Item | Value |
---|---|
geneid | 5452 |
ensemblid | ENSG00000028277.22 |
hgncid | 9213 |
symbol | POU2F2 |
name | POU class 2 homeobox 2 |
refseq_nuc | NM_001394376.1 |
refseq_prot | NP_001381305.1 |
ensembl_nuc | ENST00000692977.1 |
ensembl_prot | ENSP00000509972.1 |
mane_status | MANE Select |
chr | chr19 |
start | 42086110 |
end | 42132446 |
strand | - |
ver | v1.2 |
region | chr19:42086110-42132446 |
region5000 | chr19:42081110-42137446 |
regionname0 | POU2F2_chr19_42086110_42132446 |
regionname5000 | POU2F2_chr19_42081110_42137446 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 624 | 175 | 66 | 30 | 42 | 2 | 34 | 20 | POU2F2_chr19_42081110_42137446 | POU2F2 | MVHSS others(619): Show |
chr19 | 42081110 | 42137446 |
a0002 | 0/1 | 624 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | MVHSS others(619): Show |
chr19 | 42081110 | 42137446 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1872 | 162 | 63 | 27 | 40 | 2 | 29 | POU2F2_chr19_42081110_42137446 | POU2F2 | ATGGT others(1867): Show |
chr19 | 42081110 | 42137446 | ||
a0001c0002 | 0/0 | 1872 | 9 | 3 | 2 | 1 | 0 | 3 | POU2F2_chr19_42081110_42137446 | POU2F2 | ATGGT others(1867): Show |
chr19 | 42081110 | 42137446 | ||
a0001c0003 | 0/0 | 1872 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ATGGT others(1867): Show |
chr19 | 42081110 | 42137446 | ||
a0001c0004 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ATGGT others(1867): Show |
chr19 | 42081110 | 42137446 | ||
a0001c0006 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ATGGT others(1867): Show |
chr19 | 42081110 | 42137446 | ||
a0001c0007 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ATGGT others(1867): Show |
chr19 | 42081110 | 42137446 | ||
a0002c0005 | 0/1 | 1872 | 1 | 0 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ATGGT others(1867): Show |
chr19 | 42081110 | 42137446 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7057 | 47 | 5 | 11 | 18 | 1 | 11 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0002 | 0/0 | 7057 | 20 | 19 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0003 | 0/0 | 7059 | 14 | 1 | 0 | 7 | 0 | 6 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7054): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0004 | 0/0 | 7056 | 15 | 0 | 2 | 4 | 1 | 8 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0005 | 0/0 | 7057 | 8 | 8 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0006 | 0/0 | 7059 | 8 | 8 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7054): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0007 | 0/0 | 7058 | 7 | 0 | 5 | 2 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7053): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0008 | 0/0 | 7059 | 4 | 4 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7054): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0009 | 0/0 | 7067 | 3 | 2 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7062): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0010 | 0/0 | 7058 | 3 | 3 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7053): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0011 | 0/0 | 7057 | 2 | 0 | 1 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0012 | 0/0 | 7058 | 2 | 1 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7053): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0013 | 0/0 | 7057 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0014 | 0/0 | 7059 | 2 | 0 | 1 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7054): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0015 | 0/0 | 7061 | 2 | 2 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7056): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0016 | 0/0 | 7057 | 2 | 2 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0017 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7057): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0018 | 0/0 | 7058 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7053): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0019 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7056): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0020 | 0/0 | 7060 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7055): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0021 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0022 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0023 | 0/0 | 7058 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7053): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0025 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0026 | 0/0 | 7057 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0027 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0030 | 0/0 | 7057 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0031 | 0/0 | 7058 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7053): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0032 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7054): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0033 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7057): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0034 | 0/0 | 7061 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7056): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0035 | 0/0 | 7057 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0036 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0037 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0038 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0040 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0041 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7054): Show |
chr19 | 42081110 | 42137446 |
a0001c0001t0042 | 0/0 | 7058 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7053): Show |
chr19 | 42081110 | 42137446 |
a0001c0002t0001 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0002t0003 | 0/0 | 7059 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7054): Show |
chr19 | 42081110 | 42137446 |
a0001c0002t0005 | 0/0 | 7057 | 4 | 3 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0002t0011 | 0/0 | 7057 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0002t0024 | 0/0 | 7058 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7053): Show |
chr19 | 42081110 | 42137446 |
a0001c0002t0028 | 0/0 | 7056 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0003t0039 | 0/0 | 7056 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0004t0004 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
a0001c0006t0013 | 0/0 | 7057 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7052): Show |
chr19 | 42081110 | 42137446 |
a0001c0007t0003 | 0/0 | 7059 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7054): Show |
chr19 | 42081110 | 42137446 |
a0002c0005t0029 | 0/1 | 7056 | 1 | 0 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | ACAGT others(7051): Show |
chr19 | 42081110 | 42137446 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 6 | 0 | 1 | 2 | 0 | 2 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0007g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0011g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0012g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0012g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0013g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0014g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0014g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0015g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0016g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0018g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0019g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0020g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0021g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0022g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0023g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0025g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0026g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0027g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0030g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0031g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0032g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0033g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0034g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0035g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0036g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0037g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0038g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0040g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0041g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0001t0042g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0011g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0024g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0002t0028g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0003t0039g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0006t0013g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0001c0007t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
