026 a0001c0001t0002g0049 others(12): Show |
16 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.3260+299A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182883934 | |||||||
chr1:182884178 | G | A | 14 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(11): Show |
15 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.3261-435G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182884178 | |||||||
chr1:182884308 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3261-305C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182884308 | |||||||
chr1:182884335 | A | T | 5 | a0001c0002t0001g0009 a0001c0002t0001g0021 a0001c0002t0001g0147 others(2): Show |
8 | NA18955.hp1 NA18965.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3261-278A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | chr1 | 182884335 | |||||||
chr1:182884482 | G | GT | 8 | a0001c0002t0001g0037 a0001c0002t0001g0128 a0001c0002t0001g0129 others(5): Show |
8 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.3261-120dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr1 | 182884482 | ||||||
chr1:182884882 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.3461+69G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182884882 | |||||||
chr1:182885065 | G | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.3461+252G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182885065 | |||||||
chr1:182885356 | G | T | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3461+543G>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182885356 | |||||||
chr1:182885588 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 |
4 | HG02622.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3461+775C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182885588 | |||||||
chr1:182885704 | T | G | 1 | a0001c0002t0001g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3461+891T>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182885704 | |||||||
chr1:182885966 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3462-1117C>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182885966 | |||||||
chr1:182886173 | A | AT | 10 | a0001c0004t0001g0057 a0001c0004t0001g0210 a0001c0004t0001g0211 others(7): Show |
10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3462-901dupT | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr1 | 182886173 | ||||||
chr1:182886183 | A | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0223 a0001c0004t0001g0057 others(2): Show |
6 | HG01243.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3462-900A>T | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182886183 | |||||||
chr1:182886184 | A | AATTT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(8): Show |
14 | HG01069.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3462-874_3462-871d others(6): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr1 | 182886184 | ||||||
chr1:182886184 | AATTTATT others(1): Show |
A | 66 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(63): Show |
82 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.3462-878_3462-871d others(10): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr1 | 182886184 | ||||||
chr1:182886375 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3462-708T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182886375 | |||||||
chr1:182886484 | C | A | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3462-599C>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182886484 | |||||||
chr1:182886563 | A | G | 95 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0039 others(92): Show |
115 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.3462-520A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182886563 | |||||||
chr1:182886722 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01358.hp2 HG01952.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.3462-361A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182886722 | |||||||
chr1:182886750 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3462-333T>C | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182886750 | |||||||
chr1:182886953 | A | G | 4 | a0001c0001t0002g0026 a0001c0001t0002g0049 a0001c0001t0002g0220 others(1): Show |
5 | HG02622.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3462-130A>G | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182886953 | |||||||
chr1:182887005 | CTA | C | 50 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(47): Show |
63 | HG00140.hp2 HG00597.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.3462-77_3462-76del others(2): Show |
DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182887005 | |||||||
chr1:182887029 | G | A | 1 | a0001c0010t0004g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3462-54G>A | DHX9 | ENSG00000135829.17 | transcript | ENST00000367549.4 | protein_coding | 27/27 | chr1 | 182887029 |