| geneid | 5316 |
|---|---|
| ensemblid | ENSG00000160199.15 |
| hgncid | 9022 |
| symbol | PKNOX1 |
| name | PBX/knotted 1 homeobox 1 |
| refseq_nuc | NM_004571.5 |
| refseq_prot | NP_004562.2 |
| ensembl_nuc | ENST00000291547.10 |
| ensembl_prot | ENSP00000291547.4 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 42974562 |
| end | 43033931 |
| strand | + |
| ver | v1.2 |
| region | chr21:42974562-43033931 |
| region5000 | chr21:42969562-43038931 |
| regionname0 | PKNOX1_chr21_42974562_43033931 |
| regionname5000 | PKNOX1_chr21_42969562_43038931 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 436 | 361 | 84 | 72 | 151 | 18 | 34 | 113 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0002 | 0/0 | 436 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1311 | 287 | 74 | 59 | 105 | 18 | 30 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| c0002 | 1/0 | 1311 | 70 | 10 | 12 | 43 | 0 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| c0003 | 0/0 | 1311 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| c0004 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| c0005 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| c0006 | 0/0 | 1311 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3980 | 85 | 7 | 20 | 47 | 3 | 8 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0002 | 0/0 | 3980 | 65 | 24 | 7 | 29 | 3 | 2 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0003 | 1/0 | 3990 | 47 | 4 | 5 | 34 | 0 | 3 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0004 | 0/1 | 4002 | 21 | 0 | 5 | 8 | 1 | 6 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0005 | 0/0 | 4000 | 17 | 0 | 1 | 11 | 1 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0006 | 0/0 | 4000 | 14 | 4 | 4 | 0 | 4 | 2 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0007 | 0/0 | 3980 | 14 | 14 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0008 | 0/0 | 3973 | 14 | 1 | 5 | 0 | 4 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0009 | 0/0 | 3990 | 7 | 0 | 7 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0010 | 0/0 | 3980 | 6 | 0 | 4 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0011 | 0/0 | 3980 | 4 | 4 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0012 | 0/0 | 3980 | 4 | 3 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0013 | 0/0 | 3980 | 3 | 0 | 3 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0014 | 0/0 | 3980 | 3 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0015 | 0/0 | 3971 | 3 | 0 | 2 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0016 | 0/0 | 3980 | 3 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0017 | 0/0 | 3988 | 3 | 0 | 0 | 2 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0018 | 0/0 | 3992 | 3 | 0 | 0 | 2 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0019 | 0/0 | 3972 | 2 | 0 | 0 | 0 | 1 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0020 | 0/0 | 4000 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0021 | 0/0 | 4002 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0022 | 0/0 | 3980 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0023 | 0/0 | 3980 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0024 | 0/0 | 3982 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0025 | 0/0 | 3980 | 2 | 0 | 2 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0026 | 0/0 | 3980 | 2 | 1 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0027 | 0/0 | 3982 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0028 | 0/0 | 3990 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0029 | 0/0 | 3990 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0030 | 0/0 | 3980 | 2 | 0 | 2 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0031 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0032 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0033 | 0/0 | 4000 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0034 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0035 | 0/0 | 3978 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0036 | 0/0 | 3978 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0037 | 0/0 | 3980 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0038 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0039 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0040 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0041 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0042 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0043 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0044 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0045 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0046 | 0/0 | 3980 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0047 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0048 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0049 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0050 | 0/0 | 3982 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0051 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| t0052 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1311 | 287 | 74 | 59 | 105 | 18 | 30 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002 | 1/0 | 1311 | 70 | 10 | 12 | 43 | 0 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0003 | 0/0 | 1311 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0005 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0006 | 0/0 | 1311 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0002c0004 | 0/0 | 1311 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5290 | 85 | 7 | 20 | 47 | 3 | 8 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0002 | 0/0 | 5290 | 63 | 24 | 7 | 27 | 3 | 2 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0004 | 0/1 | 5312 | 21 | 0 | 5 | 8 | 1 | 6 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0005 | 0/0 | 5310 | 16 | 0 | 1 | 10 | 1 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0006 | 0/0 | 5310 | 14 | 4 | 4 | 0 | 4 | 2 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0007 | 0/0 | 5290 | 14 | 14 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0008 | 0/0 | 5283 | 14 | 1 | 5 | 0 | 4 | 4 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0010 | 0/0 | 5290 | 6 | 0 | 4 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0011 | 0/0 | 5290 | 4 | 4 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0012 | 0/0 | 5290 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0013 | 0/0 | 5290 | 3 | 0 | 3 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0014 | 0/0 | 5290 | 3 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0015 | 0/0 | 5281 | 3 | 0 | 2 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0017 | 0/0 | 5298 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0019 | 0/0 | 5282 | 2 | 0 | 0 | 0 | 1 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0020 | 0/0 | 5310 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0021 | 0/0 | 5312 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0022 | 0/0 | 5290 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0023 | 0/0 | 5290 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0024 | 0/0 | 5292 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0025 | 0/0 | 5290 | 2 | 0 | 2 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0026 | 0/0 | 5290 | 2 | 1 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0027 | 0/0 | 5292 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0030 | 0/0 | 5290 | 2 | 0 | 2 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0031 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0032 | 0/0 | 5282 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0033 | 0/0 | 5310 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0034 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0035 | 0/0 | 5288 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0036 | 0/0 | 5288 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0037 | 0/0 | 5290 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0038 | 0/0 | 5290 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0040 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0041 | 0/0 | 5290 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0042 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0043 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0044 | 0/0 | 5283 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0045 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0046 | 0/0 | 5290 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0047 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0048 | 0/0 | 5290 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0049 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0001t0050 | 0/0 | 5292 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0003 | 1/0 | 5300 | 46 | 4 | 5 | 33 | 0 | 3 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0009 | 0/0 | 5300 | 6 | 0 | 6 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0012 | 0/0 | 5290 | 3 | 3 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0016 | 0/0 | 5290 | 3 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0017 | 0/0 | 5298 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0018 | 0/0 | 5302 | 3 | 0 | 0 | 2 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0028 | 0/0 | 5300 | 2 | 2 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0029 | 0/0 | 5300 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0039 | 0/0 | 5290 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0051 | 0/0 | 5300 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0002t0052 | 0/0 | 5300 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0003t0002 | 0/0 | 5290 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0005t0003 | 0/0 | 5300 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0001c0006t0009 | 0/0 | 5300 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| a0002c0004t0005 | 0/0 | 5310 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | copy fasta | chr21 | 42969562 | 43038931 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0008g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0010g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0010g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0010g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0011g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0012g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0013g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0013g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0013g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0014g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0014g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0015g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0015g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0015g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0017g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0019g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0019g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0020g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0021g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0021g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0022g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0022g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0023g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0023g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0024g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0024g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0025g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0025g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0026g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0026g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0027g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0027g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0030g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0030g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0031g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0032g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0033g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0034g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0035g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0036g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0037g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0038g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0040g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0041g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0042g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0043g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0044g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0045g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0046g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0047g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0048g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0049g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0001t0050g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0001 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0009g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0009g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0009g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0009g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0009g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0009g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0012g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0012g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0012g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0016g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0016g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0016g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0017g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0017g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0018g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0018g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0018g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0028g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0028g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0029g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0029g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0039g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0051g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0002t0052g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0005t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0001c0006t0009g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| a0002c0004t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0026 | g0193 | EUR | GBR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0167 | EUR | GBR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0040 | EUR | GBR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00140 | hp2 | a0001 | c0001 | t0008 | g0271 | EUR | GBR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | FIN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0178 | EUR | FIN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00323 | hp2 | a0001 | c0001 | t0008 | g0278 | EUR | FIN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00597 | hp1 | a0001 | c0001 | t0014 | g0053 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0300 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0346 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00639 | hp1 | a0001 | c0002 | t0009 | g0323 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00639 | hp2 | a0001 | c0001 | t0025 | g0016 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00642 | hp2 | a0001 | c0001 | t0025 | g0015 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00673 | hp1 | a0001 | c0001 | t0014 | g0085 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00673 | hp2 | a0001 | c0002 | t0052 | g0332 | EAS | CHS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0177 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0176 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00735 | hp2 | a0001 | c0002 | t0051 | g0325 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00738 | hp1 | a0001 | c0002 | t0009 | g0307 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG00741 | hp2 | a0001 | c0001 | t0010 | g0033 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0269 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0272 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0274 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01081 | hp1 | a0001 | c0001 | t0037 | g0195 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0313 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0277 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01099 | hp2 | a0001 | c0001 | t0033 | g0166 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01109 | hp1 | a0001 | c0001 | t0012 | g0098 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01168 | hp2 | a0001 | c0001 | t0030 | g0075 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0034 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01243 | hp2 | a0001 | c0001 | t0046 | g0222 | AMR | PUR | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0329 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01258 | hp1 | a0001 | c0001 | t0030 | g0117 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0184 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0331 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0336 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01346 | hp2 | a0001 | c0001 | t0013 | g0112 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0316 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0258 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0190 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0283 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0205 | EUR | IBS | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01928 | hp1 | a0001 | c0006 | t0009 | g0318 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01934 | hp2 | a0001 | c0002 | t0009 | g0308 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01943 | hp2 | a0001 | c0002 | t0009 | g0297 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0185 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01975 | hp2 | a0001 | c0001 | t0013 | g0077 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01981 | hp2 | a0001 | c0001 | t0015 | g0273 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02004 | hp1 | a0001 | c0001 | t0013 | g0110 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02004 | hp2 | a0001 | c0001 | t0015 | g0276 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02015 | hp1 | a0001 | c0001 | t0014 | g0109 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0328 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02055 | hp2 | a0001 | c0001 | t0044 | g0290 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0315 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02080 | hp1 | a0001 | c0005 | t0003 | g0302 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0327 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0101 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02148 | hp1 | a0001 | c0001 | t0010 | g0032 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02148 | hp2 | a0001 | c0002 | t0009 | g0342 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CDX | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0349 | EAS | CDX | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | CDX | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02258 | hp1 | a0001 | c0001 | t0049 | g0266 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0338 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02293 | hp1 | a0001 | c0001 | t0010 | g0030 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02293 | hp2 | a0001 | c0002 | t0009 | g0306 | AMR | PEL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0263 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0102 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0324 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0333 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02647 | hp1 | a0001 | c0001 | t0040 | g0008 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0264 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0310 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02717 | hp1 | a0001 | c0001 | t0034 | g0105 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02723 | hp1 | a0001 | c0001 | t0031 | g0119 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02738 | hp2 | a0001 | c0001 | t0017 | g0238 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02809 | hp1 | a0001 | c0001 | t0027 | g0155 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02896 | hp2 | a0001 | c0002 | t0028 | g0288 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02897 | hp1 | a0001 | c0002 | t0028 | g0289 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0172 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02965 | hp1 | a0001 | c0002 | t0039 | g0355 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03098 | hp1 | a0001 | c0002 | t0012 | g0292 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03098 | hp2 | a0001 | c0001 | t0027 | g0170 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0339 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03195 | hp1 | a0001 | c0001 | t0045 | g0267 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03209 | hp2 | a0001 | c0001 | t0020 | g0154 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03225 | hp1 | a0001 | c0001 | t0043 | g0175 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03453 | hp1 | a0001 | c0001 | t0035 | g0050 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0104 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0049 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0282 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0048 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0279 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0180 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0265 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03654 | hp1 | a0001 | c0001 | t0019 | g0287 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0162 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03688 | hp1 | a0001 | c0001 | t0008 | g0280 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0163 | SAS | PJL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0174 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03831 | hp2 | a0001 | c0002 | t0018 | g0299 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0042 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03834 | hp2 | a0001 | c0001 | t0015 | g0270 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03927 | hp1 | a0001 | c0001 | t0050 | g0240 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0157 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0259 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0275 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0352 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18522 | hp2 | a0001 | c0001 | t0023 | g0052 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18906 | hp1 | a0001 | c0002 | t0012 | g0356 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18939 | hp2 | a0001 | c0002 | t0016 | g0354 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18940 | hp1 | a0002 | c0004 | t0005 | g0158 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18942 | hp1 | a0001 | c0002 | t0003 | g0326 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18944 | hp1 | a0001 | c0002 | t0029 | g0312 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18944 | hp2 | a0001 | c0001 | t0024 | g0092 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18946 | hp2 | a0001 | c0002 | t0017 | g0296 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18952 | hp2 | a0001 | c0002 | t0016 | g0294 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0348 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18960 | hp1 | a0001 | c0002 | t0003 | g0319 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18961 | hp1 | a0001 | c0002 | t0003 | g0337 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18962 | hp1 | a0001 | c0001 | t0024 | g0026 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18962 | hp2 | a0001 | c0002 | t0018 | g0305 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18963 | hp2 | a0001 | c0001 | t0021 | g0151 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18969 | hp2 | a0001 | c0002 | t0029 | g0304 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0335 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0350 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18979 | hp2 | a0001 | c0001 | t0048 | g0249 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0340 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0341 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0322 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18994 | hp1 | a0001 | c0002 | t0016 | g0295 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18995 | hp1 | a0001 | c0001 | t0038 | g0091 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18998 | hp1 | a0001 | c0001 | t0036 | g0141 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0311 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0330 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0309 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19011 | hp2 | a0001 | c0002 | t0003 | g0347 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0262 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19030 | hp2 | a0001 | c0001 | t0042 | g0120 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19043 | hp1 | a0001 | c0001 | t0022 | g0051 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19055 | hp1 | a0001 | c0002 | t0003 | g0320 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19057 | hp1 | a0001 | c0002 | t0003 | g0353 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19058 | hp2 | a0001 | c0002 | t0018 | g0334 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19060 | hp1 | a0001 | c0003 | t0002 | g0203 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0303 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19063 | hp2 | a0001 | c0001 | t0010 | g0031 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0351 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0211 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0321 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19079 | hp1 | a0001 | c0001 | t0021 | g0152 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0314 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19082 | hp1 | a0001 | c0001 | t0041 | g0058 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0317 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0301 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0344 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19091 | hp1 | a0001 | c0002 | t0017 | g0293 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19240 | hp1 | a0001 | c0002 | t0012 | g0357 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | YRI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20129 | hp1 | a0001 | c0001 | t0032 | g0291 | AFR | ASW | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | ASW | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0284 | EUR | TSI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20805 | hp1 | a0001 | c0001 | t0019 | g0286 | EUR | TSI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0179 | SAS | GIH | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0298 | SAS | GIH | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0281 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0268 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0183 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02486 | hp1 | a0001 | c0001 | t0026 | g0239 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02559 | hp1 | a0001 | c0001 | t0047 | g0216 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0115 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG03471 | hp2 | a0001 | c0001 | t0020 | g0165 | AFR | MSL | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | USA | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| HG06807 | hp2 | a0001 | c0001 | t0022 | g0022 | AFR | USA | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | USA | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | USA | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0041 | REF | REF | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0001 | REF | REF | PKNOX1_chr21_42969562_43038931 | PKNOX1 | chr21 | 42969562 | 43038931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43028761
|
C | A | 1 | a0002 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.986C>A | p.Thr329Asn | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/11 | 1145/5300 | 986/1311 | 329/436 | chr21 | 43028761 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43010215
|
T | C | 3 | a0001c0001a0001c0003a0002c0004 | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
synonymous_variant | LOW | c.342T>C | p.Thr114Thr | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/11 | 501/5300 | 342/1311 | 114/436 | chr21 | 43010215 | ||
| chr21:43016961
|
G | A | 1 | a0001c0003 | 2 | NA19060.hp1 NA19070.hp1 |
synonymous_variant | LOW | c.576G>A | p.Pro192Pro | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/11 | 735/5300 | 576/1311 | 192/436 | chr21 | 43016961 | ||
| chr21:43016985
|
C | T | 1 | a0001c0006 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.600C>T | p.Asn200Asn | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/11 | 759/5300 | 600/1311 | 200/436 | chr21 | 43016985 | ||
| chr21:43029972
|
G | A | 1 | a0001c0005 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1182G>A | p.Ala394Ala | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1341/5300 | 1182/1311 | 394/436 | chr21 | 43029972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:43004334
|