a0002c0005t0029g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0030 | EUR | FIN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | CHS | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0027 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01070 | hp2 | a0001 | c0003 | t0039 | g0031 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01109 | hp2 | a0001 | c0001 | t0012 | g0043 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01175 | hp1 | a0001 | c0001 | t0041 | g0062 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01175 | hp2 | a0001 | c0001 | t0018 | g0021 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0056 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01243 | hp2 | a0001 | c0002 | t0005 | g0081 | AMR | PUR | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01256 | hp1 | a0001 | c0001 | t0014 | g0146 | AMR | CLM | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01256 | hp2 | a0001 | c0002 | t0028 | g0083 | AMR | CLM | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01261 | hp2 | a0001 | c0001 | t0034 | g0058 | AMR | CLM | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01346 | hp1 | a0001 | c0001 | t0035 | g0038 | AMR | CLM | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01346 | hp2 | a0001 | c0001 | t0013 | g0114 | AMR | CLM | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01884 | hp1 | a0001 | c0001 | t0015 | g0011 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0035 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01891 | hp2 | a0001 | c0001 | t0020 | g0044 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01978 | hp1 | a0001 | c0001 | t0007 | g0112 | AMR | PEL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01978 | hp2 | a0001 | c0001 | t0007 | g0113 | AMR | PEL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0139 | AMR | PEL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02004 | hp1 | a0001 | c0001 | t0007 | g0087 | AMR | PEL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02004 | hp2 | a0001 | c0001 | t0007 | g0039 | AMR | PEL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02071 | hp1 | a0001 | c0001 | t0040 | g0029 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02074 | hp2 | a0001 | c0001 | t0038 | g0023 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02135 | hp1 | a0001 | c0001 | t0037 | g0028 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0161 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02155 | hp1 | a0001 | c0004 | t0004 | g0020 | EAS | CDX | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | CDX | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02257 | hp1 | a0001 | c0002 | t0005 | g0080 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0007 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0160 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02572 | hp2 | a0001 | c0001 | t0025 | g0048 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0055 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02622 | hp2 | a0001 | c0001 | t0032 | g0117 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0067 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02735 | hp1 | a0001 | c0006 | t0013 | g0151 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02738 | hp1 | a0001 | c0002 | t0024 | g0085 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02738 | hp2 | a0001 | c0001 | t0014 | g0110 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0159 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02809 | hp2 | a0001 | c0001 | t0016 | g0007 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02818 | hp1 | a0001 | c0001 | t0017 | g0098 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02976 | hp1 | a0001 | c0001 | t0021 | g0057 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0051 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03195 | hp2 | a0001 | c0001 | t0030 | g0105 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | MSL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | MSL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0076 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03704 | hp2 | a0001 | c0001 | t0031 | g0097 | SAS | PJL | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03831 | hp1 | a0001 | c0001 | t0023 | g0077 | SAS | BEB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | BEB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | BEB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | BEB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG03927 | hp2 | a0001 | c0002 | t0011 | g0016 | SAS | BEB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | STU | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0086 | SAS | STU | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | STU | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0026 | SAS | STU | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG04228 | hp2 | a0001 | c0007 | t0003 | g0158 | SAS | STU | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18747 | hp2 | a0001 | c0001 | t0007 | g0060 | EAS | CHB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18906 | hp1 | a0001 | c0001 | t0019 | g0136 | AFR | YRI | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18946 | hp1 | a0001 | c0001 | t0027 | g0134 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18946 | hp2 | a0001 | c0001 | t0042 | g0014 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18971 | hp2 | a0001 | c0001 | t0033 | g0072 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18988 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18990 | hp1 | a0001 | c0001 | t0007 | g0121 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18994 | hp1 | a0001 | c0001 | t0036 | g0143 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19030 | hp1 | a0001 | c0001 | t0015 | g0011 | AFR | LWK | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19043 | hp1 | a0001 | c0002 | t0005 | g0079 | AFR | LWK | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | LWK | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19084 | hp1 | a0001 | c0001 | t0022 | g0122 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19240 | hp1 | a0001 | c0001 | t0026 | g0125 | AFR | YRI | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | YRI | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | ASW | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | GIH | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | GIH | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0034 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0096 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | USA | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
HG06807 | hp2 | a0001 | c0002 | t0005 | g0084 | AFR | USA | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
homoSapiens | chm13v2 | a0002 | c0005 | t0029 | g0129 | REF | REF | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | POU2F2_chr19_42081110_42137446 | POU2F2 | chr19 | 42081110 | 42137446 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42091302 | G | A | 1 | a0001c0003 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.1830C>T | p.Thr610Thr | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1865/7057 | 1830/1875 | 610/624 | chr19 | 42091302 | |||
chr19:42091904 | T | C | 1 | a0001c0002 | 9 | HG01243.hp2 HG01256.hp2 HG02155.hp2 others(6): Show |
synonymous_variant | LOW | c.1503A>G | p.Pro501Pro | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 14/15 | 1538/7057 | 1503/1875 | 501/624 | chr19 | 42091904 | |||
chr19:42095424 | G | C | 1 | a0001c0004 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.1059C>G | p.Ala353Ala | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 11/15 | 1094/7057 | 1059/1875 | 353/624 | chr19 | 42095424 | |||
