| geneid | 1912 |
|---|---|
| ensemblid | ENSG00000134686.21 |
| hgncid | 3183 |
| symbol | PHC2 |
| name | polyhomeotic homolog 2 |
| refseq_nuc | NM_001385109.1 |
| refseq_prot | NP_001372038.1 |
| ensembl_nuc | ENST00000683057.1 |
| ensembl_prot | ENSP00000507877.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 33323626 |
| end | 33431095 |
| strand | - |
| ver | v1.2 |
| region | chr1:33323626-33431095 |
| region5000 | chr1:33318626-33436095 |
| regionname0 | PHC2_chr1_33323626_33431095 |
| regionname5000 | PHC2_chr1_33318626_33436095 |
| 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 | 859 | 272 | 57 | 40 | 139 | 6 | 28 | 109 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0002 | 0/0 | 859 | 60 | 1 | 9 | 32 | 5 | 13 | 25 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0003 | 0/0 | 859 | 31 | 18 | 4 | 7 | 0 | 2 | 6 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0004 | 0/0 | 859 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0005 | 0/0 | 859 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0006 | 0/0 | 859 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0007 | 0/0 | 859 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0008 | 0/0 | 859 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| 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 | 0/0 | 2580 | 104 | 40 | 6 | 42 | 2 | 14 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0002 | 1/1 | 2580 | 87 | 8 | 22 | 44 | 4 | 7 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0003 | 0/0 | 2580 | 67 | 0 | 8 | 53 | 0 | 6 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0004 | 0/0 | 2580 | 60 | 1 | 9 | 32 | 5 | 13 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0005 | 0/0 | 2580 | 31 | 18 | 4 | 7 | 0 | 2 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0006 | 0/0 | 2580 | 9 | 8 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0007 | 0/0 | 2580 | 3 | 0 | 1 | 0 | 1 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0008 | 0/0 | 2580 | 2 | 1 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0009 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0010 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0011 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0012 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0013 | 0/0 | 2580 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0014 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| c0015 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| 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 | 1/1 | 1414 | 89 | 8 | 23 | 43 | 5 | 8 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0002 | 0/0 | 1414 | 80 | 27 | 8 | 39 | 1 | 5 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0003 | 0/0 | 1414 | 67 | 2 | 8 | 50 | 0 | 7 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0004 | 0/0 | 1414 | 60 | 1 | 7 | 34 | 5 | 13 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0005 | 0/0 | 1414 | 32 | 10 | 7 | 5 | 1 | 9 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0006 | 0/0 | 1414 | 8 | 8 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0007 | 0/0 | 1414 | 3 | 3 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0008 | 0/0 | 1414 | 3 | 0 | 0 | 3 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0009 | 0/0 | 1418 | 3 | 3 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0010 | 0/0 | 1414 | 3 | 3 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0011 | 0/0 | 1414 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0012 | 0/0 | 1414 | 2 | 0 | 0 | 0 | 0 | 2 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0013 | 0/0 | 1414 | 2 | 0 | 2 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0014 | 0/0 | 1414 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0015 | 0/0 | 1414 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0016 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0017 | 0/0 | 1418 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0018 | 0/0 | 1414 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0019 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0020 | 0/0 | 1414 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0021 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0022 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0023 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0024 | 0/0 | 1414 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0025 | 0/0 | 1414 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0026 | 0/0 | 1414 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| t0027 | 0/0 | 1414 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| 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 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| 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 | 0/0 | 2580 | 104 | 40 | 6 | 42 | 2 | 14 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0002 | 1/1 | 2580 | 87 | 8 | 22 | 44 | 4 | 7 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0003 | 0/0 | 2580 | 67 | 0 | 8 | 53 | 0 | 6 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0006 | 0/0 | 2580 | 9 | 8 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0008 | 0/0 | 2580 | 2 | 1 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0011 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0013 | 0/0 | 2580 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0014 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0002c0004 | 0/0 | 2580 | 60 | 1 | 9 | 32 | 5 | 13 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0003c0005 | 0/0 | 2580 | 31 | 18 | 4 | 7 | 0 | 2 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0004c0007 | 0/0 | 2580 | 3 | 0 | 1 | 0 | 1 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0005c0015 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0006c0010 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0007c0012 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0008c0009 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 3993 | 48 | 11 | 1 | 32 | 1 | 3 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0005 | 0/0 | 3993 | 30 | 10 | 5 | 5 | 1 | 9 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0006 | 0/0 | 3993 | 3 | 3 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0007 | 0/0 | 3993 | 3 | 3 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0008 | 0/0 | 3993 | 3 | 0 | 0 | 3 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0009 | 0/0 | 3997 | 3 | 3 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0010 | 0/0 | 3993 | 3 | 3 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0011 | 0/0 | 3993 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0012 | 0/0 | 3993 | 2 | 0 | 0 | 0 | 0 | 2 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0014 | 0/0 | 3993 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0015 | 0/0 | 3993 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0017 | 0/0 | 3997 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0023 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0001t0027 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0002t0001 | 1/1 | 3993 | 84 | 8 | 22 | 41 | 4 | 7 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0002t0016 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0002t0021 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0002t0022 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0003t0001 | 0/0 | 3993 | 2 | 0 | 0 | 2 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0003t0003 | 0/0 | 3993 | 63 | 0 | 7 | 50 | 0 | 6 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0003t0005 | 0/0 | 3993 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0003t0019 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0006t0003 | 0/0 | 3993 | 3 | 2 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0006t0006 | 0/0 | 3993 | 5 | 5 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0006t0020 | 0/0 | 3993 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0008t0002 | 0/0 | 3993 | 2 | 1 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0011t0005 | 0/0 | 3993 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0013t0003 | 0/0 | 3993 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0001c0014t0001 | 0/0 | 3993 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0002c0004t0004 | 0/0 | 3993 | 58 | 1 | 7 | 32 | 5 | 13 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0002c0004t0013 | 0/0 | 3993 | 2 | 0 | 2 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0003c0005t0002 | 0/0 | 3993 | 28 | 15 | 4 | 7 | 0 | 2 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0003c0005t0024 | 0/0 | 3993 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0003c0005t0025 | 0/0 | 3993 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0003c0005t0026 | 0/0 | 3993 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0004c0007t0001 | 0/0 | 3993 | 2 | 0 | 0 | 0 | 1 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0004c0007t0018 | 0/0 | 3993 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0005c0015t0004 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0006c0010t0004 | 0/0 | 3993 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0007c0012t0002 | 0/0 | 3993 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| a0008c0009t0002 | 0/0 | 3993 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | copy fasta | chr1 | 33318626 | 33436095 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0009g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0009g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0010g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0010g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0012g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0014g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0015g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0015g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0017g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0023g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0001t0027g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0016g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0021g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0002t0022g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0003t0019g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0006t0020g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0008t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0008t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0011t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0013t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0001c0014t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0013g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0002c0004t0013g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0024g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0025g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0003c0005t0026g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0004c0007t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0004c0007t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0004c0007t0018g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0005c0015t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0006c0010t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0007c0012t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| a0008c0009t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0156 | EUR | GBR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0111 | EUR | GBR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00323 | hp1 | a0002 | c0004 | t0004 | g0025 | EUR | FIN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0146 | EUR | FIN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00408 | hp2 | a0001 | c0003 | t0003 | g0196 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00423 | hp1 | a0001 | c0003 | t0003 | g0236 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00423 | hp2 | a0003 | c0005 | t0002 | g0288 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00438 | hp2 | a0001 | c0003 | t0003 | g0193 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00558 | hp2 | a0002 | c0004 | t0004 | g0054 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00609 | hp1 | a0002 | c0004 | t0004 | g0032 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00621 | hp1 | a0001 | c0003 | t0003 | g0209 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00621 | hp2 | a0002 | c0004 | t0004 | g0059 | EAS | CHS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00639 | hp1 | a0003 | c0005 | t0002 | g0282 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00639 | hp2 | a0001 | c0008 | t0002 | g0349 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00642 | hp1 | a0003 | c0005 | t0002 | g0268 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0091 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00735 | hp1 | a0002 | c0004 | t0004 | g0045 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00738 | hp1 | a0001 | c0003 | t0003 | g0187 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0092 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01074 | hp1 | a0002 | c0004 | t0004 | g0263 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01081 | hp1 | a0004 | c0007 | t0018 | g0143 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01099 | hp2 | a0002 | c0004 | t0004 | g0060 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01106 | hp1 | a0002 | c0004 | t0004 | g0033 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01106 | hp2 | a0003 | c0005 | t0002 | g0292 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01109 | hp2 | a0001 | c0006 | t0003 | g0264 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01167 | hp1 | a0001 | c0003 | t0005 | g0237 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0191 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01175 | hp2 | a0002 | c0004 | t0004 | g0017 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0259 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01192 | hp2 | a0001 | c0003 | t0003 | g0186 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01243 | hp1 | a0008 | c0009 | t0002 | g0348 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01243 | hp2 | a0003 | c0005 | t0002 | g0350 | AMR | PUR | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01257 | hp2 | a0001 | c0003 | t0003 | g0008 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01258 | hp1 | a0001 | c0003 | t0003 | g0008 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01258 | hp2 | a0001 | c0014 | t0001 | g0127 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01346 | hp1 | a0001 | c0011 | t0005 | g0258 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0230 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01358 | hp1 | a0002 | c0004 | t0013 | g0012 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0255 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01433 | hp2 | a0002 | c0004 | t0004 | g0034 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01496 | hp1 | a0002 | c0004 | t0004 | g0019 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01515 | hp1 | a0002 | c0004 | t0004 | g0016 | EUR | IBS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01515 | hp2 | a0004 | c0007 | t0001 | g0144 | EUR | IBS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0129 | EUR | IBS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01516 | hp2 | a0002 | c0004 | t0004 | g0061 | EUR | IBS | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0357 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01884 | hp2 | a0001 | c0006 | t0003 | g0265 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01891 | hp2 | a0003 | c0005 | t0002 | g0286 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01934 | hp1 | a0007 | c0012 | t0002 | g0287 | AMR | PEL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PEL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01981 | hp2 | a0002 | c0004 | t0013 | g0013 | AMR | PEL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | PEL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PEL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02027 | hp2 | a0001 | c0003 | t0003 | g0240 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02055 | hp1 | a0003 | c0005 | t0025 | g0351 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0298 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02056 | hp2 | a0002 | c0004 | t0004 | g0003 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0205 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02074 | hp1 | a0002 | c0004 | t0004 | g0028 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02074 | hp2 | a0001 | c0003 | t0003 | g0241 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0201 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0198 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02132 | hp1 | a0001 | c0003 | t0003 | g0213 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02132 | hp2 | a0002 | c0004 | t0004 | g0040 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02155 | hp1 | a0001 | c0003 | t0003 | g0243 | EAS | CDX | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CDX | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | CDX | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02165 | hp2 | a0001 | c0003 | t0003 | g0218 | EAS | CDX | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02258 | hp1 | a0002 | c0004 | t0004 | g0052 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0082 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02523 | hp1 | a0001 | c0003 | t0003 | g0192 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | KHV | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0170 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02572 | hp2 | a0003 | c0005 | t0002 | g0269 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02622 | hp1 | a0003 | c0005 | t0024 | g0296 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02622 | hp2 | a0001 | c0006 | t0003 | g0266 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0291 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02630 | hp2 | a0003 | c0005 | t0002 | g0293 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0131 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02683 | hp2 | a0001 | c0003 | t0003 | g0227 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02698 | hp2 | a0002 | c0004 | t0004 | g0063 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0089 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02723 | hp2 | a0003 | c0005 | t0002 | g0276 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0076 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02735 | hp2 | a0002 | c0004 | t0004 | g0047 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0262 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02738 | hp2 | a0001 | c0003 | t0003 | g0189 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02809 | hp1 | a0001 | c0006 | t0006 | g0180 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02809 | hp2 | a0003 | c0005 | t0002 | g0289 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02886 | hp1 | a0003 | c0005 | t0002 | g0277 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0245 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02896 | hp1 | a0001 | c0008 | t0002 | g0347 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0344 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02922 | hp1 | a0001 | c0006 | t0020 | g0181 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02965 | hp2 | a0003 | c0005 | t0002 | g0295 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03017 | hp1 | a0002 | c0004 | t0004 | g0071 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03130 | hp1 | a0003 | c0005 | t0002 | g0290 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0342 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0307 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03239 | hp1 | a0001 | c0013 | t0003 | g0226 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03453 | hp1 | a0001 | c0001 | t0015 | g0270 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03486 | hp1 | a0003 | c0005 | t0002 | g0275 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03490 | hp2 | a0002 | c0004 | t0004 | g0066 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03516 | hp1 | a0003 | c0005 | t0002 | g0278 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03516 | hp2 | a0001 | c0006 | t0006 | g0184 | AFR | ESN | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0074 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03579 | hp1 | a0001 | c0006 | t0006 | g0185 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0248 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03654 | hp1 | a0001 | c0003 | t0003 | g0234 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0260 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03669 | hp1 | a0002 | c0004 | t0004 | g0064 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0085 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03688 | hp1 | a0003 | c0005 | t0002 | g0281 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03688 | hp2 | a0002 | c0004 | t0004 | g0048 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0088 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03704 | hp2 | a0001 | c0003 | t0003 | g0229 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0086 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03710 | hp2 | a0002 | c0004 | t0004 | g0067 | SAS | PJL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03831 | hp1 | a0002 | c0004 | t0004 | g0069 | SAS | BEB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03831 | hp2 | a0003 | c0005 | t0002 | g0271 | SAS | BEB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | BEB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | BEB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03927 | hp1 | a0002 | c0004 | t0004 | g0070 | SAS | BEB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0079 | SAS | BEB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | BEB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03942 | hp2 | a0002 | c0004 | t0004 | g0030 | SAS | BEB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0231 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0257 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG04199 | hp1 | a0001 | c0003 | t0003 | g0065 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG04199 | hp2 | a0004 | c0007 | t0001 | g0145 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0084 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG04204 | hp2 | a0002 | c0004 | t0004 | g0024 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG04228 | hp1 | a0001 | c0001 | t0012 | g0083 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG04228 | hp2 | a0002 | c0004 | t0004 | g0029 | SAS | STU | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | YRI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0171 | AFR | YRI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18612 | hp1 | a0001 | c0003 | t0003 | g0200 | EAS | CHB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18747 | hp1 | a0002 | c0004 | t0004 | g0037 | EAS | CHB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | YRI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18906 | hp2 | a0003 | c0005 | t0002 | g0273 | AFR | YRI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18939 | hp1 | a0002 | c0004 | t0004 | g0044 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0223 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18941 | hp1 | a0001 | c0003 | t0003 | g0235 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18942 | hp2 | a0002 | c0004 | t0004 | g0023 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18943 | hp2 | a0001 | c0003 | t0003 | g0222 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18944 | hp2 | a0002 | c0004 | t0004 | g0051 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18945 | hp2 | a0001 | c0002 | t0021 | g0138 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18946 | hp1 | a0002 | c0004 | t0004 | g0049 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18947 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0217 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18950 | hp1 | a0001 | c0003 | t0003 | g0220 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18950 | hp2 | a0002 | c0004 | t0004 | g0036 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18952 | hp1 | a0002 | c0004 | t0004 | g0038 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18953 | hp2 | a0001 | c0003 | t0003 | g0203 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18959 | hp1 | a0002 | c0004 | t0004 | g0056 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18959 | hp2 | a0003 | c0005 | t0002 | g0354 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18960 | hp1 | a0002 | c0004 | t0004 | g0062 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18963 | hp1 | a0001 | c0003 | t0003 | g0215 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18963 | hp2 | a0002 | c0004 | t0004 | g0031 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18965 | hp1 | a0001 | c0003 | t0003 | g0210 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18965 | hp2 | a0001 | c0001 | t0008 | g0177 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18967 | hp1 | a0001 | c0003 | t0003 | g0239 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18968 | hp1 | a0002 | c0004 | t0004 | g0042 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18969 | hp1 | a0002 | c0004 | t0004 | g0046 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18969 | hp2 | a0003 | c0005 | t0002 | g0356 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18971 | hp2 | a0003 | c0005 | t0002 | g0355 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18973 | hp1 | a0001 | c0002 | t0022 | g0103 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18973 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18975 | hp2 | a0001 | c0001 | t0008 | g0178 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18977 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18978 | hp1 | a0001 | c0001 | t0023 | g0343 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18979 | hp1 | a0001 | c0003 | t0003 | g0221 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18980 | hp1 | a0002 | c0004 | t0004 | g0058 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18983 | hp1 | a0002 | c0004 | t0004 | g0055 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18986 | hp2 | a0001 | c0003 | t0003 | g0211 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18988 | hp1 | a0001 | c0001 | t0027 | g0317 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18988 | hp2 | a0001 | c0003 | t0003 | g0233 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0219 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18991 | hp2 | a0001 | c0003 | t0003 | g0190 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18994 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18994 | hp2 | a0001 | c0002 | t0016 | g0097 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18995 | hp1 | a0002 | c0004 | t0004 | g0014 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18995 | hp2 | a0003 | c0005 | t0002 | g0283 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA18999 | hp2 | a0001 | c0003 | t0003 | g0199 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19001 | hp1 | a0003 | c0005 | t0002 | g0352 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19001 | hp2 | a0001 | c0003 | t0003 | g0197 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19003 | hp1 | a0001 | c0003 | t0003 | g0188 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19003 | hp2 | a0006 | c0010 | t0004 | g0022 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19004 | hp2 | a0002 | c0004 | t0004 | g0050 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19006 | hp1 | a0005 | c0015 | t0004 | g0026 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19006 | hp2 | a0001 | c0003 | t0003 | g0232 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0238 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19012 | hp2 | a0002 | c0004 | t0004 | g0021 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19030 | hp1 | a0001 | c0006 | t0006 | g0179 | AFR | LWK | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0249 | AFR | LWK | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19043 | hp1 | a0001 | c0006 | t0006 | g0182 | AFR | LWK | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | LWK | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19054 | hp1 | a0002 | c0004 | t0004 | g0043 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19056 | hp2 | a0002 | c0004 | t0004 | g0035 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19058 | hp1 | a0002 | c0004 | t0004 | g0039 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0176 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19060 | hp1 | a0002 | c0004 | t0004 | g0020 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19065 | hp1 | a0002 | c0004 | t0004 | g0003 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19066 | hp1 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19074 | hp2 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19078 | hp1 | a0002 | c0004 | t0004 | g0027 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19078 | hp2 | a0001 | c0003 | t0003 | g0242 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19079 | hp2 | a0001 | c0003 | t0003 | g0195 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19080 | hp2 | a0001 | c0003 | t0019 | g0224 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19081 | hp1 | a0003 | c0005 | t0002 | g0353 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19081 | hp2 | a0001 | c0003 | t0003 | g0225 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19083 | hp2 | a0001 | c0003 | t0003 | g0228 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19084 | hp2 | a0001 | c0003 | t0003 | g0206 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19085 | hp2 | a0002 | c0004 | t0004 | g0053 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19088 | hp2 | a0001 | c0003 | t0003 | g0207 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19089 | hp1 | a0001 | c0003 | t0003 | g0204 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19089 | hp2 | a0002 | c0004 | t0004 | g0041 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19090 | hp1 | a0002 | c0004 | t0004 | g0057 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | YRI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | YRI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | ASW | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | ASW | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20752 | hp1 | a0002 | c0004 | t0004 | g0015 | EUR | TSI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0306 | EUR | TSI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0261 | EUR | TSI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20805 | hp2 | a0002 | c0004 | t0004 | g0018 | EUR | TSI | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0093 | SAS | GIH | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20905 | hp2 | a0002 | c0004 | t0004 | g0068 | SAS | GIH | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01123 | hp1 | a0001 | c0003 | t0003 | g0212 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0256 | AMR | CLM | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02109 | hp2 | a0003 | c0005 | t0002 | g0280 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02486 | hp1 | a0003 | c0005 | t0002 | g0284 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0172 | AFR | ACB | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0078 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0173 | AFR | MSL | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | USA | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| HG06807 | hp2 | a0003 | c0005 | t0002 | g0294 | AFR | USA | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20300 | hp1 | a0003 | c0005 | t0002 | g0279 | AFR | USA | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| NA20300 | hp2 | a0003 | c0005 | t0026 | g0274 | AFR | USA | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0141 | REF | REF | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0135 | REF | REF | PHC2_chr1_33318626_33436095 | PHC2 | chr1 | 33318626 | 33436095 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:33330126
|
C | T | 1 | a0007 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.2093G>A | p.Arg698His | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/15 | 2267/3993 | 2093/2580 | 698/859 | chr1 | 33330126 | ||
| chr1:33330187
|
C | A | 1 | a0006 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.2032G>T | p.Val678Leu | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/15 | 2206/3993 | 2032/2580 | 678/859 | chr1 | 33330187 | ||
| chr1:33334206
|
C | T | 1 | a0007 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1645G>A | p.Ala549Thr | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/15 | 1819/3993 | 1645/2580 | 549/859 | chr1 | 33334206 | ||
| chr1:33354533
|
C | T | 3 | a0002a0005a0006 | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
missense_variant | MODERATE | c.1426G>A | p.Val476Met | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/15 | 1600/3993 | 1426/2580 | 476/859 | chr1 | 33354533 | ||
| chr1:33367332
|
G | A | 1 | a0003 | 31 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(28): Show |
missense_variant | MODERATE | c.760C>T | p.Pro254Ser | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/15 | 934/3993 | 760/2580 | 254/859 | chr1 | 33367332 | ||
| chr1:33368547
|
T | G | 1 | a0005 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.652A>C | p.Thr218Pro | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/15 | 826/3993 | 652/2580 | 218/859 | chr1 | 33368547 | ||
| chr1:33370563
|
G | A | 1 | a0004 | 3 | HG01081.hp1 HG01515.hp2 HG04199.hp2 |
missense_variant | MODERATE | c.434C>T | p.Ala145Val | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/15 | 608/3993 | 434/2580 | 145/859 | chr1 | 33370563 | ||
| chr1:33372381
|
C | T | 1 | a0008 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.241G>A | p.Ala81Thr | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/15 | 415/3993 | 241/2580 | 81/859 | chr1 | 33372381 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:33324895
|
G | A | 4 | a0001c0011a0002c0004a0005c0015others(1): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
synonymous_variant | LOW | c.2550C>T | p.Tyr850Tyr | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 2724/3993 | 2550/2580 | 850/859 | chr1 | 33324895 | ||
| chr1:33354432
|
C | T | 2 | a0001c0003a0001c0013 | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
synonymous_variant | LOW | c.1527G>A | p.Thr509Thr | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/15 | 1701/3993 | 1527/2580 | 509/859 | chr1 | 33354432 | ||
| chr1:33354483
|
T | C | 2 | a0001c0008a0008c0009 | 3 | HG00639.hp2 HG01243.hp1 HG02896.hp1 |
synonymous_variant | LOW | c.1476A>G | p.Pro492Pro | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/15 | 1650/3993 | 1476/2580 | 492/859 | chr1 | 33354483 | ||
| chr1:33354913
|