C | T | 1 | a0001c0001t0030 | 2 | HG01168.hp2 HG01258.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/11 | chr21 | 43004334 | ||||||
| chr21:43004380
|
C | A | 1 | a0001c0001t0031 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/11 | 2 | chr21 | 43004380 | |||||
| chr21:43030260
|
A | AGT | 1 | a0001c0002t0018 | 3 | HG03831.hp2 NA18962.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*191_*192dupTG | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 193 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | ||||
| chr21:43030260
|
AGT | A | 2 | a0001c0001t0017a0001c0002t0017 | 3 | HG02738.hp2 NA18946.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*191_*192delTG | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 191 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | ||||
| chr21:43030260
|
AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0024a0001c0001t0027a0001c0001t0031others(4): Show | 9 | HG02258.hp1 HG02723.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*185_*192delTGTGTG others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 185 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | ||||
| chr21:43030260
|
AGTGTGTG others(3): Show |
A | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(25): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*183_*192delTGTGTG others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 183 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | ||||
| chr21:43030260
|
AGTGTGTG others(5): Show |
A | 3 | a0001c0001t0015a0001c0001t0035a0001c0001t0036 | 5 | HG01981.hp2 HG02004.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*181_*192delTGTGTG others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 181 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | ||||
| chr21:43030260
|
AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0004a0001c0001t0021 | 23 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*179_*192delTGTGTG others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 179 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | ||||
| chr21:43030260
|
AGTGTGTG others(9): Show |
A | 5 | a0001c0001t0005a0001c0001t0006a0001c0001t0020others(2): Show | 34 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*177_*192delTGTGTG others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 177 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | ||||
| chr21:43030260
|
AGTGTGTG others(11): Show |
A | 2 | a0001c0001t0019a0001c0001t0032 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*175_*192delTGTGTG others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 175 | INFO_REALIGN_3_PRIME | chr21 | 43030260 | ||||
| chr21:43030290
|
T | C | 2 | a0001c0001t0034a0001c0001t0037 | 2 | HG01081.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*189T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 189 | chr21 | 43030290 | |||||
| chr21:43030292
|
T | C | 21 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(18): Show | 132 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 191 | chr21 | 43030292 | |||||
| chr21:43030302
|
C | T | 1 | a0001c0001t0021 | 2 | NA18963.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*201C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 201 | chr21 | 43030302 | |||||
| chr21:43030446
|
T | G | 1 | a0001c0002t0029 | 2 | NA18944.hp1 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*345T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 345 | chr21 | 43030446 | |||||
| chr21:43030828
|
T | C | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(4): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*727T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 727 | chr21 | 43030828 | |||||
| chr21:43030870
|
C | T | 1 | a0001c0001t0041 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*769C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 769 | chr21 | 43030870 | |||||
| chr21:43030890
|
A | G | 1 | a0001c0001t0048 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*789A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 789 | chr21 | 43030890 | |||||
| chr21:43030947
|
G | A | 6 | a0001c0001t0008a0001c0001t0011a0001c0001t0015others(3): Show | 24 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*846G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 846 | chr21 | 43030947 | |||||
| chr21:43031060
|
A | G | 1 | a0001c0001t0045 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*959A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 959 | chr21 | 43031060 | |||||
| chr21:43031128
|
G | A | 1 | a0001c0001t0025 | 2 | HG00639.hp2 HG00642.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1027G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1027 | chr21 | 43031128 | |||||
| chr21:43031276
|
A | T | 2 | a0001c0001t0027a0001c0001t0043 | 3 | HG02809.hp1 HG03098.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1175A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1175 | chr21 | 43031276 | |||||
| chr21:43031301
|
C | T | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(5): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1200C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1200 | chr21 | 43031301 | |||||
| chr21:43031306
|
C | T | 1 | a0001c0001t0047 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1205 | chr21 | 43031306 | |||||
| chr21:43031318
|
C | A | 2 | a0001c0001t0022a0001c0001t0035 | 3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1217C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1217 | chr21 | 43031318 | |||||
| chr21:43031395
|
T | A | 1 | a0001c0001t0043 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1294T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1294 | chr21 | 43031395 | |||||
| chr21:43031437
|
C | T | 1 | a0001c0002t0028 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1336C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1336 | chr21 | 43031437 | |||||
| chr21:43031492
|
G | C | 1 | a0001c0001t0038 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1391G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1391 | chr21 | 43031492 | |||||
| chr21:43031538
|
T | C | 1 | a0001c0002t0028 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1437T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1437 | chr21 | 43031538 | |||||
| chr21:43031642
|
C | T | 1 | a0001c0001t0040 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1541 | chr21 | 43031642 | |||||
| chr21:43031766
|
G | A | 2 | a0001c0001t0004a0001c0001t0021 | 23 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1665G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1665 | chr21 | 43031766 | |||||
| chr21:43031802
|
G | A | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(4): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1701G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1701 | chr21 | 43031802 | |||||
| chr21:43031825
|
T | TA | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(4): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1725dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1726 | INFO_REALIGN_3_PRIME | chr21 | 43031825 | ||||
| chr21:43031887
|
G | A | 8 | a0001c0001t0002a0001c0001t0025a0001c0001t0037others(5): Show | 72 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1786G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1786 | chr21 | 43031887 | |||||
| chr21:43032080
|
G | A | 1 | a0001c0001t0014 | 3 | HG00597.hp1 HG00673.hp1 HG02015.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1979G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 1979 | chr21 | 43032080 | |||||
| chr21:43032109
|
C | T | 3 | a0001c0001t0012a0001c0002t0012a0001c0002t0039 | 5 | HG01109.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2008C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2008 | chr21 | 43032109 | |||||
| chr21:43032152
|
G | A | 1 | a0001c0001t0044 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2051 | chr21 | 43032152 | |||||
| chr21:43032314
|
T | TTCCCTCA others(18): Show |
7 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(4): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2214_*2238dupTCCC others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2239 | INFO_REALIGN_3_PRIME | chr21 | 43032314 | ||||
| chr21:43032331
|
G | A | 1 | a0001c0001t0032 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2230G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2230 | chr21 | 43032331 | |||||
| chr21:43032339
|
G | A | 1 | a0001c0001t0046 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2238G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2238 | chr21 | 43032339 | |||||
| chr21:43032345
|
T | C | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(35): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*2244T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2244 | chr21 | 43032345 | |||||
| chr21:43032365
|
G | T | 1 | a0001c0002t0052 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2264G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2264 | chr21 | 43032365 | |||||
| chr21:43032540
|
C | T | 1 | a0001c0001t0043 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2439C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2439 | chr21 | 43032540 | |||||
| chr21:43032653
|
C | T | 10 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(7): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2552C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2552 | chr21 | 43032653 | |||||
| chr21:43032655
|
G | C | 2 | a0001c0001t0031a0001c0001t0042 | 2 | HG02723.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2554G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2554 | chr21 | 43032655 | |||||
| chr21:43032703
|
A | G | 10 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(7): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2602A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2602 | chr21 | 43032703 | |||||
| chr21:43032728
|
C | A | 10 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(7): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2627C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2627 | chr21 | 43032728 | |||||
| chr21:43032758
|
C | G | 7 | a0001c0001t0001a0001c0001t0014a0001c0001t0024others(4): Show | 95 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2657C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2657 | chr21 | 43032758 | |||||
| chr21:43032836
|
C | T | 1 | a0001c0001t0044 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2735C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2735 | chr21 | 43032836 | |||||
| chr21:43032838
|
G | C | 10 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(7): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2737G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2737 | chr21 | 43032838 | |||||
| chr21:43032912
|
G | A | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(21): Show | 194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*2811G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2811 | chr21 | 43032912 | |||||
| chr21:43032946
|
C | G | 3 | a0001c0001t0011a0001c0001t0045a0001c0001t0049 | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2845C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 2845 | chr21 | 43032946 | |||||
| chr21:43033167
|
C | T | 6 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(3): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3066C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3066 | chr21 | 43033167 | |||||
| chr21:43033168
|
A | G | 10 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(7): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3067A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3067 | chr21 | 43033168 | |||||
| chr21:43033262
|
G | C | 10 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(7): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3161G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3161 | chr21 | 43033262 | |||||
| chr21:43033429
|
TTTCGTTC | T | 3 | a0001c0001t0008a0001c0001t0015a0001c0001t0044 | 18 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3330_*3336delTCGT others(3): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3330 | INFO_REALIGN_3_PRIME | chr21 | 43033429 | ||||
| chr21:43033645
|
T | A | 2 | a0001c0002t0009a0001c0006t0009 | 7 | HG00639.hp1 HG00738.hp1 HG01928.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3544T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3544 | chr21 | 43033645 | |||||
| chr21:43033694
|
C | T | 1 | a0001c0001t0033 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3593C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3593 | chr21 | 43033694 | |||||
| chr21:43033743
|
A | G | 1 | a0001c0001t0010 | 6 | HG00741.hp2 HG01192.hp2 HG02148.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3642A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3642 | chr21 | 43033743 | |||||
| chr21:43033803
|
G | C | 2 | a0001c0001t0005a0002c0004t0005 | 17 | HG00099.hp2 HG00423.hp1 HG01109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3702G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3702 | chr21 | 43033803 | |||||
| chr21:43033908
|
A | G | 3 | a0001c0001t0012a0001c0002t0012a0001c0002t0039 | 5 | HG01109.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3807A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 11/11 | 3807 | chr21 | 43033908 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:42974825
|
G | C | 10 | a0001c0001t0007g0004a0001c0001t0007g0005a0001c0001t0007g0006others(7): Show | 10 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57+161G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974825 | ||||||
| chr21:42974856
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+192G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974856 | ||||||
| chr21:42974868
|
G | T | 1 | a0001c0001t0002g0285 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-57+204G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974868 | ||||||
| chr21:42974890
|
C | G | 1 | a0001c0001t0002g0285 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-57+226C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974890 | ||||||
| chr21:42974897
|
C | G | 17 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-57+233C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974897 | ||||||
| chr21:42974991
|
T | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-57+327T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42974991 | ||||||
| chr21:42975029
|
G | T | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+365G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975029 | ||||||
| chr21:42975047
|
C | CGGGGCG | 283 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-57+390_-57+395dup others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42975047 | |||||
| chr21:42975048
|
G | GGGGCGGG others(11): Show |
1 | a0001c0001t0032g0291 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+395_-57+396ins others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42975048 | |||||
| chr21:42975052
|
C | CGGGGGCG | 6 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0004g0256others(3): Show | 6 | HG01515.hp1 HG02056.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+389_-57+395dup others(7): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42975052 | |||||
| chr21:42975163
|
C | G | 15 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0245others(12): Show | 15 | NA18954.hp2 NA18966.hp2 NA18979.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57+499C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975163 | ||||||
| chr21:42975174
|
C | T | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57+510C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975174 | ||||||
| chr21:42975182
|
C | A | 2 | a0001c0001t0025g0015a0001c0001t0025g0016 | 2 | HG00639.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-57+518C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975182 | ||||||
| chr21:42975249
|
G | A | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+585G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975249 | ||||||
| chr21:42975304
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.-57+640G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975304 | ||||||
| chr21:42975372
|
G | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+708G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975372 | ||||||
| chr21:42975379
|
G | A | 17 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-57+715G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975379 | ||||||
| chr21:42975413
|
G | A | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+749G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975413 | ||||||
| chr21:42975526
|
C | G | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-57+862C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975526 | ||||||
| chr21:42975534
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-57+870T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975534 | ||||||
| chr21:42975620
|
G | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(288): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+956G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975620 | ||||||
| chr21:42975621
|
G | C | 1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-57+957G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975621 | ||||||
| chr21:42975639
|
G | A | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+975G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975639 | ||||||
| chr21:42975686
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(244): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-57+1022C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975686 | ||||||
| chr21:42975718
|
G | T | 3 | a0001c0001t0001g0153a0001c0001t0021g0151a0001c0001t0021g0152 | 3 | NA18963.hp2 NA19004.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-57+1054G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975718 | ||||||
| chr21:42975936
|
A | T | 1 | a0001c0002t0016g0354 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-57+1272A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42975936 | ||||||
| chr21:42976026
|
C | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+1362C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976026 | ||||||
| chr21:42976034
|
C | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+1370C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976034 | ||||||
| chr21:42976165
|
G | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-57+1501G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976165 | ||||||
| chr21:42976192
|
A | G | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+1528A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976192 | ||||||
| chr21:42976219
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-57+1555T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976219 | ||||||
| chr21:42976220
|
TAA | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+1558_-57+1559d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42976220 | |||||
| chr21:42976265
|
GTTAA | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+1606_-57+1609d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42976265 | |||||
| chr21:42976337
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+1673A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976337 | ||||||
| chr21:42976352
|
G | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-57+1688G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976352 | ||||||
| chr21:42976510
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-57+1846A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976510 | ||||||
| chr21:42976609
|
A | T | 1 | a0001c0002t0003g0353 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-57+1945A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976609 | ||||||
| chr21:42976657
|
T | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-57+1993T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976657 | ||||||
| chr21:42976685
|
G | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2021G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976685 | ||||||
| chr21:42976788
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+2124A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976788 | ||||||
| chr21:42976812
|
A | G | 1 | a0001c0002t0003g0352 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-57+2148A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976812 | ||||||
| chr21:42976841
|
C | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+2177C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42976841 | ||||||
| chr21:42977071
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2407A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977071 | ||||||
| chr21:42977073
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2409G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977073 | ||||||
| chr21:42977104
|
C | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2440C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977104 | ||||||
| chr21:42977119
|
G | T | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+2455G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977119 | ||||||
| chr21:42977124
|
T | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2460T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977124 | ||||||
| chr21:42977228
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-57+2564C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977228 | ||||||
| chr21:42977241
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-57+2577A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977241 | ||||||
| chr21:42977380
|
T | G | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+2716T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977380 | ||||||
| chr21:42977384
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-57+2720C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977384 | ||||||
| chr21:42977448
|
G | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+2784G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977448 | ||||||
| chr21:42977465
|
C | T | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+2801C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977465 | ||||||
| chr21:42977493
|
G | A | 1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+2829G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977493 | ||||||
| chr21:42977537
|
CT | C | 70 | a0001c0001t0002g0188a0001c0001t0002g0241a0001c0001t0002g0242others(67): Show | 71 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-57+2900delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42977537 | |||||
| chr21:42977537
|
CTT | C | 96 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(93): Show | 96 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-57+2899_-57+2900d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42977537 | |||||
| chr21:42977537
|
CTTT | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-57+2898_-57+2900d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42977537 | |||||
| chr21:42977537
|
CTTTT | C | 17 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 17 | HG01168.hp1 HG01257.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57+2897_-57+2900d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42977537 | |||||
| chr21:42977592
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-57+2928A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977592 | ||||||
| chr21:42977616
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-57+2952C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977616 | ||||||
| chr21:42977617
|
G | A | 1 | a0001c0001t0005g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-57+2953G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977617 | ||||||
| chr21:42977671
|
C | T | 1 | a0001c0002t0003g0352 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-57+3007C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977671 | ||||||
| chr21:42977731
|
T | C | 110 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+3067T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977731 | ||||||
| chr21:42977737
|
C | T | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57+3073C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977737 | ||||||
| chr21:42977776
|
C | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+3112C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42977776 | ||||||
| chr21:42978000
|
C | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+3336C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978000 | ||||||
| chr21:42978248
|
G | A | 110 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+3584G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978248 | ||||||
| chr21:42978374
|
G | A | 6 | a0001c0001t0010g0030a0001c0001t0010g0031a0001c0001t0010g0032others(3): Show | 6 | HG00741.hp2 HG01192.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+3710G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978374 | ||||||
| chr21:42978404
|
G | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-57+3740G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978404 | ||||||
| chr21:42978428
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+3764G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978428 | ||||||
| chr21:42978441
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+3777G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978441 | ||||||
| chr21:42978463
|
A | AACTTGTT others(1): Show |
110 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+3800_-57+3807d others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42978463 | |||||
| chr21:42978472
|
T | A | 1 | a0001c0001t0002g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-57+3808T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978472 | ||||||
| chr21:42978473
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-57+3809T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978473 | ||||||
| chr21:42978476
|
C | G | 1 | a0001c0001t0002g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-57+3812C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978476 | ||||||
| chr21:42978486
|
C | CT | 9 | a0001c0001t0001g0137a0001c0001t0002g0242a0001c0001t0004g0135others(6): Show | 9 | HG00544.hp1 HG01975.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+3839dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42978486 | |||||
| chr21:42978486
|
CT | C | 64 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0200others(61): Show | 64 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.-57+3839delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42978486 | |||||
| chr21:42978491
|
T | C | 9 | a0001c0001t0002g0260a0001c0001t0005g0159a0001c0001t0005g0160others(6): Show | 9 | HG02055.hp2 HG02056.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+3827T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978491 | ||||||
| chr21:42978492
|
T | C | 1 | a0001c0002t0003g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-57+3828T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978492 | ||||||
| chr21:42978496
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-57+3832T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978496 | ||||||
| chr21:42978514
|
C | T | 18 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0123others(15): Show | 18 | HG00438.hp2 HG01358.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+3850C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978514 | ||||||
| chr21:42978801
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+4137A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978801 | ||||||
| chr21:42978825
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4161A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978825 | ||||||
| chr21:42978882
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4218A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978882 | ||||||
| chr21:42978922
|
C | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4258C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978922 | ||||||
| chr21:42978990
|
C | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4326C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42978990 | ||||||
| chr21:42979178
|
G | A | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+4514G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979178 | ||||||
| chr21:42979245
|
T | A | 23 | a0001c0001t0001g0153a0001c0001t0004g0019a0001c0001t0004g0020others(20): Show | 23 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+4581T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979245 | ||||||
| chr21:42979249
|
C | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4585C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979249 | ||||||
| chr21:42979303
|
AACACAG | A | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+4645_-57+4650d others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42979303 | |||||
| chr21:42979363
|
T | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4699T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979363 | ||||||
| chr21:42979369
|
A | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4705A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979369 | ||||||
| chr21:42979381
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4717G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979381 | ||||||
| chr21:42979405
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4741G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979405 | ||||||
| chr21:42979590
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4926G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979590 | ||||||
| chr21:42979611
|
G | A | 3 | a0001c0001t0022g0022a0001c0001t0022g0051a0001c0001t0035g0050 | 3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+4947G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979611 | ||||||
| chr21:42979678
|
C | A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5014C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979678 | ||||||