chr19:42122174 | T | C | 1 | a0001c0006 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.138A>G | p.Gln46Gln | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/15 | 173/7057 | 138/1875 | 46/624 | chr19 | 42122174 | |||
chr19:42122524 | T | A | 1 | a0001c0007 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.81A>T | p.Pro27Pro | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 2/15 | 116/7057 | 81/1875 | 27/624 | chr19 | 42122524 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42087103 | T | C | 1 | a0001c0001t0009 | 3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4154A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 4154 | chr19 | 42087103 | ||||||
chr19:42087134 | G | A | 1 | a0001c0001t0040 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4123C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 4123 | chr19 | 42087134 | ||||||
chr19:42087138 | GT | G | 4 | a0001c0001t0009 a0001c0001t0021 a0001c0001t0025 others(1): Show |
6 | HG01070.hp2 HG01243.hp1 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4118delA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 4118 | chr19 | 42087138 | ||||||
chr19:42087332 | G | A | 34 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(31): Show |
107 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*3925C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 3925 | chr19 | 42087332 | ||||||
chr19:42087386 | G | T | 1 | a0001c0001t0022 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3871C>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 3871 | chr19 | 42087386 | ||||||
chr19:42087541 | C | A | 1 | a0001c0001t0026 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3716G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 3716 | chr19 | 42087541 | ||||||
chr19:42087594 | AT | A | 11 | a0001c0001t0004 a0001c0001t0022 a0001c0001t0027 others(8): Show |
25 | HG00323.hp2 HG00597.hp1 HG01071.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3662delA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 3662 | chr19 | 42087594 | ||||||
chr19:42087773 | C | T | 1 | a0001c0001t0038 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3484G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 3484 | chr19 | 42087773 | ||||||
chr19:42087936 | C | G | 1 | a0001c0001t0023 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3321G>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 3321 | chr19 | 42087936 | ||||||
chr19:42087952 | A | C | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(2): Show |
28 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3305T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 3305 | chr19 | 42087952 | ||||||
chr19:42088497 | C | CT | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0012 others(6): Show |
19 | HG01109.hp2 HG01175.hp1 HG01891.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2759dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 2759 | chr19 | 42088497 | ||||||
chr19:42088851 | C | T | 2 | a0001c0001t0006 a0001c0001t0020 |
9 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2406G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 2406 | chr19 | 42088851 | ||||||
chr19:42088985 | T | C | 2 | a0001c0001t0013 a0001c0006t0013 |
2 | HG01346.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2272A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 2272 | chr19 | 42088985 | ||||||
chr19:42089446 | T | A | 2 | a0001c0001t0030 a0001c0001t0032 |
2 | HG02622.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1811A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1811 | chr19 | 42089446 | ||||||
chr19:42089564 | A | G | 16 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0009 others(13): Show |
36 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1693T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1693 | chr19 | 42089564 | ||||||
chr19:42089710 | T | TTA | 11 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0014 others(8): Show |
32 | HG01175.hp1 HG01256.hp1 HG01891.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1545_*1546dupTA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1546 | chr19 | 42089710 | ||||||
chr19:42089710 | T | TTATA | 4 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0033 others(1): Show |
5 | HG01261.hp2 HG01884.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1543_*1546dupTATA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1546 | chr19 | 42089710 | ||||||
chr19:42089848 | G | A | 1 | a0001c0001t0035 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1409C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1409 | chr19 | 42089848 | ||||||
chr19:42089897 | G | A | 1 | a0001c0001t0016 | 2 | HG02257.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1360C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1360 | chr19 | 42089897 | ||||||
chr19:42089955 | C | T | 1 | a0001c0001t0021 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1302 | chr19 | 42089955 | ||||||
chr19:42089994 | G | A | 1 | a0001c0001t0036 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1263C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 1263 | chr19 | 42089994 | ||||||
chr19:42090331 | G | C | 1 | a0001c0001t0008 | 4 | HG01891.hp1 HG02109.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*926C>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 926 | chr19 | 42090331 | ||||||
chr19:42090696 | C | T | 1 | a0001c0001t0017 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 561 | chr19 | 42090696 | ||||||
chr19:42090742 | T | G | 10 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0037 others(7): Show |
25 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*515A>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 515 | chr19 | 42090742 | ||||||
chr19:42091094 | C | CT | 6 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0017 others(3): Show |
11 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*162dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 162 | chr19 | 42091094 | ||||||
chr19:42091094 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0009 | 3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*152_*162dupAAAAAA others(5): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 15/15 | 162 | chr19 | 42091094 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42091639 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1541-48C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 14/14 | chr19 | 42091639 | |||||||
chr19:42091689 | C | T | 1 | a0001c0001t0005g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1541-98G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 14/14 | chr19 | 42091689 | |||||||
chr19:42091839 | G | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0153 |
3 | HG01070.hp1 HG01071.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1540+28C>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 14/14 | chr19 | 42091839 | |||||||
chr19:42092369 | G | A | 1 | a0001c0001t0021g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1265-99C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42092369 | |||||||
chr19:42092539 | G | A | 1 | a0001c0001t0022g0122 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1265-269C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42092539 | |||||||
chr19:42092987 | G | GTATA | 2 | a0001c0001t0008g0034 a0001c0001t0008g0037 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1265-721_1265-718d others(6): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42092987 | |||||||
chr19:42092987 | GTA | G | 71 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0061 others(68): Show |
78 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.1265-719_1265-718d others(4): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42092987 | |||||||
chr19:42092987 | GTATA | G | 3 | a0001c0001t0009g0054 a0001c0002t0005g0079 a0001c0002t0028g0083 |
3 | HG01256.hp2 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1265-721_1265-718d others(6): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42092987 | |||||||
chr19:42092989 | A | G | 1 | a0001c0001t0017g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1265-719T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42092989 | |||||||
chr19:42093006 | TA | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0109 others(2): Show |
5 | HG00558.hp1 HG00597.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1265-737delT | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093006 | |||||||