G | A | 1 | a0007c0012 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.1317C>T | p.Gly439Gly | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 8/15 | 1491/3993 | 1317/2580 | 439/859 | chr1 | 33354913 | ||
| chr1:33354919
|
G | A | 1 | a0001c0006 | 9 | HG01109.hp2 HG01884.hp2 HG02622.hp2 others(6): Show |
synonymous_variant | LOW | c.1311C>T | p.Pro437Pro | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 8/15 | 1485/3993 | 1311/2580 | 437/859 | chr1 | 33354919 | ||
| chr1:33355030
|
C | T | 1 | a0001c0014 | 1 | HG01258.hp2 | synonymous_variant | LOW | c.1200G>A | p.Pro400Pro | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 8/15 | 1374/3993 | 1200/2580 | 400/859 | chr1 | 33355030 | ||
| chr1:33367129
|
G | C | 1 | a0001c0013 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.963C>G | p.Pro321Pro | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/15 | 1137/3993 | 963/2580 | 321/859 | chr1 | 33367129 | ||
| chr1:33367264
|
A | G | 12 | a0001c0001a0001c0003a0001c0006others(9): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
synonymous_variant | LOW | c.828T>C | p.Pro276Pro | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/15 | 1002/3993 | 828/2580 | 276/859 | chr1 | 33367264 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:33323759
|
C | T | 1 | a0001c0003t0019 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1106G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 1106 | chr1 | 33323759 | |||||
| chr1:33323781
|
C | T | 18 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(15): Show | 128 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1084G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 1084 | chr1 | 33323781 | |||||
| chr1:33323782
|
G | A | 1 | a0001c0006t0020 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1083C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 1083 | chr1 | 33323782 | |||||
| chr1:33323790
|
T | C | 1 | a0004c0007t0018 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1075A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 1075 | chr1 | 33323790 | |||||
| chr1:33323811
|
A | C | 1 | a0003c0005t0025 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1054T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 1054 | chr1 | 33323811 | |||||
| chr1:33323901
|
G | C | 3 | a0001c0001t0006a0001c0006t0006a0001c0006t0020 | 9 | HG02257.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*964C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 964 | chr1 | 33323901 | |||||
| chr1:33323909
|
T | C | 1 | a0001c0001t0014 | 2 | HG02886.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*956A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 956 | chr1 | 33323909 | |||||
| chr1:33323918
|
G | A | 1 | a0003c0005t0026 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*947C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 947 | chr1 | 33323918 | |||||
| chr1:33323919
|
C | A | 33 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(30): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*946G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 946 | chr1 | 33323919 | |||||
| chr1:33323987
|
T | C | 33 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(30): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*878A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 878 | chr1 | 33323987 | |||||
| chr1:33323995
|
T | C | 1 | a0001c0002t0021 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 870 | chr1 | 33323995 | |||||
| chr1:33324037
|
C | T | 1 | a0001c0001t0007 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*828G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 828 | chr1 | 33324037 | |||||
| chr1:33324047
|
G | A | 1 | a0001c0001t0012 | 2 | HG02735.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*818C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 818 | chr1 | 33324047 | |||||
| chr1:33324069
|
G | A | 5 | a0001c0001t0008a0002c0004t0004a0002c0004t0013others(2): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*796C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 796 | chr1 | 33324069 | |||||
| chr1:33324086
|
A | T | 1 | a0003c0005t0024 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*779T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 779 | chr1 | 33324086 | |||||
| chr1:33324199
|
C | CTGTT | 2 | a0001c0001t0009a0001c0001t0017 | 4 | HG02055.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*665dupAACA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 665 | chr1 | 33324199 | |||||
| chr1:33324319
|
C | T | 1 | a0001c0001t0007 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 546 | chr1 | 33324319 | |||||
| chr1:33324363
|
G | A | 1 | a0001c0001t0010 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*502C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 502 | chr1 | 33324363 | |||||
| chr1:33324367
|
G | C | 1 | a0001c0002t0022 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 498 | chr1 | 33324367 | |||||
| chr1:33324367
|
G | T | 3 | a0002c0004t0004a0005c0015t0004a0006c0010t0004 | 60 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*498C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 498 | chr1 | 33324367 | |||||
| chr1:33324456
|
G | A | 1 | a0001c0001t0014 | 2 | HG02886.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 409 | chr1 | 33324456 | |||||
| chr1:33324580
|
A | C | 1 | a0001c0002t0016 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*285T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 285 | chr1 | 33324580 | |||||
| chr1:33324749
|
T | C | 1 | a0001c0001t0027 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 116 | chr1 | 33324749 | |||||
| chr1:33324835
|
C | T | 1 | a0001c0001t0011 | 2 | HG02486.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*30G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 30 | chr1 | 33324835 | |||||
| chr1:33324848
|
C | T | 1 | a0001c0001t0015 | 2 | HG02630.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 15/15 | 17 | chr1 | 33324848 | |||||
| chr1:33375563
|
G | T | 1 | a0001c0001t0023 | 1 | NA18978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-24C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/15 | 24 | chr1 | 33375563 | |||||
| chr1:33375570
|
G | A | 1 | a0001c0001t0008 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-31C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/15 | chr1 | 33375570 | ||||||
| chr1:33431053
|
G | A | 13 | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(10): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/15 | chr1 | 33431053 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:33325051
|
C | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2426-32G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325051 | ||||||
| chr1:33325149
|
T | G | 4 | a0001c0006t0006g0179a0001c0006t0006g0180a0001c0006t0006g0182others(1): Show | 4 | HG02809.hp1 HG02922.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2426-130A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325149 | ||||||
| chr1:33325172
|
T | C | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2426-153A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325172 | ||||||
| chr1:33325234
|
A | G | 1 | a0002c0004t0004g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2426-215T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325234 | ||||||
| chr1:33325272
|
G | A | 1 | a0001c0002t0001g0147 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2426-253C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325272 | ||||||
| chr1:33325298
|
G | A | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2426-279C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325298 | ||||||
| chr1:33325474
|
C | T | 2 | a0001c0002t0001g0118a0001c0002t0001g0157 | 2 | HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2426-455G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325474 | ||||||
| chr1:33325475
|
G | A | 1 | a0001c0003t0003g0230 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2426-456C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325475 | ||||||
| chr1:33325476
|
T | G | 1 | a0001c0001t0002g0301 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2426-457A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325476 | ||||||
| chr1:33325583
|
G | C | 1 | a0001c0002t0001g0130 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2426-564C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325583 | ||||||
| chr1:33325608
|
T | G | 2 | a0001c0003t0003g0203a0001c0003t0003g0207 | 2 | NA18953.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2426-589A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325608 | ||||||
| chr1:33325648
|
A | G | 1 | a0003c0005t0002g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2426-629T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33325648 | ||||||
| chr1:33326055
|
G | T | 1 | a0002c0004t0004g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2426-1036C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326055 | ||||||
| chr1:33326081
|
A | C | 2 | a0001c0001t0014g0245a0001c0001t0014g0249 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2426-1062T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326081 | ||||||
| chr1:33326129
|
G | A | 2 | a0002c0004t0004g0060a0002c0004t0004g0061 | 2 | HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2426-1110C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326129 | ||||||
| chr1:33326165
|
T | C | 1 | a0007c0012t0002g0287 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2426-1146A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326165 | ||||||
| chr1:33326317
|
G | C | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2426-1298C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326317 | ||||||
| chr1:33326364
|
C | T | 1 | a0006c0010t0004g0022 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2426-1345G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326364 | ||||||
| chr1:33326368
|
T | C | 1 | a0001c0002t0022g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2426-1349A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326368 | ||||||
| chr1:33326444
|
G | C | 1 | a0001c0001t0005g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2426-1425C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326444 | ||||||
| chr1:33326756
|
C | G | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2426-1737G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326756 | ||||||
| chr1:33326846
|
A | G | 4 | a0001c0006t0006g0179a0001c0006t0006g0180a0001c0006t0006g0182others(1): Show | 4 | HG02809.hp1 HG02922.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2426-1827T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326846 | ||||||
| chr1:33326916
|
A | G | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2426-1897T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326916 | ||||||
| chr1:33326930
|
T | C | 2 | a0001c0001t0014g0245a0001c0001t0014g0249 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2426-1911A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326930 | ||||||
| chr1:33326955
|
A | C | 1 | a0006c0010t0004g0022 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2425+1915T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33326955 | ||||||
| chr1:33327097
|
G | C | 60 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(57): Show | 61 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2425+1773C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327097 | ||||||
| chr1:33327176
|
G | A | 1 | a0001c0001t0015g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2425+1694C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327176 | ||||||
| chr1:33327191
|
C | T | 1 | a0006c0010t0004g0022 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2425+1679G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327191 | ||||||
| chr1:33327242
|
C | T | 4 | a0001c0001t0005g0183a0001c0008t0002g0347a0001c0008t0002g0349others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2425+1628G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327242 | ||||||
| chr1:33327244
|
T | C | 2 | a0001c0006t0006g0184a0001c0006t0006g0185 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2425+1626A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327244 | ||||||
| chr1:33327403
|
G | A | 1 | a0001c0001t0005g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2425+1467C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327403 | ||||||
| chr1:33327415
|
C | T | 3 | a0001c0002t0001g0161a0001c0002t0001g0162a0001c0002t0001g0168 | 3 | HG00408.hp1 HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2425+1455G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327415 | ||||||
| chr1:33327567
|
T | C | 1 | a0003c0005t0026g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2425+1303A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327567 | ||||||
| chr1:33327610
|
G | A | 1 | a0001c0001t0002g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2425+1260C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327610 | ||||||
| chr1:33327656
|
C | G | 1 | a0002c0004t0004g0045 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2425+1214G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327656 | ||||||
| chr1:33327715
|
C | T | 4 | a0001c0001t0005g0183a0001c0008t0002g0347a0001c0008t0002g0349others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2425+1155G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327715 | ||||||
| chr1:33327774
|
G | T | 1 | a0002c0004t0004g0045 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2425+1096C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327774 | ||||||
| chr1:33327841
|
G | A | 1 | a0001c0003t0003g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2425+1029C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327841 | ||||||
| chr1:33327842
|
T | G | 1 | a0002c0004t0004g0045 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2425+1028A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33327842 | ||||||
| chr1:33328081
|
A | G | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.2425+789T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328081 | ||||||
| chr1:33328103
|
G | A | 1 | a0003c0005t0002g0289 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2425+767C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328103 | ||||||
| chr1:33328207
|
C | T | 7 | a0002c0004t0004g0020a0002c0004t0004g0021a0002c0004t0004g0023others(4): Show | 7 | HG00609.hp1 NA18942.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.2425+663G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328207 | ||||||
| chr1:33328329
|
A | C | 1 | a0006c0010t0004g0022 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2425+541T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328329 | ||||||
| chr1:33328378
|
A | AT | 148 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(145): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.2425+491dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328378 | ||||||
| chr1:33328378
|
A | ATT | 73 | a0001c0001t0002g0314a0001c0001t0002g0330a0001c0001t0002g0337others(70): Show | 74 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.2425+490_2425+491d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328378 | ||||||
| chr1:33328378
|
A | ATTT | 120 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(117): Show | 121 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.2425+489_2425+491d others(5): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328378 | ||||||
| chr1:33328378
|
A | ATTTT | 7 | a0001c0001t0002g0303a0001c0001t0002g0309a0001c0001t0002g0316others(4): Show | 7 | HG03486.hp2 HG03669.hp2 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.2425+488_2425+491d others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328378 | ||||||
| chr1:33328467
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2425+403G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328467 | ||||||
| chr1:33328555
|
TCTAC | T | 87 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(84): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2425+311_2425+314d others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328555 | ||||||
| chr1:33328773
|
A | C | 1 | a0006c0010t0004g0022 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2425+97T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328773 | ||||||
| chr1:33328815
|
T | C | 59 | a0001c0003t0003g0001a0001c0003t0003g0002a0001c0003t0003g0008others(56): Show | 65 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2425+55A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 14/14 | chr1 | 33328815 | ||||||
| chr1:33329251
|
C | T | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2149-105G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329251 | ||||||
| chr1:33329252
|
A | G | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.2149-106T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329252 | ||||||
| chr1:33329452
|
C | T | 59 | a0001c0003t0003g0001a0001c0003t0003g0002a0001c0003t0003g0008others(56): Show | 65 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2149-306G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329452 | ||||||
| chr1:33329473
|
C | A | 1 | a0006c0010t0004g0022 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2149-327G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329473 | ||||||
| chr1:33329490
|
CA | C | 130 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(127): Show | 131 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.2149-345delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329490 | ||||||
| chr1:33329610
|
A | G | 4 | a0001c0003t0003g0229a0001c0003t0003g0230a0001c0003t0003g0231others(1): Show | 4 | HG01346.hp2 HG03239.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.2148+461T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329610 | ||||||
| chr1:33329691
|
G | C | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2148+380C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329691 | ||||||
| chr1:33329930
|
G | C | 127 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(124): Show | 128 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.2148+141C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329930 | ||||||
| chr1:33329971
|
G | A | 69 | a0001c0002t0001g0006a0001c0002t0001g0009a0001c0002t0001g0011others(66): Show | 71 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.2148+100C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329971 | ||||||
| chr1:33329989
|
A | T | 87 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(84): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2148+82T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33329989 | ||||||
| chr1:33330061
|
C | T | 2 | a0001c0002t0001g0129a0001c0002t0001g0131 | 2 | HG01516.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2148+10G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 13/14 | chr1 | 33330061 | ||||||
| chr1:33330480
|
A | C | 173 | a0001c0001t0002g0272a0001c0001t0002g0285a0001c0001t0002g0297others(170): Show | 179 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.2007-268T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330480 | ||||||
| chr1:33330501
|
C | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2007-289G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330501 | ||||||
| chr1:33330548
|
G | A | 2 | a0001c0001t0010g0010a0001c0001t0010g0344 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2007-336C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330548 | ||||||
| chr1:33330581
|
G | A | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2007-369C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330581 | ||||||
| chr1:33330628
|
T | C | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.2007-416A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330628 | ||||||
| chr1:33330705
|
A | G | 2 | a0001c0001t0014g0245a0001c0001t0014g0249 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2007-493T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330705 | ||||||
| chr1:33330747
|
G | A | 1 | a0001c0002t0001g0142 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2007-535C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330747 | ||||||
| chr1:33330939
|
G | A | 12 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(9): Show | 12 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2006+409C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330939 | ||||||
| chr1:33330953
|
G | A | 200 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(197): Show | 207 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.2006+395C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33330953 | ||||||
| chr1:33331087
|
G | A | 1 | a0002c0004t0004g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2006+261C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33331087 | ||||||
| chr1:33331202
|
G | A | 2 | a0001c0001t0014g0245a0001c0001t0014g0249 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2006+146C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33331202 | ||||||
| chr1:33331206
|
T | C | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2006+142A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33331206 | ||||||
| chr1:33331233
|
GA | G | 87 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(84): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2006+114delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33331233 | ||||||
| chr1:33331290
|
C | A | 59 | a0001c0003t0003g0001a0001c0003t0003g0002a0001c0003t0003g0008others(56): Show | 65 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2006+58G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 12/14 | chr1 | 33331290 | ||||||
| chr1:33331820
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1892-358G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 11/14 | chr1 | 33331820 | ||||||
| chr1:33331967
|
G | A | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1891+308C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 11/14 | chr1 | 33331967 | ||||||
| chr1:33332198
|
C | G | 1 | a0001c0001t0002g0285 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1891+77G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 11/14 | chr1 | 33332198 | ||||||
| chr1:33332250
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1891+25C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 11/14 | chr1 | 33332250 | ||||||
| chr1:33332490
|
A | G | 2 | a0001c0001t0014g0245a0001c0001t0014g0249 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1762-86T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332490 | ||||||
| chr1:33332525
|
T | G | 3 | a0001c0003t0003g0008a0001c0003t0003g0186a0001c0003t0003g0187 | 4 | HG00738.hp1 HG01192.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-121A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332525 | ||||||
| chr1:33332603
|
G | T | 2 | a0001c0003t0003g0191a0001c0003t0003g0227 | 2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1762-199C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332603 | ||||||
| chr1:33332789
|
C | T | 1 | a0001c0003t0003g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1762-385G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332789 | ||||||
| chr1:33332796
|
G | C | 1 | a0001c0006t0020g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1762-392C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332796 | ||||||
| chr1:33332797
|
A | T | 1 | a0001c0006t0020g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1762-393T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332797 | ||||||
| chr1:33332832
|
C | G | 1 | a0001c0001t0011g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1762-428G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332832 | ||||||
| chr1:33332841
|
A | T | 1 | a0001c0002t0001g0142 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1762-437T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332841 | ||||||
| chr1:33332844
|
C | T | 1 | a0002c0004t0004g0059 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1762-440G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332844 | ||||||
| chr1:33332907
|
T | C | 1 | a0001c0001t0002g0309 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1762-503A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332907 | ||||||
| chr1:33332908
|
G | T | 1 | a0001c0001t0002g0309 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1762-504C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332908 | ||||||
| chr1:33332935
|
T | A | 14 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1762-531A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332935 | ||||||
| chr1:33332964
|
C | T | 1 | a0001c0001t0005g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1762-560G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33332964 | ||||||
| chr1:33333125
|
G | C | 141 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(138): Show | 142 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1762-721C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333125 | ||||||
| chr1:33333223
|
C | T | 69 | a0001c0001t0002g0285a0001c0001t0002g0322a0001c0001t0005g0072others(66): Show | 70 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1762-819G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333223 | ||||||
| chr1:33333252
|
A | T | 1 | a0001c0001t0002g0309 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1761+838T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333252 | ||||||
| chr1:33333327
|
G | A | 69 | a0001c0001t0002g0285a0001c0001t0002g0322a0001c0001t0005g0072others(66): Show | 70 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.1761+763C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333327 | ||||||
| chr1:33333356
|
G | C | 1 | a0001c0002t0001g0147 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1761+734C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333356 | ||||||
| chr1:33333419
|
TC | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1761+670delG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333419 | ||||||
| chr1:33333656
|
C | G | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1761+434G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333656 | ||||||
| chr1:33333663
|
G | T | 269 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(266): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1761+427C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333663 | ||||||
| chr1:33333947
|
C | T | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1761+143G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 10/14 | chr1 | 33333947 | ||||||
| chr1:33334299
|
G | A | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
splice_region_variant&intron_variant | LOW | c.1559-7C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33334299 | ||||||
| chr1:33334433
|
C | T | 4 | a0001c0001t0005g0183a0001c0008t0002g0347a0001c0008t0002g0349others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-141G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33334433 | ||||||
| chr1:33334585
|
G | A | 1 | a0001c0001t0002g0324 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1559-293C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33334585 | ||||||
| chr1:33334719
|
G | A | 2 | a0001c0001t0015g0270a0001c0001t0015g0291 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1559-427C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33334719 | ||||||
| chr1:33335028
|
T | A | 1 | a0001c0003t0003g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1559-736A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335028 | ||||||
| chr1:33335432
|
A | G | 1 | a0001c0003t0003g0214 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1559-1140T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335432 | ||||||
| chr1:33335537
|
C | T | 75 | a0001c0001t0002g0285a0001c0001t0002g0322a0001c0001t0005g0072others(72): Show | 76 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1559-1245G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335537 | ||||||
| chr1:33335640
|
A | G | 1 | a0001c0001t0002g0302 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1559-1348T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335640 | ||||||
| chr1:33335679
|
A | T | 6 | a0001c0002t0001g0101a0001c0002t0001g0107a0001c0002t0001g0108others(3): Show | 6 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1559-1387T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335679 | ||||||
| chr1:33335861
|
C | A | 1 | a0001c0006t0006g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1559-1569G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335861 | ||||||
| chr1:33335869
|
C | G | 2 | a0002c0004t0004g0063a0002c0004t0004g0067 | 2 | HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1559-1577G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335869 | ||||||
| chr1:33335878
|
C | T | 1 | a0001c0003t0003g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1559-1586G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335878 | ||||||
| chr1:33335902
|
G | C | 2 | a0001c0001t0002g0357a0001c0001t0005g0082 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1559-1610C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335902 | ||||||
| chr1:33335908
|
AG | A | 70 | a0001c0002t0001g0106a0001c0002t0001g0116a0001c0002t0001g0126others(67): Show | 76 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1559-1617delC | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335908 | ||||||
| chr1:33335910
|
G | A | 1 | a0003c0005t0002g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1559-1618C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335910 | ||||||
| chr1:33335996
|
G | GT | 60 | a0001c0002t0001g0120a0001c0003t0003g0001a0001c0003t0003g0002others(57): Show | 66 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1559-1705dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335996 | ||||||
| chr1:33335996
|
G | T | 11 | a0001c0002t0001g0009a0001c0002t0001g0132a0001c0002t0001g0133others(8): Show | 12 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1559-1704C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335996 | ||||||
| chr1:33335998
|
T | TGTTG | 4 | a0001c0006t0006g0184a0001c0006t0006g0185a0003c0005t0002g0273others(1): Show | 4 | HG02965.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559-1707_1559-170 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335998 | ||||||
| chr1:33335998
|
T | TGTTGTTG | 3 | a0001c0001t0005g0090a0001c0006t0006g0180a0003c0005t0002g0292 | 3 | HG01106.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1559-1707_1559-170 others(11): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335998 | ||||||
| chr1:33335998
|
T | TGTTGTTG others(3): Show |
62 | a0001c0001t0002g0285a0001c0001t0005g0072a0001c0001t0005g0073others(59): Show | 63 | HG00423.hp2 HG00639.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1559-1707_1559-170 others(14): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335998 | ||||||
| chr1:33335998
|
T | TGTTGTTG others(6): Show |
12 | a0001c0001t0002g0322a0001c0001t0005g0087a0001c0001t0005g0260others(9): Show | 12 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1559-1707_1559-170 others(17): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335998 | ||||||
| chr1:33335999
|
T | G | 16 | a0001c0001t0002g0297a0001c0001t0002g0301a0001c0001t0002g0314others(13): Show | 16 | HG00597.hp1 HG01109.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1559-1707A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33335999 | ||||||
| chr1:33336001
|
T | G | 80 | a0001c0001t0002g0285a0001c0001t0002g0322a0001c0001t0005g0072others(77): Show | 81 | HG00423.hp2 HG00639.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1559-1709A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336001 | ||||||
| chr1:33336002
|
T | G | 2 | a0001c0001t0008g0177a0001c0001t0008g0178 | 2 | NA18965.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1559-1710A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336002 | ||||||
| chr1:33336030
|
C | T | 1 | a0001c0003t0003g0212 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1559-1738G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336030 | ||||||
| chr1:33336051
|
C | T | 1 | a0001c0001t0015g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1559-1759G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336051 | ||||||
| chr1:33336105
|
T | C | 214 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(211): Show | 222 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.1559-1813A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336105 | ||||||
| chr1:33336106
|
G | A | 1 | a0001c0001t0005g0256 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1559-1814C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336106 | ||||||
| chr1:33336327
|
A | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1559-2035T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336327 | ||||||
| chr1:33336406
|
A | G | 6 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1559-2114T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336406 | ||||||
| chr1:33336458
|
G | GT | 347 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(344): Show | 360 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.1559-2167dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336458 | ||||||
| chr1:33336694
|
G | C | 37 | a0001c0001t0002g0297a0001c0001t0002g0301a0001c0001t0002g0302others(34): Show | 37 | HG00558.hp1 HG00597.hp1 HG02027.hp1 others(34): Show |
intron_variant | MODIFIER | c.1559-2402C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336694 | ||||||
| chr1:33336745
|
A | C | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1559-2453T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336745 | ||||||
| chr1:33336750
|
C | T | 127 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(124): Show | 128 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1559-2458G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336750 | ||||||
| chr1:33336787
|
G | A | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1559-2495C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336787 | ||||||
| chr1:33336853
|
G | A | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1559-2561C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336853 | ||||||
| chr1:33336878
|
T | C | 1 | a0001c0002t0001g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1559-2586A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33336878 | ||||||
| chr1:33337216
|
A | G | 74 | a0001c0002t0001g0006a0001c0002t0001g0009a0001c0002t0001g0011others(71): Show | 76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1559-2924T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337216 | ||||||
| chr1:33337334
|
C | T | 141 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(138): Show | 142 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1559-3042G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337334 | ||||||
| chr1:33337335
|
A | G | 200 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(197): Show | 207 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.1559-3043T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337335 | ||||||
| chr1:33337462
|
C | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1559-3170G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337462 | ||||||
| chr1:33337547
|
C | T | 200 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(197): Show | 207 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.1559-3255G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337547 | ||||||
| chr1:33337570
|
C | T | 127 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(124): Show | 128 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1559-3278G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337570 | ||||||
| chr1:33337719
|
T | G | 1 | a0001c0001t0015g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1559-3427A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337719 | ||||||
| chr1:33337852
|
A | G | 1 | a0001c0001t0005g0262 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1559-3560T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337852 | ||||||
| chr1:33337970
|
G | C | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1559-3678C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33337970 | ||||||
| chr1:33338366
|
T | C | 4 | a0001c0003t0005g0237a0003c0005t0002g0276a0003c0005t0002g0277others(1): Show | 4 | HG01167.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559-4074A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338366 | ||||||
| chr1:33338533
|
C | T | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1559-4241G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338533 | ||||||
| chr1:33338546
|
G | A | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1559-4254C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338546 | ||||||
| chr1:33338576
|
A | G | 1 | a0001c0003t0003g0225 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1559-4284T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338576 | ||||||
| chr1:33338612
|
C | T | 1 | a0001c0001t0014g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1559-4320G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338612 | ||||||
| chr1:33338759
|
G | A | 1 | a0001c0006t0006g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1559-4467C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338759 | ||||||
| chr1:33338786
|
G | A | 2 | a0002c0004t0013g0012a0002c0004t0013g0013 | 2 | HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1559-4494C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338786 | ||||||
| chr1:33338809
|
C | G | 1 | a0001c0003t0003g0198 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1559-4517G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338809 | ||||||
| chr1:33338836
|
T | C | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1559-4544A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338836 | ||||||
| chr1:33338913
|
C | T | 1 | a0001c0002t0001g0102 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1559-4621G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33338913 | ||||||
| chr1:33339158
|
G | A | 1 | a0001c0013t0003g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1559-4866C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33339158 | ||||||
| chr1:33339886
|
A | C | 2 | a0001c0006t0006g0184a0001c0006t0006g0185 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1559-5594T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33339886 | ||||||
| chr1:33339923
|
T | C | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1559-5631A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33339923 | ||||||
| chr1:33340194
|
A | C | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.1559-5902T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340194 | ||||||
| chr1:33340196
|
T | G | 2 | a0001c0001t0002g0333a0003c0005t0002g0280 | 2 | HG02109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1559-5904A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340196 | ||||||
| chr1:33340200
|
A | G | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.1559-5908T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340200 | ||||||
| chr1:33340337
|
C | T | 2 | a0001c0003t0003g0195a0001c0003t0003g0225 | 2 | NA19079.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1559-6045G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340337 | ||||||
| chr1:33340570
|
T | C | 3 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248 | 3 | HG02257.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1559-6278A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340570 | ||||||
| chr1:33340833
|
G | A | 14 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1559-6541C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340833 | ||||||
| chr1:33340862
|
C | T | 127 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(124): Show | 128 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1559-6570G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340862 | ||||||
| chr1:33340955
|
G | A | 269 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(266): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1559-6663C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340955 | ||||||
| chr1:33340986
|
A | G | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1559-6694T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33340986 | ||||||
| chr1:33341000
|
T | C | 2 | a0001c0006t0006g0184a0001c0006t0006g0185 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1559-6708A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341000 | ||||||
| chr1:33341045
|
A | G | 1 | a0003c0005t0002g0294 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1559-6753T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341045 | ||||||
| chr1:33341153
|
T | TG | 11 | a0001c0001t0002g0305a0001c0001t0002g0336a0001c0001t0005g0078others(8): Show | 11 | HG01496.hp1 HG02698.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1559-6862dupC | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341153 | ||||||
| chr1:33341178
|
A | G | 4 | a0001c0001t0005g0183a0001c0008t0002g0347a0001c0008t0002g0349others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-6886T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341178 | ||||||
| chr1:33341311
|
G | A | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1559-7019C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341311 | ||||||
| chr1:33341335
|
G | T | 1 | a0001c0001t0005g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1559-7043C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341335 | ||||||
| chr1:33341426
|
G | A | 1 | a0001c0003t0003g0216 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1559-7134C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341426 | ||||||
| chr1:33341437
|
T | C | 1 | a0001c0001t0007g0171 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1559-7145A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341437 | ||||||
| chr1:33341462
|
T | C | 1 | a0003c0005t0002g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1559-7170A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341462 | ||||||
| chr1:33341534
|
A | C | 1 | a0001c0001t0008g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1559-7242T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341534 | ||||||
| chr1:33341535
|
C | T | 1 | a0001c0001t0008g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1559-7243G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341535 | ||||||
| chr1:33341539
|
C | T | 1 | a0001c0001t0008g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1559-7247G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341539 | ||||||
| chr1:33341623
|
T | C | 1 | a0001c0002t0001g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1559-7331A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341623 | ||||||
| chr1:33341668
|
A | C | 1 | a0001c0002t0001g0174 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1559-7376T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341668 | ||||||
| chr1:33341919
|
G | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1559-7627C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33341919 | ||||||
| chr1:33342283
|
T | C | 1 | a0001c0002t0001g0155 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1559-7991A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33342283 | ||||||
| chr1:33342442
|
A | G | 2 | a0001c0001t0005g0259a0001c0011t0005g0258 | 2 | HG01192.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1559-8150T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33342442 | ||||||
| chr1:33342524
|
C | T | 2 | a0001c0003t0003g0188a0001c0003t0003g0216 | 2 | NA18974.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1559-8232G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33342524 | ||||||
| chr1:33342525
|
C | G | 1 | a0003c0005t0002g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1559-8233G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33342525 | ||||||
| chr1:33342525
|
C | T | 2 | a0001c0001t0010g0010a0001c0001t0010g0344 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1559-8233G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33342525 | ||||||
| chr1:33342733
|
A | G | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1559-8441T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33342733 | ||||||
| chr1:33343056
|
C | T | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0099others(3): Show | 8 | HG01891.hp1 HG02723.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1559-8764G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343056 | ||||||
| chr1:33343098
|
A | G | 1 | a0001c0002t0001g0121 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1559-8806T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343098 | ||||||
| chr1:33343126
|
C | T | 4 | a0002c0004t0004g0028a0002c0004t0004g0044a0002c0004t0004g0051others(1): Show | 4 | HG00558.hp2 HG02074.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559-8834G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343126 | ||||||
| chr1:33343314
|
A | AAT | 59 | a0001c0003t0003g0001a0001c0003t0003g0002a0001c0003t0003g0008others(56): Show | 65 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1559-9023_1559-902 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343314 | ||||||
| chr1:33343337
|
G | A | 144 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(141): Show | 145 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.1559-9045C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343337 | ||||||
| chr1:33343395
|
T | C | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1559-9103A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343395 | ||||||
| chr1:33343423
|
T | C | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1559-9131A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343423 | ||||||
| chr1:33343468
|
C | CA | 92 | a0001c0001t0002g0303a0001c0001t0002g0308a0001c0001t0002g0309others(89): Show | 97 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1559-9177dupT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343468 | ||||||
| chr1:33343468
|
C | CAA | 59 | a0001c0001t0008g0176a0001c0002t0001g0099a0001c0002t0001g0101others(56): Show | 60 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1559-9178_1559-917 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343468 | ||||||
| chr1:33343468
|
C | CAAA | 18 | a0001c0001t0008g0177a0001c0001t0008g0178a0001c0002t0001g0116others(15): Show | 18 | HG00558.hp2 HG01175.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.1559-9179_1559-917 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343468 | ||||||
| chr1:33343468
|
CA | C | 12 | a0001c0001t0002g0312a0001c0001t0002g0327a0001c0001t0027g0317others(9): Show | 12 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1559-9177delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343468 | ||||||
| chr1:33343836
|
A | G | 57 | a0001c0002t0001g0006a0001c0002t0001g0009a0001c0002t0001g0011others(54): Show | 59 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1559-9544T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343836 | ||||||
| chr1:33343937
|
C | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1559-9645G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33343937 | ||||||
| chr1:33344012
|
G | T | 1 | a0001c0002t0001g0175 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1559-9720C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344012 | ||||||
| chr1:33344137
|
A | T | 127 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(124): Show | 128 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1559-9845T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344137 | ||||||
| chr1:33344183
|
C | A | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1559-9891G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344183 | ||||||
| chr1:33344331
|
A | G | 2 | a0001c0001t0010g0010a0001c0001t0010g0344 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1559-10039T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344331 | ||||||
| chr1:33344373
|
A | T | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1558+10028T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344373 | ||||||
| chr1:33344389
|
A | G | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.1558+10012T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344389 | ||||||
| chr1:33344586
|
A | G | 269 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(266): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1558+9815T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344586 | ||||||
| chr1:33344615
|
A | T | 6 | a0001c0002t0001g0098a0001c0002t0001g0114a0001c0002t0001g0123others(3): Show | 6 | HG01358.hp2 HG01361.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558+9786T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344615 | ||||||
| chr1:33344726
|
C | T | 1 | a0001c0001t0005g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1558+9675G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344726 | ||||||
| chr1:33344740
|
A | G | 2 | a0003c0005t0002g0273a0003c0005t0002g0295 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1558+9661T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344740 | ||||||
| chr1:33344838
|
C | A | 2 | a0001c0006t0006g0184a0001c0006t0006g0185 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1558+9563G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344838 | ||||||
| chr1:33344883
|
G | A | 2 | a0002c0004t0004g0024a0002c0004t0004g0025 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1558+9518C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344883 | ||||||
| chr1:33344908
|
A | T | 127 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(124): Show | 128 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.1558+9493T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344908 | ||||||
| chr1:33344918
|
C | T | 1 | a0001c0002t0001g0007 | 2 | NA19056.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1558+9483G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33344918 | ||||||
| chr1:33345038
|
G | C | 3 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0016g0097 | 3 | NA18957.hp1 NA18971.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1558+9363C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345038 | ||||||
| chr1:33345259
|
G | A | 14 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1558+9142C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345259 | ||||||
| chr1:33345343
|
T | C | 14 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1558+9058A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345343 | ||||||
| chr1:33345346
|
C | T | 2 | a0001c0001t0010g0010a0001c0001t0010g0344 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1558+9055G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345346 | ||||||
| chr1:33345446
|
G | A | 1 | a0001c0001t0005g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1558+8955C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345446 | ||||||
| chr1:33345478
|
A | G | 128 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(125): Show | 129 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1558+8923T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345478 | ||||||
| chr1:33345511
|
A | T | 2 | a0001c0001t0010g0010a0001c0001t0010g0344 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1558+8890T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345511 | ||||||
| chr1:33345560
|
T | A | 1 | a0001c0001t0005g0262 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1558+8841A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345560 | ||||||
| chr1:33345579
|
G | T | 1 | a0001c0003t0003g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1558+8822C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345579 | ||||||
| chr1:33345731
|
T | G | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1558+8670A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33345731 | ||||||
| chr1:33346200
|
C | T | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1558+8201G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33346200 | ||||||
| chr1:33346392
|
A | G | 1 | a0002c0004t0004g0015 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1558+8009T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33346392 | ||||||
| chr1:33346483
|
T | A | 128 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(125): Show | 129 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1558+7918A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33346483 | ||||||
| chr1:33346579
|
A | T | 1 | a0001c0002t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1558+7822T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33346579 | ||||||
| chr1:33347017
|
C | G | 6 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558+7384G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33347017 | ||||||
| chr1:33347389
|
G | A | 2 | a0002c0004t0004g0050a0002c0004t0004g0062 | 2 | NA18960.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1558+7012C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33347389 | ||||||
| chr1:33347448
|
T | C | 1 | a0001c0002t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1558+6953A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33347448 | ||||||
| chr1:33347507
|
T | C | 1 | a0002c0004t0004g0044 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1558+6894A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33347507 | ||||||
| chr1:33347726
|
T | C | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1558+6675A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33347726 | ||||||
| chr1:33347910
|
G | C | 3 | a0001c0002t0001g0136a0001c0002t0001g0159a0001c0002t0001g0166 | 3 | HG00735.hp2 HG02004.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1558+6491C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33347910 | ||||||
| chr1:33348079
|
A | C | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1558+6322T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348079 | ||||||
| chr1:33348129
|
A | C | 4 | a0001c0001t0005g0074a0001c0001t0005g0077a0001c0001t0005g0078others(1): Show | 4 | HG02818.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558+6272T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348129 | ||||||
| chr1:33348154
|
C | T | 66 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(63): Show | 67 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1558+6247G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348154 | ||||||
| chr1:33348224
|
C | G | 1 | a0007c0012t0002g0287 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1558+6177G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348224 | ||||||
| chr1:33348250
|
C | T | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1558+6151G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348250 | ||||||
| chr1:33348366
|
T | C | 5 | a0002c0004t0004g0030a0002c0004t0004g0033a0002c0004t0004g0034others(2): Show | 5 | HG01106.hp1 HG01433.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558+6035A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348366 | ||||||
| chr1:33348367
|
A | T | 5 | a0002c0004t0004g0030a0002c0004t0004g0033a0002c0004t0004g0034others(2): Show | 5 | HG01106.hp1 HG01433.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558+6034T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348367 | ||||||
| chr1:33348420
|
C | G | 1 | a0001c0001t0002g0318 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1558+5981G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348420 | ||||||
| chr1:33348553
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1558+5848T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348553 | ||||||
| chr1:33348572
|
A | C | 1 | a0001c0001t0002g0318 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1558+5829T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348572 | ||||||
| chr1:33348632
|
G | T | 1 | a0002c0004t0004g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1558+5769C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348632 | ||||||
| chr1:33348743
|
A | G | 9 | a0001c0002t0001g0112a0001c0002t0001g0115a0001c0002t0001g0116others(6): Show | 9 | HG00438.hp1 NA18941.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558+5658T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33348743 | ||||||
| chr1:33349147
|
G | A | 1 | a0001c0002t0001g0106 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1558+5254C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349147 | ||||||
| chr1:33349191
|
CAGGCGCC others(8): Show |
C | 1 | a0003c0005t0002g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1558+5195_1558+520 others(19): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349191 | ||||||
| chr1:33349206
|
T | C | 1 | a0001c0003t0003g0204 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1558+5195A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349206 | ||||||
| chr1:33349215
|
C | T | 1 | a0001c0003t0003g0241 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1558+5186G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349215 | ||||||
| chr1:33349260
|
C | G | 129 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(126): Show | 130 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.1558+5141G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349260 | ||||||
| chr1:33349269
|
C | G | 2 | a0001c0002t0001g0004a0001c0002t0001g0005 | 4 | HG01891.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558+5132G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349269 | ||||||
| chr1:33349321
|
G | GT | 4 | a0001c0003t0005g0237a0003c0005t0002g0276a0003c0005t0002g0277others(1): Show | 4 | HG01167.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558+5079dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349321 | ||||||
| chr1:33349338
|
T | G | 3 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248 | 3 | HG02257.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1558+5063A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349338 | ||||||
| chr1:33349424
|
G | A | 1 | a0002c0004t0004g0051 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1558+4977C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349424 | ||||||
| chr1:33349671
|
T | G | 1 | a0001c0003t0001g0194 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1558+4730A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349671 | ||||||
| chr1:33349754
|
C | T | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1558+4647G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349754 | ||||||
| chr1:33349802
|
G | C | 1 | a0001c0002t0001g0147 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1558+4599C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349802 | ||||||
| chr1:33349939
|
GGCGGGGC others(6): Show |
G | 1 | a0001c0001t0008g0177 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1558+4449_1558+446 others(17): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33349939 | ||||||
| chr1:33350014
|
T | C | 1 | a0001c0001t0015g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1558+4387A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350014 | ||||||
| chr1:33350021
|
G | A | 1 | a0001c0001t0014g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1558+4380C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350021 | ||||||
| chr1:33350030
|
G | GC | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1558+4370dupG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350030 | ||||||
| chr1:33350098
|
A | T | 87 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(84): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1558+4303T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350098 | ||||||
| chr1:33350120
|
C | T | 1 | a0001c0003t0003g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1558+4281G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350120 | ||||||
| chr1:33350177
|
C | T | 62 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1558+4224G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350177 | ||||||
| chr1:33350247
|
C | T | 1 | a0003c0005t0002g0284 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1558+4154G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350247 | ||||||
| chr1:33350599
|
G | C | 3 | a0001c0002t0001g0011a0001c0002t0001g0125a0001c0002t0001g0244 | 3 | HG00609.hp2 NA18747.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1558+3802C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350599 | ||||||
| chr1:33350612
|
C | T | 11 | a0001c0002t0001g0009a0001c0002t0001g0110a0001c0002t0001g0132others(8): Show | 12 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1558+3789G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350612 | ||||||
| chr1:33350659
|
G | T | 1 | a0001c0001t0011g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1558+3742C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350659 | ||||||
| chr1:33350744
|
C | A | 5 | a0001c0003t0003g0192a0001c0003t0003g0193a0001c0003t0003g0241others(2): Show | 5 | HG00438.hp2 HG02074.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558+3657G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350744 | ||||||
| chr1:33350756
|
T | C | 1 | a0002c0004t0004g0043 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1558+3645A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350756 | ||||||
| chr1:33350855
|
TCTC | T | 6 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558+3543_1558+354 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33350855 | ||||||
| chr1:33351059
|
C | G | 1 | a0007c0012t0002g0287 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1558+3342G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351059 | ||||||
| chr1:33351125
|
G | A | 83 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(80): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1558+3276C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351125 | ||||||
| chr1:33351254
|
T | C | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1558+3147A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351254 | ||||||
| chr1:33351263
|
A | G | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1558+3138T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351263 | ||||||
| chr1:33351305
|
A | T | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1558+3096T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351305 | ||||||
| chr1:33351404
|
A | G | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1558+2997T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351404 | ||||||
| chr1:33351411
|
C | T | 6 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558+2990G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351411 | ||||||
| chr1:33351424
|
A | C | 4 | a0002c0004t0004g0035a0002c0004t0004g0036a0002c0004t0004g0038others(1): Show | 4 | NA18950.hp2 NA18952.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558+2977T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351424 | ||||||
| chr1:33351533
|
A | G | 1 | a0001c0001t0005g0095 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1558+2868T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351533 | ||||||
| chr1:33351545
|
T | C | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1558+2856A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351545 | ||||||
| chr1:33351585
|
G | C | 4 | a0001c0003t0003g0198a0001c0003t0003g0221a0001c0003t0003g0222others(1): Show | 4 | HG02129.hp2 NA18939.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558+2816C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351585 | ||||||
| chr1:33351625
|
C | T | 1 | a0001c0003t0003g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1558+2776G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351625 | ||||||
| chr1:33351951
|
C | CA | 100 | a0001c0002t0001g0165a0001c0002t0001g0166a0001c0003t0001g0194others(97): Show | 106 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1558+2449dupT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351951 | ||||||
| chr1:33351951
|
C | CAA | 22 | a0001c0003t0003g0065a0001c0003t0003g0197a0001c0003t0003g0205others(19): Show | 23 | HG00323.hp1 HG00609.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1558+2448_1558+244 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351951 | ||||||
| chr1:33351951
|
C | CAAA | 9 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(6): Show | 9 | HG00621.hp2 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558+2447_1558+244 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351951 | ||||||
| chr1:33351951
|
CA | C | 119 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(116): Show | 121 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1558+2449delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351951 | ||||||
| chr1:33351956
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1558+2445T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351956 | ||||||
| chr1:33351975
|
C | A | 3 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0016g0097 | 3 | NA18957.hp1 NA18971.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1558+2426G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351975 | ||||||
| chr1:33351979
|
C | G | 1 | a0001c0001t0002g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1558+2422G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351979 | ||||||
| chr1:33351985
|
A | G | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1558+2416T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351985 | ||||||
| chr1:33351988
|
G | GAT | 14 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(11): Show | 14 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1558+2411_1558+241 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33351988 | ||||||
| chr1:33352036
|
T | C | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1558+2365A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33352036 | ||||||
| chr1:33352813
|
C | T | 266 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(263): Show | 274 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.1558+1588G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33352813 | ||||||
| chr1:33352850
|
C | T | 1 | a0003c0005t0002g0275 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1558+1551G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33352850 | ||||||
| chr1:33353000
|
G | A | 1 | a0002c0004t0004g0028 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1558+1401C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33353000 | ||||||
| chr1:33353573
|
T | G | 1 | a0004c0007t0018g0143 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1558+828A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33353573 | ||||||
| chr1:33353671
|
G | A | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558+730C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33353671 | ||||||
| chr1:33353821
|
C | T | 1 | a0001c0003t0003g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1558+580G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33353821 | ||||||
| chr1:33353919
|
G | A | 1 | a0001c0002t0001g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1558+482C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33353919 | ||||||
| chr1:33353961
|
C | T | 204 | a0001c0001t0002g0272a0001c0001t0002g0285a0001c0001t0002g0297others(201): Show | 206 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.1558+440G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33353961 | ||||||
| chr1:33354049
|
T | C | 1 | a0001c0002t0001g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1558+352A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33354049 | ||||||
| chr1:33354169
|
G | A | 1 | a0001c0002t0001g0251 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1558+232C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33354169 | ||||||
| chr1:33354172
|
C | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1558+229G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33354172 | ||||||
| chr1:33354189
|
T | C | 6 | a0001c0001t0005g0074a0001c0001t0005g0077a0001c0001t0005g0078others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558+212A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33354189 | ||||||
| chr1:33354213
|
T | G | 126 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(123): Show | 127 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.1558+188A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33354213 | ||||||
| chr1:33354229
|
A | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.1558+172T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 9/14 | chr1 | 33354229 | ||||||
| chr1:33354579
|
AGGACAGA others(5): Show |
A | 1 | a0001c0003t0003g0232 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1393-25_1393-14del others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 8/14 | chr1 | 33354579 | ||||||
| chr1:33355263
|
G | C | 1 | a0001c0003t0003g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.977-10C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33355263 | ||||||
| chr1:33355600
|
C | T | 1 | a0001c0001t0005g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.977-347G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33355600 | ||||||
| chr1:33355826
|
G | A | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.977-573C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33355826 | ||||||
| chr1:33356187
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.977-934C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356187 | ||||||
| chr1:33356206
|
T | C | 269 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(266): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.977-953A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356206 | ||||||
| chr1:33356249
|
T | TTATATAT others(3): Show |
2 | a0001c0003t0001g0194a0001c0003t0003g0234 | 2 | HG03654.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.977-1006_977-997du others(11): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
T | TTATATAT others(5): Show |
2 | a0001c0003t0003g0195a0001c0003t0005g0237 | 2 | HG01167.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.977-1008_977-997du others(13): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
T | TTATATAT others(17): Show |
3 | a0002c0004t0004g0029a0002c0004t0004g0035a0002c0004t0004g0038 | 3 | HG04228.hp2 NA18952.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.977-997_977-996ins others(24): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