| chr21:42979720
|
T | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-57+5056T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979720 | ||||||
| chr21:42979843
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5179G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979843 | ||||||
| chr21:42979869
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5205G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979869 | ||||||
| chr21:42979927
|
T | C | 1 | a0001c0001t0005g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-57+5263T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979927 | ||||||
| chr21:42979935
|
G | A | 35 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.-57+5271G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979935 | ||||||
| chr21:42979978
|
C | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-57+5314C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979978 | ||||||
| chr21:42979988
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57+5324C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42979988 | ||||||
| chr21:42980005
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5341A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980005 | ||||||
| chr21:42980072
|
A | G | 3 | a0001c0001t0006g0183a0001c0001t0006g0184a0001c0001t0006g0186 | 3 | HG01261.hp1 HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-57+5408A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980072 | ||||||
| chr21:42980139
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5475G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980139 | ||||||
| chr21:42980166
|
A | G | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+5502A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980166 | ||||||
| chr21:42980179
|
C | T | 1 | a0001c0002t0003g0337 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-57+5515C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980179 | ||||||
| chr21:42980201
|
C | T | 2 | a0001c0001t0031g0119a0001c0001t0042g0120 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-57+5537C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980201 | ||||||
| chr21:42980356
|
A | C | 10 | a0001c0001t0002g0189a0001c0001t0002g0198a0001c0001t0002g0199others(7): Show | 10 | HG01257.hp2 HG01258.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57+5692A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980356 | ||||||
| chr21:42980382
|
G | GA | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+5727dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42980382 | |||||
| chr21:42980427
|
C | T | 2 | a0001c0001t0031g0119a0001c0001t0042g0120 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-57+5763C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980427 | ||||||
| chr21:42980431
|
T | G | 17 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-57+5767T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980431 | ||||||
| chr21:42980479
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57+5815A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980479 | ||||||
| chr21:42980551
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+5887A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980551 | ||||||
| chr21:42980718
|
C | G | 2 | a0001c0001t0004g0048a0001c0001t0004g0049 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+6054C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980718 | ||||||
| chr21:42980719
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6055G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980719 | ||||||
| chr21:42980764
|
AT | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6106delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42980764 | |||||
| chr21:42980777
|
C | G | 36 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-57+6113C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980777 | ||||||
| chr21:42980793
|
A | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6129A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980793 | ||||||
| chr21:42980857
|
G | A | 10 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0245others(7): Show | 10 | NA18954.hp2 NA18966.hp2 NA18979.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57+6193G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42980857 | ||||||
| chr21:42981014
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-57+6350C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981014 | ||||||
| chr21:42981015
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6351G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981015 | ||||||
| chr21:42981111
|
C | T | 3 | a0001c0001t0022g0022a0001c0001t0022g0051a0001c0001t0035g0050 | 3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+6447C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981111 | ||||||
| chr21:42981176
|
G | A | 1 | a0001c0001t0023g0052 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-57+6512G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981176 | ||||||
| chr21:42981207
|
C | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+6543C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981207 | ||||||
| chr21:42981329
|
G | A | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+6665G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981329 | ||||||
| chr21:42981369
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6705A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981369 | ||||||
| chr21:42981382
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6718G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981382 | ||||||
| chr21:42981386
|
T | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+6722T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981386 | ||||||
| chr21:42981459
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+6795A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981459 | ||||||
| chr21:42981553
|
TTTAATTT others(3): Show |
T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+6892_-57+6901d others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42981553 | |||||
| chr21:42981556
|
A | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-57+6892A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981556 | ||||||
| chr21:42981584
|
G | A | 3 | a0001c0001t0006g0183a0001c0001t0006g0184a0001c0001t0006g0186 | 3 | HG01261.hp1 HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-57+6920G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981584 | ||||||
| chr21:42981586
|
G | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+6922G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981586 | ||||||
| chr21:42981700
|
C | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7036C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981700 | ||||||
| chr21:42981701
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7037A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981701 | ||||||
| chr21:42981749
|
T | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7085T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981749 | ||||||
| chr21:42981856
|
G | A | 1 | a0001c0001t0005g0257 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-57+7192G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981856 | ||||||
| chr21:42981937
|
T | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7273T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981937 | ||||||
| chr21:42981980
|
C | T | 15 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0123others(12): Show | 15 | HG00438.hp2 HG00621.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57+7316C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42981980 | ||||||
| chr21:42982017
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7353A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982017 | ||||||
| chr21:42982074
|
C | T | 2 | a0001c0001t0027g0155a0001c0001t0027g0170 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-57+7410C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982074 | ||||||
| chr21:42982137
|
C | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7473C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982137 | ||||||
| chr21:42982352
|
T | G | 1 | a0001c0002t0003g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-57+7688T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982352 | ||||||
| chr21:42982367
|
C | T | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+7703C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982367 | ||||||
| chr21:42982384
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-57+7720G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982384 | ||||||
| chr21:42982435
|
A | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7771A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982435 | ||||||
| chr21:42982468
|
G | A | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57+7804G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982468 | ||||||
| chr21:42982483
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-57+7819A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982483 | ||||||
| chr21:42982524
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7860A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982524 | ||||||
| chr21:42982588
|
G | A | 5 | a0001c0001t0014g0053a0001c0001t0019g0286a0001c0001t0019g0287others(2): Show | 5 | HG00597.hp1 HG02055.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+7924G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982588 | ||||||
| chr21:42982612
|
T | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7948T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982612 | ||||||
| chr21:42982686
|
G | A | 3 | a0001c0001t0005g0159a0001c0001t0005g0160a0002c0004t0005g0158 | 3 | NA18940.hp1 NA18999.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-57+8022G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982686 | ||||||
| chr21:42982695
|
C | T | 1 | a0001c0001t0030g0117 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-57+8031C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982695 | ||||||
| chr21:42982731
|
C | CA | 37 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0001t0002g0250others(34): Show | 38 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.-57+8083dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42982731 | |||||
| chr21:42982731
|
C | CAA | 238 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(235): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-57+8082_-57+8083d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42982731 | |||||
| chr21:42982731
|
C | CAAA | 7 | a0001c0001t0001g0054a0001c0001t0002g0204a0001c0001t0004g0038others(4): Show | 7 | HG00609.hp2 HG00741.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+8081_-57+8083d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42982731 | |||||
| chr21:42982731
|
CAAAAAAA | C | 7 | a0001c0001t0006g0183a0001c0001t0006g0184a0001c0001t0006g0186others(4): Show | 7 | HG01261.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+8077_-57+8083d others(9): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42982731 | |||||
| chr21:42982805
|
G | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8141G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982805 | ||||||
| chr21:42982820
|
T | C | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8156T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982820 | ||||||
| chr21:42982848
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+8184T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982848 | ||||||
| chr21:42982914
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8250A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982914 | ||||||
| chr21:42982949
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8285A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982949 | ||||||
| chr21:42982965
|
A | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8301A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42982965 | ||||||
| chr21:42983018
|
C | T | 1 | a0001c0001t0050g0240 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-57+8354C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983018 | ||||||
| chr21:42983050
|
G | T | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+8386G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983050 | ||||||
| chr21:42983059
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+8395T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983059 | ||||||
| chr21:42983073
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+8409G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983073 | ||||||
| chr21:42983099
|
T | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-57+8435T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983099 | ||||||
| chr21:42983109
|
CT | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-57+8453delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42983109 | |||||
| chr21:42983253
|
C | G | 34 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(31): Show | 35 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+8589C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983253 | ||||||
| chr21:42983309
|
GA | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+8647delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42983309 | |||||
| chr21:42983486
|
GCTGAATA | G | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+8825_-57+8831d others(9): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42983486 | |||||
| chr21:42983528
|
C | T | 1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+8864C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983528 | ||||||
| chr21:42983630
|
A | AT | 15 | a0001c0001t0002g0197a0001c0001t0002g0201a0001c0001t0002g0202others(12): Show | 15 | HG01167.hp2 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57+8973dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42983630 | |||||
| chr21:42983849
|
A | C | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+9185A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983849 | ||||||
| chr21:42983929
|
C | T | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+9265C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983929 | ||||||
| chr21:42983930
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-57+9266A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983930 | ||||||
| chr21:42983934
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+9270T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983934 | ||||||
| chr21:42983993
|
A | G | 1 | a0001c0001t0002g0248 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-57+9329A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42983993 | ||||||
| chr21:42984065
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+9401C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984065 | ||||||
| chr21:42984083
|
CGT | C | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG03098.hp1 NA18906.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+9444_-57+9445d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984083 | |||||
| chr21:42984083
|
CGTGT | C | 13 | a0001c0001t0001g0123a0001c0001t0002g0243a0001c0001t0002g0244others(10): Show | 13 | HG02055.hp2 NA18950.hp1 NA18954.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57+9442_-57+9445d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984083 | |||||
| chr21:42984083
|
CGTGTGT | C | 275 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-57+9440_-57+9445d others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984083 | |||||
| chr21:42984120
|
CA | C | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+9457delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984120 | ||||||
| chr21:42984222
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57+9558T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984222 | ||||||
| chr21:42984245
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-57+9581T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984245 | ||||||
| chr21:42984284
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-57+9620T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984284 | ||||||
| chr21:42984483
|
G | A | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+9819G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984483 | ||||||
| chr21:42984740
|
T | C | 2 | a0001c0001t0004g0135a0001c0001t0041g0058 | 2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-57+10076T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984740 | ||||||
| chr21:42984909
|
T | TGA | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+10251_-57+1025 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984909 | |||||
| chr21:42984961
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57+10297C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42984961 | ||||||
| chr21:42984974
|
C | CT | 14 | a0001c0001t0007g0013a0001c0002t0003g0298a0001c0002t0003g0333others(11): Show | 14 | HG00621.hp1 HG00673.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+10337dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | |||||
| chr21:42984974
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57+10326_-57+1033 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | |||||
| chr21:42984974
|
CT | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(146): Show | 151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-57+10337delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | |||||
| chr21:42984974
|
CTT | C | 114 | a0001c0001t0001g0023a0001c0001t0001g0059a0001c0001t0001g0147others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.-57+10336_-57+1033 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | |||||
| chr21:42984974
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+10326_-57+1033 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | |||||
| chr21:42984974
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0005g0159a0001c0001t0005g0160a0001c0001t0005g0161others(1): Show | 4 | NA18940.hp1 NA18963.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+10322_-57+1033 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42984974 | |||||
| chr21:42985590
|
C | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02129.hp2 HG02523.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-57+10926C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985590 | ||||||
| chr21:42985630
|
C | T | 1 | a0001c0001t0013g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-57+10966C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985630 | ||||||
| chr21:42985656
|
G | A | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57+10992G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985656 | ||||||
| chr21:42985762
|
G | A | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57+11098G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985762 | ||||||
| chr21:42985841
|
A | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+11177A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985841 | ||||||
| chr21:42985872
|
G | A | 1 | a0001c0001t0020g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57+11208G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42985872 | ||||||
| chr21:42986002
|
G | GA | 7 | a0001c0001t0007g0007a0001c0001t0007g0009a0001c0001t0007g0010others(4): Show | 7 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+11353dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986002 | |||||
| chr21:42986002
|
G | GAA | 69 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0027others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-57+11352_-57+1135 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986002 | |||||
| chr21:42986002
|
G | GAAA | 96 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0024others(93): Show | 97 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-57+11351_-57+1135 others(7): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986002 | |||||
| chr21:42986017
|
A | AAT | 30 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(27): Show | 31 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+11353_-57+1135 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986017 | ||||||
| chr21:42986017
|
A | ATT | 80 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(77): Show | 80 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-57+11354_-57+1135 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986017 | |||||
| chr21:42986020
|
A | T | 76 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-57+11356A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986020 | ||||||
| chr21:42986021
|
A | T | 2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | NA18951.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-57+11357A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986021 | ||||||
| chr21:42986160
|
T | G | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+11496T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986160 | ||||||
| chr21:42986228
|
C | T | 4 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0248others(1): Show | 4 | NA18954.hp2 NA18983.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+11564C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986228 | ||||||
| chr21:42986229
|
G | A | 1 | a0001c0001t0010g0030 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-57+11565G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986229 | ||||||
| chr21:42986334
|
C | G | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+11670C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986334 | ||||||
| chr21:42986400
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-57+11736C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986400 | ||||||
| chr21:42986442
|
A | G | 16 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(13): Show | 16 | HG00099.hp2 HG00423.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+11778A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986442 | ||||||
| chr21:42986484
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-57+11820G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986484 | ||||||
| chr21:42986760
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+12096T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986760 | ||||||
| chr21:42986774
|
G | A | 2 | a0001c0001t0008g0283a0001c0001t0008g0284 | 2 | HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-57+12110G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986774 | ||||||
| chr21:42986821
|
ATAAATGC others(8): Show |
A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+12160_-57+1217 others(19): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42986821 | |||||
| chr21:42986847
|
T | C | 3 | a0001c0002t0003g0300a0001c0002t0003g0301a0001c0005t0003g0302 | 3 | HG00597.hp2 HG02080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-57+12183T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986847 | ||||||
| chr21:42986958
|
C | T | 5 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(2): Show | 5 | HG02055.hp2 HG03654.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+12294C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42986958 | ||||||
| chr21:42987031
|
G | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-57+12367G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987031 | ||||||
| chr21:42987195
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-57+12531A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987195 | ||||||
| chr21:42987296
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-57+12632C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987296 | ||||||
| chr21:42987345
|
A | G | 2 | a0001c0002t0003g0331a0001c0002t0003g0336 | 2 | HG01261.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-57+12681A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987345 | ||||||
| chr21:42987382
|
CA | C | 26 | a0001c0001t0001g0025a0001c0001t0001g0063a0001c0001t0001g0090others(23): Show | 26 | HG00639.hp1 HG01255.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.-57+12741delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | |||||
| chr21:42987382
|
CAA | C | 64 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0054others(61): Show | 64 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-57+12740_-57+1274 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | |||||
| chr21:42987382
|
CAAA | C | 9 | a0001c0001t0001g0094a0001c0001t0001g0113a0001c0001t0001g0114others(6): Show | 9 | HG01069.hp1 HG01928.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+12739_-57+1274 others(7): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | |||||
| chr21:42987382
|
CAAAA | C | 9 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0207others(6): Show | 9 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+12738_-57+1274 others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | |||||
| chr21:42987382
|
CAAAAA | C | 20 | a0001c0001t0002g0194a0001c0001t0005g0157a0001c0001t0005g0159others(17): Show | 20 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.-57+12737_-57+1274 others(9): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | |||||
| chr21:42987382
|
CAAAAAA | C | 53 | a0001c0001t0001g0200a0001c0001t0002g0171a0001c0001t0002g0187others(50): Show | 53 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.-57+12736_-57+1274 others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987382 | |||||
| chr21:42987394
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57+12730A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987394 | ||||||
| chr21:42987395
|
A | T | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+12731A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987395 | ||||||
| chr21:42987396
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57+12732A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987396 | ||||||
| chr21:42987396
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0002g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57+12734_-57+1274 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987396 | |||||
| chr21:42987398
|
A | AATATATA others(3): Show |
2 | a0001c0001t0008g0268a0001c0001t0049g0266 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-57+12735_-57+1273 others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | |||||
| chr21:42987398
|
A | AATATATA others(7): Show |
1 | a0001c0001t0011g0265 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-57+12735_-57+1273 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | |||||
| chr21:42987398
|
A | AATATATA others(9): Show |
1 | a0001c0001t0011g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57+12735_-57+1273 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | |||||
| chr21:42987398
|
A | AATATATA others(11): Show |
2 | a0001c0001t0011g0262a0001c0001t0045g0267 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-57+12735_-57+1273 others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | |||||
| chr21:42987398
|
A | AATATATA others(15): Show |
1 | a0001c0001t0011g0263 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-57+12735_-57+1273 others(26): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987398 | |||||
| chr21:42987398
|
A | T | 4 | a0001c0001t0001g0023a0001c0001t0002g0217a0001c0001t0002g0218others(1): Show | 4 | HG02630.hp1 HG02630.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+12734A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987398 | ||||||
| chr21:42987400
|
A | T | 14 | a0001c0001t0001g0023a0001c0001t0002g0014a0001c0001t0002g0217others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+12736A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987400 | ||||||
| chr21:42987402
|
A | AATATATA others(11): Show |
2 | a0001c0001t0001g0153a0001c0001t0004g0108 | 2 | NA19004.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-57+12739_-57+1274 others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987402 | |||||
| chr21:42987402
|
A | AATATATA others(13): Show |
2 | a0001c0001t0001g0107a0001c0001t0004g0135 | 2 | HG01167.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-57+12739_-57+1274 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987402 | |||||
| chr21:42987402
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0004g0046a0001c0001t0004g0047 | 2 | HG01175.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-57+12738_-57+1273 others(23): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987402 | ||||||
| chr21:42987402
|
A | T | 20 | a0001c0001t0001g0023a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 20 | HG01261.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-57+12738A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987402 | ||||||
| chr21:42987402
|
AAAATATA others(7): Show |
A | 1 | a0001c0001t0004g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1275 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987402 | |||||
| chr21:42987404
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0012g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(34): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(47): Show |
1 | a0001c0001t0019g0287 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(58): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(46): Show |
1 | a0001c0001t0019g0286 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(57): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0012g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0007g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(32): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(42): Show |
1 | a0001c0001t0032g0291 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(53): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(9): Show |
3 | a0001c0002t0012g0292a0001c0002t0012g0357a0001c0002t0039g0355 | 3 | HG02965.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0007g0007 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(28): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0015g0270 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(30): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0008g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(27): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0007g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0007g0101a0001c0001t0008g0274 | 2 | HG01074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0100a0001c0001t0007g0006 | 2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(30): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(21): Show |