chr19:42093006 | TATA | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0149 a0001c0001t0001g0155 others(13): Show |
16 | HG00544.hp1 HG01243.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1265-739_1265-737d others(5): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093006 | |||||||
chr19:42093007 | A | T | 3 | a0001c0001t0001g0132 a0001c0001t0002g0006 a0001c0002t0001g0082 |
3 | HG00673.hp2 HG02155.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1265-737T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093007 | |||||||
chr19:42093007 | ATAT | A | 16 | a0001c0001t0002g0095 a0001c0001t0002g0138 a0001c0001t0003g0068 others(13): Show |
19 | HG01891.hp2 HG01993.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1265-740_1265-738d others(5): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093007 | |||||||
chr19:42093008 | TA | T | 6 | a0001c0001t0001g0099 a0001c0001t0001g0123 a0001c0001t0001g0130 others(3): Show |
6 | HG00639.hp2 HG00738.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1265-739delT | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093008 | |||||||
chr19:42093009 | A | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0033 others(42): Show |
48 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1265-739T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093009 | |||||||
chr19:42093009 | AT | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0124 others(13): Show |
18 | HG00558.hp2 HG00597.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1265-740delA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093009 | |||||||
chr19:42093009 | ATT | A | 7 | a0001c0001t0001g0102 a0001c0001t0002g0040 a0001c0001t0002g0091 others(4): Show |
7 | HG01981.hp2 HG02074.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1265-741_1265-740d others(4): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093009 | |||||||
chr19:42093009 | ATTT | A | 5 | a0001c0001t0001g0147 a0001c0001t0004g0030 a0001c0001t0017g0098 others(2): Show |
5 | HG00323.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1265-742_1265-740d others(5): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093009 | |||||||
chr19:42093010 | T | TATA | 2 | a0001c0001t0008g0035 a0001c0001t0008g0036 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1265-741_1265-740i others(5): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093010 | |||||||
chr19:42093011 | T | A | 5 | a0001c0001t0001g0075 a0001c0001t0001g0128 a0001c0001t0008g0034 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1265-741A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093011 | |||||||
chr19:42093012 | T | A | 3 | a0001c0001t0008g0035 a0001c0001t0008g0036 a0001c0001t0019g0136 |
3 | HG01891.hp1 HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1265-742A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093012 | |||||||
chr19:42093013 | T | A | 4 | a0001c0001t0002g0040 a0001c0001t0008g0034 a0001c0001t0008g0037 others(1): Show |
4 | HG02109.hp2 HG02818.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265-743A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093013 | |||||||
chr19:42093014 | T | A | 1 | a0001c0001t0019g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1265-744A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093014 | |||||||
chr19:42093015 | T | A | 2 | a0001c0001t0008g0034 a0001c0001t0008g0037 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1265-745A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093015 | |||||||
chr19:42093135 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1264+694G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 12/14 | chr19 | 42093135 | |||||||
chr19:42093994 | A | G | 1 | a0001c0001t0005g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1198-99T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 11/14 | chr19 | 42093994 | |||||||
chr19:42094437 | C | T | 4 | a0001c0002t0005g0081 a0001c0002t0005g0084 a0001c0002t0024g0085 others(1): Show |
4 | HG01243.hp2 HG01256.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1198-542G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 11/14 | chr19 | 42094437 | |||||||
chr19:42094499 | A | G | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1198-604T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 11/14 | chr19 | 42094499 | |||||||
chr19:42095101 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1197+185A>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 11/14 | chr19 | 42095101 | |||||||
chr19:42096387 | C | T | 1 | a0001c0003t0039g0031 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.568-144G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42096387 | |||||||
chr19:42096388 | C | T | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.568-145G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42096388 | |||||||
chr19:42096802 | A | T | 1 | a0001c0001t0002g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.568-559T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42096802 | |||||||
chr19:42096832 | G | A | 8 | a0001c0002t0003g0086 a0001c0002t0005g0079 a0001c0002t0005g0080 others(5): Show |
8 | HG01243.hp2 HG01256.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-589C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42096832 | |||||||
chr19:42096859 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.568-616C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42096859 | |||||||
chr19:42097064 | A | C | 1 | a0001c0001t0004g0018 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.568-821T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42097064 | |||||||
chr19:42097160 | A | G | 5 | a0001c0001t0001g0063 a0001c0001t0001g0126 a0001c0001t0007g0039 others(2): Show |
5 | HG01346.hp1 HG01978.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-917T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42097160 | |||||||
chr19:42097192 | G | GT | 7 | a0001c0001t0001g0119 a0001c0001t0001g0144 a0001c0001t0005g0009 others(4): Show |
8 | HG01175.hp2 HG02145.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.568-950dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42097192 | |||||||
chr19:42097192 | GT | G | 31 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0004g0002 others(28): Show |
33 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.568-950delA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42097192 | |||||||
chr19:42097417 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.568-1174C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42097417 | |||||||
chr19:42097495 | C | CT | 10 | a0001c0001t0001g0109 a0001c0001t0004g0022 a0001c0001t0004g0024 others(7): Show |
10 | HG01071.hp2 HG01243.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.568-1253dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42097495 | |||||||
chr19:42097878 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0155 |
2 | HG02040.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.568-1635G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42097878 | |||||||
chr19:42098324 | A | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0111 a0001c0001t0001g0115 |
3 | HG00738.hp1 HG01981.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.567+1203T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42098324 | |||||||
chr19:42098412 | C | CA | 18 | a0001c0001t0001g0124 a0001c0001t0001g0141 a0001c0001t0002g0047 others(15): Show |
19 | HG01070.hp2 HG02027.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.567+1114dupT | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42098412 | |||||||
chr19:42098429 | AC | A | 2 | a0001c0001t0008g0036 a0001c0001t0008g0037 |
2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.567+1097delG | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42098429 | |||||||
chr19:42098430 | C | A | 4 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0017g0098 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.567+1097G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42098430 | |||||||
chr19:42098724 | C | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0153 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.567+803G>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42098724 | |||||||
chr19:42098891 | G | A | 1 | a0001c0001t0017g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.567+636C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42098891 | |||||||
chr19:42098921 | T | A | 23 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0012 others(20): Show |