T | TTATATAT others(19): Show |
1 | a0002c0004t0004g0037 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.977-997_977-996ins others(26): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
T | TTATATAT others(21): Show |
1 | a0002c0004t0004g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.977-997_977-996ins others(28): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
T | TTATATAT others(47): Show |
1 | a0002c0004t0004g0036 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.977-997_977-996ins others(54): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
T | TTATATAT others(77): Show |
1 | a0002c0004t0004g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.977-997_977-996ins others(84): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
TTA | T | 14 | a0001c0001t0002g0323a0001c0002t0001g0104a0001c0002t0001g0105others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.977-998_977-997del others(2): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
TTATA | T | 77 | a0001c0001t0002g0272a0001c0001t0002g0300a0001c0001t0002g0308others(74): Show | 82 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.977-1000_977-997de others(5): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356249
|
TTATATAT others(21): Show |
T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.977-1024_977-997de others(29): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356249 | ||||||
| chr1:33356251
|
A | ATATATAT others(17): Show |
1 | a0001c0002t0001g0142 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.977-999_977-998ins others(24): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356251 | ||||||
| chr1:33356253
|
A | ATATATAT others(13): Show |
5 | a0001c0002t0001g0175a0001c0014t0001g0127a0004c0007t0001g0144others(2): Show | 5 | HG01081.hp1 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.977-1001_977-1000i others(22): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356253 | ||||||
| chr1:33356253
|
A | ATATATAT others(13): Show |
1 | a0002c0004t0013g0012 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.977-1001_977-1000i others(22): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356253 | ||||||
| chr1:33356253
|
ATATATAT others(17): Show |
A | 2 | a0001c0001t0002g0299a0001c0001t0002g0357 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.977-1024_977-1001d others(26): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356253 | ||||||
| chr1:33356255
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.977-1024_977-1003d others(24): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356255 | ||||||
| chr1:33356267
|
A | G | 1 | a0001c0001t0005g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.977-1014T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356267 | ||||||
| chr1:33356267
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.977-1024_977-1015d others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356267 | ||||||
| chr1:33356269
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0015g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.977-1017_977-1016i others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356269 | ||||||
| chr1:33356270
|
T | TGTATATA others(21): Show |
1 | a0002c0004t0004g0031 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.977-1018_977-1017i others(30): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356270 | ||||||
| chr1:33356271
|
A | G | 52 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(49): Show | 53 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.977-1018T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356271 | ||||||
| chr1:33356271
|
ATATATG | A | 7 | a0001c0001t0002g0332a0001c0001t0002g0333a0001c0001t0002g0334others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.977-1024_977-1019d others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356271 | ||||||
| chr1:33356273
|
A | ACG | 3 | a0002c0004t0004g0029a0002c0004t0004g0037a0002c0004t0013g0012 | 3 | HG01358.hp1 HG04228.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.977-1021_977-1020i others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(19): Show |
1 | a0002c0004t0004g0039 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.977-1021_977-1020i others(28): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(17): Show |
4 | a0002c0004t0004g0015a0002c0004t0004g0020a0002c0004t0004g0027others(1): Show | 4 | HG01981.hp2 NA19060.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.977-1021_977-1020i others(26): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(19): Show |
13 | a0002c0004t0004g0003a0002c0004t0004g0021a0002c0004t0004g0023others(10): Show | 14 | HG00323.hp1 HG01106.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.977-1021_977-1020i others(28): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(21): Show |
14 | a0002c0004t0004g0014a0002c0004t0004g0032a0002c0004t0004g0040others(11): Show | 14 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.977-1021_977-1020i others(30): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(69): Show |
1 | a0002c0004t0004g0049 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.977-1021_977-1020i others(78): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(23): Show |
5 | a0002c0004t0004g0028a0002c0004t0004g0053a0002c0004t0004g0054others(2): Show | 5 | HG00558.hp2 HG02074.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.977-1021_977-1020i others(32): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(25): Show |
2 | a0002c0004t0004g0044a0002c0004t0004g0051 | 2 | NA18939.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.977-1021_977-1020i others(34): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(47): Show |
1 | a0002c0004t0004g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.977-1021_977-1020i others(56): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATAT others(5): Show |
1 | a0001c0003t0003g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.977-1021_977-1020i others(14): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATATATG | 4 | a0001c0001t0005g0074a0001c0001t0005g0078a0001c0001t0005g0080others(1): Show | 4 | HG02896.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.977-1021_977-1020i others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | ATG | 3 | a0001c0001t0002g0315a0003c0005t0002g0273a0003c0005t0002g0295 | 3 | HG00558.hp1 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.977-1021_977-1020i others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356273
|
A | G | 48 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0081others(45): Show | 48 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.977-1020T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356273 | ||||||
| chr1:33356275
|
A | AATATATA others(14): Show |
1 | a0001c0003t0003g0232 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.977-1023_977-1022i others(23): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ACG | 3 | a0002c0004t0004g0035a0002c0004t0004g0036a0002c0004t0004g0038 | 3 | NA18950.hp2 NA18952.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.977-1023_977-1022i others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(17): Show |
6 | a0002c0004t0004g0018a0002c0004t0004g0024a0002c0004t0004g0042others(3): Show | 6 | HG00621.hp2 HG01099.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.977-1023_977-1022i others(26): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(19): Show |
4 | a0002c0004t0004g0016a0002c0004t0004g0017a0002c0004t0004g0019others(1): Show | 4 | HG01175.hp2 HG01496.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.977-1023_977-1022i others(28): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(19): Show |
1 | a0001c0003t0003g0205 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.977-1023_977-1022i others(28): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(17): Show |
3 | a0001c0003t0003g0192a0001c0003t0003g0209a0001c0003t0003g0213 | 3 | HG00621.hp1 HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.977-1023_977-1022i others(26): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(15): Show |
4 | a0001c0003t0003g0210a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02074.hp2 HG02155.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.977-1023_977-1022i others(24): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(45): Show |
1 | a0002c0004t0004g0071 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.977-1023_977-1022i others(54): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(11): Show |
2 | a0001c0003t0003g0186a0001c0003t0003g0222 | 2 | HG01192.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.977-1023_977-1022i others(20): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(9): Show |
6 | a0001c0003t0003g0208a0001c0003t0003g0212a0001c0003t0003g0229others(3): Show | 6 | HG01123.hp1 HG01346.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.977-1023_977-1022i others(18): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(7): Show |
5 | a0001c0003t0003g0065a0001c0003t0003g0219a0001c0003t0003g0225others(2): Show | 5 | HG02683.hp2 HG03239.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-1023_977-1022i others(16): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(5): Show |
6 | a0001c0003t0003g0197a0001c0003t0003g0198a0001c0003t0003g0203others(3): Show | 6 | HG02129.hp2 NA18948.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.977-1023_977-1022i others(14): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(33): Show |
2 | a0001c0003t0003g0221a0001c0003t0003g0223 | 2 | NA18939.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.977-1023_977-1022i others(42): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATATAT others(3): Show |
16 | a0001c0003t0001g0201a0001c0003t0003g0001a0001c0003t0003g0008others(13): Show | 20 | HG00423.hp1 HG00738.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.977-1023_977-1022i others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATATG | 3 | a0001c0001t0005g0077a0001c0008t0002g0347a0008c0009t0002g0348 | 3 | HG01243.hp1 HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.977-1023_977-1022i others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | ATCTATAT others(5): Show |
7 | a0001c0003t0003g0002a0001c0003t0003g0190a0001c0003t0003g0199others(4): Show | 9 | NA18612.hp1 NA18945.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.977-1023_977-1022i others(14): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
A | G | 44 | a0001c0001t0002g0285a0001c0001t0002g0297a0001c0001t0002g0301others(41): Show | 44 | HG00597.hp1 HG00639.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.977-1022T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356275
|
ATG | A | 46 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0081others(43): Show | 46 | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.977-1024_977-1023d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356275 | ||||||
| chr1:33356277
|
G | A | 178 | a0001c0001t0002g0285a0001c0001t0002g0297a0001c0001t0002g0301others(175): Show | 185 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.977-1024C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356277 | ||||||
| chr1:33356277
|
G | GTA | 5 | a0001c0001t0002g0302a0001c0001t0002g0325a0001c0001t0002g0331others(2): Show | 5 | HG00639.hp2 HG02027.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.977-1026_977-1025d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356277 | ||||||
| chr1:33356279
|
A | ATATATAT others(39): Show |
1 | a0001c0003t0003g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.977-1027_977-1026i others(48): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356279 | ||||||
| chr1:33356279
|
A | G | 4 | a0001c0001t0002g0332a0001c0001t0002g0333a0001c0001t0002g0334others(1): Show | 4 | HG02647.hp2 HG02818.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.977-1026T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356279 | ||||||
| chr1:33356281
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0011g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.977-1029_977-1028i others(24): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356281 | ||||||
| chr1:33356281
|
A | G | 4 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(1): Show | 4 | HG02486.hp2 HG02572.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.977-1028T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356281 | ||||||
| chr1:33356291
|
A | T | 5 | a0001c0001t0006g0247a0001c0001t0014g0245a0001c0001t0014g0249others(2): Show | 5 | HG02647.hp1 HG02886.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.977-1038T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356291 | ||||||
| chr1:33356295
|
T | A | 1 | a0002c0004t0004g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.977-1042A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356295 | ||||||
| chr1:33356375
|
G | T | 1 | a0007c0012t0002g0287 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.977-1122C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356375 | ||||||
| chr1:33356483
|
C | T | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.977-1230G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356483 | ||||||
| chr1:33356509
|
G | A | 57 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(54): Show | 63 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.977-1256C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356509 | ||||||
| chr1:33356546
|
C | T | 201 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(198): Show | 203 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.977-1293G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356546 | ||||||
| chr1:33356621
|
A | C | 85 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(82): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.977-1368T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356621 | ||||||
| chr1:33356686
|
ACTT | A | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.977-1436_977-1434d others(5): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356686 | ||||||
| chr1:33356722
|
T | C | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.977-1469A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356722 | ||||||
| chr1:33356781
|
G | A | 1 | a0001c0014t0001g0127 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.977-1528C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356781 | ||||||
| chr1:33356819
|
C | CG | 5 | a0001c0001t0002g0310a0001c0001t0027g0317a0001c0002t0016g0097others(2): Show | 5 | NA18957.hp2 NA18988.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.977-1567dupC | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356819 | ||||||
| chr1:33356865
|
G | A | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.977-1612C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356865 | ||||||
| chr1:33356889
|
C | G | 1 | a0001c0001t0014g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.977-1636G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356889 | ||||||
| chr1:33356941
|
A | C | 1 | a0001c0001t0002g0318 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.977-1688T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33356941 | ||||||
| chr1:33357106
|
T | G | 1 | a0001c0006t0003g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.977-1853A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33357106 | ||||||
| chr1:33357287
|
A | C | 4 | a0001c0001t0005g0183a0001c0008t0002g0347a0001c0008t0002g0349others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.977-2034T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33357287 | ||||||
| chr1:33357521
|
T | C | 1 | a0001c0001t0005g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.977-2268A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33357521 | ||||||
| chr1:33357668
|
T | C | 269 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(266): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.977-2415A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33357668 | ||||||
| chr1:33357993
|
G | C | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.977-2740C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33357993 | ||||||
| chr1:33358061
|
T | G | 1 | a0002c0004t0004g0061 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.977-2808A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33358061 | ||||||
| chr1:33358336
|
T | C | 6 | a0001c0002t0001g0175a0001c0014t0001g0127a0003c0005t0002g0288others(3): Show | 6 | HG00423.hp2 HG01081.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.977-3083A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33358336 | ||||||
| chr1:33358373
|
T | C | 1 | a0001c0002t0001g0147 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.977-3120A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33358373 | ||||||
| chr1:33358646
|
A | G | 12 | a0001c0002t0001g0009a0001c0002t0001g0110a0001c0002t0001g0132others(9): Show | 13 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.977-3393T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33358646 | ||||||
| chr1:33358648
|
C | T | 1 | a0001c0001t0002g0306 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.977-3395G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33358648 | ||||||
| chr1:33358649
|
G | A | 2 | a0003c0005t0002g0273a0003c0005t0002g0295 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.977-3396C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33358649 | ||||||
| chr1:33358712
|
C | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.977-3459G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33358712 | ||||||
| chr1:33358910
|
T | C | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.977-3657A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33358910 | ||||||
| chr1:33359010
|
G | A | 2 | a0001c0003t0003g0195a0001c0003t0003g0225 | 2 | NA19079.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.977-3757C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359010 | ||||||
| chr1:33359201
|
CTGAA | C | 128 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(125): Show | 129 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.977-3952_977-3949d others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359201 | ||||||
| chr1:33359231
|
G | A | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.977-3978C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359231 | ||||||
| chr1:33359520
|
C | G | 1 | a0001c0001t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.977-4267G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359520 | ||||||
| chr1:33359699
|
G | A | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.977-4446C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359699 | ||||||
| chr1:33359700
|
G | A | 2 | a0001c0001t0005g0090a0001c0001t0017g0089 | 2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.977-4447C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359700 | ||||||
| chr1:33359704
|
A | C | 1 | a0002c0004t0004g0043 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.977-4451T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359704 | ||||||
| chr1:33359727
|
A | T | 1 | a0003c0005t0025g0351 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.977-4474T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359727 | ||||||
| chr1:33359763
|
C | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.977-4510G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359763 | ||||||
| chr1:33359915
|
T | C | 4 | a0001c0001t0005g0183a0001c0008t0002g0347a0001c0008t0002g0349others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.977-4662A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359915 | ||||||
| chr1:33359934
|
G | A | 8 | a0001c0002t0001g0006a0001c0002t0001g0109a0001c0002t0001g0113others(5): Show | 9 | HG00597.hp2 NA18964.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.977-4681C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33359934 | ||||||
| chr1:33360107
|
G | A | 1 | a0001c0003t0003g0220 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.977-4854C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33360107 | ||||||
| chr1:33360167
|
T | C | 1 | a0001c0002t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.977-4914A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33360167 | ||||||
| chr1:33360478
|
TTAGA | T | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.977-5229_977-5226d others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33360478 | ||||||
| chr1:33360530
|
TGACACAT others(8): Show |
T | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.977-5292_977-5278d others(17): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33360530 | ||||||
| chr1:33360592
|
C | A | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.977-5339G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33360592 | ||||||
| chr1:33360694
|
G | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.977-5441C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33360694 | ||||||
| chr1:33360965
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.977-5712G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33360965 | ||||||
| chr1:33361344
|
T | G | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.976+5772A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33361344 | ||||||
| chr1:33361622
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+5494G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33361622 | ||||||
| chr1:33361838
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+5278G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33361838 | ||||||
| chr1:33361898
|
T | G | 12 | a0001c0002t0001g0009a0001c0002t0001g0110a0001c0002t0001g0132others(9): Show | 13 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.976+5218A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33361898 | ||||||
| chr1:33361956
|
A | C | 1 | a0001c0001t0005g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.976+5160T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33361956 | ||||||
| chr1:33362005
|
T | G | 1 | a0001c0001t0005g0256 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.976+5111A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362005 | ||||||
| chr1:33362117
|
A | C | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.976+4999T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362117 | ||||||
| chr1:33362170
|
T | C | 5 | a0001c0002t0001g0114a0001c0002t0001g0123a0001c0002t0001g0128others(2): Show | 5 | HG01358.hp2 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.976+4946A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362170 | ||||||
| chr1:33362335
|
G | A | 1 | a0001c0003t0003g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.976+4781C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362335 | ||||||
| chr1:33362394
|
A | G | 5 | a0003c0005t0002g0279a0003c0005t0002g0280a0003c0005t0002g0282others(2): Show | 5 | HG00639.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+4722T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362394 | ||||||
| chr1:33362611
|
G | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.976+4505C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362611 | ||||||
| chr1:33362658
|
C | A | 85 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(82): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.976+4458G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362658 | ||||||
| chr1:33362659
|
G | A | 269 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(266): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.976+4457C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362659 | ||||||
| chr1:33362748
|
C | T | 1 | a0001c0001t0005g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.976+4368G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362748 | ||||||
| chr1:33362759
|
CTT | C | 202 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(199): Show | 204 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.976+4355_976+4356d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362759 | ||||||
| chr1:33362765
|
C | A | 202 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(199): Show | 204 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.976+4351G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362765 | ||||||
| chr1:33362769
|
T | C | 35 | a0001c0001t0002g0285a0001c0001t0005g0072a0001c0001t0005g0073others(32): Show | 35 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.976+4347A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362769 | ||||||
| chr1:33362791
|
C | T | 51 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(48): Show | 51 | HG00558.hp1 HG00597.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.976+4325G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362791 | ||||||
| chr1:33362874
|
G | C | 4 | a0001c0001t0002g0311a0001c0001t0002g0316a0001c0001t0002g0330others(1): Show | 4 | NA18942.hp1 NA18964.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.976+4242C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33362874 | ||||||
| chr1:33363031
|
A | G | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.976+4085T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363031 | ||||||
| chr1:33363061
|
A | G | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.976+4055T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363061 | ||||||
| chr1:33363066
|
C | G | 7 | a0003c0005t0002g0269a0003c0005t0002g0275a0003c0005t0002g0284others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.976+4050G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363066 | ||||||
| chr1:33363084
|
ATAG | A | 202 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(199): Show | 204 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.976+4029_976+4031d others(5): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363084 | ||||||
| chr1:33363116
|
C | T | 2 | a0001c0002t0001g0124a0001c0002t0001g0134 | 2 | NA18612.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.976+4000G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363116 | ||||||
| chr1:33363199
|
C | T | 1 | a0003c0005t0002g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.976+3917G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363199 | ||||||
| chr1:33363233
|
C | T | 269 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(266): Show | 277 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.976+3883G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363233 | ||||||
| chr1:33363373
|
C | T | 2 | a0001c0001t0005g0259a0001c0011t0005g0258 | 2 | HG01192.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.976+3743G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363373 | ||||||
| chr1:33363481
|
C | T | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.976+3635G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363481 | ||||||
| chr1:33363912
|
A | C | 67 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(64): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.976+3204T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33363912 | ||||||
| chr1:33364130
|
C | G | 1 | a0001c0001t0005g0095 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.976+2986G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364130 | ||||||
| chr1:33364248
|
C | T | 1 | a0001c0002t0001g0118 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.976+2868G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364248 | ||||||
| chr1:33364336
|
G | A | 202 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(199): Show | 204 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.976+2780C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364336 | ||||||
| chr1:33364359
|
G | GAC | 20 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(17): Show | 21 | HG00609.hp1 HG00621.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.976+2755_976+2756d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364359 | ||||||
| chr1:33364359
|
GAC | G | 168 | a0001c0001t0002g0332a0001c0001t0005g0072a0001c0001t0005g0075others(165): Show | 177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.976+2755_976+2756d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364359 | ||||||
| chr1:33364359
|
GACAC | G | 8 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.976+2753_976+2756d others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364359 | ||||||
| chr1:33364390
|
TCA | T | 4 | a0001c0001t0010g0010a0001c0001t0010g0344a0001c0002t0001g0101others(1): Show | 5 | HG00733.hp2 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+2724_976+2725d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364390 | ||||||
| chr1:33364390
|
TCACACAC others(3): Show |
T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+2716_976+2725d others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364390 | ||||||
| chr1:33364390
|
TCACACAC others(5): Show |
T | 1 | a0001c0003t0003g0232 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.976+2714_976+2725d others(14): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364390 | ||||||
| chr1:33364390
|
TCACACAC others(7): Show |
T | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.976+2712_976+2725d others(16): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364390 | ||||||
| chr1:33364410
|
A | ACACACAC others(5): Show |
3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.976+2705_976+2706i others(14): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364410 | ||||||
| chr1:33364410
|
A | ACACACG | 62 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(59): Show | 62 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.976+2705_976+2706i others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364410 | ||||||
| chr1:33364410
|
A | ACACG | 123 | a0001c0001t0002g0285a0001c0001t0005g0072a0001c0001t0005g0073others(120): Show | 124 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.976+2705_976+2706i others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364410 | ||||||
| chr1:33364410
|
A | ACACGCG | 5 | a0003c0005t0002g0269a0003c0005t0002g0275a0003c0005t0002g0284others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+2705_976+2706i others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364410 | ||||||
| chr1:33364410
|
A | G | 2 | a0001c0001t0010g0010a0001c0001t0010g0344 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.976+2706T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364410 | ||||||
| chr1:33364418
|
A | C | 1 | a0001c0002t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.976+2698T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364418 | ||||||
| chr1:33364422
|
A | ACACACAC others(7): Show |
1 | a0001c0002t0001g0159 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.976+2693_976+2694i others(16): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364422 | ||||||
| chr1:33364422
|
A | ACACACAC others(5): Show |
1 | a0001c0002t0001g0168 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.976+2693_976+2694i others(14): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364422 | ||||||
| chr1:33364422
|
A | ACACACAC others(3): Show |
6 | a0001c0002t0001g0007a0001c0002t0001g0136a0001c0002t0001g0160others(3): Show | 7 | HG00735.hp2 HG02300.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.976+2693_976+2694i others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364422 | ||||||
| chr1:33364422
|
A | ACACACAC others(1): Show |
4 | a0001c0002t0001g0158a0001c0002t0001g0161a0001c0002t0001g0162others(1): Show | 4 | HG02071.hp2 HG02080.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.976+2693_976+2694i others(10): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364422 | ||||||
| chr1:33364422
|
A | ACACG | 3 | a0001c0002t0001g0100a0001c0002t0001g0153a0001c0002t0001g0154 | 3 | HG02723.hp1 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.976+2690_976+2693d others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364422 | ||||||
| chr1:33364422
|
A | ACG | 17 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(14): Show | 20 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.976+2693_976+2694i others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364422 | ||||||
| chr1:33364422
|
A | G | 53 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0098others(50): Show | 54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.976+2694T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364422 | ||||||
| chr1:33364435
|
C | T | 1 | a0001c0006t0006g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.976+2681G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364435 | ||||||
| chr1:33364537
|
C | G | 1 | a0001c0001t0002g0326 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.976+2579G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364537 | ||||||
| chr1:33364812
|
T | C | 202 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(199): Show | 204 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.976+2304A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364812 | ||||||
| chr1:33364919
|
A | C | 1 | a0002c0004t0004g0031 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.976+2197T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364919 | ||||||
| chr1:33364977
|
C | T | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.976+2139G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33364977 | ||||||
| chr1:33365023
|
T | A | 1 | a0001c0001t0002g0324 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.976+2093A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365023 | ||||||
| chr1:33365035
|
G | C | 5 | a0001c0001t0002g0323a0001c0001t0002g0327a0001c0001t0002g0332others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.976+2081C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365035 | ||||||
| chr1:33365129
|
G | A | 91 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(88): Show | 92 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.976+1987C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365129 | ||||||
| chr1:33365261
|
C | T | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.976+1855G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365261 | ||||||
| chr1:33365262
|
G | A | 2 | a0001c0006t0006g0180a0001c0006t0020g0181 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.976+1854C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365262 | ||||||
| chr1:33365283
|
G | A | 5 | a0001c0003t0003g0198a0001c0003t0003g0221a0001c0003t0003g0222others(2): Show | 5 | HG02129.hp2 NA18939.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+1833C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365283 | ||||||
| chr1:33365445
|
G | C | 1 | a0002c0004t0004g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.976+1671C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365445 | ||||||
| chr1:33365566
|
A | G | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.976+1550T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365566 | ||||||
| chr1:33365593
|
C | T | 1 | a0001c0001t0015g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.976+1523G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365593 | ||||||
| chr1:33365723
|
G | A | 1 | a0001c0001t0002g0346 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.976+1393C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365723 | ||||||