3 | a0001c0001t0007g0005a0001c0001t0008g0272a0001c0001t0015g0273 | 3 | HG01071.hp1 HG01981.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(32): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(25): Show |
2 | a0001c0001t0001g0060a0001c0001t0007g0004 | 2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(36): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(38): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAT others(6): Show |
2 | a0001c0001t0007g0103a0001c0001t0007g0104 | 2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(17): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAT others(20): Show |
2 | a0001c0001t0007g0009a0001c0001t0008g0275 | 2 | HG04199.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(31): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAAAT others(24): Show |
1 | a0001c0001t0040g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(35): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0007g0106 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAATA others(7): Show |
1 | a0001c0001t0034g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAATA others(13): Show |
1 | a0001c0001t0008g0277 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAATA others(15): Show |
1 | a0001c0001t0001g0027 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(26): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAATA others(21): Show |
2 | a0001c0001t0001g0024a0001c0001t0007g0011 | 2 | HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(32): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAATA others(23): Show |
1 | a0001c0001t0015g0276 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(34): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAATA others(25): Show |
1 | a0001c0001t0007g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(36): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAAATA others(27): Show |
1 | a0001c0001t0008g0280 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(38): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAAATAT others(14): Show |
1 | a0001c0001t0004g0039 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(25): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0008g0281 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0138 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAATATA others(17): Show |
2 | a0001c0001t0004g0040a0001c0001t0004g0041 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(28): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAATATA others(19): Show |
2 | a0001c0001t0008g0283a0001c0001t0008g0284 | 2 | HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(30): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAAATATA others(23): Show |
2 | a0001c0001t0007g0012a0001c0001t0008g0278 | 2 | HG00323.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-57+12741_-57+1274 others(34): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAATATAT others(18): Show |
1 | a0001c0001t0004g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(29): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AAATATAT others(20): Show |
1 | a0001c0001t0008g0279 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-57+12741_-57+1274 others(31): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AATATATA others(7): Show |
1 | a0001c0001t0004g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-57+12751_-57+1276 others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AATATATA others(11): Show |
2 | a0001c0001t0004g0019a0001c0001t0004g0139 | 2 | HG01168.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-57+12747_-57+1276 others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AATATATA others(13): Show |
1 | a0001c0001t0021g0151 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-57+12745_-57+1276 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AATATATA others(15): Show |
2 | a0001c0001t0004g0020a0001c0001t0031g0119 | 2 | HG02723.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-57+12743_-57+1276 others(26): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AATATATA others(17): Show |
2 | a0001c0001t0004g0043a0001c0001t0004g0136 | 2 | HG00544.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-57+12741_-57+1276 others(28): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AATATATA others(19): Show |
2 | a0001c0001t0004g0038a0001c0001t0008g0282 | 2 | HG02080.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-57+12764_-57+1276 others(30): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987404 | |||||
| chr21:42987404
|
A | AT | 4 | a0001c0001t0021g0152a0001c0002t0003g0337a0001c0005t0003g0302others(1): Show | 4 | HG01928.hp1 HG02080.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+12740_-57+1274 others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | ||||||
| chr21:42987404
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0045 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1274 others(19): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | ||||||
| chr21:42987404
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0004g0049 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1274 others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | ||||||
| chr21:42987404
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0021 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1274 others(27): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | ||||||
| chr21:42987404
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0004g0256 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-57+12740_-57+1274 others(29): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | ||||||
| chr21:42987404
|
A | T | 88 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0028others(85): Show | 88 | HG00099.hp1 HG00609.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.-57+12740A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987404 | ||||||
| chr21:42987406
|
T | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0002t0003g0346others(5): Show | 8 | HG00544.hp2 HG00621.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+12742T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987406 | ||||||
| chr21:42987407
|
A | G | 2 | a0001c0001t0019g0287a0001c0001t0032g0291 | 2 | HG03654.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-57+12743A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987407 | ||||||
| chr21:42987408
|
T | A | 5 | a0001c0001t0001g0018a0001c0001t0023g0052a0001c0001t0044g0290others(2): Show | 5 | HG01496.hp1 HG02055.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+12744T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987408 | ||||||
| chr21:42987409
|
A | C | 1 | a0001c0001t0004g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-57+12745A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987409 | ||||||
| chr21:42987409
|
A | G | 1 | a0001c0001t0019g0286 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-57+12745A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987409 | ||||||
| chr21:42987410
|
T | A | 3 | a0001c0001t0023g0052a0001c0002t0028g0288a0001c0002t0028g0289 | 3 | HG02896.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-57+12746T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987410 | ||||||
| chr21:42987449
|
T | G | 1 | a0001c0001t0020g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57+12785T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987449 | ||||||
| chr21:42987450
|
C | A | 1 | a0001c0001t0020g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-57+12786C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987450 | ||||||
| chr21:42987467
|
G | A | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57+12803G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987467 | ||||||
| chr21:42987496
|
A | T | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+12832A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987496 | ||||||
| chr21:42987553
|
A | T | 1 | a0001c0001t0032g0291 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+12889A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987553 | ||||||
| chr21:42987557
|
C | A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+12893C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987557 | ||||||
| chr21:42987618
|
CT | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(205): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-57+12971delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42987618 | |||||
| chr21:42987680
|
G | A | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+13016G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987680 | ||||||
| chr21:42987779
|
T | G | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+13115T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42987779 | ||||||
| chr21:42988065
|
TG | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-57+13402delG | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988065 | ||||||
| chr21:42988066
|
G | T | 111 | a0001c0001t0001g0130a0001c0001t0001g0200a0001c0001t0002g0014others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-57+13402G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988066 | ||||||
| chr21:42988254
|
T | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0142 | 3 | NA18983.hp1 NA18988.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-57+13590T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988254 | ||||||
| chr21:42988292
|
G | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-57+13628G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988292 | ||||||
| chr21:42988343
|
C | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(246): Show | 250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-57+13679C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988343 | ||||||
| chr21:42988659
|
G | A | 1 | a0001c0001t0008g0277 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-57+13995G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988659 | ||||||
| chr21:42988774
|
G | A | 1 | a0001c0002t0003g0353 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-57+14110G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988774 | ||||||
| chr21:42988949
|
T | A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+14285T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42988949 | ||||||
| chr21:42989079
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0089 | 3 | HG01074.hp1 HG01243.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-57+14415C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989079 | ||||||
| chr21:42989129
|
C | T | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+14465C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989129 | ||||||
| chr21:42989130
|
G | A | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-57+14466G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989130 | ||||||
| chr21:42989285
|
CA | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+14623delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42989285 | |||||
| chr21:42989290
|
T | C | 75 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-57+14626T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989290 | ||||||
| chr21:42989308
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-57+14644T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989308 | ||||||
| chr21:42989318
|
T | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-57+14654T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989318 | ||||||
| chr21:42989564
|
G | A | 1 | a0001c0001t0004g0049 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-56-14762G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989564 | ||||||
| chr21:42989575
|
C | T | 1 | a0001c0001t0006g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-14751C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989575 | ||||||
| chr21:42989577
|
C | T | 1 | a0001c0001t0005g0169 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-56-14749C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989577 | ||||||
| chr21:42989654
|
A | G | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-14672A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989654 | ||||||
| chr21:42989691
|
T | C | 1 | a0001c0001t0002g0251 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-56-14635T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989691 | ||||||
| chr21:42989699
|
G | A | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG03654.hp1 NA18960.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-14627G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989699 | ||||||
| chr21:42989713
|
C | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-56-14613C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989713 | ||||||
| chr21:42989716
|
G | C | 1 | a0001c0001t0006g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-56-14610G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989716 | ||||||
| chr21:42989877
|
T | C | 3 | a0001c0001t0022g0022a0001c0001t0022g0051a0001c0001t0035g0050 | 3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-14449T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989877 | ||||||
| chr21:42989958
|
G | A | 105 | a0001c0001t0002g0014a0001c0001t0002g0187a0001c0001t0002g0188others(102): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-56-14368G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989958 | ||||||
| chr21:42989992
|
C | T | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-56-14334C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42989992 | ||||||
| chr21:42990076
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-56-14250A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990076 | ||||||
| chr21:42990096
|
CA | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-56-14217delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42990096 | |||||
| chr21:42990107
|
A | T | 11 | a0001c0001t0001g0200a0001c0001t0002g0204a0001c0001t0002g0214others(8): Show | 11 | HG00609.hp2 HG01496.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-14219A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990107 | ||||||
| chr21:42990292
|
C | T | 35 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.-56-14034C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990292 | ||||||
| chr21:42990299
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-14027C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990299 | ||||||
| chr21:42990312
|
G | A | 1 | a0001c0001t0030g0075 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-56-14014G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990312 | ||||||
| chr21:42990388
|
T | C | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-13938T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990388 | ||||||
| chr21:42990615
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-13711C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990615 | ||||||
| chr21:42990796
|
A | G | 1 | a0001c0001t0004g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-56-13530A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990796 | ||||||
| chr21:42990984
|
G | A | 3 | a0001c0001t0002g0210a0001c0003t0002g0203a0001c0003t0002g0211 | 3 | HG02040.hp2 NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-56-13342G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42990984 | ||||||
| chr21:42991209
|
G | A | 1 | a0001c0002t0003g0316 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-56-13117G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991209 | ||||||
| chr21:42991285
|
G | A | 3 | a0001c0001t0005g0173a0001c0001t0005g0182a0001c0001t0005g0257 | 3 | NA18950.hp1 NA18951.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-56-13041G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991285 | ||||||
| chr21:42991369
|
C | G | 1 | a0001c0002t0003g0315 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-56-12957C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991369 | ||||||
| chr21:42991443
|
T | G | 1 | a0001c0001t0043g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-56-12883T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991443 | ||||||
| chr21:42991510
|
A | C | 111 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-56-12816A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991510 | ||||||
| chr21:42991645
|
G | A | 16 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0113others(13): Show | 16 | HG00741.hp2 HG01168.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-12681G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991645 | ||||||
| chr21:42991660
|
G | A | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-56-12666G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42991660 | ||||||
| chr21:42991733
|
CA | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-56-12580delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42991733 | |||||
| chr21:42992082
|
G | A | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-12244G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992082 | ||||||
| chr21:42992148
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-56-12178A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992148 | ||||||
| chr21:42992329
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-56-11997A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992329 | ||||||
| chr21:42992566
|
C | T | 33 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(30): Show | 34 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.-56-11760C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992566 | ||||||
| chr21:42992625
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-11701C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992625 | ||||||
| chr21:42992699
|
A | G | 10 | a0001c0001t0006g0003a0001c0001t0006g0174a0001c0001t0006g0176others(7): Show | 11 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-56-11627A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992699 | ||||||
| chr21:42992714
|
TTCACAGC others(13): Show |
T | 5 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0209others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-11596_-56-1157 others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42992714 | |||||
| chr21:42992769
|
G | A | 1 | a0001c0001t0005g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-56-11557G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992769 | ||||||
| chr21:42992828
|
GGGGGCCT others(33): Show |
G | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-56-11493_-56-1145 others(44): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42992828 | |||||
| chr21:42992843
|
G | A | 290 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-56-11483G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992843 | ||||||
| chr21:42992888
|
T | C | 1 | a0001c0001t0004g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-56-11438T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992888 | ||||||
| chr21:42992943
|
T | G | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-11383T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992943 | ||||||
| chr21:42992991
|
A | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-11335A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42992991 | ||||||
| chr21:42993000
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-56-11326C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993000 | ||||||
| chr21:42993073
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-56-11253G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993073 | ||||||
| chr21:42993291
|
G | A | 1 | a0001c0001t0005g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-56-11035G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993291 | ||||||
| chr21:42993347
|
G | A | 6 | a0001c0001t0006g0003a0001c0001t0006g0176a0001c0001t0006g0177others(3): Show | 7 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-10979G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993347 | ||||||
| chr21:42993351
|
C | T | 1 | a0001c0001t0023g0052 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-56-10975C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993351 | ||||||
| chr21:42993381
|
C | T | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10945C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993381 | ||||||
| chr21:42993396
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG03688.hp2 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-56-10930C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993396 | ||||||
| chr21:42993521
|
CT | C | 7 | a0001c0001t0001g0063a0001c0001t0001g0097a0001c0001t0001g0113others(4): Show | 7 | HG02602.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-10791delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993521 | |||||
| chr21:42993548
|
A | G | 1 | a0001c0001t0004g0046 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-56-10778A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993548 | ||||||
| chr21:42993603
|
C | G | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10723C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993603 | ||||||
| chr21:42993607
|
C | T | 1 | a0001c0001t0008g0275 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-56-10719C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993607 | ||||||
| chr21:42993646
|
CTTTGTTT others(2): Show |
C | 32 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(29): Show | 33 | HG00323.hp1 HG00423.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-56-10667_-56-1065 others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993646 | |||||
| chr21:42993650
|
GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10667_-56-1065 others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993650 | |||||
| chr21:42993651
|
TTTTTTTT others(1): Show |
T | 169 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-56-10667_-56-1066 others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993651 | |||||
| chr21:42993652
|
TTTTTTTG | T | 78 | a0001c0001t0001g0027a0001c0001t0001g0076a0001c0001t0001g0093others(75): Show | 78 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-56-10667_-56-1066 others(11): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993652 | |||||
| chr21:42993659
|
G | GT | 7 | a0001c0002t0003g0313a0001c0002t0003g0314a0001c0002t0003g0324others(4): Show | 7 | HG01081.hp2 HG02027.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-10652dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993659 | |||||
| chr21:42993714
|
A | G | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-10612A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993714 | ||||||
| chr21:42993723
|
CTCTTTTT others(3): Show |
C | 254 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-56-10591_-56-1058 others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993723 | |||||
| chr21:42993725
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0093a0001c0001t0001g0116a0001c0001t0002g0252others(1): Show | 4 | HG01516.hp1 NA18942.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10591_-56-1058 others(15): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993725 | |||||
| chr21:42993726
|
TTTTTTTT others(2): Show |
T | 26 | a0001c0001t0001g0029a0001c0001t0001g0128a0001c0001t0001g0129others(23): Show | 27 | HG00423.hp1 HG00735.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-56-10591_-56-1058 others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993726 | |||||
| chr21:42993733
|
TTC | T | 7 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(4): Show | 7 | HG03098.hp1 HG03654.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-10591_-56-1059 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42993733 | |||||
| chr21:42993734
|
TC | T | 53 | a0001c0002t0003g0300a0001c0002t0003g0301a0001c0002t0003g0309others(50): Show | 53 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-56-10591delC | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993734 | ||||||
| chr21:42993735
|
C | T | 4 | a0001c0001t0044g0290a0001c0002t0003g0298a0001c0002t0003g0311others(1): Show | 4 | HG02055.hp2 NA18944.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-10591C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993735 | ||||||
| chr21:42993819
|
G | A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10507G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993819 | ||||||
| chr21:42993826
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-56-10500G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993826 | ||||||
| chr21:42993857
|
G | A | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-56-10469G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993857 | ||||||
| chr21:42993978
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-56-10348T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993978 | ||||||
| chr21:42993996
|
T | C | 1 | a0001c0001t0011g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-10330T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42993996 | ||||||
| chr21:42994018
|
C | T | 1 | a0001c0001t0024g0092 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-56-10308C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994018 | ||||||
| chr21:42994023
|
C | T | 1 | a0001c0001t0013g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-56-10303C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994023 | ||||||
| chr21:42994031
|
C | CT | 6 | a0001c0001t0007g0101a0001c0002t0003g0310a0001c0002t0003g0315others(3): Show | 6 | HG01496.hp2 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-10273dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994031 | |||||
| chr21:42994031
|
CT | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(162): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-56-10273delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994031 | |||||
| chr21:42994031
|
CTT | C | 107 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(104): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-56-10274_-56-1027 others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994031 | |||||
| chr21:42994194
|
T | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-10132T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994194 | ||||||
| chr21:42994294
|
A | AGCCTCCC others(2141): Show |
1 | a0001c0001t0001g0123 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2152): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2167): Show |
1 | a0001c0001t0006g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2178): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2166): Show |
1 | a0001c0001t0006g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2177): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0002g0247 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0046g0222 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0005g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2163): Show |
1 | a0001c0001t0006g0178 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2174): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0006g0177 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2163): Show |
3 | a0001c0001t0006g0003a0001c0001t0006g0179a0001c0001t0006g0258 | 4 | HG01515.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2174): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0006g0174 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0006g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2163): Show |
1 | a0001c0001t0005g0161 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2174): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2164): Show |
3 | a0001c0001t0005g0159a0001c0001t0005g0160a0002c0004t0005g0158 | 3 | NA18940.hp1 NA18999.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2166): Show |
1 | a0001c0001t0005g0173 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2177): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0005g0182 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2166): Show |
1 | a0001c0001t0037g0195 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2177): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2169): Show |
1 | a0001c0001t0002g0191 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2180): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2155): Show |
1 | a0001c0001t0002g0209 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2166): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2164): Show |
1 | a0001c0001t0002g0192 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2175): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2159): Show |
1 | a0001c0001t0002g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2170): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0026g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2156): Show |
1 | a0001c0001t0002g0217 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2167): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2158): Show |
1 | a0001c0001t0002g0250 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2169): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2159): Show |
1 | a0001c0001t0002g0218 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2170): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0002g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2157): Show |
5 | a0001c0001t0002g0196a0001c0001t0002g0210a0001c0001t0002g0219others(2): Show | 5 | HG02040.hp2 HG02886.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2168): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2158): Show |
21 | a0001c0001t0002g0171a0001c0001t0002g0194a0001c0001t0002g0197others(18): Show | 21 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2169): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2159): Show |