25 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.567+606A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 7/14 | chr19 | 42098921 | |||||||
chr19:42099624 | A | G | 98 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0041 others(95): Show |
106 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(103): Show |
splice_region_variant&intron_variant | LOW | c.476-6T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 6/14 | chr19 | 42099624 | |||||||
chr19:42099640 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0111 a0001c0001t0001g0115 |
3 | HG00738.hp1 HG01981.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.476-22G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 6/14 | chr19 | 42099640 | |||||||
chr19:42100085 | C | CT | 60 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0099 others(57): Show |
62 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.370-265dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42100085 | |||||||
chr19:42100085 | C | CTT | 6 | a0001c0001t0004g0024 a0001c0001t0005g0096 a0001c0001t0009g0054 others(3): Show |
6 | HG01071.hp2 HG01175.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-266_370-265dup others(2): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42100085 | |||||||
chr19:42100178 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.370-357C>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42100178 | |||||||
chr19:42100449 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.370-628A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42100449 | |||||||
chr19:42100895 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.370-1074G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42100895 | |||||||
chr19:42100944 | A | G | 1 | a0001c0001t0021g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.370-1123T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42100944 | |||||||
chr19:42101310 | C | T | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.370-1489G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42101310 | |||||||
chr19:42101885 | G | A | 22 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0012 others(19): Show |
24 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.370-2064C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42101885 | |||||||
chr19:42102217 | T | C | 33 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0012 others(30): Show |
35 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.370-2396A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42102217 | |||||||
chr19:42102231 | A | T | 1 | a0001c0001t0025g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.370-2410T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42102231 | |||||||
chr19:42102408 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.370-2587A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42102408 | |||||||
chr19:42102507 | A | T | 1 | a0001c0001t0002g0065 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.370-2686T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42102507 | |||||||
chr19:42103028 | G | GT | 5 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0150 others(2): Show |
5 | HG03490.hp1 HG03669.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-3208dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42103028 | |||||||
chr19:42103347 | G | C | 1 | a0001c0001t0002g0052 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.370-3526C>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42103347 | |||||||
chr19:42103627 | C | CT | 22 | a0001c0001t0001g0075 a0001c0001t0001g0102 a0001c0001t0001g0109 others(19): Show |
22 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.370-3807dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42103627 | |||||||
chr19:42103627 | CT | C | 20 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0041 others(17): Show |
23 | HG01109.hp2 HG01884.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.370-3807delA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42103627 | |||||||
chr19:42103738 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.370-3917A>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42103738 | |||||||
chr19:42103842 | C | G | 1 | a0001c0003t0039g0031 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.370-4021G>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42103842 | |||||||
chr19:42104000 | A | G | 1 | a0001c0007t0003g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.370-4179T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42104000 | |||||||
chr19:42104137 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.370-4316C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42104137 | |||||||
chr19:42104363 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.370-4542T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42104363 | |||||||
chr19:42104652 | A | C | 3 | a0001c0001t0004g0019 a0001c0001t0011g0013 a0001c0004t0004g0020 |
3 | HG00597.hp1 HG02155.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.370-4831T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42104652 | |||||||
chr19:42104723 | C | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0154 others(1): Show |
4 | HG00544.hp2 HG00673.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-4902G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42104723 | |||||||
chr19:42105550 | TAG | T | 13 | a0001c0001t0003g0008 a0001c0001t0003g0064 a0001c0001t0003g0068 others(10): Show |
14 | HG02027.hp1 HG02074.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.370-5731_370-5730d others(4): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105550 | |||||||
chr19:42105923 | T | A | 1 | a0001c0001t0007g0087 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.370-6102A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105923 | |||||||
chr19:42105999 | T | TC | 2 | a0001c0001t0001g0120 a0001c0001t0005g0009 |
2 | HG01358.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.370-6179_370-6178i others(3): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | T | TCTTTC | 3 | a0001c0001t0006g0004 a0001c0001t0017g0098 a0001c0001t0022g0122 |
3 | HG02723.hp1 HG02818.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.370-6179_370-6178i others(7): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0007g0060 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.370-6179_370-6178i others(12): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | T | TTTCTTTC others(4): Show |
1 | a0001c0002t0005g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.370-6179_370-6178i others(13): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | T | TTTTC | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0075 others(41): Show |
46 | HG00639.hp1 HG01070.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.370-6182_370-6179d others(6): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | T | TTTTCTTT others(1): Show |
28 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0061 others(25): Show |
28 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.370-6186_370-6179d others(10): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | T | TTTTCTTT others(5): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0070 others(10): Show |
13 | HG00323.hp1 HG01109.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.370-6190_370-6179d others(14): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | T | TTTTCTTT others(9): Show |
3 | a0001c0001t0001g0074 a0001c0001t0002g0047 a0001c0001t0002g0050 |
3 | HG02071.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.370-6194_370-6179d others(18): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | T | TTTTCTTT others(3): Show |
1 | a0001c0002t0011g0016 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.370-6179_370-6178i others(12): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | TTTTC | T | 20 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0002g0049 others(17): Show |
20 | HG00323.hp2 HG01346.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.370-6182_370-6179d others(6): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | TTTTCTTT others(17): Show |
T | 2 | a0001c0001t0009g0054 a0001c0001t0009g0055 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.370-6202_370-6179d others(26): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42105999 | TTTTCTTT others(25): Show |