| chr1:33365871
|
CTCTG | C | 91 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(88): Show | 92 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.976+1241_976+1244d others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365871 | ||||||
| chr1:33365872
|
T | C | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.976+1244A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33365872 | ||||||
| chr1:33366068
|
A | T | 1 | a0002c0004t0004g0059 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.976+1048T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33366068 | ||||||
| chr1:33366143
|
A | G | 1 | a0001c0002t0022g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.976+973T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33366143 | ||||||
| chr1:33366153
|
C | T | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.976+963G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33366153 | ||||||
| chr1:33366191
|
G | A | 3 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0016g0097 | 3 | NA18957.hp1 NA18971.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.976+925C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33366191 | ||||||
| chr1:33366233
|
C | T | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.976+883G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33366233 | ||||||
| chr1:33366432
|
C | T | 67 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(64): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.976+684G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33366432 | ||||||
| chr1:33366856
|
C | T | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.976+260G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33366856 | ||||||
| chr1:33366982
|
T | C | 5 | a0001c0001t0005g0074a0001c0001t0005g0077a0001c0001t0005g0078others(2): Show | 5 | HG02818.hp2 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.976+134A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33366982 | ||||||
| chr1:33367046
|
G | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.976+70C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33367046 | ||||||
| chr1:33367068
|
C | A | 1 | a0001c0002t0001g0147 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.976+48G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 7/14 | chr1 | 33367068 | ||||||
| chr1:33367455
|
C | G | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.664-27G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367455 | ||||||
| chr1:33367571
|
G | C | 6 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(3): Show | 6 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-143C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367571 | ||||||
| chr1:33367609
|
A | T | 8 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0129others(5): Show | 8 | HG00323.hp2 HG01081.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-181T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367609 | ||||||
| chr1:33367610
|
G | A | 8 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0129others(5): Show | 8 | HG00323.hp2 HG01081.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-182C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367610 | ||||||
| chr1:33367638
|
C | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.664-210G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367638 | ||||||
| chr1:33367649
|
G | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.664-221C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367649 | ||||||
| chr1:33367687
|
C | T | 1 | a0002c0004t0004g0020 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.664-259G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367687 | ||||||
| chr1:33367696
|
G | A | 3 | a0004c0007t0001g0144a0004c0007t0001g0145a0004c0007t0018g0143 | 3 | HG01081.hp1 HG01515.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.664-268C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367696 | ||||||
| chr1:33367943
|
C | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.664-515G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33367943 | ||||||
| chr1:33368023
|
C | T | 1 | a0001c0002t0022g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.663+513G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33368023 | ||||||
| chr1:33368053
|
A | G | 1 | a0001c0002t0021g0138 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.663+483T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33368053 | ||||||
| chr1:33368087
|
C | G | 1 | a0001c0003t0003g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.663+449G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33368087 | ||||||
| chr1:33368345
|
C | T | 5 | a0003c0005t0002g0269a0003c0005t0002g0275a0003c0005t0002g0284others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+191G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33368345 | ||||||
| chr1:33368374
|
T | C | 1 | a0003c0005t0002g0355 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.663+162A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33368374 | ||||||
| chr1:33368393
|
G | A | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.663+143C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33368393 | ||||||
| chr1:33368413
|
G | T | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.663+123C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 6/14 | chr1 | 33368413 | ||||||
| chr1:33368710
|
C | T | 2 | a0001c0003t0003g0229a0001c0003t0003g0231 | 2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.577-88G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368710 | ||||||
| chr1:33368768
|
C | T | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.577-146G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368768 | ||||||
| chr1:33368809
|
G | C | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.577-187C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368809 | ||||||
| chr1:33368811
|
G | A | 1 | a0003c0005t0025g0351 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.577-189C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368811 | ||||||
| chr1:33368815
|
T | C | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.577-193A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368815 | ||||||
| chr1:33368831
|
G | C | 1 | a0001c0002t0001g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.577-209C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368831 | ||||||
| chr1:33368852
|
G | A | 2 | a0002c0004t0004g0024a0002c0004t0004g0025 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.577-230C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368852 | ||||||
| chr1:33368854
|
A | G | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.577-232T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368854 | ||||||
| chr1:33368871
|
G | C | 1 | a0004c0007t0001g0145 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.577-249C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368871 | ||||||
| chr1:33368979
|
C | T | 1 | a0001c0002t0001g0155 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.577-357G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33368979 | ||||||
| chr1:33369101
|
C | A | 1 | a0003c0005t0002g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.577-479G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369101 | ||||||
| chr1:33369182
|
G | A | 1 | a0003c0005t0002g0275 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.577-560C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369182 | ||||||
| chr1:33369372
|
A | T | 67 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(64): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.577-750T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369372 | ||||||
| chr1:33369594
|
C | T | 4 | a0002c0004t0004g0016a0002c0004t0004g0017a0002c0004t0004g0018others(1): Show | 4 | HG01175.hp2 HG01496.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+827G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369594 | ||||||
| chr1:33369634
|
C | T | 1 | a0007c0012t0002g0287 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.576+787G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369634 | ||||||
| chr1:33369791
|
G | A | 66 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(63): Show | 67 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.576+630C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369791 | ||||||
| chr1:33369805
|
T | C | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.576+616A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369805 | ||||||
| chr1:33369890
|
T | C | 52 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(49): Show | 52 | HG00558.hp1 HG00597.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.576+531A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369890 | ||||||
| chr1:33369894
|
TG | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.576+526delC | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369894 | ||||||
| chr1:33369953
|
C | T | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.576+468G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369953 | ||||||
| chr1:33369954
|
G | A | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.576+467C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33369954 | ||||||
| chr1:33370045
|
G | A | 3 | a0001c0001t0002g0267a0001c0001t0002g0299a0001c0001t0002g0357 | 3 | HG01884.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.576+376C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 5/14 | chr1 | 33370045 | ||||||
| chr1:33370666
|
C | G | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.412-81G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 4/14 | chr1 | 33370666 | ||||||
| chr1:33370705
|
C | T | 2 | a0001c0002t0001g0129a0001c0002t0001g0131 | 2 | HG01516.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.412-120G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 4/14 | chr1 | 33370705 | ||||||
| chr1:33370867
|
G | T | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.411+150C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 4/14 | chr1 | 33370867 | ||||||
| chr1:33370918
|
A | G | 3 | a0001c0001t0002g0332a0001c0001t0002g0333a0001c0001t0002g0334 | 3 | HG02647.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.411+99T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 4/14 | chr1 | 33370918 | ||||||
| chr1:33370932
|
C | T | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.411+85G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 4/14 | chr1 | 33370932 | ||||||
| chr1:33370954
|
G | T | 1 | a0001c0002t0022g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.411+63C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 4/14 | chr1 | 33370954 | ||||||
| chr1:33371131
|
A | T | 1 | a0002c0004t0004g0027 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.334-37T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371131 | ||||||
| chr1:33371195
|
C | G | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.334-101G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371195 | ||||||
| chr1:33371341
|
AGCACTC | A | 86 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(83): Show | 91 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-253_334-248del others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371341 | ||||||
| chr1:33371406
|
C | T | 1 | a0001c0001t0010g0344 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.334-312G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371406 | ||||||
| chr1:33371426
|
A | G | 2 | a0001c0002t0001g0119a0001c0002t0001g0120 | 2 | NA19004.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.334-332T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371426 | ||||||
| chr1:33371502
|
G | A | 37 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(34): Show | 38 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.334-408C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371502 | ||||||
| chr1:33371508
|
C | T | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-414G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371508 | ||||||
| chr1:33371590
|
C | T | 1 | a0001c0001t0002g0312 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.334-496G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371590 | ||||||
| chr1:33371639
|
G | A | 1 | a0002c0004t0004g0049 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.334-545C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371639 | ||||||
| chr1:33371676
|
A | G | 1 | a0003c0005t0002g0279 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.334-582T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371676 | ||||||
| chr1:33371733
|
C | A | 85 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(82): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.333+556G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371733 | ||||||
| chr1:33371792
|
T | C | 2 | a0001c0001t0005g0090a0001c0001t0017g0089 | 2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.333+497A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371792 | ||||||
| chr1:33371816
|
G | A | 1 | a0001c0001t0005g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.333+473C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371816 | ||||||
| chr1:33371869
|
C | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.333+420G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371869 | ||||||
| chr1:33371978
|
G | A | 3 | a0001c0001t0002g0332a0001c0001t0002g0333a0001c0001t0002g0334 | 3 | HG02647.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.333+311C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371978 | ||||||
| chr1:33371987
|
C | T | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.333+302G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33371987 | ||||||
| chr1:33372101
|
A | G | 1 | a0001c0001t0005g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.333+188T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33372101 | ||||||
| chr1:33372173
|
T | G | 1 | a0001c0001t0027g0317 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.333+116A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 3/14 | chr1 | 33372173 | ||||||
| chr1:33372564
|
TGTGACCA others(5): Show |
T | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-129_175-118del others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372564 | ||||||
| chr1:33372572
|
C | T | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.175-125G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372572 | ||||||
| chr1:33372578
|
C | G | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-131G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372578 | ||||||
| chr1:33372579
|
A | G | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-132T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372579 | ||||||
| chr1:33372582
|
C | A | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-135G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372582 | ||||||
| chr1:33372583
|
A | G | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-136T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372583 | ||||||
| chr1:33372584
|
A | T | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-137T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372584 | ||||||
| chr1:33372585
|
T | G | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-138A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372585 | ||||||
| chr1:33372586
|
T | G | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-139A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372586 | ||||||
| chr1:33372588
|
T | A | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-141A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372588 | ||||||
| chr1:33372591
|
C | A | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.175-144G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372591 | ||||||
| chr1:33372688
|
C | T | 1 | a0002c0004t0004g0027 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.175-241G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372688 | ||||||
| chr1:33372762
|
C | T | 67 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(64): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.175-315G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372762 | ||||||
| chr1:33372944
|
G | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.175-497C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372944 | ||||||
| chr1:33372951
|
T | C | 6 | a0002c0004t0004g0015a0002c0004t0004g0030a0002c0004t0004g0033others(3): Show | 6 | HG01106.hp1 HG01433.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-504A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33372951 | ||||||
| chr1:33373014
|
A | G | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.175-567T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373014 | ||||||
| chr1:33373028
|
C | T | 1 | a0001c0001t0005g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.175-581G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373028 | ||||||
| chr1:33373120
|
C | CT | 205 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(202): Show | 207 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.175-674dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373120 | ||||||
| chr1:33373147
|
C | T | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.175-700G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373147 | ||||||
| chr1:33373179
|
G | A | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-732C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373179 | ||||||
| chr1:33373323
|
G | A | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.175-876C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373323 | ||||||
| chr1:33373367
|
C | T | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.175-920G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373367 | ||||||
| chr1:33373386
|
G | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0131 | 2 | HG01516.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.175-939C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373386 | ||||||
| chr1:33373403
|
G | A | 1 | a0002c0004t0004g0016 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.175-956C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373403 | ||||||
| chr1:33373666
|
C | T | 3 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248 | 3 | HG02257.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.175-1219G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373666 | ||||||
| chr1:33373940
|
T | C | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.174+1426A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373940 | ||||||
| chr1:33373969
|
C | T | 9 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0111others(6): Show | 9 | HG00140.hp2 HG00323.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+1397G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373969 | ||||||
| chr1:33373990
|
C | T | 66 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(63): Show | 67 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.174+1376G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33373990 | ||||||
| chr1:33374280
|
C | T | 1 | a0003c0005t0002g0275 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174+1086G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33374280 | ||||||
| chr1:33374418
|
T | C | 2 | a0001c0001t0011g0172a0001c0001t0011g0173 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.174+948A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33374418 | ||||||
| chr1:33374749
|
C | A | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.174+617G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33374749 | ||||||
| chr1:33374888
|
T | A | 1 | a0001c0001t0005g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.174+478A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33374888 | ||||||
| chr1:33374923
|
G | A | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.174+443C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33374923 | ||||||
| chr1:33375028
|
G | A | 43 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(40): Show | 43 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.174+338C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33375028 | ||||||
| chr1:33375061
|
G | A | 2 | a0001c0001t0002g0319a0001c0001t0002g0320 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.174+305C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33375061 | ||||||
| chr1:33375194
|
T | G | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.174+172A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33375194 | ||||||
| chr1:33375257
|
G | A | 67 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(64): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.174+109C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33375257 | ||||||
| chr1:33375262
|
A | T | 2 | a0003c0005t0002g0293a0003c0005t0002g0294 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.174+104T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33375262 | ||||||
| chr1:33375353
|
A | G | 2 | a0001c0001t0012g0076a0001c0001t0012g0083 | 2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.174+13T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 2/14 | chr1 | 33375353 | ||||||
| chr1:33375682
|
C | T | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-54-89G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33375682 | ||||||
| chr1:33375729
|
C | T | 8 | a0001c0002t0001g0006a0001c0002t0001g0109a0001c0002t0001g0113others(5): Show | 9 | HG00597.hp2 NA18964.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54-136G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33375729 | ||||||
| chr1:33375751
|
A | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-158T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33375751 | ||||||
| chr1:33375876
|
G | A | 1 | a0001c0001t0002g0346 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-54-283C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33375876 | ||||||
| chr1:33376195
|
C | T | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-54-602G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376195 | ||||||
| chr1:33376226
|
G | C | 67 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(64): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-54-633C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376226 | ||||||
| chr1:33376258
|
C | T | 204 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(201): Show | 206 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.-54-665G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376258 | ||||||
| chr1:33376419
|
C | T | 2 | a0002c0004t0004g0070a0002c0004t0004g0071 | 2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-54-826G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376419 | ||||||
| chr1:33376452
|
T | C | 272 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(269): Show | 280 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.-54-859A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376452 | ||||||
| chr1:33376543
|
C | T | 1 | a0001c0001t0015g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-54-950G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376543 | ||||||
| chr1:33376577
|
A | G | 1 | a0001c0002t0001g0118 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-54-984T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376577 | ||||||
| chr1:33376668
|
T | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-1075A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376668 | ||||||
| chr1:33376726
|
C | T | 2 | a0002c0004t0004g0024a0002c0004t0004g0025 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-54-1133G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33376726 | ||||||
| chr1:33377010
|
T | G | 1 | a0001c0001t0005g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-54-1417A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33377010 | ||||||
| chr1:33377030
|
TG | T | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54-1438delC | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33377030 | ||||||
| chr1:33377040
|
G | A | 1 | a0001c0001t0002g0341 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-54-1447C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33377040 | ||||||
| chr1:33377064
|
A | G | 1 | a0001c0002t0001g0161 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-54-1471T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33377064 | ||||||
| chr1:33377134
|
C | T | 272 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(269): Show | 280 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.-54-1541G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33377134 | ||||||
| chr1:33377162
|
T | G | 53 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(50): Show | 53 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-54-1569A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33377162 | ||||||
| chr1:33377165
|
C | T | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-54-1572G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33377165 | ||||||
| chr1:33377467
|
G | A | 67 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(64): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-54-1874C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33377467 | ||||||
| chr1:33378043
|
T | C | 1 | a0001c0002t0021g0138 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-54-2450A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33378043 | ||||||
| chr1:33378647
|
A | T | 1 | a0001c0001t0002g0328 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-54-3054T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33378647 | ||||||
| chr1:33379101
|
A | G | 1 | a0001c0001t0005g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-54-3508T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379101 | ||||||
| chr1:33379156
|
G | A | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54-3563C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379156 | ||||||
| chr1:33379185
|
C | T | 4 | a0001c0002t0001g0142a0001c0006t0003g0264a0001c0006t0003g0265others(1): Show | 4 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54-3592G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379185 | ||||||
| chr1:33379244
|
C | T | 68 | a0001c0001t0005g0082a0001c0001t0006g0246a0001c0001t0006g0247others(65): Show | 74 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-54-3651G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379244 | ||||||
| chr1:33379293
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-54-3700C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379293 | ||||||
| chr1:33379309
|
A | AC | 14 | a0001c0001t0002g0300a0001c0001t0002g0311a0001c0001t0005g0084others(11): Show | 14 | HG01496.hp1 HG01515.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-54-3717dupG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379309 | ||||||
| chr1:33379309
|
A | C | 3 | a0001c0001t0005g0262a0001c0002t0001g0174a0002c0004t0004g0045 | 3 | HG00735.hp1 HG02738.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-54-3716T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379309 | ||||||
| chr1:33379312
|
C | T | 1 | a0003c0005t0002g0279 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-54-3719G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379312 | ||||||
| chr1:33379319
|
TGCCCCCC others(19): Show |
T | 1 | a0001c0003t0003g0231 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-54-3752_-54-3727d others(28): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379319 | ||||||
| chr1:33379320
|
G | GC | 7 | a0001c0001t0009g0298a0001c0002t0001g0142a0001c0002t0001g0163others(4): Show | 7 | HG00621.hp2 HG01167.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-54-3728dupG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379320 | ||||||
| chr1:33379328
|
GCCCCCCA others(1): Show |
G | 8 | a0001c0003t0003g0198a0001c0003t0003g0203a0001c0003t0003g0204others(5): Show | 8 | HG02129.hp2 NA18939.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-54-3743_-54-3736d others(10): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379328 | ||||||
| chr1:33379335
|
A | AC | 28 | a0001c0001t0002g0301a0001c0001t0002g0319a0001c0001t0002g0326others(25): Show | 28 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.-54-3743dupG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379335 | ||||||
| chr1:33379345
|
C | T | 1 | a0003c0005t0002g0268 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-54-3752G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379345 | ||||||
| chr1:33379353
|
G | GC | 17 | a0001c0001t0002g0332a0001c0001t0005g0072a0001c0001t0005g0079others(14): Show | 17 | HG01106.hp1 HG01192.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.-54-3761dupG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379353 | ||||||
| chr1:33379353
|
GC | G | 12 | a0001c0002t0001g0156a0001c0002t0001g0158a0001c0002t0001g0159others(9): Show | 12 | HG00140.hp1 HG00408.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54-3761delG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379353 | ||||||
| chr1:33379356
|
C | A | 1 | a0001c0001t0005g0091 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-54-3763G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379356 | ||||||
| chr1:33379357
|
C | T | 87 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(84): Show | 88 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.-54-3764G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379357 | ||||||
| chr1:33379372
|
T | TC | 15 | a0001c0001t0002g0300a0001c0001t0005g0259a0001c0001t0005g0260others(12): Show | 15 | HG00558.hp2 HG01192.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-54-3780dupG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379372 | ||||||
| chr1:33379373
|
C | G | 74 | a0001c0001t0002g0323a0001c0001t0002g0327a0001c0001t0002g0332others(71): Show | 80 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-54-3780G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379373 | ||||||
| chr1:33379413
|
T | C | 267 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(264): Show | 275 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.-54-3820A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379413 | ||||||
| chr1:33379445
|
A | G | 205 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(202): Show | 207 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(204): Show |
intron_variant | MODIFIER | c.-54-3852T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379445 | ||||||
| chr1:33379446
|
T | TC | 43 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-54-3854dupG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379446 | ||||||
| chr1:33379527
|
G | A | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-54-3934C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379527 | ||||||
| chr1:33379597
|
C | T | 1 | a0001c0003t0001g0201 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-54-4004G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379597 | ||||||
| chr1:33379710
|
C | A | 1 | a0003c0005t0002g0284 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-54-4117G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379710 | ||||||
| chr1:33379744
|
C | T | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-54-4151G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379744 | ||||||
| chr1:33379759
|
C | T | 1 | a0001c0003t0003g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-54-4166G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379759 | ||||||
| chr1:33379778
|
T | A | 44 | a0001c0001t0002g0332a0001c0001t0005g0072a0001c0001t0005g0073others(41): Show | 44 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-54-4185A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379778 | ||||||
| chr1:33379862
|
C | CCTT | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-4270_-54-4269i others(5): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33379862 | ||||||
| chr1:33380027
|
C | A | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-54-4434G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33380027 | ||||||
| chr1:33380057
|
G | A | 91 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(88): Show | 92 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.-54-4464C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33380057 | ||||||
| chr1:33380095
|
G | T | 1 | a0003c0005t0002g0293 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-54-4502C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33380095 | ||||||
| chr1:33380177
|
A | G | 2 | a0003c0005t0002g0283a0003c0005t0002g0288 | 2 | HG00423.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-54-4584T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33380177 | ||||||
| chr1:33380218
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-54-4625T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33380218 | ||||||
| chr1:33380460
|
A | G | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-54-4867T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33380460 | ||||||
| chr1:33381220
|
C | T | 1 | a0003c0005t0002g0275 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-54-5627G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33381220 | ||||||
| chr1:33381576
|
A | G | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-5983T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33381576 | ||||||
| chr1:33381994
|
C | T | 1 | a0002c0004t0004g0029 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-54-6401G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33381994 | ||||||
| chr1:33382098
|
C | G | 1 | a0001c0001t0002g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-54-6505G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382098 | ||||||
| chr1:33382139
|
T | G | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-6546A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382139 | ||||||
| chr1:33382235
|
C | T | 1 | a0001c0001t0005g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-54-6642G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382235 | ||||||
| chr1:33382399
|
C | T | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-54-6806G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382399 | ||||||
| chr1:33382468
|
C | T | 1 | a0001c0003t0003g0216 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-54-6875G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382468 | ||||||
| chr1:33382470
|
T | C | 1 | a0001c0003t0003g0216 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-54-6877A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382470 | ||||||
| chr1:33382471
|
C | T | 1 | a0001c0003t0003g0216 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-54-6878G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382471 | ||||||
| chr1:33382534
|
A | G | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-54-6941T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382534 | ||||||
| chr1:33382997
|
C | T | 1 | a0001c0003t0003g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-54-7404G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33382997 | ||||||
| chr1:33383038
|