2 | a0001c0001t0002g0237a0001c0001t0002g0254 | 2 | HG02818.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2170): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0047g0216 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2158): Show |
6 | a0001c0001t0001g0200a0001c0001t0002g0187a0001c0001t0002g0188others(3): Show | 6 | HG02145.hp1 HG02602.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2169): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0017g0238 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2158): Show |
2 | a0001c0001t0002g0233a0001c0001t0002g0234 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2169): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0005g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2159): Show |
1 | a0001c0001t0033g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2170): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2162): Show |
1 | a0001c0001t0005g0169 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2173): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0005g0257 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2161): Show |
1 | a0001c0001t0005g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2172): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0043g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2157): Show |
1 | a0001c0001t0006g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2168): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2160): Show |
2 | a0001c0001t0005g0167a0001c0001t0005g0259 | 2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2154): Show |
1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2154): Show |
1 | a0001c0001t0002g0014 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0002g0253 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2154): Show |
12 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0221others(9): Show | 12 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2155): Show |
1 | a0001c0001t0050g0240 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2166): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0004g0020 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2154): Show |
11 | a0001c0001t0001g0153a0001c0001t0002g0199a0001c0001t0002g0202others(8): Show | 11 | HG02056.hp1 HG02071.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2152): Show |
1 | a0001c0001t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2163): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2153): Show |
2 | a0001c0001t0007g0101a0001c0001t0007g0102 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2154): Show |
1 | a0001c0001t0007g0104 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2165): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2160): Show |
1 | a0001c0001t0005g0164 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2171): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0006g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2157): Show |
2 | a0001c0001t0005g0168a0001c0001t0005g0181 | 2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2168): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2151): Show |
1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2162): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2148): Show |
1 | a0001c0001t0020g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2159): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2150): Show |
1 | a0001c0001t0027g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2150): Show |
1 | a0001c0001t0027g0170 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0006g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2155): Show |
1 | a0001c0001t0006g0184 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2166): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2151): Show |
2 | a0001c0001t0004g0139a0001c0001t0023g0115 | 2 | HG01981.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2162): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2152): Show |
2 | a0001c0001t0001g0024a0001c0001t0004g0140 | 2 | HG02965.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2163): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2153): Show |
2 | a0001c0001t0002g0189a0001c0001t0002g0198 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2149): Show |
3 | a0001c0001t0001g0093a0001c0001t0004g0019a0001c0001t0004g0041 | 3 | HG01168.hp1 NA18969.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2160): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2150): Show |
14 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0143others(11): Show | 14 | HG01175.hp1 HG01361.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2151): Show |
3 | a0001c0001t0001g0089a0001c0001t0002g0241a0001c0001t0004g0046 | 3 | HG01192.hp1 HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2162): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2148): Show |
1 | a0001c0001t0031g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2159): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2150): Show |
4 | a0001c0001t0001g0064a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG00544.hp1 HG00609.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2151): Show |
1 | a0001c0001t0001g0072 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2162): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2149): Show |
1 | a0001c0001t0034g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2160): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2150): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0004g0135others(1): Show | 4 | HG02027.hp2 NA18522.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2150): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0078 | 2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2152): Show |
1 | a0001c0001t0005g0156 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2163): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0001g0079 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2147): Show |
1 | a0001c0001t0041g0058 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2145): Show |
2 | a0001c0001t0022g0051a0001c0001t0035g0050 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0001g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2148): Show |
1 | a0001c0001t0001g0124 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2159): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0060others(5): Show | 9 | HG01168.hp2 HG01258.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2147): Show |
2 | a0001c0001t0001g0107a0001c0001t0001g0125 | 2 | HG01167.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2148): Show |
4 | a0001c0001t0001g0076a0001c0001t0001g0097a0001c0001t0001g0138others(1): Show | 4 | HG01109.hp1 HG02602.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2159): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2149): Show |
1 | a0001c0001t0001g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2160): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2150): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0094 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2161): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2145): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0142a0001c0001t0010g0031 | 3 | HG00733.hp1 NA19063.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
26 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0054others(23): Show | 26 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2147): Show |
7 | a0001c0001t0007g0004a0001c0001t0007g0005a0001c0001t0007g0009others(4): Show | 7 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2149): Show |
1 | a0001c0001t0001g0130 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2160): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2145): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0147 | 2 | HG01358.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
21 | a0001c0001t0001g0028a0001c0001t0001g0056a0001c0001t0001g0067others(18): Show | 21 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2147): Show |
5 | a0001c0001t0001g0027a0001c0001t0001g0087a0001c0001t0001g0096others(2): Show | 5 | HG02258.hp2 HG02897.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2145): Show |
1 | a0001c0001t0001g0113 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2145): Show |
1 | a0001c0001t0001g0116 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
5 | a0001c0001t0001g0059a0001c0001t0001g0137a0001c0001t0001g0144others(2): Show | 5 | HG02015.hp1 NA18965.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0042g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0001g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0001g0145 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2153): Show |
1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2164): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
3 | a0001c0001t0008g0271a0001c0001t0008g0277a0001c0001t0008g0281 | 3 | HG00140.hp2 HG01099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2145): Show |
3 | a0001c0001t0008g0269a0001c0001t0008g0280a0001c0001t0008g0282 | 3 | HG01070.hp2 HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2156): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
7 | a0001c0001t0008g0272a0001c0001t0008g0274a0001c0001t0008g0278others(4): Show | 7 | HG00323.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2147): Show |
3 | a0001c0001t0008g0275a0001c0001t0015g0273a0001c0001t0015g0276 | 3 | HG01981.hp2 HG02004.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2158): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2152): Show |
1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2163): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2144): Show |
1 | a0001c0001t0001g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2155): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2142): Show |
2 | a0001c0001t0001g0018a0001c0001t0011g0265 | 2 | HG01496.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2153): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2140): Show |
4 | a0001c0001t0011g0262a0001c0001t0011g0264a0001c0001t0045g0267others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2151): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2140): Show |
1 | a0001c0001t0011g0263 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2151): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2124): Show |
6 | a0001c0002t0003g0313a0001c0002t0003g0333a0001c0002t0003g0338others(3): Show | 6 | HG00621.hp1 HG01081.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2125): Show |
2 | a0001c0002t0003g0298a0001c0002t0003g0315 | 2 | HG02071.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2136): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2126): Show |
1 | a0001c0002t0003g0344 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2137): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2123): Show |
3 | a0001c0002t0009g0297a0001c0002t0028g0288a0001c0002t0028g0289 | 3 | HG01943.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2134): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2124): Show |
40 | a0001c0002t0003g0300a0001c0002t0003g0301a0001c0002t0003g0303others(37): Show | 40 | HG00597.hp2 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2122): Show |
4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2133): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2124): Show |
2 | a0001c0002t0003g0309a0001c0002t0003g0314 | 2 | NA19009.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2124): Show |
1 | a0001c0002t0003g0343 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2130): Show |
1 | a0001c0002t0016g0294 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2141): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2124): Show |
2 | a0001c0002t0016g0295a0001c0002t0016g0354 | 2 | NA18939.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2127): Show |
2 | a0001c0001t0019g0286a0001c0001t0032g0291 | 2 | NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2138): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2125): Show |
1 | a0001c0001t0019g0287 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2136): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2139): Show |
1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2150): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2124): Show |
1 | a0001c0002t0003g0324 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2137): Show |
1 | a0001c0001t0022g0022 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2148): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2124): Show |
1 | a0001c0005t0003g0302 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2135): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994294
|
A | AGCCTCCC others(2146): Show |
1 | a0001c0001t0013g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-56-10005_-56-1000 others(2157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994294 | |||||
| chr21:42994330
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-9996C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994330 | ||||||
| chr21:42994901
|
T | C | 1 | a0001c0001t0002g0253 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-56-9425T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994901 | ||||||
| chr21:42994911
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-56-9415C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994911 | ||||||
| chr21:42994918
|
C | CT | 146 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(143): Show | 147 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-56-9387dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994918 | |||||
| chr21:42994918
|
C | CTT | 16 | a0001c0001t0004g0047a0001c0001t0008g0269a0001c0001t0008g0272others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-56-9388_-56-9387d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994918 | |||||
| chr21:42994918
|
CT | C | 85 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(82): Show | 85 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-56-9387delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994918 | |||||
| chr21:42994918
|
CTT | C | 31 | a0001c0001t0002g0219a0001c0001t0002g0250a0001c0001t0002g0253others(28): Show | 32 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.-56-9388_-56-9387d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42994918 | |||||
| chr21:42994945
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-56-9381A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994945 | ||||||
| chr21:42994980
|
G | A | 1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-9346G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994980 | ||||||
| chr21:42994983
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(153): Show | 157 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.-56-9343G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42994983 | ||||||
| chr21:42995111
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-56-9215G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995111 | ||||||
| chr21:42995161
|
G | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-56-9165G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995161 | ||||||
| chr21:42995222
|
G | A | 7 | a0001c0002t0003g0316a0001c0002t0003g0317a0001c0002t0003g0335others(4): Show | 7 | HG01496.hp2 NA18939.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-9104G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995222 | ||||||
| chr21:42995235
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-56-9091T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995235 | ||||||
| chr21:42995241
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-56-9085A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995241 | ||||||
| chr21:42995356
|
T | C | 36 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56-8970T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995356 | ||||||
| chr21:42995529
|
T | TTAGCCAG others(19): Show |
17 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-56-8793_-56-8768d others(28): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42995529 | |||||
| chr21:42995532
|
G | A | 111 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-56-8794G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995532 | ||||||
| chr21:42995726
|
G | A | 1 | a0001c0001t0004g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-56-8600G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995726 | ||||||
| chr21:42995774
|
C | A | 1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-8552C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995774 | ||||||
| chr21:42995775
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-56-8551G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995775 | ||||||
| chr21:42995799
|
A | G | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-8527A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995799 | ||||||
| chr21:42995800
|
C | T | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-8526C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995800 | ||||||
| chr21:42995852
|
G | A | 3 | a0001c0001t0027g0155a0001c0001t0027g0170a0001c0001t0043g0175 | 3 | HG02809.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-56-8474G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995852 | ||||||
| chr21:42995872
|
T | C | 5 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0209others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-8454T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995872 | ||||||
| chr21:42995902
|
T | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-56-8424T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995902 | ||||||
| chr21:42995951
|
T | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-56-8375T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995951 | ||||||
| chr21:42995989
|
C | T | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-8337C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42995989 | ||||||
| chr21:42996251
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-56-8075G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996251 | ||||||
| chr21:42996314
|
A | G | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-8012A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996314 | ||||||
| chr21:42996317
|
G | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-56-8009G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996317 | ||||||
| chr21:42996442
|
A | AT | 36 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56-7883dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996442 | |||||
| chr21:42996540
|
T | TAAAAATG others(142): Show |
1 | a0001c0001t0002g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-56-7769_-56-7768i others(151): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996540 | |||||
| chr21:42996540
|
T | TAAAAATG others(143): Show |
1 | a0001c0001t0002g0202 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-56-7769_-56-7768i others(152): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996540 | |||||
| chr21:42996540
|
T | TAAAAATG others(148): Show |
1 | a0001c0001t0002g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-56-7769_-56-7768i others(157): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996540 | |||||
| chr21:42996547
|
G | A | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-7779G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996547 | ||||||
| chr21:42996730
|
A | G | 1 | a0001c0001t0020g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-56-7596A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996730 | ||||||
| chr21:42996819
|
T | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-7507T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996819 | ||||||
| chr21:42996891
|
A | AT | 204 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(201): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.-56-7422dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42996891 | |||||
| chr21:42996943
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-56-7383C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996943 | ||||||
| chr21:42996949
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-7377C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42996949 | ||||||
| chr21:42997077
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0044g0290 | 2 | HG02055.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-56-7249C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997077 | ||||||
| chr21:42997304
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-56-7022C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997304 | ||||||
| chr21:42997422
|
C | T | 2 | a0001c0001t0010g0031a0001c0001t0010g0035 | 2 | NA18950.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-56-6904C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997422 | ||||||
| chr21:42997454
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(146): Show | 150 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.-56-6872A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997454 | ||||||
| chr21:42997513
|
A | G | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-6813A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997513 | ||||||
| chr21:42997539
|
TTTG | T | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0082others(2): Show | 5 | HG00423.hp2 HG01257.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-6785_-56-6783d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42997539 | |||||
| chr21:42997654
|
A | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-56-6672A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997654 | ||||||
| chr21:42997855
|
G | A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-6471G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997855 | ||||||
| chr21:42997871
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-56-6455C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997871 | ||||||
| chr21:42997909
|
G | T | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-6417G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42997909 | ||||||
| chr21:42998211
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-6115A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998211 | ||||||
| chr21:42998326
|
C | T | 36 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56-6000C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998326 | ||||||
| chr21:42998542
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-56-5784T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998542 | ||||||
| chr21:42998650
|
A | G | 1 | a0001c0002t0009g0308 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-56-5676A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998650 | ||||||
| chr21:42998803
|
G | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-5523G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998803 | ||||||
| chr21:42998810
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-56-5516G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998810 | ||||||
| chr21:42998895
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02129.hp2 HG02523.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-56-5431A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42998895 | ||||||
| chr21:42999021
|
G | A | 2 | a0001c0001t0023g0052a0001c0001t0023g0115 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-56-5305G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999021 | ||||||
| chr21:42999031
|
G | C | 1 | a0001c0002t0016g0294 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-56-5295G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999031 | ||||||
| chr21:42999040
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-56-5286G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999040 | ||||||
| chr21:42999048
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0131 | 2 | NA18939.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-56-5278A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999048 | ||||||
| chr21:42999074
|
C | T | 2 | a0001c0002t0003g0338a0001c0002t0003g0339 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-56-5252C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999074 | ||||||
| chr21:42999157
|
T | C | 299 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-56-5169T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999157 | ||||||
| chr21:42999474
|
ATTTTC | A | 75 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-56-4842_-56-4838d others(7): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 42999474 | |||||
| chr21:42999484
|
C | T | 10 | a0001c0001t0006g0003a0001c0001t0006g0174a0001c0001t0006g0176others(7): Show | 11 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.-56-4842C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999484 | ||||||
| chr21:42999545
|
A | G | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-56-4781A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999545 | ||||||
| chr21:42999592
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-56-4734C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999592 | ||||||
| chr21:42999666
|
A | G | 4 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291others(1): Show | 4 | HG02055.hp2 HG03654.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-4660A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 42999666 | ||||||
| chr21:43000275
|
C | G | 10 | a0001c0001t0007g0004a0001c0001t0007g0005a0001c0001t0007g0006others(7): Show | 10 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-4051C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000275 | ||||||
| chr21:43000360
|
G | A | 2 | a0001c0001t0027g0155a0001c0001t0027g0170 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-56-3966G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000360 | ||||||
| chr21:43000419
|
G | T | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-3907G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000419 | ||||||
| chr21:43000504
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-56-3822A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000504 | ||||||
| chr21:43000576
|
G | A | 1 | a0001c0002t0003g0352 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-56-3750G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000576 | ||||||
| chr21:43000651
|
C | T | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-3675C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000651 | ||||||
| chr21:43000729
|
AT | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-56-3594delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43000729 | |||||
| chr21:43000782
|
C | T | 1 | a0001c0002t0003g0352 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-56-3544C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000782 | ||||||
| chr21:43000816
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-56-3510G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000816 | ||||||
| chr21:43000856
|
C | G | 1 | a0001c0001t0008g0281 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-56-3470C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000856 | ||||||
| chr21:43000937
|
A | G | 23 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(20): Show | 23 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-56-3389A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43000937 | ||||||
| chr21:43001057
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-56-3269G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001057 | ||||||
| chr21:43001123
|
C | T | 1 | a0001c0002t0012g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-3203C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001123 | ||||||
| chr21:43001136
|
G | A | 10 | a0001c0001t0007g0004a0001c0001t0007g0005a0001c0001t0007g0006others(7): Show | 10 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-3190G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001136 | ||||||
| chr21:43001408
|
A | ACTCTTCC others(15): Show |
1 | a0001c0001t0027g0170 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-56-2898_-56-2877d others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43001408 | |||||
| chr21:43001498
|
C | T | 1 | a0001c0001t0005g0259 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-56-2828C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001498 | ||||||
| chr21:43001540
|
G | T | 1 | a0001c0002t0003g0352 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-56-2786G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001540 | ||||||
| chr21:43001654
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0095others(1): Show | 4 | HG00609.hp1 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-2672A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001654 | ||||||
| chr21:43001703
|
A | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(291): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-56-2623A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001703 | ||||||
| chr21:43001720
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-56-2606G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001720 | ||||||
| chr21:43001756
|
C | G | 1 | a0001c0001t0007g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-56-2570C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001756 | ||||||
| chr21:43001756
|
C | T | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-2570C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001756 | ||||||
| chr21:43001827
|
G | A | 110 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-56-2499G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001827 | ||||||
| chr21:43001916
|
G | A | 1 | a0001c0001t0004g0256 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-2410G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001916 | ||||||
| chr21:43001917
|
C | T | 17 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-56-2409C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001917 | ||||||
| chr21:43001955
|
C | T | 1 | a0001c0001t0007g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-56-2371C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001955 | ||||||