T | 1 | a0001c0001t0009g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.370-6210_370-6179d others(34): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42105999 | |||||||
chr19:42106051 | C | CT | 2 | a0001c0001t0001g0152 a0001c0001t0002g0041 |
2 | HG00558.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.370-6231dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106051 | |||||||
chr19:42106054 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.370-6233G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106054 | |||||||
chr19:42106054 | CT | C | 2 | a0001c0001t0001g0131 a0001c0001t0004g0012 |
2 | HG01358.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.370-6234delA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106054 | |||||||
chr19:42106055 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.370-6234A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106055 | |||||||
chr19:42106055 | T | TTC | 2 | a0001c0001t0001g0010 a0001c0001t0002g0041 |
2 | HG01884.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.370-6235_370-6234i others(4): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106055 | |||||||
chr19:42106342 | C | A | 1 | a0001c0001t0009g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.370-6521G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106342 | |||||||
chr19:42106465 | G | A | 1 | a0001c0001t0014g0146 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.370-6644C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106465 | |||||||
chr19:42106573 | C | T | 1 | a0001c0001t0004g0017 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.370-6752G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106573 | |||||||
chr19:42106821 | A | G | 1 | a0001c0001t0030g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.370-7000T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106821 | |||||||
chr19:42106830 | G | GAGGAGAA others(8): Show |
1 | a0001c0001t0021g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.370-7010_370-7009i others(17): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106830 | |||||||
chr19:42106921 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.370-7100C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42106921 | |||||||
chr19:42107050 | A | T | 5 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-7229T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42107050 | |||||||
chr19:42107228 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.370-7407C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42107228 | |||||||
chr19:42107253 | G | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.370-7432C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42107253 | |||||||
chr19:42107419 | A | T | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.370-7598T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42107419 | |||||||
chr19:42107672 | T | C | 7 | a0001c0002t0001g0082 a0001c0002t0003g0086 a0001c0002t0005g0081 others(4): Show |
7 | HG01243.hp2 HG01256.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.370-7851A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42107672 | |||||||
chr19:42108068 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.370-8247C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42108068 | |||||||
chr19:42108175 | C | T | 1 | a0001c0001t0004g0018 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.370-8354G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42108175 | |||||||
chr19:42108374 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.370-8553A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42108374 | |||||||
chr19:42108445 | C | T | 1 | a0001c0001t0021g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.370-8624G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42108445 | |||||||
chr19:42108824 | T | C | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.369+8426A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42108824 | |||||||
chr19:42109043 | G | A | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0154 others(1): Show |
4 | HG00544.hp2 HG00673.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+8207C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42109043 | |||||||
chr19:42109270 | G | A | 7 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0092 others(4): Show |
8 | HG02257.hp2 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+7980C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42109270 | |||||||
chr19:42109470 | G | A | 1 | a0001c0001t0006g0005 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.369+7780C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42109470 | |||||||
chr19:42109481 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.369+7769A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42109481 | |||||||
chr19:42109606 | G | C | 1 | a0001c0002t0024g0085 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.369+7644C>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42109606 | |||||||
chr19:42109956 | T | C | 5 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+7294A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42109956 | |||||||
chr19:42109992 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.369+7258G>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42109992 | |||||||
chr19:42110100 | T | A | 2 | a0001c0001t0009g0054 a0001c0001t0009g0055 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.369+7150A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42110100 | |||||||
chr19:42110246 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.369+7004A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42110246 | |||||||
chr19:42110269 | G | A | 1 | a0001c0001t0017g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.369+6981C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42110269 | |||||||
chr19:42110374 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.369+6876G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42110374 | |||||||
chr19:42110471 | G | C | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.369+6779C>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42110471 | |||||||
chr19:42111032 | G | A | 1 | a0001c0001t0035g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.369+6218C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42111032 | |||||||
chr19:42111327 | G | C | 1 | a0001c0001t0003g0137 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.369+5923C>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42111327 | |||||||
chr19:42111741 | A | C | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.369+5509T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42111741 | |||||||
chr19:42111957 | C | T | 1 | a0001c0001t0012g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.369+5293G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42111957 | |||||||
chr19:42113182 | T | A | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0012g0067 |
3 | HG02630.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.369+4068A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113182 | |||||||
chr19:42113204 | T | C | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.369+4046A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113204 | |||||||
chr19:42113267 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.369+3983G>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113267 | |||||||
chr19:42113307 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.369+3943A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113307 | |||||||
chr19:42113319 | C | T | 4 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+3931G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113319 | |||||||
chr19:42113346 | A | C | 1 | a0001c0001t0005g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.369+3904T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113346 | |||||||
chr19:42113390 | T | C | 1 | a0001c0002t0003g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.369+3860A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113390 | |||||||
chr19:42113392 | G | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.369+3858C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113392 | |||||||
chr19:42113613 | A | G | 4 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+3637T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42113613 | |||||||
chr19:42114019 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.369+3231G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42114019 | |||||||