G | A | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-54-7445C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383038 | ||||||
| chr1:33383103
|
C | T | 1 | a0001c0001t0005g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-54-7510G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383103 | ||||||
| chr1:33383263
|
G | A | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54-7670C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383263 | ||||||
| chr1:33383386
|
G | A | 7 | a0001c0002t0001g0111a0001c0002t0001g0129a0001c0002t0001g0131others(4): Show | 7 | HG00140.hp2 HG00323.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.-54-7793C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383386 | ||||||
| chr1:33383789
|
C | T | 1 | a0002c0004t0004g0020 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-54-8196G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383789 | ||||||
| chr1:33383796
|
G | A | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-54-8203C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383796 | ||||||
| chr1:33383903
|
CAG | C | 48 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(45): Show | 48 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-54-8312_-54-8311d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383903 | ||||||
| chr1:33383911
|
G | T | 43 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(40): Show | 43 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-54-8318C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383911 | ||||||
| chr1:33383948
|
C | T | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-54-8355G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383948 | ||||||
| chr1:33383957
|
C | T | 2 | a0003c0005t0002g0290a0003c0005t0025g0351 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-54-8364G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33383957 | ||||||
| chr1:33384002
|
G | C | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-54-8409C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33384002 | ||||||
| chr1:33384017
|
G | A | 1 | a0001c0002t0001g0148 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-54-8424C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33384017 | ||||||
| chr1:33384053
|
C | T | 1 | a0001c0001t0011g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-54-8460G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33384053 | ||||||
| chr1:33384122
|
G | A | 1 | a0001c0008t0002g0347 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-54-8529C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33384122 | ||||||
| chr1:33384323
|
G | C | 1 | a0001c0002t0001g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-54-8730C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33384323 | ||||||
| chr1:33384371
|
A | C | 1 | a0002c0004t0004g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-54-8778T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33384371 | ||||||
| chr1:33384674
|
G | A | 1 | a0001c0001t0005g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-54-9081C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33384674 | ||||||
| chr1:33384965
|
C | G | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-9372G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33384965 | ||||||
| chr1:33385155
|
A | C | 52 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(49): Show | 52 | HG00558.hp1 HG00597.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-54-9562T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385155 | ||||||
| chr1:33385289
|
T | C | 48 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(45): Show | 48 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-54-9696A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385289 | ||||||
| chr1:33385318
|
C | A | 1 | a0001c0001t0002g0339 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-54-9725G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385318 | ||||||
| chr1:33385329
|
A | G | 3 | a0001c0001t0002g0267a0001c0001t0002g0299a0001c0001t0002g0357 | 3 | HG01884.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-54-9736T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385329 | ||||||
| chr1:33385347
|
A | G | 2 | a0001c0006t0006g0180a0001c0006t0020g0181 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-54-9754T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385347 | ||||||
| chr1:33385368
|
A | G | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-54-9775T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385368 | ||||||
| chr1:33385444
|
G | C | 11 | a0001c0002t0001g0007a0001c0002t0001g0158a0001c0002t0001g0159others(8): Show | 12 | HG00408.hp1 HG00735.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54-9851C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385444 | ||||||
| chr1:33385539
|
G | T | 4 | a0001c0001t0002g0297a0001c0001t0002g0336a0001c0001t0002g0340others(1): Show | 4 | NA18953.hp1 NA18974.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54-9946C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385539 | ||||||
| chr1:33385565
|
A | T | 1 | a0001c0002t0001g0112 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-54-9972T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385565 | ||||||
| chr1:33385766
|
A | G | 3 | a0001c0008t0002g0347a0001c0008t0002g0349a0008c0009t0002g0348 | 3 | HG00639.hp2 HG01243.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-54-10173T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385766 | ||||||
| chr1:33385798
|
A | AT | 62 | a0001c0001t0005g0183a0001c0001t0008g0177a0001c0001t0008g0178others(59): Show | 63 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-54-10206_-54-1020 others(5): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385798 | ||||||
| chr1:33385798
|
A | ATT | 3 | a0002c0004t0004g0021a0002c0004t0004g0028a0002c0004t0004g0054 | 3 | HG00558.hp2 HG02074.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-54-10206_-54-1020 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385798 | ||||||
| chr1:33385799
|
A | T | 116 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(113): Show | 117 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.-54-10206T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385799 | ||||||
| chr1:33385944
|
G | A | 1 | a0001c0006t0006g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-54-10351C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33385944 | ||||||
| chr1:33386077
|
G | A | 1 | a0002c0004t0004g0049 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-54-10484C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386077 | ||||||
| chr1:33386181
|
A | G | 85 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(82): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-54-10588T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386181 | ||||||
| chr1:33386184
|
G | C | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-10591C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386184 | ||||||
| chr1:33386205
|
C | T | 43 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(40): Show | 43 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-54-10612G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386205 | ||||||
| chr1:33386256
|
G | A | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-10663C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386256 | ||||||
| chr1:33386388
|
C | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-54-10795G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386388 | ||||||
| chr1:33386409
|
C | G | 174 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(171): Show | 181 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.-54-10816G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386409 | ||||||
| chr1:33386803
|
C | T | 3 | a0001c0001t0005g0257a0001c0001t0011g0172a0001c0001t0011g0173 | 3 | HG02486.hp2 HG03471.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-54-11210G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386803 | ||||||
| chr1:33386855
|
T | C | 174 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(171): Show | 181 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.-54-11262A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33386855 | ||||||
| chr1:33387051
|
T | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-54-11458A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387051 | ||||||
| chr1:33387272
|
G | T | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-54-11679C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387272 | ||||||
| chr1:33387345
|
C | T | 4 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0153others(1): Show | 6 | HG01891.hp1 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54-11752G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387345 | ||||||
| chr1:33387464
|
C | A | 1 | a0001c0001t0002g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-54-11871G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387464 | ||||||
| chr1:33387707
|
G | A | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-54-12114C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387707 | ||||||
| chr1:33387812
|
C | T | 3 | a0001c0008t0002g0347a0001c0008t0002g0349a0008c0009t0002g0348 | 3 | HG00639.hp2 HG01243.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-54-12219G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387812 | ||||||
| chr1:33387857
|
G | A | 6 | a0001c0003t0003g0198a0001c0003t0003g0204a0001c0003t0003g0221others(3): Show | 6 | HG02129.hp2 NA18939.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54-12264C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387857 | ||||||
| chr1:33387905
|
C | CCCT | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54-12315_-54-1231 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387905 | ||||||
| chr1:33387922
|
G | C | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-54-12329C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33387922 | ||||||
| chr1:33388103
|
G | A | 1 | a0001c0006t0006g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-54-12510C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388103 | ||||||
| chr1:33388318
|
A | AT | 71 | a0001c0001t0002g0300a0001c0001t0005g0080a0001c0001t0005g0256others(68): Show | 73 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-54-12726dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388318 | ||||||
| chr1:33388318
|
A | ATT | 11 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(8): Show | 11 | HG00621.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-54-12727_-54-1272 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388318 | ||||||
| chr1:33388318
|
AT | A | 15 | a0001c0001t0002g0327a0001c0001t0002g0328a0001c0001t0005g0075others(12): Show | 15 | HG00323.hp2 HG00738.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-54-12726delA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388318 | ||||||
| chr1:33388347
|
G | T | 1 | a0001c0003t0003g0208 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-54-12754C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388347 | ||||||
| chr1:33388348
|
A | T | 1 | a0001c0003t0003g0208 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-54-12755T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388348 | ||||||
| chr1:33388412
|
C | T | 85 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006others(82): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-54-12819G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388412 | ||||||
| chr1:33388431
|
C | G | 1 | a0002c0004t0004g0042 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-54-12838G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388431 | ||||||
| chr1:33388451
|
G | A | 1 | a0001c0003t0003g0216 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-54-12858C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388451 | ||||||
| chr1:33388810
|
GTTCTGAG others(12): Show |
G | 1 | a0001c0001t0014g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-54-13236_-54-1321 others(23): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33388810 | ||||||
| chr1:33389059
|
T | TA | 93 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(90): Show | 94 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-54-13467dupT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389059 | ||||||
| chr1:33389059
|
T | TAA | 66 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(63): Show | 72 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-54-13468_-54-1346 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389059 | ||||||
| chr1:33389072
|
A | AAG | 103 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(100): Show | 104 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-54-13480_-54-1347 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389072 | ||||||
| chr1:33389072
|
A | G | 1 | a0002c0004t0004g0053 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-54-13479T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389072 | ||||||
| chr1:33389092
|
AC | A | 4 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(1): Show | 4 | HG02572.hp1 HG03471.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54-13500delG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389092 | ||||||
| chr1:33389093
|
C | A | 10 | a0001c0001t0005g0183a0001c0006t0003g0264a0001c0006t0003g0265others(7): Show | 10 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54-13500G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389093 | ||||||
| chr1:33389097
|
C | T | 3 | a0002c0004t0004g0045a0002c0004t0004g0052a0002c0004t0004g0263 | 3 | HG00735.hp1 HG01074.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-54-13504G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389097 | ||||||
| chr1:33389545
|
C | CCCTGGCA others(6): Show |
1 | a0001c0002t0001g0244 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-54-13965_-54-1395 others(17): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389545 | ||||||
| chr1:33389603
|
A | G | 1 | a0001c0001t0011g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-54-14010T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389603 | ||||||
| chr1:33389648
|
C | T | 9 | a0001c0002t0001g0112a0001c0002t0001g0115a0001c0002t0001g0116others(6): Show | 9 | HG00438.hp1 NA18941.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-54-14055G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389648 | ||||||
| chr1:33389731
|
G | A | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-54-14138C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33389731 | ||||||
| chr1:33390050
|
A | G | 1 | a0001c0002t0021g0138 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-54-14457T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390050 | ||||||
| chr1:33390122
|
C | T | 2 | a0001c0001t0015g0270a0001c0001t0015g0291 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-54-14529G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390122 | ||||||
| chr1:33390202
|
A | G | 1 | a0003c0005t0002g0295 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-54-14609T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390202 | ||||||
| chr1:33390222
|
T | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-14629A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390222 | ||||||
| chr1:33390255
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-14662G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390255 | ||||||
| chr1:33390363
|
T | C | 1 | a0001c0006t0020g0181 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-54-14770A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390363 | ||||||
| chr1:33390392
|
C | T | 2 | a0002c0004t0013g0012a0002c0004t0013g0013 | 2 | HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-54-14799G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390392 | ||||||
| chr1:33390411
|
C | G | 1 | a0001c0003t0003g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-54-14818G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390411 | ||||||
| chr1:33390436
|
CTG | C | 6 | a0001c0003t0003g0001a0001c0003t0003g0206a0001c0003t0003g0219others(3): Show | 9 | HG00423.hp1 HG02027.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-54-14845_-54-1484 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390436 | ||||||
| chr1:33390482
|
A | C | 1 | a0001c0001t0002g0309 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-54-14889T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390482 | ||||||
| chr1:33390570
|
A | G | 1 | a0001c0006t0003g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-54-14977T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390570 | ||||||
| chr1:33390605
|
C | T | 1 | a0001c0003t0003g0205 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-54-15012G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390605 | ||||||
| chr1:33390685
|
AT | A | 105 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(102): Show | 108 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.-54-15093delA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390685 | ||||||
| chr1:33390685
|
ATT | A | 104 | a0001c0001t0002g0333a0001c0001t0005g0072a0001c0001t0005g0073others(101): Show | 110 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-54-15094_-54-1509 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390685 | ||||||
| chr1:33390685
|
ATTT | A | 66 | a0001c0001t0005g0183a0001c0001t0008g0176a0001c0001t0008g0177others(63): Show | 67 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.-54-15095_-54-1509 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390685 | ||||||
| chr1:33390700
|
T | C | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-54-15107A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390700 | ||||||
| chr1:33390862
|
GC | G | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-15270delG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33390862 | ||||||
| chr1:33391023
|
C | T | 1 | a0002c0004t0004g0045 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-54-15430G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33391023 | ||||||
| chr1:33391146
|
G | C | 7 | a0003c0005t0002g0269a0003c0005t0002g0275a0003c0005t0002g0284others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54-15553C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33391146 | ||||||
| chr1:33391394
|
A | C | 3 | a0001c0003t0003g0190a0001c0003t0003g0200a0001c0003t0003g0232 | 3 | NA18612.hp1 NA18991.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-54-15801T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33391394 | ||||||
| chr1:33391427
|
G | A | 6 | a0001c0001t0005g0183a0001c0006t0003g0264a0001c0006t0003g0265others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54-15834C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33391427 | ||||||
| chr1:33391506
|
C | T | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-54-15913G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33391506 | ||||||
| chr1:33391551
|
T | C | 2 | a0001c0006t0006g0180a0001c0006t0020g0181 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-54-15958A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33391551 | ||||||
| chr1:33391641
|
T | G | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-54-16048A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33391641 | ||||||
| chr1:33391653
|
GA | G | 98 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(95): Show | 99 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.-54-16061delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33391653 | ||||||
| chr1:33392165
|
G | A | 1 | a0001c0001t0005g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-54-16572C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392165 | ||||||
| chr1:33392167
|
G | GCA | 120 | a0001c0001t0002g0285a0001c0001t0005g0074a0001c0001t0005g0075others(117): Show | 127 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-54-16576_-54-1657 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392167 | ||||||
| chr1:33392167
|
G | GCACA | 18 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0081others(15): Show | 18 | HG01123.hp2 HG01192.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.-54-16578_-54-1657 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392167 | ||||||
| chr1:33392167
|
GCA | G | 65 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(62): Show | 65 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.-54-16576_-54-1657 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392167 | ||||||
| chr1:33392193
|
A | C | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-16600T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392193 | ||||||
| chr1:33392207
|
A | G | 1 | a0001c0001t0005g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-54-16614T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392207 | ||||||
| chr1:33392291
|
C | T | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-54-16698G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392291 | ||||||
| chr1:33392359
|
T | G | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-16766A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392359 | ||||||
| chr1:33392387
|
C | G | 1 | a0001c0001t0005g0256 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-54-16794G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392387 | ||||||
| chr1:33392422
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-16829G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392422 | ||||||
| chr1:33392926
|
C | A | 1 | a0001c0002t0001g0174 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-54-17333G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392926 | ||||||
| chr1:33392992
|
T | C | 1 | a0001c0003t0003g0205 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-54-17399A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33392992 | ||||||
| chr1:33393059
|
C | G | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-54-17466G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393059 | ||||||
| chr1:33393100
|
G | A | 53 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(50): Show | 53 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-54-17507C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393100 | ||||||
| chr1:33393195
|
C | T | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-54-17602G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393195 | ||||||
| chr1:33393216
|
C | T | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-54-17623G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393216 | ||||||
| chr1:33393272
|
C | T | 276 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(273): Show | 284 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.-54-17679G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393272 | ||||||
| chr1:33393463
|
G | GT | 154 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(151): Show | 156 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.-54-17871dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393463 | ||||||
| chr1:33393463
|
G | GTT | 105 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(102): Show | 111 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-54-17872_-54-1787 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393463 | ||||||
| chr1:33393463
|
G | GTTT | 7 | a0001c0001t0005g0094a0001c0001t0005g0262a0001c0001t0008g0176others(4): Show | 7 | HG01175.hp1 HG02738.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-54-17873_-54-1787 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393463 | ||||||
| chr1:33393666
|
C | A | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-54-18073G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393666 | ||||||
| chr1:33393724
|
A | AAACGATG others(41): Show |
271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-18132_-54-1813 others(52): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393724 | ||||||
| chr1:33393798
|
T | G | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-54-18205A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393798 | ||||||
| chr1:33393886
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-18293G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393886 | ||||||
| chr1:33393981
|
A | G | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54-18388T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33393981 | ||||||
| chr1:33394079
|
T | C | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-54-18486A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394079 | ||||||
| chr1:33394080
|
A | T | 1 | a0002c0004t0004g0066 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-54-18487T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394080 | ||||||
| chr1:33394129
|
A | C | 1 | a0003c0005t0026g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-54-18536T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394129 | ||||||
| chr1:33394138
|
C | T | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-18545G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394138 | ||||||
| chr1:33394170
|
T | A | 1 | a0001c0001t0005g0095 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-54-18577A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394170 | ||||||
| chr1:33394174
|
T | TA | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54-18582dupT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394174 | ||||||
| chr1:33394355
|
T | TA | 64 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-54-18763dupT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394355 | ||||||
| chr1:33394355
|
TA | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-18763delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394355 | ||||||
| chr1:33394449
|
C | A | 2 | a0001c0002t0001g0104a0001c0002t0001g0105 | 2 | HG03017.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-54-18856G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394449 | ||||||
| chr1:33394700
|
G | A | 1 | a0001c0001t0005g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-54-19107C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394700 | ||||||
| chr1:33394829
|
C | T | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-54-19236G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33394829 | ||||||
| chr1:33395288
|
G | A | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-54-19695C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395288 | ||||||
| chr1:33395294
|
C | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-19701G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395294 | ||||||
| chr1:33395357
|
G | A | 1 | a0001c0003t0003g0218 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-54-19764C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395357 | ||||||
| chr1:33395449
|
AAAAT | A | 164 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(161): Show | 169 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.-54-19860_-54-1985 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395449 | ||||||
| chr1:33395449
|
AAAATAAA others(1): Show |
A | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-54-19864_-54-1985 others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395449 | ||||||
| chr1:33395583
|
G | C | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-19990C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395583 | ||||||
| chr1:33395626
|
T | C | 1 | a0001c0002t0001g0254 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-54-20033A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395626 | ||||||
| chr1:33395676
|
G | A | 1 | a0001c0001t0005g0095 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-54-20083C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395676 | ||||||
| chr1:33395746
|
C | T | 1 | a0001c0001t0005g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-54-20153G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395746 | ||||||
| chr1:33395826
|
T | C | 1 | a0001c0003t0003g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-54-20233A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33395826 | ||||||
| chr1:33396252
|
A | G | 154 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(151): Show | 161 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.-54-20659T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396252 | ||||||
| chr1:33396343
|
C | T | 1 | a0003c0005t0002g0268 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-54-20750G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396343 | ||||||
| chr1:33396384
|
A | G | 1 | a0001c0006t0006g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-54-20791T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396384 | ||||||
| chr1:33396389
|
G | T | 2 | a0003c0005t0002g0275a0003c0005t0002g0284 | 2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-54-20796C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396389 | ||||||
| chr1:33396436
|
C | T | 63 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(60): Show | 64 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-54-20843G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396436 | ||||||
| chr1:33396443
|
A | G | 1 | a0003c0005t0002g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-54-20850T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396443 | ||||||
| chr1:33396491
|
A | T | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-54-20898T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396491 | ||||||
| chr1:33396678
|
C | T | 44 | a0001c0001t0002g0272a0001c0001t0002g0297a0001c0001t0002g0300others(41): Show | 44 | HG00558.hp1 HG00597.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.-54-21085G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396678 | ||||||
| chr1:33396693
|
G | A | 61 | a0002c0004t0004g0003a0002c0004t0004g0014a0002c0004t0004g0015others(58): Show | 62 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-54-21100C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396693 | ||||||
| chr1:33396803
|
G | C | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-54-21210C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396803 | ||||||
| chr1:33396864
|
C | T | 2 | a0001c0003t0003g0191a0001c0003t0003g0227 | 2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-54-21271G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396864 | ||||||
| chr1:33396916
|
A | G | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-21323T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33396916 | ||||||
| chr1:33397290
|
G | A | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-54-21697C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33397290 | ||||||
| chr1:33397504
|
A | C | 2 | a0001c0003t0003g0203a0001c0003t0003g0207 | 2 | NA18953.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-54-21911T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33397504 | ||||||
| chr1:33397910
|
A | G | 3 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248 | 3 | HG02257.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-54-22317T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33397910 | ||||||
| chr1:33397972
|
G | A | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-54-22379C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33397972 | ||||||
| chr1:33397973
|
C | A | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-54-22380G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33397973 | ||||||
| chr1:33398095
|
T | C | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-22502A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33398095 | ||||||
| chr1:33398136
|
C | T | 1 | a0001c0006t0006g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-54-22543G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33398136 | ||||||
| chr1:33398541
|
T | G | 1 | a0002c0004t0004g0049 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-54-22948A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33398541 | ||||||
| chr1:33398745
|
C | A | 1 | a0001c0002t0001g0155 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-54-23152G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33398745 | ||||||
| chr1:33398837
|
G | A | 1 | a0001c0001t0005g0262 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-54-23244C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33398837 | ||||||
| chr1:33398896
|
C | T | 1 | a0001c0003t0003g0205 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-54-23303G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33398896 | ||||||
| chr1:33398921
|
C | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-23328G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33398921 | ||||||
| chr1:33398996
|
G | T | 1 | a0002c0004t0004g0051 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-54-23403C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33398996 | ||||||
| chr1:33399138
|
C | T | 1 | a0002c0004t0004g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-54-23545G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399138 | ||||||
| chr1:33399141
|
G | A | 1 | a0001c0001t0002g0321 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-54-23548C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399141 | ||||||
| chr1:33399229
|
G | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-54-23636C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399229 | ||||||
| chr1:33399336
|
GCTCACA | G | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-54-23749_-54-2374 others(10): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399336 | ||||||
| chr1:33399407
|
G | A | 3 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248 | 3 | HG02257.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-54-23814C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399407 | ||||||
| chr1:33399467
|
C | T | 32 | a0001c0001t0002g0285a0003c0005t0002g0268a0003c0005t0002g0269others(29): Show | 32 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-54-23874G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399467 | ||||||
| chr1:33399502
|
T | C | 1 | a0001c0001t0005g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-54-23909A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399502 | ||||||
| chr1:33399648
|
C | T | 1 | a0001c0002t0001g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-54-24055G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399648 | ||||||
| chr1:33399702
|
G | T | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-54-24109C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399702 | ||||||
| chr1:33399809
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-24216G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399809 | ||||||
| chr1:33399843
|
CA | C | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-24251delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399843 | ||||||
| chr1:33399954
|
T | G | 4 | a0001c0003t0003g0198a0001c0003t0003g0221a0001c0003t0003g0222others(1): Show | 4 | HG02129.hp2 NA18939.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54-24361A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33399954 | ||||||
| chr1:33400031
|
T | TA | 14 | a0001c0001t0005g0093a0001c0002t0001g0009a0001c0002t0001g0110others(11): Show | 15 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-54-24439dupT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400031 | ||||||