| chr21:43001960
|
C | CAAAT | 278 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0023others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-56-2342_-56-2339d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43001960 | |||||
| chr21:43001960
|
C | CAAATAAA others(1): Show |
5 | a0001c0001t0001g0018a0001c0001t0004g0044a0001c0001t0006g0186others(2): Show | 5 | HG01496.hp1 HG02486.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-2346_-56-2339d others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43001960 | |||||
| chr21:43001984
|
T | C | 1 | a0001c0005t0003g0302 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-56-2342T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43001984 | ||||||
| chr21:43002073
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-2253A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002073 | ||||||
| chr21:43002126
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-56-2200A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002126 | ||||||
| chr21:43002161
|
G | A | 1 | a0001c0001t0005g0182 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-56-2165G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002161 | ||||||
| chr21:43002163
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-56-2163G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002163 | ||||||
| chr21:43002186
|
C | T | 37 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(34): Show | 38 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.-56-2140C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002186 | ||||||
| chr21:43002404
|
G | GC | 6 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0209others(3): Show | 6 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-1917dupC | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr21 | 43002404 | |||||
| chr21:43002405
|
C | A | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-1921C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002405 | ||||||
| chr21:43002409
|
CT | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(225): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.-56-1916delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002409 | ||||||
| chr21:43002410
|
T | C | 63 | a0001c0001t0001g0200a0001c0001t0002g0171a0001c0001t0002g0187others(60): Show | 63 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.-56-1916T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002410 | ||||||
| chr21:43002485
|
C | G | 35 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.-56-1841C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43002485 | ||||||
| chr21:43003172
|
T | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(245): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-56-1154T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003172 | ||||||
| chr21:43003255
|
C | T | 3 | a0001c0001t0002g0215a0001c0001t0002g0218a0001c0001t0047g0216 | 3 | HG02559.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-56-1071C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003255 | ||||||
| chr21:43003259
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-56-1067C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003259 | ||||||
| chr21:43003271
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01358.hp1 HG01928.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1055C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003271 | ||||||
| chr21:43003420
|
G | A | 2 | a0001c0002t0003g0313a0001c0002t0003g0324 | 2 | HG01081.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-56-906G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003420 | ||||||
| chr21:43003457
|
C | T | 1 | a0001c0001t0004g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-56-869C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003457 | ||||||
| chr21:43003543
|
C | T | 75 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-56-783C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003543 | ||||||
| chr21:43003552
|
C | T | 110 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-56-774C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003552 | ||||||
| chr21:43003561
|
A | G | 2 | a0001c0001t0027g0155a0001c0001t0027g0170 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-56-765A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003561 | ||||||
| chr21:43003576
|
C | G | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-56-750C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003576 | ||||||
| chr21:43003693
|
G | A | 1 | a0001c0001t0008g0274 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-56-633G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003693 | ||||||
| chr21:43003931
|
G | T | 36 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56-395G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43003931 | ||||||
| chr21:43004027
|
C | T | 1 | a0001c0001t0002g0244 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-56-299C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004027 | ||||||
| chr21:43004035
|
C | T | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-291C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004035 | ||||||
| chr21:43004038
|
G | A | 22 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(19): Show | 22 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-56-288G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004038 | ||||||
| chr21:43004045
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-56-281C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004045 | ||||||
| chr21:43004223
|
G | A | 7 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(4): Show | 7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-103G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 1/10 | chr21 | 43004223 | ||||||
| chr21:43004489
|
G | A | 1 | a0001c0001t0043g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.51+57G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004489 | ||||||
| chr21:43004571
|
C | T | 1 | a0001c0001t0006g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+139C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004571 | ||||||
| chr21:43004579
|
G | GA | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.51+154dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 43004579 | |||||
| chr21:43004776
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.51+344G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004776 | ||||||
| chr21:43004864
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.51+432T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004864 | ||||||
| chr21:43004877
|
A | G | 1 | a0001c0001t0008g0280 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.51+445A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004877 | ||||||
| chr21:43004924
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.51+492C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004924 | ||||||
| chr21:43004927
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.51+495G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43004927 | ||||||
| chr21:43005091
|
T | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.51+659T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005091 | ||||||
| chr21:43005232
|
G | A | 1 | a0001c0001t0008g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.51+800G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005232 | ||||||
| chr21:43005249
|
C | T | 1 | a0001c0001t0015g0270 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.51+817C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005249 | ||||||
| chr21:43005278
|
C | T | 2 | a0001c0001t0027g0155a0001c0001t0027g0170 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.51+846C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005278 | ||||||
| chr21:43005289
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(243): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.51+857C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005289 | ||||||
| chr21:43005413
|
G | A | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.51+981G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005413 | ||||||
| chr21:43005431
|
G | GT | 272 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.51+1008dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 43005431 | |||||
| chr21:43005534
|
CT | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(185): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.51+1116delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr21 | 43005534 | |||||
| chr21:43005659
|
C | T | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.51+1227C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005659 | ||||||
| chr21:43005939
|
C | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.51+1507C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43005939 | ||||||
| chr21:43006024
|
C | G | 1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52-1467C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006024 | ||||||
| chr21:43006160
|
G | T | 1 | a0001c0001t0002g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.52-1331G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006160 | ||||||
| chr21:43006177
|
G | A | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.52-1314G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006177 | ||||||
| chr21:43006369
|
G | A | 35 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.52-1122G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006369 | ||||||
| chr21:43006613
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.52-878A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006613 | ||||||
| chr21:43006617
|
G | A | 16 | a0001c0001t0008g0269a0001c0001t0008g0271a0001c0001t0008g0272others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.52-874G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006617 | ||||||
| chr21:43006717
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.52-774C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006717 | ||||||
| chr21:43006774
|
C | T | 15 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0245others(12): Show | 15 | NA18954.hp2 NA18966.hp2 NA18979.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-717C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43006774 | ||||||
| chr21:43007083
|
T | C | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52-408T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43007083 | ||||||
| chr21:43007090
|
C | T | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.52-401C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43007090 | ||||||
| chr21:43007400
|
A | G | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.52-91A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43007400 | ||||||
| chr21:43007449
|
A | T | 1 | a0001c0001t0014g0109 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.52-42A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 2/10 | chr21 | 43007449 | ||||||
| chr21:43007705
|
G | A | 1 | a0001c0001t0002g0255 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.179+87G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43007705 | ||||||
| chr21:43007909
|
C | T | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.179+291C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43007909 | ||||||
| chr21:43007988
|
G | C | 2 | a0001c0001t0021g0151a0001c0001t0021g0152 | 2 | NA18963.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.179+370G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43007988 | ||||||
| chr21:43008002
|
T | G | 1 | a0001c0001t0023g0115 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.179+384T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008002 | ||||||
| chr21:43008052
|
A | G | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.179+434A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008052 | ||||||
| chr21:43008061
|
T | TCA | 12 | a0001c0001t0002g0220a0001c0001t0002g0230a0001c0001t0002g0232others(9): Show | 12 | HG00735.hp2 HG02056.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.179+478_179+479dup others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCACA | 53 | a0001c0001t0001g0200a0001c0001t0002g0187a0001c0001t0002g0188others(50): Show | 53 | HG00438.hp1 HG00609.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.179+476_179+479dup others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCACACA | 14 | a0001c0001t0002g0014a0001c0001t0002g0190a0001c0001t0002g0191others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.179+474_179+479dup others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCACACAC others(1): Show |
3 | a0001c0001t0002g0171a0001c0001t0023g0115a0001c0001t0025g0015 | 3 | HG00642.hp2 HG03471.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.179+472_179+479dup others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCA | 17 | a0001c0001t0007g0004a0001c0001t0007g0005a0001c0001t0007g0006others(14): Show | 17 | HG00140.hp2 HG01074.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCACA | 5 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0047others(2): Show | 5 | HG01168.hp1 HG01175.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCACAC others(1): Show |
13 | a0001c0001t0001g0099a0001c0001t0007g0101a0001c0001t0007g0102others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(8): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCACAC others(3): Show |
28 | a0001c0001t0001g0027a0001c0001t0004g0021a0001c0001t0004g0039others(25): Show | 28 | HG00140.hp1 HG00544.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCACAC others(5): Show |
8 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0100others(5): Show | 8 | HG00642.hp1 HG01167.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCACAC others(7): Show |
4 | a0001c0001t0006g0184a0001c0001t0006g0186a0001c0001t0027g0155others(1): Show | 4 | HG01261.hp1 HG02486.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCACAC others(9): Show |
2 | a0001c0001t0001g0138a0001c0001t0008g0268 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.179+444_179+445ins others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCTCAC others(3): Show |
4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCTCAC others(5): Show |
3 | a0001c0001t0005g0159a0001c0001t0005g0160a0002c0004t0005g0158 | 3 | NA18940.hp1 NA18999.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.179+444_179+445ins others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCTCAC others(7): Show |
3 | a0001c0001t0006g0179a0001c0001t0006g0180a0001c0001t0033g0166 | 3 | HG01099.hp2 HG03579.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.179+444_179+445ins others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCTCAC others(9): Show |
8 | a0001c0001t0005g0156a0001c0001t0005g0161a0001c0001t0005g0163others(5): Show | 8 | HG00099.hp2 HG00423.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.179+444_179+445ins others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCTCAC others(11): Show |
3 | a0001c0001t0005g0157a0001c0001t0005g0164a0001c0001t0005g0168 | 3 | HG01109.hp2 HG03942.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.179+444_179+445ins others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCTCAC others(13): Show |
2 | a0001c0001t0005g0162a0001c0001t0005g0169 | 2 | HG02132.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.179+444_179+445ins others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCTCAC others(15): Show |
2 | a0001c0001t0006g0172a0001c0001t0006g0174 | 2 | HG02922.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.179+444_179+445ins others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
T | TCTCTCTC others(9): Show |
1 | a0001c0001t0005g0257 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.179+444_179+445ins others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
TCA | T | 19 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0073others(16): Show | 19 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.179+478_179+479del others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
TCACA | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 94 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.179+476_179+479del others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0002g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.179+470_179+479del others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008061
|
TCACACAC others(5): Show |
T | 1 | a0001c0003t0002g0211 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.179+468_179+479del others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008061 | |||||
| chr21:43008063
|
A | T | 3 | a0001c0001t0008g0277a0001c0001t0019g0286a0001c0001t0019g0287 | 3 | HG01099.hp1 HG03654.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.179+445A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008063 | ||||||
| chr21:43008065
|
A | T | 16 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0073others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.179+447A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008065 | ||||||
| chr21:43008067
|
A | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 94 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.179+449A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008067 | ||||||
| chr21:43008069
|
A | T | 2 | a0001c0001t0006g0176a0001c0001t0006g0185 | 2 | HG00735.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.179+451A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008069 | ||||||
| chr21:43008158
|
C | T | 1 | a0001c0001t0008g0278 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.179+540C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008158 | ||||||
| chr21:43008237
|
G | A | 36 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.179+619G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008237 | ||||||
| chr21:43008424
|
A | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(153): Show | 157 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.179+806A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008424 | ||||||
| chr21:43008622
|
T | C | 2 | a0001c0001t0002g0213a0001c0001t0002g0260 | 2 | HG00438.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.179+1004T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008622 | ||||||
| chr21:43008678
|
C | T | 6 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.179+1060C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008678 | ||||||
| chr21:43008770
|
G | A | 2 | a0001c0001t0006g0180a0001c0001t0033g0166 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.179+1152G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008770 | ||||||
| chr21:43008780
|
C | CA | 21 | a0001c0001t0001g0111a0001c0001t0001g0145a0001c0001t0008g0269others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.179+1174dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43008780 | |||||
| chr21:43008919
|
C | T | 1 | a0001c0002t0003g0337 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.180-1134C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43008919 | ||||||
| chr21:43009118
|
A | C | 1 | a0001c0002t0003g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.180-935A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009118 | ||||||
| chr21:43009226
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.180-827T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009226 | ||||||
| chr21:43009280
|
T | TCTA | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.180-772_180-770dup others(3): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009280 | |||||
| chr21:43009286
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.180-767G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009286 | ||||||
| chr21:43009335
|
C | G | 3 | a0001c0001t0022g0022a0001c0001t0022g0051a0001c0001t0035g0050 | 3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.180-718C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009335 | ||||||
| chr21:43009604
|
C | A | 1 | a0001c0001t0017g0238 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.180-449C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009604 | ||||||
| chr21:43009610
|
C | CA | 34 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0005g0157others(31): Show | 35 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.180-423dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009610 | |||||
| chr21:43009610
|
C | CAA | 157 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(154): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.180-424_180-423dup others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009610 | |||||
| chr21:43009610
|
C | CAAA | 27 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0001g0111others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.180-425_180-423dup others(3): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009610 | |||||
| chr21:43009610
|
C | CAAAA | 72 | a0001c0001t0002g0014a0001c0001t0002g0171a0001c0001t0002g0187others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.180-426_180-423dup others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr21 | 43009610 | |||||
| chr21:43009749
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.180-304G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009749 | ||||||
| chr21:43009800
|
G | A | 1 | a0001c0001t0008g0274 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.180-253G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009800 | ||||||
| chr21:43009974
|
G | A | 1 | a0001c0001t0045g0267 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.180-79G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43009974 | ||||||
| chr21:43010029
|
T | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.180-24T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43010029 | ||||||
| chr21:43010039
|
T | C | 1 | a0001c0002t0003g0327 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.180-14T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 3/10 | chr21 | 43010039 | ||||||
| chr21:43010267
|
T | C | 1 | a0001c0001t0004g0049 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.351+43T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010267 | ||||||
| chr21:43010478
|
C | T | 16 | a0001c0001t0008g0269a0001c0001t0008g0271a0001c0001t0008g0272others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.351+254C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010478 | ||||||
| chr21:43010489
|
A | C | 3 | a0001c0001t0002g0207a0001c0001t0025g0015a0001c0001t0025g0016 | 3 | HG00639.hp2 HG00642.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.351+265A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010489 | ||||||
| chr21:43010599
|
C | T | 2 | a0001c0001t0027g0155a0001c0001t0027g0170 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.351+375C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010599 | ||||||
| chr21:43010627
|
A | G | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+403A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010627 | ||||||
| chr21:43010632
|
A | G | 1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.351+408A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010632 | ||||||
| chr21:43010648
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.351+424G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010648 | ||||||
| chr21:43010787
|
G | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.351+563G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43010787 | ||||||
| chr21:43010998
|
T | TGTGTCTG others(14): Show |
1 | a0001c0001t0004g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.351+775_351+795dup others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr21 | 43010998 | |||||
| chr21:43011066
|
CT | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.351+861delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr21 | 43011066 | |||||
| chr21:43011154
|
G | A | 1 | a0001c0002t0052g0332 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.351+930G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011154 | ||||||
| chr21:43011193
|
G | A | 1 | a0001c0001t0006g0174 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.351+969G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011193 | ||||||
| chr21:43011248
|
T | G | 36 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.351+1024T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011248 | ||||||
| chr21:43011271
|
G | A | 1 | a0001c0001t0044g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.351+1047G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011271 | ||||||
| chr21:43011290
|
C | T | 1 | a0001c0001t0026g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.351+1066C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011290 | ||||||
| chr21:43011291
|
G | A | 1 | a0001c0001t0020g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.351+1067G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011291 | ||||||
| chr21:43011361
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.351+1137G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011361 | ||||||
| chr21:43011372
|
G | A | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+1148G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011372 | ||||||
| chr21:43011438
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.351+1214C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011438 | ||||||
| chr21:43011504
|
T | C | 111 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.351+1280T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011504 | ||||||
| chr21:43011573
|
C | T | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.351+1349C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011573 | ||||||
| chr21:43011613
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(144): Show | 148 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.351+1389G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011613 | ||||||
| chr21:43011841
|
C | T | 1 | a0001c0002t0003g0301 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.352-1227C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43011841 | ||||||
| chr21:43012052
|
TTTGACAC others(3): Show |
T | 1 | a0001c0001t0007g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.352-1015_352-1006d others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012052 | ||||||
| chr21:43012140
|
A | G | 1 | a0001c0001t0023g0052 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.352-928A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012140 | ||||||
| chr21:43012259
|
T | C | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.352-809T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012259 | ||||||
| chr21:43012605
|
A | G | 17 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.352-463A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012605 | ||||||
| chr21:43012638
|
C | G | 1 | a0001c0001t0001g0145 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.352-430C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012638 | ||||||
| chr21:43012742
|
G | T | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-326G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012742 | ||||||
| chr21:43012770
|
G | C | 36 | a0001c0001t0005g0156a0001c0001t0005g0157a0001c0001t0005g0159others(33): Show | 37 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.352-298G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012770 | ||||||
| chr21:43012784
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.352-284G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012784 | ||||||
| chr21:43012806
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.352-262C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 4/10 | chr21 | 43012806 | ||||||
| chr21:43013344
|
C | G | 75 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.522+106C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013344 | ||||||
| chr21:43013385
|
G | C | 2 | a0001c0001t0031g0119a0001c0001t0042g0120 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.522+147G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013385 | ||||||
| chr21:43013571
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(175): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.522+333A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013571 | ||||||
| chr21:43013611
|
A | C | 1 | a0001c0001t0020g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.522+373A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013611 | ||||||
| chr21:43013669
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.522+431A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013669 | ||||||
| chr21:43013859
|
C | A | 114 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.522+621C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013859 | ||||||
| chr21:43013890
|
T | C | 2 | a0001c0001t0027g0155a0001c0001t0027g0170 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.522+652T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013890 | ||||||
| chr21:43013891
|
G | C | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.522+653G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013891 | ||||||
| chr21:43013892
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.522+654A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013892 | ||||||
| chr21:43013906
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.522+668T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013906 | ||||||
| chr21:43013907
|
A | T | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.522+669A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43013907 | ||||||
| chr21:43014019
|
C | CT | 80 | a0001c0001t0001g0066a0001c0001t0001g0128a0001c0001t0001g0129others(77): Show | 80 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(77): Show |
intron_variant | MODIFIER | c.522+801dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr21 | 43014019 | |||||
| chr21:43014053
|
G | A | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.522+815G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014053 | ||||||
| chr21:43014078
|