chr19:42114830 | A | G | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.369+2420T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42114830 | |||||||
chr19:42114991 | T | C | 3 | a0001c0001t0010g0159 a0001c0001t0010g0160 a0001c0001t0010g0161 |
3 | HG02145.hp1 HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.369+2259A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42114991 | |||||||
chr19:42115312 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.369+1938G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42115312 | |||||||
chr19:42115324 | G | C | 1 | a0001c0001t0021g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.369+1926C>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42115324 | |||||||
chr19:42116046 | G | T | 1 | a0001c0001t0003g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.369+1204C>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42116046 | |||||||
chr19:42116107 | T | C | 1 | a0001c0001t0015g0011 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.369+1143A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42116107 | |||||||
chr19:42116368 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.369+882G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42116368 | |||||||
chr19:42116464 | T | C | 1 | a0001c0001t0004g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.369+786A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42116464 | |||||||
chr19:42116532 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.369+718G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42116532 | |||||||
chr19:42116889 | G | A | 2 | a0001c0001t0007g0139 a0001c0002t0011g0016 |
2 | HG01981.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.369+361C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 5/14 | chr19 | 42116889 | |||||||
chr19:42117754 | C | A | 1 | a0001c0001t0002g0094 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187-322G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42117754 | |||||||
chr19:42118001 | T | C | 1 | a0001c0003t0039g0031 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.187-569A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42118001 | |||||||
chr19:42118396 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.187-964G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42118396 | |||||||
chr19:42118611 | C | T | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.187-1179G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42118611 | |||||||
chr19:42118693 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02040.hp2 HG02135.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.187-1261C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42118693 | |||||||
chr19:42118737 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0014g0146 |
2 | HG01256.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.187-1305C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42118737 | |||||||
chr19:42118748 | G | A | 1 | a0001c0007t0003g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.187-1316C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42118748 | |||||||
chr19:42118889 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.187-1457C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42118889 | |||||||
chr19:42119348 | T | TG | 4 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-1917_187-1916i others(3): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42119348 | |||||||
chr19:42119598 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187-2166C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42119598 | |||||||
chr19:42119616 | G | A | 1 | a0001c0001t0017g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.187-2184C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42119616 | |||||||
chr19:42119634 | C | T | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.187-2202G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42119634 | |||||||
chr19:42119751 | G | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.187-2319C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42119751 | |||||||
chr19:42119779 | T | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.186+2347A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42119779 | |||||||
chr19:42119784 | A | G | 1 | a0001c0001t0021g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186+2342T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42119784 | |||||||
chr19:42119955 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.186+2171C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42119955 | |||||||
chr19:42120021 | C | T | 1 | a0001c0001t0004g0012 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.186+2105G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120021 | |||||||
chr19:42120146 | A | C | 1 | a0001c0001t0031g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.186+1980T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120146 | |||||||
chr19:42120218 | C | CT | 6 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+1907dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120218 | |||||||
chr19:42120253 | G | A | 1 | a0001c0001t0004g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.186+1873C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120253 | |||||||
chr19:42120347 | A | G | 1 | a0001c0001t0005g0096 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.186+1779T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120347 | |||||||
chr19:42120421 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.186+1705C>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120421 | |||||||
chr19:42120510 | G | T | 32 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0041 others(29): Show |
36 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.186+1616C>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120510 | |||||||
chr19:42120631 | A | G | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.186+1495T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120631 | |||||||
chr19:42120711 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.186+1415C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42120711 | |||||||
chr19:42121002 | G | A | 1 | a0001c0001t0009g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.186+1124C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42121002 | |||||||
chr19:42121197 | A | G | 1 | a0001c0001t0007g0087 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.186+929T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42121197 | |||||||
chr19:42121358 | A | G | 5 | a0001c0001t0006g0004 a0001c0001t0006g0005 a0001c0001t0006g0045 others(2): Show |
7 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+768T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42121358 | |||||||
chr19:42121780 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.186+346G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42121780 | |||||||
chr19:42121952 | C | A | 1 | a0001c0002t0003g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.186+174G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42121952 | |||||||
chr19:42122047 | C | A | 1 | a0001c0001t0003g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.186+79G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42122047 | |||||||
chr19:42122055 | C | T | 8 | a0001c0002t0001g0082 a0001c0002t0003g0086 a0001c0002t0005g0079 others(5): Show |
8 | HG01243.hp2 HG01256.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+71G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 4/14 | chr19 | 42122055 | |||||||
chr19:42122247 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.130-65G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 3/14 | chr19 | 42122247 | |||||||
chr19:42122264 | C | T | 1 | a0001c0001t0012g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.129+80G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 3/14 | chr19 | 42122264 | |||||||
chr19:42122462 | C | A | 1 | a0001c0001t0010g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94+49G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 2/14 | chr19 | 42122462 | |||||||
chr19:42122806 | C | T | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-230G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42122806 | |||||||
chr19:42122902 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.29-326C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42122902 | |||||||