| chr1:33400031
|
TA | T | 10 | a0001c0001t0002g0336a0001c0001t0005g0255a0001c0001t0006g0246others(7): Show | 10 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-54-24439delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400031 | ||||||
| chr1:33400273
|
T | C | 5 | a0002c0004t0004g0035a0002c0004t0004g0036a0002c0004t0004g0037others(2): Show | 5 | NA18747.hp1 NA18950.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54-24680A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400273 | ||||||
| chr1:33400408
|
A | C | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-24815T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400408 | ||||||
| chr1:33400507
|
A | C | 4 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0153others(1): Show | 6 | HG01891.hp1 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54-24914T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400507 | ||||||
| chr1:33400604
|
G | C | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-54-25011C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400604 | ||||||
| chr1:33400633
|
A | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-25040T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400633 | ||||||
| chr1:33400650
|
C | A | 1 | a0001c0002t0001g0134 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-54-25057G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400650 | ||||||
| chr1:33400939
|
T | TAATAAAT others(1): Show |
3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-54-25354_-54-2534 others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400939 | ||||||
| chr1:33400986
|
T | G | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-54-25393A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33400986 | ||||||
| chr1:33401101
|
C | T | 1 | a0001c0006t0006g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-54-25508G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401101 | ||||||
| chr1:33401181
|
C | T | 1 | a0001c0003t0003g0198 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-54-25588G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401181 | ||||||
| chr1:33401269
|
T | A | 1 | a0001c0001t0005g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-54-25676A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401269 | ||||||
| chr1:33401334
|
A | G | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-54-25741T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401334 | ||||||
| chr1:33401424
|
T | C | 1 | a0001c0006t0006g0180 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-54-25831A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401424 | ||||||
| chr1:33401501
|
T | C | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-54-25908A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401501 | ||||||
| chr1:33401501
|
TCTAA | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-25912_-54-2590 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401501 | ||||||
| chr1:33401693
|
T | C | 1 | a0002c0004t0004g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-54-26100A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401693 | ||||||
| chr1:33401694
|
C | G | 43 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(40): Show | 43 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-54-26101G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401694 | ||||||
| chr1:33401711
|
C | T | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-54-26118G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401711 | ||||||
| chr1:33401846
|
C | A | 43 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(40): Show | 43 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-54-26253G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401846 | ||||||
| chr1:33401913
|
T | G | 1 | a0001c0001t0002g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-54-26320A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401913 | ||||||
| chr1:33401980
|
A | C | 1 | a0001c0003t0019g0224 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-54-26387T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33401980 | ||||||
| chr1:33402064
|
C | T | 4 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0094others(1): Show | 4 | NA18944.hp1 NA18981.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54-26471G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402064 | ||||||
| chr1:33402153
|
T | C | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-26560A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402153 | ||||||
| chr1:33402313
|
T | C | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-54-26720A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402313 | ||||||
| chr1:33402368
|
A | G | 1 | a0001c0001t0005g0092 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-54-26775T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402368 | ||||||
| chr1:33402388
|
T | G | 3 | a0003c0005t0002g0352a0003c0005t0002g0353a0003c0005t0002g0354 | 3 | NA18959.hp2 NA19001.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-54-26795A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402388 | ||||||
| chr1:33402464
|
C | T | 7 | a0001c0001t0002g0272a0001c0001t0002g0300a0001c0001t0002g0308others(4): Show | 7 | HG01071.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54-26871G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402464 | ||||||
| chr1:33402465
|
A | G | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-54-26872T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402465 | ||||||
| chr1:33402558
|
CA | C | 3 | a0001c0002t0001g0161a0001c0002t0001g0162a0001c0002t0001g0168 | 3 | HG00408.hp1 HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-54-26966delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402558 | ||||||
| chr1:33402673
|
C | T | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-54-27080G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402673 | ||||||
| chr1:33402835
|
C | CTTT | 168 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(165): Show | 175 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.-54-27245_-54-2724 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402835 | ||||||
| chr1:33402868
|
C | G | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-54-27275G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402868 | ||||||
| chr1:33402933
|
C | T | 43 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(40): Show | 43 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-54-27340G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402933 | ||||||
| chr1:33402934
|
A | G | 174 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(171): Show | 181 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.-54-27341T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402934 | ||||||
| chr1:33402947
|
T | G | 2 | a0003c0005t0002g0290a0003c0005t0025g0351 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-54-27354A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402947 | ||||||
| chr1:33402977
|
T | A | 3 | a0001c0001t0002g0332a0001c0001t0002g0333a0001c0001t0002g0334 | 3 | HG02647.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-54-27384A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33402977 | ||||||
| chr1:33403123
|
C | CT | 181 | a0001c0001t0002g0272a0001c0001t0002g0285a0001c0001t0002g0297others(178): Show | 183 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(180): Show |
intron_variant | MODIFIER | c.-54-27531dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403123 | ||||||
| chr1:33403123
|
C | CTT | 74 | a0001c0001t0002g0267a0001c0001t0002g0302a0001c0001t0002g0335others(71): Show | 80 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-54-27532_-54-2753 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403123 | ||||||
| chr1:33403123
|
C | CTTT | 10 | a0001c0003t0003g0189a0001c0003t0003g0191a0001c0003t0003g0197others(7): Show | 10 | HG00423.hp1 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-54-27533_-54-2753 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403123 | ||||||
| chr1:33403179
|
T | G | 6 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0099others(3): Show | 8 | HG01891.hp1 HG02723.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-54-27586A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403179 | ||||||
| chr1:33403189
|
C | T | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-54-27596G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403189 | ||||||
| chr1:33403251
|
C | T | 1 | a0001c0003t0003g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-54-27658G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403251 | ||||||
| chr1:33403270
|
C | G | 174 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(171): Show | 181 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.-54-27677G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403270 | ||||||
| chr1:33403283
|
C | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-54-27690G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403283 | ||||||
| chr1:33403360
|
C | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-55+27616G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403360 | ||||||
| chr1:33403376
|
C | T | 65 | a0001c0003t0003g0002a0001c0003t0003g0065a0001c0003t0003g0199others(62): Show | 68 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-55+27600G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403376 | ||||||
| chr1:33403423
|
C | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+27553G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403423 | ||||||
| chr1:33403459
|
T | A | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+27517A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403459 | ||||||
| chr1:33403623
|
G | T | 1 | a0001c0001t0002g0301 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-55+27353C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403623 | ||||||
| chr1:33403695
|
T | C | 3 | a0003c0005t0002g0268a0003c0005t0002g0290a0003c0005t0025g0351 | 3 | HG00642.hp1 HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-55+27281A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403695 | ||||||
| chr1:33403718
|
T | G | 1 | a0001c0002t0001g0250 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-55+27258A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403718 | ||||||
| chr1:33403739
|
A | G | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+27237T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33403739 | ||||||
| chr1:33404067
|
G | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-55+26909C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404067 | ||||||
| chr1:33404075
|
T | A | 1 | a0001c0003t0019g0224 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-55+26901A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404075 | ||||||
| chr1:33404098
|
T | C | 4 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0153others(1): Show | 6 | HG01891.hp1 HG03130.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-55+26878A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404098 | ||||||
| chr1:33404119
|
A | C | 2 | a0001c0001t0010g0010a0001c0001t0010g0344 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-55+26857T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404119 | ||||||
| chr1:33404205
|
C | T | 2 | a0001c0002t0001g0107a0001c0002t0001g0108 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-55+26771G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404205 | ||||||
| chr1:33404329
|
G | A | 2 | a0002c0004t0004g0024a0002c0004t0004g0025 | 2 | HG00323.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-55+26647C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404329 | ||||||
| chr1:33404792
|
T | G | 1 | a0001c0006t0006g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-55+26184A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404792 | ||||||
| chr1:33404893
|
T | A | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+26083A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404893 | ||||||
| chr1:33404971
|
T | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+26005A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33404971 | ||||||
| chr1:33405096
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+25880G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405096 | ||||||
| chr1:33405184
|
CT | C | 13 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0081others(10): Show | 13 | HG00323.hp2 HG01516.hp2 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.-55+25791delA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405184 | ||||||
| chr1:33405198
|
T | C | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+25778A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405198 | ||||||
| chr1:33405252
|
G | A | 2 | a0002c0004t0004g0042a0002c0004t0004g0043 | 2 | NA18968.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-55+25724C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405252 | ||||||
| chr1:33405387
|
C | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-55+25589G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405387 | ||||||
| chr1:33405471
|
G | A | 93 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(90): Show | 94 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-55+25505C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405471 | ||||||
| chr1:33405645
|
T | C | 4 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | HG00733.hp1 HG01071.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-55+25331A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405645 | ||||||
| chr1:33405684
|
C | T | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-55+25292G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405684 | ||||||
| chr1:33405707
|
T | C | 1 | a0001c0001t0005g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-55+25269A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405707 | ||||||
| chr1:33405808
|
TC | T | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+25167delG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405808 | ||||||
| chr1:33405907
|
G | C | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+25069C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33405907 | ||||||
| chr1:33406028
|
TCTTA | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+24944_-55+2494 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406028 | ||||||
| chr1:33406125
|
T | C | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-55+24851A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406125 | ||||||
| chr1:33406185
|
A | T | 356 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(353): Show | 369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.-55+24791T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406185 | ||||||
| chr1:33406393
|
T | C | 2 | a0001c0006t0003g0265a0001c0006t0003g0266 | 2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-55+24583A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406393 | ||||||
| chr1:33406585
|
G | C | 1 | a0001c0002t0001g0150 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-55+24391C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406585 | ||||||
| chr1:33406613
|
T | A | 2 | a0001c0001t0008g0177a0001c0001t0008g0178 | 2 | NA18965.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-55+24363A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406613 | ||||||
| chr1:33406643
|
TAGTCCAT others(4273): Show |
T | 1 | a0001c0002t0001g0098 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-55+20053_-55+2433 others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406643 | ||||||
| chr1:33406748
|
T | C | 1 | a0001c0003t0003g0240 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-55+24228A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406748 | ||||||
| chr1:33406761
|
T | C | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-55+24215A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406761 | ||||||
| chr1:33406770
|
G | A | 1 | a0001c0001t0002g0306 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-55+24206C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406770 | ||||||
| chr1:33406830
|
T | C | 1 | a0001c0001t0002g0341 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-55+24146A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406830 | ||||||
| chr1:33406872
|
CTCTT | C | 37 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0010g0344others(34): Show | 38 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.-55+24100_-55+2410 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406872 | ||||||
| chr1:33406992
|
T | C | 105 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(102): Show | 106 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.-55+23984A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33406992 | ||||||
| chr1:33407024
|
T | G | 1 | a0001c0003t0003g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-55+23952A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33407024 | ||||||
| chr1:33407374
|
A | T | 179 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(176): Show | 186 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.-55+23602T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33407374 | ||||||
| chr1:33407409
|
T | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+23567A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33407409 | ||||||
| chr1:33407413
|
G | T | 1 | a0001c0002t0001g0153 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-55+23563C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33407413 | ||||||
| chr1:33407414
|
A | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+23562T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33407414 | ||||||
| chr1:33407433
|
A | G | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+23543T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33407433 | ||||||
| chr1:33407434
|
C | A | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+23542G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33407434 | ||||||
| chr1:33407910
|
C | A | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+23066G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33407910 | ||||||
| chr1:33408158
|
C | T | 1 | a0003c0005t0002g0281 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-55+22818G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408158 | ||||||
| chr1:33408211
|
G | A | 1 | a0001c0001t0006g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-55+22765C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408211 | ||||||
| chr1:33408374
|
A | G | 1 | a0001c0001t0002g0328 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-55+22602T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408374 | ||||||
| chr1:33408428
|
C | G | 2 | a0001c0001t0002g0332a0001c0001t0002g0333 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-55+22548G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408428 | ||||||
| chr1:33408448
|
T | TG | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+22527_-55+2252 others(5): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408448 | ||||||
| chr1:33408448
|
T | TTTTTG | 179 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(176): Show | 186 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.-55+22523_-55+2252 others(9): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408448 | ||||||
| chr1:33408530
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-55+22446C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408530 | ||||||
| chr1:33408621
|
C | T | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+22355G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408621 | ||||||
| chr1:33408655
|
C | A | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+22321G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408655 | ||||||
| chr1:33408882
|
A | C | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+22094T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33408882 | ||||||
| chr1:33409461
|
C | A | 2 | a0001c0001t0015g0270a0001c0001t0015g0291 | 2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-55+21515G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33409461 | ||||||
| chr1:33409529
|
C | A | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-55+21447G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33409529 | ||||||
| chr1:33409876
|
T | C | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+21100A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33409876 | ||||||
| chr1:33410030
|
T | A | 1 | a0003c0005t0002g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-55+20946A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33410030 | ||||||
| chr1:33410030
|
T | C | 1 | a0001c0001t0009g0342 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-55+20946A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33410030 | ||||||
| chr1:33410550
|
C | T | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+20426G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33410550 | ||||||
| chr1:33410709
|
C | CCT | 3 | a0001c0008t0002g0347a0001c0008t0002g0349a0008c0009t0002g0348 | 3 | HG00639.hp2 HG01243.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-55+20265_-55+2026 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33410709 | ||||||
| chr1:33410788
|
A | G | 40 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(37): Show | 40 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.-55+20188T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33410788 | ||||||
| chr1:33410968
|
T | C | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+20008A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33410968 | ||||||
| chr1:33410972
|
A | G | 1 | a0003c0005t0002g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-55+20004T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33410972 | ||||||
| chr1:33411019
|
T | G | 1 | a0001c0002t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-55+19957A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411019 | ||||||
| chr1:33411446
|
G | GT | 10 | a0001c0001t0002g0323a0001c0001t0002g0346a0001c0001t0006g0246others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-55+19529dupA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411446 | ||||||
| chr1:33411453
|
G | T | 270 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(267): Show | 278 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.-55+19523C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411453 | ||||||
| chr1:33411456
|
G | T | 263 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(260): Show | 270 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.-55+19520C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411456 | ||||||
| chr1:33411459
|
G | T | 91 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(88): Show | 91 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-55+19517C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411459 | ||||||
| chr1:33411616
|
A | G | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-55+19360T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411616 | ||||||
| chr1:33411707
|
C | T | 1 | a0001c0001t0002g0306 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-55+19269G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411707 | ||||||
| chr1:33411710
|
G | A | 1 | a0001c0003t0003g0235 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-55+19266C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411710 | ||||||
| chr1:33411729
|
T | A | 1 | a0001c0002t0001g0147 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-55+19247A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411729 | ||||||
| chr1:33411855
|
G | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+19121C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33411855 | ||||||
| chr1:33412090
|
A | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+18886T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412090 | ||||||
| chr1:33412145
|
C | T | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-55+18831G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412145 | ||||||
| chr1:33412151
|
T | G | 1 | a0001c0001t0002g0328 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-55+18825A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412151 | ||||||
| chr1:33412207
|
C | T | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-55+18769G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412207 | ||||||
| chr1:33412275
|
G | C | 1 | a0002c0004t0004g0050 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-55+18701C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412275 | ||||||
| chr1:33412317
|
G | C | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+18659C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412317 | ||||||
| chr1:33412403
|
C | T | 1 | a0001c0001t0005g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-55+18573G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412403 | ||||||
| chr1:33412414
|
G | A | 1 | a0001c0002t0001g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-55+18562C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412414 | ||||||
| chr1:33412457
|
TACC | T | 52 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(49): Show | 52 | HG00558.hp1 HG00597.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-55+18516_-55+1851 others(7): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412457 | ||||||
| chr1:33412754
|
C | G | 5 | a0003c0005t0002g0279a0003c0005t0002g0280a0003c0005t0002g0282others(2): Show | 5 | HG00639.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+18222G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412754 | ||||||
| chr1:33412780
|
G | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+18196C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412780 | ||||||
| chr1:33412875
|
G | C | 1 | a0001c0001t0009g0342 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-55+18101C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412875 | ||||||
| chr1:33412927
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-55+18049C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412927 | ||||||
| chr1:33412946
|
GT | G | 36 | a0001c0001t0002g0285a0001c0001t0010g0010a0001c0001t0015g0270others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-55+18029delA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412946 | ||||||
| chr1:33412953
|
T | G | 107 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(104): Show | 113 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-55+18023A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33412953 | ||||||
| chr1:33413020
|
G | A | 1 | a0001c0001t0002g0329 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-55+17956C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413020 | ||||||
| chr1:33413118
|
C | T | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+17858G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413118 | ||||||
| chr1:33413139
|
G | A | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+17837C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413139 | ||||||
| chr1:33413235
|
G | A | 3 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248 | 3 | HG02257.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-55+17741C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413235 | ||||||
| chr1:33413292
|
G | C | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-55+17684C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413292 | ||||||
| chr1:33413715
|
T | A | 2 | a0002c0004t0013g0012a0002c0004t0013g0013 | 2 | HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-55+17261A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413715 | ||||||
| chr1:33413801
|
A | T | 1 | a0001c0001t0002g0305 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-55+17175T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413801 | ||||||
| chr1:33413844
|
T | C | 2 | a0003c0005t0002g0273a0003c0005t0002g0295 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-55+17132A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413844 | ||||||
| chr1:33413988
|
G | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+16988C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33413988 | ||||||
| chr1:33414116
|
A | G | 2 | a0001c0002t0001g0004a0001c0002t0001g0005 | 4 | HG01891.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-55+16860T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414116 | ||||||
| chr1:33414164
|
TTC | T | 4 | a0001c0003t0003g0190a0001c0003t0003g0202a0001c0003t0003g0203others(1): Show | 4 | NA18953.hp2 NA18978.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-55+16810_-55+1681 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414164 | ||||||
| chr1:33414172
|
C | CTG | 3 | a0001c0003t0003g0187a0001c0003t0003g0225a0001c0003t0003g0242 | 3 | HG00738.hp1 NA19078.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-55+16803_-55+1680 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414172 | ||||||
| chr1:33414173
|
T | TGTCA | 5 | a0001c0003t0003g0227a0001c0003t0003g0228a0001c0003t0003g0229others(2): Show | 5 | HG01346.hp2 HG02683.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+16802_-55+1680 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414173 | ||||||
| chr1:33414174
|
C | G | 48 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(45): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-55+16802G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414174 | ||||||
| chr1:33414175
|
T | A | 9 | a0001c0003t0003g0187a0001c0003t0003g0225a0001c0003t0003g0227others(6): Show | 9 | HG00738.hp1 HG01346.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.-55+16801A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414175 | ||||||
| chr1:33414175
|
TGTCA | T | 7 | a0001c0003t0003g0002a0001c0003t0003g0192a0001c0003t0003g0199others(4): Show | 9 | HG02074.hp2 HG02523.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-55+16797_-55+1680 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414175 | ||||||
| chr1:33414176
|
G | C | 49 | a0001c0003t0001g0194a0001c0003t0003g0001a0001c0003t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-55+16800C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414176 | ||||||
| chr1:33414176
|
G | GTCAC | 4 | a0001c0001t0002g0346a0001c0008t0002g0347a0001c0008t0002g0349others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-55+16796_-55+1679 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414176 | ||||||
| chr1:33414177
|
T | A | 49 | a0001c0003t0001g0194a0001c0003t0003g0001a0001c0003t0003g0008others(46): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-55+16799A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
T | TCA | 37 | a0001c0001t0002g0285a0001c0001t0005g0073a0001c0001t0005g0084others(34): Show | 37 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.-55+16797_-55+1679 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
T | TCACA | 27 | a0001c0001t0005g0086a0001c0001t0005g0183a0001c0002t0001g0104others(24): Show | 27 | HG00323.hp2 HG00423.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-55+16795_-55+1679 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
T | TCACACA | 11 | a0001c0001t0010g0010a0001c0001t0015g0270a0001c0002t0001g0007others(8): Show | 13 | HG00408.hp1 HG02071.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-55+16793_-55+1679 others(10): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0015g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-55+16789_-55+1679 others(14): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
T | TCTCA | 33 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0015others(30): Show | 34 | HG00609.hp1 HG00621.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-55+16798_-55+1679 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
T | TCTCACA | 6 | a0002c0004t0004g0045a0002c0004t0004g0046a0002c0004t0004g0047others(3): Show | 6 | HG00735.hp1 HG02735.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-55+16798_-55+1679 others(10): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
T | TCTCACAC others(1): Show |
9 | a0002c0004t0004g0014a0002c0004t0004g0051a0002c0004t0004g0052others(6): Show | 9 | HG00558.hp2 HG02258.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.-55+16798_-55+1679 others(12): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
T | TCTCACAC others(5): Show |
1 | a0002c0004t0004g0058 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-55+16798_-55+1679 others(16): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
TCA | T | 36 | a0001c0001t0002g0304a0001c0001t0005g0075a0001c0001t0005g0079others(33): Show | 36 | HG00140.hp1 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-55+16797_-55+1679 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
TCACA | T | 8 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0303others(5): Show | 8 | HG00597.hp1 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-55+16795_-55+1679 others(8): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
TCACACA | T | 3 | a0003c0005t0002g0279a0003c0005t0002g0293a0003c0005t0002g0294 | 3 | HG02630.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-55+16793_-55+1679 others(10): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414177
|
TCACACAC others(5): Show |
T | 1 | a0001c0002t0001g0106 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-55+16787_-55+1679 others(16): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414177 | ||||||
| chr1:33414179
|
A | ACT | 3 | a0001c0001t0002g0330a0001c0001t0002g0331a0001c0001t0023g0343 | 3 | HG02027.hp1 NA18942.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-55+16796_-55+1679 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414179 | ||||||
| chr1:33414179
|
A | T | 1 | a0002c0004t0004g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-55+16797T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414179 | ||||||
| chr1:33414181
|
A | T | 50 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(47): Show | 50 | HG00558.hp1 HG01071.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.-55+16795T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414181 | ||||||
| chr1:33414183
|
A | T | 1 | a0001c0001t0002g0304 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-55+16793T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414183 | ||||||
| chr1:33414185
|
A | T | 3 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0303 | 3 | HG00597.hp1 NA18956.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-55+16791T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414185 | ||||||
| chr1:33414220
|
A | C | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02572.hp1 HG03017.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-55+16756T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414220 | ||||||
| chr1:33414237
|
A | C | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+16739T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414237 | ||||||
| chr1:33414368
|
G | C | 1 | a0001c0001t0005g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-55+16608C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414368 | ||||||
| chr1:33414532
|
C | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+16444G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414532 | ||||||
| chr1:33414575
|
G | C | 2 | a0001c0006t0006g0180a0001c0006t0020g0181 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-55+16401C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414575 | ||||||
| chr1:33414755
|
C | T | 105 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(102): Show | 106 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.-55+16221G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414755 | ||||||
| chr1:33414834
|
A | C | 3 | a0003c0005t0002g0276a0003c0005t0002g0277a0003c0005t0002g0278 | 3 | HG02723.hp2 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-55+16142T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414834 | ||||||
| chr1:33414948
|
A | T | 1 | a0001c0002t0022g0103 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-55+16028T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33414948 | ||||||
| chr1:33415123
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+15853G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415123 | ||||||
| chr1:33415131
|
C | T | 1 | a0001c0003t0003g0198 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-55+15845G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415131 | ||||||
| chr1:33415212
|
C | T | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+15764G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415212 | ||||||
| chr1:33415227
|
G | T | 1 | a0001c0002t0001g0102 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-55+15749C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415227 | ||||||
| chr1:33415237
|
C | G | 12 | a0001c0002t0001g0007a0001c0002t0001g0158a0001c0002t0001g0159others(9): Show | 13 | HG00408.hp1 HG00735.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.-55+15739G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415237 | ||||||
| chr1:33415333
|
T | G | 2 | a0001c0006t0006g0180a0001c0006t0020g0181 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-55+15643A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415333 | ||||||
| chr1:33415443
|
C | T | 1 | a0001c0003t0003g0197 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-55+15533G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415443 | ||||||
| chr1:33415585
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-55+15391T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415585 | ||||||
| chr1:33415686
|
C | T | 3 | a0001c0008t0002g0347a0001c0008t0002g0349a0008c0009t0002g0348 | 3 | HG00639.hp2 HG01243.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-55+15290G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33415686 | ||||||
| chr1:33416107
|
G | A | 1 | a0001c0001t0014g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-55+14869C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416107 | ||||||
| chr1:33416295
|
C | T | 64 | a0001c0001t0005g0183a0001c0003t0001g0194a0001c0003t0001g0201others(61): Show | 70 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-55+14681G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416295 | ||||||
| chr1:33416296
|
G | A | 65 | a0001c0003t0003g0065a0001c0006t0006g0180a0001c0006t0006g0182others(62): Show | 66 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-55+14680C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416296 | ||||||
| chr1:33416370
|
T | A | 261 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(258): Show | 269 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.-55+14606A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416370 | ||||||
| chr1:33416411
|
CA | C | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+14564delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416411 | ||||||
| chr1:33416474
|
G | A | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+14502C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416474 | ||||||
| chr1:33416551
|
G | T | 1 | a0003c0005t0002g0355 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-55+14425C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416551 | ||||||
| chr1:33416584
|
G | GA | 168 | a0001c0001t0002g0299a0001c0001t0005g0072a0001c0001t0005g0073others(165): Show | 175 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.-55+14391dupT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416584 | ||||||
| chr1:33416584
|
G | GAA | 99 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(96): Show | 100 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.-55+14390_-55+1439 others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416584 | ||||||
| chr1:33416733
|
A | T | 1 | a0002c0004t0004g0020 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-55+14243T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416733 | ||||||
| chr1:33416876
|
G | A | 3 | a0001c0001t0002g0332a0001c0001t0002g0333a0001c0001t0002g0334 | 3 | HG02647.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-55+14100C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416876 | ||||||
| chr1:33416893
|
G | A | 1 | a0001c0002t0001g0150 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-55+14083C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33416893 | ||||||
| chr1:33417067
|
T | C | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+13909A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417067 | ||||||
| chr1:33417075
|
A | G | 1 | a0002c0004t0004g0020 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-55+13901T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417075 | ||||||
| chr1:33417100
|
G | T | 1 | a0001c0002t0001g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-55+13876C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417100 | ||||||
| chr1:33417101
|
A | C | 1 | a0001c0002t0001g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-55+13875T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417101 | ||||||
| chr1:33417293
|
C | T | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-55+13683G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417293 | ||||||
| chr1:33417523
|
GC | G | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-55+13452delG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417523 | ||||||
| chr1:33417525
|
C | G | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-55+13451G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417525 | ||||||
| chr1:33417642
|
A | G | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+13334T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417642 | ||||||
| chr1:33417672
|
C | A | 8 | a0001c0001t0002g0297a0001c0001t0002g0335a0001c0001t0002g0336others(5): Show | 8 | NA18953.hp1 NA18974.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.-55+13304G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417672 | ||||||
| chr1:33417706
|
G | C | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+13270C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417706 | ||||||
| chr1:33417748
|
A | G | 3 | a0001c0006t0006g0180a0001c0006t0006g0182a0001c0006t0020g0181 | 3 | HG02809.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-55+13228T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417748 | ||||||
| chr1:33417787
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-55+13189A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417787 | ||||||
| chr1:33417831
|
T | C | 2 | a0001c0006t0006g0180a0001c0006t0020g0181 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-55+13145A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417831 | ||||||
| chr1:33417906
|
C | T | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-55+13070G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33417906 | ||||||
| chr1:33418026
|
C | A | 1 | a0001c0001t0005g0087 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-55+12950G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418026 | ||||||
| chr1:33418145
|
T | C | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+12831A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418145 | ||||||
| chr1:33418201
|
C | G | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-55+12775G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418201 | ||||||
| chr1:33418282
|
G | C | 1 | a0001c0001t0005g0095 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-55+12694C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418282 | ||||||
| chr1:33418305
|
A | G | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+12671T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418305 | ||||||
| chr1:33418346
|
C | A | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+12630G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418346 | ||||||
| chr1:33418377
|
GAGAGAA | G | 169 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(166): Show | 176 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.-55+12593_-55+1259 others(10): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418377 | ||||||
| chr1:33418456
|
A | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+12520T>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418456 | ||||||
| chr1:33418649
|
A | G | 1 | a0003c0005t0026g0274 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-55+12327T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418649 | ||||||
| chr1:33418693
|
T | C | 1 | a0003c0005t0002g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-55+12283A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418693 | ||||||
| chr1:33418963
|
T | C | 108 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(105): Show | 109 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-55+12013A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33418963 | ||||||
| chr1:33419051
|
T | A | 1 | a0001c0002t0001g0167 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-55+11925A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419051 | ||||||
| chr1:33419224
|
C | T | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+11752G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419224 | ||||||
| chr1:33419302
|
T | C | 55 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(52): Show | 55 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-55+11674A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419302 | ||||||
| chr1:33419446
|
C | T | 1 | a0001c0001t0011g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-55+11530G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419446 | ||||||
| chr1:33419648
|
T | C | 261 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(258): Show | 269 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.-55+11328A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419648 | ||||||
| chr1:33419649
|
G | A | 1 | a0001c0001t0005g0088 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-55+11327C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419649 | ||||||
| chr1:33419673
|
G | A | 1 | a0001c0003t0003g0236 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-55+11303C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419673 | ||||||
| chr1:33419702
|
C | T | 12 | a0001c0002t0001g0007a0001c0002t0001g0158a0001c0002t0001g0159others(9): Show | 13 | HG00408.hp1 HG00735.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.-55+11274G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419702 | ||||||
| chr1:33419717
|
C | T | 2 | a0001c0001t0005g0090a0001c0001t0017g0089 | 2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-55+11259G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419717 | ||||||
| chr1:33419771
|
G | A | 35 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(32): Show | 35 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-55+11205C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419771 | ||||||
| chr1:33419844
|
C | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+11132G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419844 | ||||||
| chr1:33419898
|
C | T | 1 | a0001c0003t0003g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-55+11078G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419898 | ||||||
| chr1:33419947
|
G | A | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-55+11029C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33419947 | ||||||
| chr1:33420162
|
T | G | 1 | a0001c0006t0006g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-55+10814A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33420162 | ||||||
| chr1:33420221
|
G | C | 2 | a0003c0005t0002g0293a0003c0005t0002g0294 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-55+10755C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33420221 | ||||||
| chr1:33420330
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-55+10646C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33420330 | ||||||
| chr1:33420831
|
A | G | 289 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(286): Show | 300 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.-55+10145T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33420831 | ||||||
| chr1:33420888
|
G | A | 1 | a0001c0003t0005g0237 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-55+10088C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33420888 | ||||||
| chr1:33420920
|
C | T | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+10056G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33420920 | ||||||
| chr1:33421127
|
ATGT | A | 108 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(105): Show | 109 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-55+9846_-55+9848d others(5): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33421127 | ||||||
| chr1:33421287
|
C | A | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+9689G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33421287 | ||||||
| chr1:33421475
|
C | T | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+9501G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33421475 | ||||||
| chr1:33421634
|
G | A | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+9342C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33421634 | ||||||
| chr1:33421869
|
C | G | 108 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(105): Show | 109 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-55+9107G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33421869 | ||||||
| chr1:33422092
|
A | G | 2 | a0003c0005t0002g0273a0003c0005t0002g0295 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-55+8884T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422092 | ||||||
| chr1:33422159
|
T | C | 261 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(258): Show | 269 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.-55+8817A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422159 | ||||||
| chr1:33422271
|
CT | C | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+8704delA | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422271 | ||||||
| chr1:33422338
|
G | A | 1 | a0002c0004t0004g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-55+8638C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422338 | ||||||
| chr1:33422472
|
C | T | 52 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0297others(49): Show | 52 | HG00558.hp1 HG00597.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-55+8504G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422472 | ||||||
| chr1:33422583
|
C | A | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+8393G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422583 | ||||||
| chr1:33422597
|
C | T | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+8379G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422597 | ||||||
| chr1:33422605
|
T | C | 2 | a0002c0004t0004g0060a0002c0004t0004g0061 | 2 | HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-55+8371A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422605 | ||||||
| chr1:33422646
|
C | A | 1 | a0001c0002t0001g0152 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-55+8330G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422646 | ||||||
| chr1:33422746
|
C | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+8230G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422746 | ||||||
| chr1:33422769
|
C | T | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+8207G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33422769 | ||||||
| chr1:33423059
|
G | A | 1 | a0001c0003t0003g0238 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-55+7917C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423059 | ||||||
| chr1:33423112
|
T | G | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+7864A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423112 | ||||||
| chr1:33423132
|
C | G | 3 | a0001c0008t0002g0347a0001c0008t0002g0349a0008c0009t0002g0348 | 3 | HG00639.hp2 HG01243.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-55+7844G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423132 | ||||||
| chr1:33423178
|
T | C | 1 | a0001c0006t0006g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-55+7798A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423178 | ||||||
| chr1:33423207
|
T | C | 62 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(59): Show | 68 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-55+7769A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423207 | ||||||
| chr1:33423287
|
G | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+7689C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423287 | ||||||
| chr1:33423432
|
G | T | 1 | a0001c0001t0002g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-55+7544C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423432 | ||||||
| chr1:33423514
|
C | T | 1 | a0001c0001t0002g0357 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-55+7462G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423514 | ||||||
| chr1:33423542
|
A | G | 2 | a0001c0001t0005g0072a0001c0001t0005g0073 | 2 | NA18944.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-55+7434T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423542 | ||||||
| chr1:33423730
|
C | T | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+7246G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423730 | ||||||
| chr1:33423768
|
C | T | 3 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171 | 3 | HG02572.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-55+7208G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423768 | ||||||
| chr1:33423797
|
T | C | 1 | a0003c0005t0002g0295 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-55+7179A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423797 | ||||||
| chr1:33423821
|
C | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+7155G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423821 | ||||||
| chr1:33423896
|
A | C | 4 | a0002c0004t0004g0016a0002c0004t0004g0017a0002c0004t0004g0018others(1): Show | 4 | HG01175.hp2 HG01496.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-55+7080T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423896 | ||||||
| chr1:33423959
|
T | C | 1 | a0001c0001t0009g0342 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-55+7017A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33423959 | ||||||
| chr1:33424011
|
G | T | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-55+6965C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424011 | ||||||
| chr1:33424033
|
TGG | T | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+6941_-55+6942d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424033 | ||||||
| chr1:33424073
|
G | C | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+6903C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424073 | ||||||
| chr1:33424092
|
C | T | 6 | a0001c0002t0001g0009a0001c0002t0001g0250a0001c0002t0001g0251others(3): Show | 7 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-55+6884G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424092 | ||||||
| chr1:33424093
|
G | A | 5 | a0001c0001t0005g0090a0001c0001t0005g0091a0001c0001t0005g0092others(2): Show | 5 | HG00733.hp1 HG01071.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-55+6883C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424093 | ||||||
| chr1:33424097
|
C | CA | 6 | a0001c0001t0023g0343a0001c0002t0001g0153a0001c0002t0001g0154others(3): Show | 6 | HG00408.hp1 HG02622.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-55+6878dupT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424097 | ||||||
| chr1:33424097
|
CA | C | 162 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(159): Show | 169 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.-55+6878delT | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424097 | ||||||
| chr1:33424097
|
CAA | C | 6 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-55+6877_-55+6878d others(4): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424097 | ||||||
| chr1:33424111
|
A | C | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+6865T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424111 | ||||||
| chr1:33424112
|
C | A | 3 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178 | 3 | NA18965.hp2 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-55+6864G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424112 | ||||||
| chr1:33424117
|
A | G | 1 | a0001c0001t0002g0297 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-55+6859T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424117 | ||||||
| chr1:33424121
|
C | A | 2 | a0001c0002t0001g0156a0001c0002t0001g0157 | 2 | HG00140.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-55+6855G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424121 | ||||||
| chr1:33424159
|
A | G | 3 | a0003c0005t0002g0352a0003c0005t0002g0353a0003c0005t0002g0354 | 3 | NA18959.hp2 NA19001.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-55+6817T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424159 | ||||||
| chr1:33424197
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-55+6779G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424197 | ||||||
| chr1:33424238
|
C | T | 42 | a0001c0001t0002g0285a0001c0001t0006g0246a0001c0001t0006g0247others(39): Show | 43 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-55+6738G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424238 | ||||||
| chr1:33424313
|
AC | A | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-55+6662delG | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424313 | ||||||
| chr1:33424397
|
T | C | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-55+6579A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424397 | ||||||
| chr1:33424430
|
T | C | 3 | a0001c0008t0002g0347a0001c0008t0002g0349a0008c0009t0002g0348 | 3 | HG00639.hp2 HG01243.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-55+6546A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424430 | ||||||
| chr1:33424594
|
C | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+6382G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424594 | ||||||
| chr1:33424676
|
C | T | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+6300G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424676 | ||||||
| chr1:33424723
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-55+6253T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424723 | ||||||
| chr1:33424802
|
C | T | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-55+6174G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424802 | ||||||
| chr1:33424879
|
C | T | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+6097G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424879 | ||||||
| chr1:33424988
|
CTAAG | C | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+5984_-55+5987d others(6): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33424988 | ||||||
| chr1:33425032
|
G | C | 5 | a0001c0003t0003g0192a0001c0003t0003g0193a0001c0003t0003g0241others(2): Show | 5 | HG00438.hp2 HG02074.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.-55+5944C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425032 | ||||||
| chr1:33425133
|
T | C | 2 | a0001c0001t0010g0010a0001c0001t0010g0344 | 3 | HG02896.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-55+5843A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425133 | ||||||
| chr1:33425505
|
C | T | 1 | a0002c0004t0004g0016 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-55+5471G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425505 | ||||||
| chr1:33425530
|
A | G | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+5446T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425530 | ||||||
| chr1:33425548
|
G | A | 271 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(268): Show | 279 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-55+5428C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425548 | ||||||
| chr1:33425608
|
G | A | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-55+5368C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425608 | ||||||
| chr1:33425619
|
G | A | 1 | a0002c0004t0004g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-55+5357C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425619 | ||||||
| chr1:33425619
|
G | C | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+5357C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425619 | ||||||
| chr1:33425634
|
G | A | 7 | a0001c0003t0003g0065a0002c0004t0004g0063a0002c0004t0004g0064others(4): Show | 7 | HG02698.hp2 HG03490.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.-55+5342C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425634 | ||||||
| chr1:33425705
|
G | A | 43 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(40): Show | 43 | HG00733.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-55+5271C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425705 | ||||||
| chr1:33425790
|
G | A | 2 | a0002c0004t0004g0070a0002c0004t0004g0071 | 2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-55+5186C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425790 | ||||||
| chr1:33425992
|
G | A | 1 | a0001c0008t0002g0349 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-55+4984C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33425992 | ||||||
| chr1:33426018
|
C | A | 1 | a0003c0005t0025g0351 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-55+4958G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426018 | ||||||
| chr1:33426027
|
T | C | 12 | a0001c0002t0001g0007a0001c0002t0001g0158a0001c0002t0001g0159others(9): Show | 13 | HG00408.hp1 HG00735.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.-55+4949A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426027 | ||||||
| chr1:33426157
|
C | T | 1 | a0003c0005t0002g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-55+4819G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426157 | ||||||
| chr1:33426276
|
C | T | 5 | a0001c0001t0007g0169a0001c0001t0007g0170a0001c0001t0007g0171others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+4700G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426276 | ||||||
| chr1:33426317
|
T | TG | 70 | a0001c0001t0002g0345a0001c0001t0002g0346a0001c0001t0005g0095others(67): Show | 76 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-55+4658dupC | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426317 | ||||||
| chr1:33426317
|
TG | T | 66 | a0001c0001t0015g0270a0001c0003t0003g0065a0001c0006t0003g0264others(63): Show | 67 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.-55+4658delC | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426317 | ||||||
| chr1:33426434
|
G | A | 1 | a0001c0001t0005g0096 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-55+4542C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426434 | ||||||
| chr1:33426589
|
T | A | 1 | a0001c0002t0001g0175 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-55+4387A>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426589 | ||||||
| chr1:33426737
|
T | C | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+4239A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426737 | ||||||
| chr1:33426802
|
TTCAGGAG others(15): Show |
T | 4 | a0001c0001t0005g0183a0001c0002t0016g0097a0001c0006t0006g0184others(1): Show | 4 | HG02451.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-55+4152_-55+4173d others(24): Show |
PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33426802 | ||||||
| chr1:33427166
|
T | C | 3 | a0001c0001t0005g0183a0001c0006t0006g0184a0001c0006t0006g0185 | 3 | HG02451.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-55+3810A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33427166 | ||||||
| chr1:33427234
|
G | T | 3 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248 | 3 | HG02257.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-55+3742C>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33427234 | ||||||
| chr1:33427363
|
T | G | 261 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(258): Show | 269 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.-55+3613A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33427363 | ||||||
| chr1:33427526
|
G | A | 3 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248 | 3 | HG02257.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-55+3450C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33427526 | ||||||
| chr1:33427582
|
C | A | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+3394G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33427582 | ||||||
| chr1:33427689
|
G | A | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+3287C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33427689 | ||||||
| chr1:33427703
|
C | T | 1 | a0002c0004t0004g0015 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-55+3273G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33427703 | ||||||
| chr1:33427757
|
G | A | 1 | a0003c0005t0002g0350 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-55+3219C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33427757 | ||||||
| chr1:33428030
|
T | C | 1 | a0001c0003t0003g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-55+2946A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33428030 | ||||||
| chr1:33428229
|
C | T | 33 | a0001c0001t0005g0072a0001c0001t0005g0073a0001c0001t0005g0074others(30): Show | 33 | HG00733.hp1 HG01071.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-55+2747G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33428229 | ||||||
| chr1:33428415
|
C | T | 1 | a0002c0004t0004g0014 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-55+2561G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33428415 | ||||||
| chr1:33428464
|
C | A | 1 | a0001c0006t0006g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-55+2512G>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33428464 | ||||||
| chr1:33428786
|
A | G | 3 | a0001c0003t0003g0008a0001c0003t0003g0186a0001c0003t0003g0187 | 4 | HG00738.hp1 HG01192.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-55+2190T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33428786 | ||||||
| chr1:33428817
|
T | C | 1 | a0001c0001t0014g0249 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-55+2159A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33428817 | ||||||
| chr1:33428927
|
A | G | 1 | a0001c0002t0001g0250 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-55+2049T>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33428927 | ||||||
| chr1:33429048
|
T | C | 61 | a0001c0003t0001g0194a0001c0003t0001g0201a0001c0003t0003g0001others(58): Show | 67 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55+1928A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33429048 | ||||||
| chr1:33429436
|
C | G | 1 | a0003c0005t0002g0269 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-55+1540G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33429436 | ||||||
| chr1:33429529
|
G | A | 2 | a0002c0004t0013g0012a0002c0004t0013g0013 | 2 | HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-55+1447C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33429529 | ||||||
| chr1:33429836
|
C | G | 62 | a0001c0003t0003g0065a0002c0004t0004g0003a0002c0004t0004g0014others(59): Show | 63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-55+1140G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33429836 | ||||||
| chr1:33429897
|
T | C | 1 | a0003c0005t0025g0351 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-55+1079A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33429897 | ||||||
| chr1:33429920
|
T | G | 1 | a0001c0002t0001g0244 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-55+1056A>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33429920 | ||||||
| chr1:33430023
|
G | C | 5 | a0001c0001t0006g0246a0001c0001t0006g0247a0001c0001t0006g0248others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+953C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430023 | ||||||
| chr1:33430117
|
A | C | 2 | a0002c0004t0013g0012a0002c0004t0013g0013 | 2 | HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-55+859T>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430117 | ||||||
| chr1:33430174
|
C | T | 1 | a0003c0005t0002g0268 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-55+802G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430174 | ||||||
| chr1:33430333
|
T | C | 6 | a0001c0002t0001g0009a0001c0002t0001g0250a0001c0002t0001g0251others(3): Show | 7 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-55+643A>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430333 | ||||||
| chr1:33430451
|
C | T | 1 | a0001c0002t0001g0011 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-55+525G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430451 | ||||||
| chr1:33430467
|
G | A | 5 | a0003c0005t0002g0352a0003c0005t0002g0353a0003c0005t0002g0354others(2): Show | 5 | NA18959.hp2 NA18969.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.-55+509C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430467 | ||||||
| chr1:33430474
|
G | C | 8 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0001t0005g0257others(5): Show | 8 | HG01123.hp2 HG01192.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.-55+502C>G | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430474 | ||||||
| chr1:33430546
|
C | T | 91 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(88): Show | 92 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.-55+430G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430546 | ||||||
| chr1:33430684
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-55+292G>A | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430684 | ||||||
| chr1:33430845
|
G | A | 1 | a0002c0004t0004g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-55+131C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430845 | ||||||
| chr1:33430925
|
G | A | 3 | a0001c0006t0003g0264a0001c0006t0003g0265a0001c0006t0003g0266 | 3 | HG01109.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-55+51C>T | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430925 | ||||||
| chr1:33430931
|
C | G | 92 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0285others(89): Show | 93 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-55+45G>C | PHC2 | ENSG00000134686.21 | transcript | ENST00000683057.1 | protein_coding | 1/14 | chr1 | 33430931 |