G | A | 63 | a0001c0001t0002g0014a0001c0001t0002g0171a0001c0001t0002g0187others(60): Show | 63 | HG00438.hp1 HG00609.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.522+840G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014078 | ||||||
| chr21:43014107
|
C | T | 35 | a0001c0001t0005g0157a0001c0001t0005g0159a0001c0001t0005g0160others(32): Show | 36 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.522+869C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014107 | ||||||
| chr21:43014176
|
C | T | 1 | a0001c0001t0050g0240 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.522+938C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014176 | ||||||
| chr21:43014225
|
A | G | 6 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0071others(3): Show | 6 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+987A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014225 | ||||||
| chr21:43014243
|
G | C | 2 | a0001c0001t0005g0168a0001c0001t0005g0181 | 2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.522+1005G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014243 | ||||||
| chr21:43014264
|
G | A | 2 | a0001c0001t0005g0168a0001c0001t0005g0181 | 2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.522+1026G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014264 | ||||||
| chr21:43014298
|
A | T | 1 | a0001c0001t0002g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.522+1060A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014298 | ||||||
| chr21:43014301
|
A | G | 1 | a0001c0001t0002g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.522+1063A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014301 | ||||||
| chr21:43014341
|
T | C | 5 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0234others(2): Show | 5 | HG02257.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+1103T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014341 | ||||||
| chr21:43014345
|
A | AT | 10 | a0001c0001t0006g0003a0001c0001t0006g0174a0001c0001t0006g0176others(7): Show | 11 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.522+1116dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr21 | 43014345 | |||||
| chr21:43014385
|
T | C | 18 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(15): Show | 18 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.522+1147T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014385 | ||||||
| chr21:43014478
|
CTT | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.522+1244_522+1245d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr21 | 43014478 | |||||
| chr21:43014501
|
A | G | 1 | a0001c0002t0039g0355 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.522+1263A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014501 | ||||||
| chr21:43014505
|
T | C | 1 | a0001c0001t0043g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.522+1267T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014505 | ||||||
| chr21:43014726
|
C | A | 61 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0004g0019others(58): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.522+1488C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014726 | ||||||
| chr21:43014888
|
C | G | 61 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0001g0200others(58): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.522+1650C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014888 | ||||||
| chr21:43014922
|
T | C | 1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.522+1684T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43014922 | ||||||
| chr21:43015845
|
G | C | 18 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(15): Show | 18 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-1063G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43015845 | ||||||
| chr21:43015995
|
G | A | 3 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0181 | 3 | HG00423.hp1 HG02132.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.523-913G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43015995 | ||||||
| chr21:43016039
|
A | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0100 | 3 | HG02965.hp2 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.523-869A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016039 | ||||||
| chr21:43016067
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(151): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.523-841G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016067 | ||||||
| chr21:43016260
|
A | T | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-648A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016260 | ||||||
| chr21:43016398
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.523-510G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016398 | ||||||
| chr21:43016510
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.523-398C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016510 | ||||||
| chr21:43016609
|
C | T | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.523-299C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016609 | ||||||
| chr21:43016679
|
G | A | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.523-229G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016679 | ||||||
| chr21:43016897
|
C | T | 1 | a0001c0001t0008g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.523-11C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 5/10 | chr21 | 43016897 | ||||||
| chr21:43017032
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(115): Show | 119 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.622+25A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017032 | ||||||
| chr21:43017057
|
T | C | 3 | a0001c0001t0011g0262a0001c0001t0011g0264a0001c0001t0045g0267 | 3 | HG02647.hp2 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.622+50T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017057 | ||||||
| chr21:43017066
|
G | A | 1 | a0001c0001t0011g0265 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.622+59G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017066 | ||||||
| chr21:43017112
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.622+105C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017112 | ||||||
| chr21:43017378
|
G | A | 2 | a0001c0001t0004g0040a0001c0001t0004g0041 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.622+371G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017378 | ||||||
| chr21:43017481
|
G | A | 1 | a0001c0001t0019g0287 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.622+474G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017481 | ||||||
| chr21:43017486
|
C | T | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.622+479C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017486 | ||||||
| chr21:43017490
|
A | G | 289 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.622+483A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017490 | ||||||
| chr21:43017556
|
G | GA | 64 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0002g0247others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.622+559dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43017556 | |||||
| chr21:43017643
|
C | CTAATTTT others(4): Show |
1 | a0001c0001t0001g0145 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.623-489_623-479dup others(11): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43017643 | |||||
| chr21:43017672
|
G | A | 1 | a0001c0001t0041g0058 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.623-461G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | chr21 | 43017672 | ||||||
| chr21:43018047
|
C | CA | 60 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0004g0019others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.623-63dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | |||||
| chr21:43018047
|
C | CAA | 13 | a0001c0001t0004g0108a0001c0001t0005g0173a0001c0001t0005g0181others(10): Show | 13 | HG00423.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.623-64_623-63dupAA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | |||||
| chr21:43018047
|
C | CAAA | 27 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0001t0001g0083others(24): Show | 27 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.623-65_623-63dupAA others(1): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | |||||
| chr21:43018047
|
C | CAAAA | 164 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(161): Show | 165 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.623-66_623-63dupAA others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | |||||
| chr21:43018047
|
C | CAAAAA | 30 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0069others(27): Show | 30 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.623-67_623-63dupAA others(3): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr21 | 43018047 | |||||
| chr21:43018378
|
C | G | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.720+148C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018378 | ||||||
| chr21:43018467
|
CT | C | 5 | a0001c0001t0002g0199a0001c0001t0002g0232a0001c0001t0002g0234others(2): Show | 5 | HG02886.hp2 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+238delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018467 | ||||||
| chr21:43018468
|
T | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.720+238T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018468 | ||||||
| chr21:43018469
|
G | C | 6 | a0001c0001t0002g0171a0001c0001t0002g0189a0001c0001t0002g0198others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+239G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018469 | ||||||
| chr21:43018470
|
C | CG | 28 | a0001c0001t0001g0080a0001c0001t0004g0019a0001c0001t0004g0021others(25): Show | 28 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.720+240_720+241ins others(1): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018470 | ||||||
| chr21:43018470
|
CCA | C | 13 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(10): Show | 13 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+242_720+243del others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | |||||
| chr21:43018470
|
CCACCCAC others(3): Show |
C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01074.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.720+244_720+253del others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | |||||
| chr21:43018470
|
CCACCCAC others(5): Show |
C | 4 | a0001c0001t0001g0067a0001c0001t0001g0132a0001c0001t0001g0144others(1): Show | 4 | HG01928.hp2 NA18522.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+244_720+255del others(12): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | |||||
| chr21:43018470
|
CCACCCAC others(7): Show |
C | 18 | a0001c0001t0001g0086a0001c0001t0001g0093a0001c0001t0001g0118others(15): Show | 18 | HG00323.hp2 HG00597.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.720+244_720+257del others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | |||||
| chr21:43018470
|
CCACCCAC others(9): Show |
C | 38 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(35): Show | 38 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.720+244_720+259del others(16): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | |||||
| chr21:43018470
|
CCACCCAC others(11): Show |
C | 15 | a0001c0001t0001g0028a0001c0001t0001g0057a0001c0001t0001g0062others(12): Show | 15 | HG00280.hp1 HG00738.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+244_720+261del others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | |||||
| chr21:43018470
|
CCACCCAC others(13): Show |
C | 4 | a0001c0001t0007g0011a0001c0001t0011g0263a0001c0001t0023g0052others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+244_720+263del others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018470 | |||||
| chr21:43018471
|
C | G | 32 | a0001c0001t0001g0094a0001c0001t0004g0020a0001c0001t0004g0040others(29): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.720+241C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018471 | ||||||
| chr21:43018472
|
A | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0024others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.720+242A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018472 | ||||||
| chr21:43018474
|
C | CCA | 15 | a0001c0002t0003g0300a0001c0002t0003g0301a0001c0002t0003g0303others(12): Show | 15 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.720+293_720+294dup others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018474
|
C | CCACA | 11 | a0001c0002t0003g0320a0001c0002t0003g0321a0001c0002t0003g0322others(8): Show | 11 | HG02083.hp2 HG02280.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.720+291_720+294dup others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018474
|
C | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0024others(57): Show | 61 | HG00423.hp2 HG00621.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.720+244C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018474 | ||||||
| chr21:43018474
|
CCA | C | 3 | a0001c0002t0003g0315a0001c0002t0003g0344a0001c0002t0003g0353 | 3 | HG02071.hp2 NA19057.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.720+293_720+294del others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018474
|
CCACA | C | 3 | a0001c0002t0018g0299a0001c0002t0028g0288a0001c0002t0028g0289 | 3 | HG02896.hp2 HG02897.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.720+291_720+294del others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018474
|
CCACACAC others(7): Show |
C | 1 | a0001c0002t0009g0307 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.720+281_720+294del others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018474
|
CCACACAC others(11): Show |
C | 2 | a0001c0001t0019g0286a0001c0001t0019g0287 | 2 | HG03654.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.720+277_720+294del others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018474
|
CCACACAC others(15): Show |
C | 2 | a0001c0001t0002g0196a0001c0001t0017g0238 | 2 | HG02738.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.720+273_720+294del others(22): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018474
|
CCACACAC others(17): Show |
C | 8 | a0001c0001t0002g0187a0001c0001t0002g0194a0001c0001t0002g0213others(5): Show | 8 | HG00438.hp1 HG00642.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+271_720+294del others(24): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018474
|
CCACACAC others(19): Show |
C | 13 | a0001c0001t0002g0197a0001c0001t0002g0202a0001c0001t0002g0217others(10): Show | 13 | HG00099.hp1 HG01243.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.720+269_720+294del others(26): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43018474 | |||||
| chr21:43018475
|
CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0079 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.720+246_720+256del others(11): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018475
|
CACACACA others(6): Show |
C | 9 | a0001c0001t0001g0018a0001c0001t0001g0056a0001c0001t0001g0061others(6): Show | 9 | HG01070.hp1 HG01496.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.720+246_720+258del others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018475
|
CACACACA others(8): Show |
C | 19 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0037others(16): Show | 19 | HG00423.hp2 HG00621.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.720+246_720+260del others(15): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018475
|
CACACACA others(10): Show |
C | 22 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0059others(19): Show | 23 | HG01168.hp2 HG01192.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.720+246_720+262del others(17): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018475
|
CACACACA others(12): Show |
C | 11 | a0001c0001t0005g0182a0001c0001t0005g0259a0001c0001t0006g0186others(8): Show | 11 | HG02258.hp1 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.720+246_720+264del others(19): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018475
|
CACACACA others(14): Show |
C | 25 | a0001c0001t0005g0156a0001c0001t0005g0159a0001c0001t0005g0162others(22): Show | 26 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.720+246_720+266del others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018475
|
CACACACA others(16): Show |
C | 15 | a0001c0001t0001g0094a0001c0001t0002g0189a0001c0001t0002g0198others(12): Show | 15 | HG00140.hp1 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.720+246_720+268del others(23): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018475
|
CACACACA others(18): Show |
C | 29 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(26): Show | 29 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.720+246_720+270del others(25): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018475
|
CACACACA others(20): Show |
C | 2 | a0001c0001t0002g0221a0001c0001t0002g0231 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.720+246_720+272del others(27): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018475 | ||||||
| chr21:43018476
|
A | C | 12 | a0001c0001t0001g0133a0001c0001t0002g0243a0001c0001t0002g0244others(9): Show | 12 | HG02129.hp2 NA18966.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+246A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018476 | ||||||
| chr21:43018477
|
CACACACA others(6): Show |
C | 7 | a0001c0001t0008g0271a0001c0001t0008g0277a0001c0001t0008g0279others(4): Show | 7 | HG00140.hp2 HG01099.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+248_720+260del others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018477 | ||||||
| chr21:43018477
|
CACACACA others(8): Show |
C | 5 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0272others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+248_720+262del others(15): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018477 | ||||||
| chr21:43018477
|
CACACACA others(14): Show |
C | 5 | a0001c0001t0005g0157a0001c0001t0005g0160a0001c0001t0005g0161others(2): Show | 5 | HG00423.hp1 HG00733.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+248_720+268del others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018477 | ||||||
| chr21:43018477
|
CACACACA others(16): Show |
C | 23 | a0001c0001t0001g0080a0001c0001t0004g0019a0001c0001t0004g0021others(20): Show | 23 | HG00544.hp1 HG00642.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.720+248_720+270del others(23): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018477 | ||||||
| chr21:43018478
|
A | C | 12 | a0001c0001t0001g0133a0001c0001t0002g0243a0001c0001t0002g0244others(9): Show | 12 | HG02129.hp2 NA18966.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+248A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018478 | ||||||
| chr21:43018480
|
A | C | 12 | a0001c0001t0001g0133a0001c0001t0002g0243a0001c0001t0002g0244others(9): Show | 12 | HG02129.hp2 NA18966.hp2 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+250A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018480 | ||||||
| chr21:43018482
|
A | C | 16 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0133others(13): Show | 16 | HG01074.hp1 HG01361.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.720+252A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018482 | ||||||
| chr21:43018484
|
A | C | 6 | a0001c0001t0001g0067a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG01928.hp2 HG02129.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+254A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018484 | ||||||
| chr21:43018484
|
A | G | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0002g0243others(9): Show | 12 | HG01074.hp1 HG01361.hp1 NA18966.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+254A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018484 | ||||||
| chr21:43018485
|
CACACACA others(18): Show |
C | 10 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0245others(7): Show | 10 | NA18966.hp2 NA18983.hp2 NA18986.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+256_720+280del others(25): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018485 | ||||||
| chr21:43018486
|
A | C | 17 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0086others(14): Show | 17 | HG00323.hp2 HG00597.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.720+256A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018486 | ||||||
| chr21:43018486
|
A | G | 5 | a0001c0001t0001g0067a0001c0001t0001g0132a0001c0001t0001g0144others(2): Show | 5 | HG01928.hp2 NA18522.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+256A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018486 | ||||||
| chr21:43018487
|
CACACACA others(16): Show |
C | 1 | a0001c0001t0002g0285 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.720+258_720+280del others(23): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018487 | ||||||
| chr21:43018488
|
A | C | 47 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(44): Show | 47 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.720+258A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018488 | ||||||
| chr21:43018488
|
A | G | 12 | a0001c0001t0001g0086a0001c0001t0001g0093a0001c0001t0001g0118others(9): Show | 12 | HG00597.hp1 HG00673.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+258A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018488 | ||||||
| chr21:43018490
|
A | C | 46 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0056others(43): Show | 46 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.720+260A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018490 | ||||||
| chr21:43018490
|
A | G | 35 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0029others(32): Show | 35 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.720+260A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018490 | ||||||
| chr21:43018491
|
CACACACA others(10): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.720+262_720+278del others(17): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018491 | ||||||
| chr21:43018492
|
A | C | 99 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(96): Show | 99 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.720+262A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018492 | ||||||
| chr21:43018492
|
A | G | 14 | a0001c0001t0001g0028a0001c0001t0001g0057a0001c0001t0001g0062others(11): Show | 14 | HG00280.hp1 HG00738.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.720+262A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018492 | ||||||
| chr21:43018494
|
A | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(136): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.720+264A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018494 | ||||||
| chr21:43018494
|
A | G | 4 | a0001c0001t0007g0011a0001c0001t0011g0263a0001c0001t0023g0052others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+264A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018494 | ||||||
| chr21:43018496
|
A | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(148): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.720+266A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018496 | ||||||
| chr21:43018498
|
A | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(153): Show | 157 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.720+268A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018498 | ||||||
| chr21:43018500
|
A | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(201): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.720+270A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018500 | ||||||
| chr21:43018502
|
A | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(269): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.720+272A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018502 | ||||||
| chr21:43018502
|
A | T | 1 | a0001c0001t0007g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.720+272A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018502 | ||||||
| chr21:43018504
|
A | C | 275 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.720+274A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018504 | ||||||
| chr21:43018506
|
A | C | 276 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.720+276A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018506 | ||||||
| chr21:43018508
|
A | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(267): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.720+278A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018508 | ||||||
| chr21:43018508
|
A | G | 4 | a0001c0001t0002g0250a0001c0001t0002g0253a0001c0001t0002g0261others(1): Show | 4 | NA18954.hp2 NA18979.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+278A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018508 | ||||||
| chr21:43018509
|
CA | C | 4 | a0001c0001t0002g0250a0001c0001t0002g0253a0001c0001t0002g0261others(1): Show | 4 | NA18954.hp2 NA18979.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+280delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018509 | ||||||
| chr21:43018510
|
A | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(210): Show | 215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.720+280A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018510 | ||||||
| chr21:43018512
|
A | C | 90 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0027others(87): Show | 91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.720+282A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018512 | ||||||
| chr21:43018514
|
A | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0081others(5): Show | 8 | HG00280.hp1 HG00733.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+284A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018514 | ||||||
| chr21:43018516
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.720+286A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018516 | ||||||
| chr21:43018529
|
T | C | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+299T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018529 | ||||||
| chr21:43018679
|
A | G | 60 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0004g0019others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.720+449A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018679 | ||||||
| chr21:43018726
|
G | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(66): Show | 70 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.720+496G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018726 | ||||||
| chr21:43018746
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.720+516C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018746 | ||||||
| chr21:43018895
|
C | G | 25 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0004g0019others(22): Show | 25 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.720+665C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018895 | ||||||
| chr21:43018958
|
G | A | 1 | a0001c0002t0052g0332 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.720+728G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018958 | ||||||
| chr21:43018994
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.720+764A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43018994 | ||||||
| chr21:43019063
|
C | T | 1 | a0001c0002t0003g0335 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.720+833C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019063 | ||||||
| chr21:43019084
|
C | CA | 11 | a0001c0001t0004g0047a0001c0001t0005g0163a0001c0001t0005g0168others(8): Show | 11 | HG00673.hp2 HG01175.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.720+870dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019084 | |||||
| chr21:43019084
|
CA | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(218): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.720+870delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019084 | |||||
| chr21:43019196
|
G | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.720+966G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019196 | ||||||
| chr21:43019222
|
G | A | 75 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.720+992G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019222 | ||||||
| chr21:43019234
|
G | A | 299 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.720+1004G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019234 | ||||||
| chr21:43019302
|
G | A | 1 | a0001c0002t0009g0308 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.720+1072G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019302 | ||||||
| chr21:43019306
|
T | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.720+1076T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019306 | ||||||
| chr21:43019379
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(284): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.720+1149A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019379 | ||||||
| chr21:43019409
|
C | CA | 247 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.720+1189dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019409 | |||||
| chr21:43019409
|
C | CAA | 36 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0134others(33): Show | 36 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.720+1188_720+1189d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019409 | |||||
| chr21:43019419
|
AC | A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+1190delC | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019419 | ||||||
| chr21:43019420
|
C | A | 287 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(284): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.720+1190C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019420 | ||||||
| chr21:43019420
|
C | CAA | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.720+1191_720+1192i others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019420 | |||||
| chr21:43019427
|
T | G | 1 | a0001c0001t0017g0238 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.720+1197T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019427 | ||||||