chr19:42123238 | C | T | 1 | a0001c0001t0023g0077 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.29-662G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42123238 | |||||||
chr19:42123263 | C | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-687G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42123263 | |||||||
chr19:42123459 | G | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-883C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42123459 | |||||||
chr19:42123598 | A | T | 1 | a0001c0001t0004g0017 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.29-1022T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42123598 | |||||||
chr19:42124175 | G | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-1599C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42124175 | |||||||
chr19:42124319 | G | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-1743C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42124319 | |||||||
chr19:42124320 | A | G | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-1744T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42124320 | |||||||
chr19:42124379 | T | TA | 21 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0004g0002 others(18): Show |
23 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.29-1804dupT | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42124379 | |||||||
chr19:42124379 | TA | T | 5 | a0001c0001t0001g0075 a0001c0001t0005g0076 a0001c0001t0009g0054 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1804delT | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42124379 | |||||||
chr19:42124671 | G | A | 18 | a0001c0001t0002g0006 a0001c0001t0002g0047 a0001c0001t0002g0049 others(15): Show |
21 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.29-2095C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42124671 | |||||||
chr19:42124703 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.29-2127T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42124703 | |||||||
chr19:42124836 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.29-2260T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42124836 | |||||||
chr19:42125686 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(1): Show |
4 | HG00558.hp1 HG00597.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-3110G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42125686 | |||||||
chr19:42125697 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.29-3121G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42125697 | |||||||
chr19:42126173 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.29-3597C>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42126173 | |||||||
chr19:42126388 | A | G | 1 | a0001c0001t0005g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-3812T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42126388 | |||||||
chr19:42126399 | T | C | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-3823A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42126399 | |||||||
chr19:42126423 | A | G | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0012g0067 |
3 | HG02630.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.29-3847T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42126423 | |||||||
chr19:42126455 | A | G | 2 | a0001c0001t0008g0034 a0001c0001t0010g0159 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.29-3879T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42126455 | |||||||
chr19:42126530 | T | C | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-3954A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42126530 | |||||||
chr19:42126593 | A | G | 1 | a0001c0001t0003g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.29-4017T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42126593 | |||||||
chr19:42126626 | C | A | 1 | a0001c0001t0003g0156 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.29-4050G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42126626 | |||||||
chr19:42127124 | A | T | 1 | a0001c0001t0005g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-4548T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42127124 | |||||||
chr19:42127125 | T | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-4549A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42127125 | |||||||
chr19:42127338 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.29-4762G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42127338 | |||||||
chr19:42127686 | C | G | 1 | a0001c0001t0041g0062 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.28+4698G>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42127686 | |||||||
chr19:42128331 | T | A | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.28+4053A>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42128331 | |||||||
chr19:42128838 | C | CT | 5 | a0001c0001t0001g0061 a0001c0001t0007g0060 a0001c0001t0009g0054 others(2): Show |
5 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+3545dupA | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42128838 | |||||||
chr19:42128945 | G | C | 1 | a0001c0001t0005g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.28+3439C>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42128945 | |||||||
chr19:42129358 | A | T | 2 | a0001c0001t0002g0059 a0001c0001t0034g0058 |
2 | HG01261.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.28+3026T>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42129358 | |||||||
chr19:42129427 | T | C | 18 | a0001c0001t0002g0006 a0001c0001t0002g0047 a0001c0001t0002g0049 others(15): Show |
21 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.28+2957A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42129427 | |||||||
chr19:42129580 | C | T | 1 | a0001c0001t0021g0057 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.28+2804G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42129580 | |||||||
chr19:42129583 | C | T | 1 | a0001c0001t0035g0038 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.28+2801G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42129583 | |||||||
chr19:42129717 | C | A | 1 | a0001c0007t0003g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.28+2667G>T | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42129717 | |||||||
chr19:42130202 | CAT | C | 1 | a0001c0001t0004g0003 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.28+2180_28+2181del others(2): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42130202 | |||||||
chr19:42130429 | A | C | 3 | a0001c0001t0009g0054 a0001c0001t0009g0055 a0001c0001t0009g0056 |
3 | HG01243.hp1 HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.28+1955T>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42130429 | |||||||
chr19:42130831 | C | T | 20 | a0001c0001t0002g0006 a0001c0001t0002g0040 a0001c0001t0002g0041 others(17): Show |
23 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.28+1553G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42130831 | |||||||
chr19:42131051 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0035g0038 |
2 | HG01346.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.28+1333G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42131051 | |||||||
chr19:42131096 | A | G | 4 | a0001c0001t0008g0034 a0001c0001t0008g0035 a0001c0001t0008g0036 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+1288T>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42131096 | |||||||
chr19:42131112 | T | TTCTGCCT others(28): Show |
1 | a0001c0001t0004g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.28+1237_28+1271dup others(35): Show |
POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42131112 | |||||||
chr19:42131200 | C | G | 1 | a0001c0001t0001g0033 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.28+1184G>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42131200 | |||||||
chr19:42131471 | C | T | 23 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0012 others(20): Show |
25 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.28+913G>A | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42131471 | |||||||
chr19:42131492 | T | G | 1 | a0001c0001t0010g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.28+892A>C | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42131492 | |||||||
chr19:42132174 | T | C | 3 | a0001c0001t0010g0159 a0001c0001t0010g0160 a0001c0001t0010g0161 |
3 | HG02145.hp1 HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.28+210A>G | POU2F2 | ENSG00000028277.22 | transcript | ENST00000692977.1 | protein_coding | 1/14 | chr19 | 42132174 |