| chr21:43019468
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.720+1238T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019468 | ||||||
| chr21:43019507
|
T | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.720+1277T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019507 | ||||||
| chr21:43019743
|
C | T | 6 | a0001c0001t0008g0269a0001c0001t0008g0272a0001c0001t0008g0275others(3): Show | 6 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+1513C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019743 | ||||||
| chr21:43019762
|
G | A | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.720+1532G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019762 | ||||||
| chr21:43019779
|
C | T | 3 | a0001c0002t0003g0303a0001c0002t0003g0311a0001c0002t0003g0341 | 3 | NA18988.hp2 NA18999.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.721-1524C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019779 | ||||||
| chr21:43019831
|
T | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(285): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.721-1472T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019831 | ||||||
| chr21:43019914
|
C | T | 228 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(225): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.721-1389C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43019914 | ||||||
| chr21:43019925
|
A | AT | 6 | a0001c0002t0003g0311a0001c0002t0003g0330a0001c0002t0003g0337others(3): Show | 6 | HG02080.hp1 HG02148.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1353dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | |||||
| chr21:43019925
|
AT | A | 38 | a0001c0001t0002g0221a0001c0001t0002g0232a0001c0001t0002g0234others(35): Show | 38 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.721-1353delT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | |||||
| chr21:43019925
|
ATT | A | 142 | a0001c0001t0001g0037a0001c0001t0001g0064a0001c0001t0001g0068others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.721-1354_721-1353d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | |||||
| chr21:43019925
|
ATTT | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(108): Show | 112 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.721-1355_721-1353d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | |||||
| chr21:43019925
|
ATTTT | A | 6 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0145others(3): Show | 6 | HG00280.hp1 HG01074.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-1356_721-1353d others(6): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr21 | 43019925 | |||||
| chr21:43020309
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.721-994C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020309 | ||||||
| chr21:43020332
|
G | A | 1 | a0001c0001t0008g0277 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.721-971G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020332 | ||||||
| chr21:43020373
|
A | T | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-930A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020373 | ||||||
| chr21:43020416
|
C | T | 60 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0004g0019others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.721-887C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020416 | ||||||
| chr21:43020532
|
G | A | 1 | a0001c0002t0003g0344 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.721-771G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020532 | ||||||
| chr21:43020655
|
C | G | 6 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-648C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020655 | ||||||
| chr21:43020905
|
A | G | 1 | a0001c0002t0003g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.721-398A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020905 | ||||||
| chr21:43020929
|
G | A | 1 | a0001c0001t0002g0171 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.721-374G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020929 | ||||||
| chr21:43020989
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.721-314G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43020989 | ||||||
| chr21:43021081
|
C | T | 1 | a0001c0001t0006g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.721-222C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43021081 | ||||||
| chr21:43021143
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.721-160G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43021143 | ||||||
| chr21:43021182
|
G | A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-121G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 7/10 | chr21 | 43021182 | ||||||
| chr21:43021549
|
A | G | 3 | a0001c0001t0002g0215a0001c0001t0002g0218a0001c0001t0047g0216 | 3 | HG02559.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.849+118A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021549 | ||||||
| chr21:43021625
|
C | T | 2 | a0001c0001t0010g0033a0001c0001t0010g0034 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.849+194C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021625 | ||||||
| chr21:43021647
|
T | A | 1 | a0001c0001t0026g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.849+216T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021647 | ||||||
| chr21:43021795
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.849+364G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021795 | ||||||
| chr21:43021858
|
A | C | 289 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.849+427A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021858 | ||||||
| chr21:43021871
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0153 | 2 | NA18956.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.849+440T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43021871 | ||||||
| chr21:43022086
|
C | G | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.849+655C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022086 | ||||||
| chr21:43022204
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.849+773C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022204 | ||||||
| chr21:43022229
|
G | A | 2 | a0001c0001t0004g0046a0001c0001t0008g0277 | 2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.849+798G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022229 | ||||||
| chr21:43022278
|
G | A | 75 | a0001c0001t0001g0200a0001c0001t0002g0014a0001c0001t0002g0171others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.849+847G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022278 | ||||||
| chr21:43022281
|
C | T | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.849+850C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022281 | ||||||
| chr21:43022515
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.849+1084G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022515 | ||||||
| chr21:43022776
|
G | A | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1345G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022776 | ||||||
| chr21:43022792
|
A | G | 1 | a0001c0001t0008g0271 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.849+1361A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022792 | ||||||
| chr21:43022799
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.849+1368T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022799 | ||||||
| chr21:43022999
|
A | T | 2 | a0001c0001t0023g0052a0001c0001t0023g0115 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.849+1568A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43022999 | ||||||
| chr21:43023046
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.849+1615G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023046 | ||||||
| chr21:43023048
|
G | A | 22 | a0001c0001t0008g0268a0001c0001t0008g0269a0001c0001t0008g0271others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.849+1617G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023048 | ||||||
| chr21:43023079
|
C | T | 2 | a0001c0001t0004g0021a0001c0001t0004g0043 | 2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.849+1648C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023079 | ||||||
| chr21:43023084
|
C | A | 1 | a0001c0002t0003g0353 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.849+1653C>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023084 | ||||||
| chr21:43023383
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.850-1488C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023383 | ||||||
| chr21:43023541
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.850-1330G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023541 | ||||||
| chr21:43023629
|
A | AT | 197 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(194): Show | 198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.850-1230dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr21 | 43023629 | |||||
| chr21:43023641
|
T | A | 1 | a0001c0002t0003g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.850-1230T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023641 | ||||||
| chr21:43023684
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.850-1187G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023684 | ||||||
| chr21:43023700
|
C | T | 55 | a0001c0001t0001g0027a0001c0001t0004g0019a0001c0001t0004g0020others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.850-1171C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023700 | ||||||
| chr21:43023761
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.850-1110T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023761 | ||||||
| chr21:43023771
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.850-1100T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023771 | ||||||
| chr21:43023916
|
A | AT | 12 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0002g0250others(9): Show | 12 | HG00423.hp1 HG02040.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-940dupT | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr21 | 43023916 | |||||
| chr21:43023954
|
G | A | 1 | a0001c0001t0008g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.850-917G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43023954 | ||||||
| chr21:43024062
|
G | A | 3 | a0001c0001t0002g0215a0001c0001t0002g0218a0001c0001t0047g0216 | 3 | HG02559.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.850-809G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024062 | ||||||
| chr21:43024068
|
A | G | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.850-803A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024068 | ||||||
| chr21:43024169
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(116): Show | 120 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.850-702C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024169 | ||||||
| chr21:43024261
|
T | C | 6 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-610T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024261 | ||||||
| chr21:43024421
|
G | A | 1 | a0001c0002t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.850-450G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024421 | ||||||
| chr21:43024456
|
C | T | 7 | a0001c0001t0011g0262a0001c0001t0011g0263a0001c0001t0011g0264others(4): Show | 7 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-415C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024456 | ||||||
| chr21:43024571
|
C | T | 1 | a0001c0001t0007g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850-300C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024571 | ||||||
| chr21:43024623
|
C | T | 1 | a0001c0001t0005g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.850-248C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024623 | ||||||
| chr21:43024665
|
G | A | 290 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.850-206G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024665 | ||||||
| chr21:43024666
|
C | T | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.850-205C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024666 | ||||||
| chr21:43024667
|
A | G | 290 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(287): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.850-204A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 8/10 | chr21 | 43024667 | ||||||
| chr21:43025039
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.926+92T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025039 | ||||||
| chr21:43025049
|
C | G | 3 | a0001c0001t0027g0155a0001c0001t0027g0170a0001c0001t0043g0175 | 3 | HG02809.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.926+102C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025049 | ||||||
| chr21:43025075
|
C | T | 56 | a0001c0001t0001g0027a0001c0001t0004g0019a0001c0001t0004g0020others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.926+128C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025075 | ||||||
| chr21:43025182
|
C | T | 138 | a0001c0001t0001g0027a0001c0001t0002g0014a0001c0001t0002g0171others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.926+235C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025182 | ||||||
| chr21:43025410
|
G | T | 2 | a0001c0001t0031g0119a0001c0001t0042g0120 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.926+463G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025410 | ||||||
| chr21:43025452
|
G | A | 1 | a0001c0001t0008g0274 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.926+505G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025452 | ||||||
| chr21:43025454
|
G | A | 7 | a0001c0002t0009g0297a0001c0002t0009g0306a0001c0002t0009g0307others(4): Show | 7 | HG00639.hp1 HG00738.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+507G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025454 | ||||||
| chr21:43025523
|
C | T | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.926+576C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025523 | ||||||
| chr21:43025677
|
A | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.926+730A>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025677 | ||||||
| chr21:43025855
|
G | A | 1 | a0001c0001t0010g0032 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.926+908G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025855 | ||||||
| chr21:43025920
|
G | T | 58 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.926+973G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43025920 | ||||||
| chr21:43026231
|
C | T | 1 | a0001c0002t0003g0309 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.926+1284C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026231 | ||||||
| chr21:43026345
|
T | A | 59 | a0001c0001t0001g0027a0001c0001t0004g0019a0001c0001t0004g0020others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.926+1398T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026345 | ||||||
| chr21:43026485
|
G | A | 4 | a0001c0001t0027g0155a0001c0001t0027g0170a0001c0002t0028g0288others(1): Show | 4 | HG02809.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+1538G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026485 | ||||||
| chr21:43026490
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.926+1543G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026490 | ||||||
| chr21:43026711
|
C | T | 1 | a0001c0002t0003g0314 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.926+1764C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026711 | ||||||
| chr21:43026818
|
C | T | 64 | a0001c0001t0001g0027a0001c0001t0004g0019a0001c0001t0004g0020others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.926+1871C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026818 | ||||||
| chr21:43026847
|
GC | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(198): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.927-1854delC | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026847 | ||||||
| chr21:43026906
|
A | G | 1 | a0001c0001t0002g0196 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.927-1796A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026906 | ||||||
| chr21:43026971
|
A | G | 1 | a0001c0001t0020g0154 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.927-1731A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43026971 | ||||||
| chr21:43027101
|
C | T | 56 | a0001c0001t0001g0027a0001c0001t0004g0019a0001c0001t0004g0020others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.927-1601C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027101 | ||||||
| chr21:43027132
|
A | C | 1 | a0001c0001t0006g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.927-1570A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027132 | ||||||
| chr21:43027133
|
G | C | 57 | a0001c0001t0001g0027a0001c0001t0004g0019a0001c0001t0004g0020others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.927-1569G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027133 | ||||||
| chr21:43027149
|
T | C | 1 | a0001c0001t0019g0286 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.927-1553T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027149 | ||||||
| chr21:43027237
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(236): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.927-1465A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027237 | ||||||
| chr21:43027289
|
C | T | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-1413C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027289 | ||||||
| chr21:43027302
|
G | A | 56 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.927-1400G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027302 | ||||||
| chr21:43027678
|
C | G | 56 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.927-1024C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027678 | ||||||
| chr21:43027746
|
C | CCT | 56 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.927-956_927-955ins others(2): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027746 | ||||||
| chr21:43027746
|
C | T | 1 | a0001c0001t0014g0109 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.927-956C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027746 | ||||||
| chr21:43027768
|
G | T | 56 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.927-934G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027768 | ||||||
| chr21:43027829
|
T | A | 1 | a0001c0001t0013g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.927-873T>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027829 | ||||||
| chr21:43027840
|
C | T | 4 | a0001c0002t0012g0292a0001c0002t0012g0356a0001c0002t0012g0357others(1): Show | 4 | HG02965.hp1 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.927-862C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027840 | ||||||
| chr21:43027910
|
C | T | 1 | a0001c0001t0043g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.927-792C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43027910 | ||||||
| chr21:43028035
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0090a0001c0001t0001g0137others(2): Show | 5 | HG00673.hp1 HG01934.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-667C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028035 | ||||||
| chr21:43028217
|
T | C | 3 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0032g0291 | 3 | HG03654.hp1 NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.927-485T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028217 | ||||||
| chr21:43028274
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(111): Show | 115 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.927-428C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028274 | ||||||
| chr21:43028298
|
G | A | 1 | a0001c0001t0007g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.927-404G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028298 | ||||||
| chr21:43028449
|
C | CA | 240 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(237): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.927-242dupA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 43028449 | |||||
| chr21:43028449
|
CA | C | 55 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.927-242delA | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr21 | 43028449 | |||||
| chr21:43028470
|
C | T | 3 | a0001c0001t0022g0022a0001c0001t0022g0051a0001c0001t0035g0050 | 3 | HG03453.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.927-232C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028470 | ||||||
| chr21:43028524
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.927-178C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028524 | ||||||
| chr21:43028608
|
C | T | 75 | a0001c0001t0002g0014a0001c0001t0002g0171a0001c0001t0002g0187others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.927-94C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028608 | ||||||
| chr21:43028619
|
G | A | 2 | a0001c0001t0020g0154a0001c0001t0020g0165 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.927-83G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028619 | ||||||
| chr21:43028653
|
G | C | 74 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.927-49G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028653 | ||||||
| chr21:43028662
|
G | A | 2 | a0001c0001t0010g0033a0001c0001t0010g0034 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.927-40G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028662 | ||||||
| chr21:43028665
|
G | A | 74 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.927-37G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 9/10 | chr21 | 43028665 | ||||||
| chr21:43028918
|
G | T | 1 | a0001c0001t0011g0265 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1099+44G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43028918 | ||||||
| chr21:43028967
|
A | AG | 3 | a0001c0001t0001g0056a0001c0001t0001g0065a0001c0001t0001g0067 | 3 | NA18970.hp1 NA18971.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1099+95dupG | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43028967 | |||||
| chr21:43028985
|
G | A | 284 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(281): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1099+111G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43028985 | ||||||
| chr21:43028990
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1099+116C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43028990 | ||||||
| chr21:43029098
|
A | G | 1 | a0001c0002t0003g0316 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1099+224A>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029098 | ||||||
| chr21:43029194
|
G | T | 2 | a0001c0001t0019g0287a0001c0001t0032g0291 | 2 | HG03654.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1099+320G>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029194 | ||||||
| chr21:43029231
|
C | T | 74 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0001g0200others(71): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1099+357C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029231 | ||||||
| chr21:43029279
|
G | A | 74 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0002g0189others(71): Show | 75 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1099+405G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029279 | ||||||
| chr21:43029311
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099+437C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029311 | ||||||
| chr21:43029312
|
G | A | 5 | a0001c0001t0008g0268a0001c0001t0019g0286a0001c0001t0019g0287others(2): Show | 5 | HG02109.hp1 HG03471.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+438G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029312 | ||||||
| chr21:43029424
|
G | GTTTTTTT | 33 | a0001c0001t0019g0287a0001c0001t0032g0291a0001c0002t0003g0301others(30): Show | 33 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1100-451_1100-445d others(9): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
G | GTTTTTTT others(1): Show |
25 | a0001c0001t0001g0023a0001c0001t0008g0269a0001c0001t0008g0271others(22): Show | 25 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1100-452_1100-445d others(10): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
G | GTTTTTTT others(4): Show |
1 | a0001c0002t0028g0289 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1100-455_1100-445d others(13): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0044g0290a0001c0002t0028g0288 | 2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1100-456_1100-445d others(14): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
G | GTTTTTTT others(8): Show |
3 | a0001c0002t0003g0314a0001c0002t0003g0317a0001c0002t0003g0344 | 3 | NA19080.hp1 NA19085.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1100-459_1100-445d others(17): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
G | GTTTTTTT others(9): Show |
3 | a0001c0002t0003g0313a0001c0002t0003g0324a0001c0002t0003g0347 | 3 | HG01081.hp2 HG02615.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1100-460_1100-445d others(18): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
G | GTTTTTTT others(10): Show |
5 | a0001c0002t0003g0298a0001c0002t0003g0309a0001c0002t0003g0316others(2): Show | 5 | HG01496.hp2 HG04204.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100-461_1100-445d others(19): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0017g0238 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1100-462_1100-445d others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
G | GTTTTTTT others(12): Show |
1 | a0001c0002t0052g0332 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1100-463_1100-445d others(21): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
GTT | G | 11 | a0001c0001t0001g0028a0001c0001t0001g0126a0001c0001t0001g0137others(8): Show | 11 | HG00438.hp2 HG02056.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1100-446_1100-445d others(4): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029424
|
GTTT | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1100-447_1100-445d others(5): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029424 | |||||
| chr21:43029433
|
T | G | 2 | a0001c0001t0002g0201a0001c0001t0002g0228 | 2 | HG01167.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1100-457T>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029433 | ||||||
| chr21:43029561
|
C | G | 56 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1100-329C>G | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029561 | ||||||
| chr21:43029580
|
T | C | 5 | a0001c0001t0019g0286a0001c0001t0019g0287a0001c0001t0025g0015others(2): Show | 5 | HG00639.hp2 HG00642.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100-310T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029580 | ||||||
| chr21:43029732
|
A | ACCCCGCC others(11): Show |
1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-158_1100-157i others(20): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029732 | ||||||
| chr21:43029732
|
A | AGAAACAG others(644): Show |
2 | a0001c0001t0019g0286a0001c0001t0032g0291 | 2 | NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1100-148_1100-147i others(653): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029732 | |||||
| chr21:43029732
|
A | AGAAACAG others(646): Show |
1 | a0001c0001t0019g0287 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1100-148_1100-147i others(655): Show |
PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr21 | 43029732 | |||||
| chr21:43029733
|
G | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-157G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029733 | ||||||
| chr21:43029734
|
A | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-156A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029734 | ||||||
| chr21:43029735
|
A | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-155A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029735 | ||||||
| chr21:43029736
|
A | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-154A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029736 | ||||||
| chr21:43029738
|
A | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-152A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029738 | ||||||
| chr21:43029741
|
T | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-149T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029741 | ||||||
| chr21:43029744
|
T | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-146T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029744 | ||||||
| chr21:43029745
|
T | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-145T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029745 | ||||||
| chr21:43029747
|
A | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-143A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029747 | ||||||
| chr21:43029748
|
A | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-142A>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029748 | ||||||
| chr21:43029749
|
T | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-141T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029749 | ||||||
| chr21:43029753
|
T | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-137T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029753 | ||||||
| chr21:43029754
|
G | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-136G>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029754 | ||||||
| chr21:43029755
|
T | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-135T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029755 | ||||||
| chr21:43029763
|
T | C | 1 | a0001c0002t0003g0329 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1100-127T>C | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029763 | ||||||
| chr21:43029806
|
C | T | 2 | a0001c0002t0028g0288a0001c0002t0028g0289 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1100-84C>T | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029806 | ||||||
| chr21:43029807
|
G | A | 56 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1100-83G>A | PKNOX1 | ENSG00000160199.15 | transcript | ENST00000291547.10 | protein_coding | 10/10 | chr21 | 43029807 |