Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84457 |
|---|---|
| ensemblid | ENSG00000165443.12 |
| hgncid | 29378 |
| symbol | PHYHIPL |
| name | phytanoyl-CoA 2-hydroxylase interacting protein like |
| refseq_nuc | NM_032439.4 |
| refseq_prot | NP_115815.2 |
| ensembl_nuc | ENST00000373880.9 |
| ensembl_prot | ENSP00000362987.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 59176643 |
| end | 59247770 |
| strand | + |
| ver | v1.2 |
| region | chr10:59176643-59247770 |
| region5000 | chr10:59171643-59252770 |
| regionname0 | PHYHIPL_chr10_59176643_59247770 |
| regionname5000 | PHYHIPL_chr10_59171643_59252770 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 376 | 110 | 55 | 7 | 34 | 1 | 13 | 27 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0002 | 0/0 | 376 | 92 | 29 | 15 | 36 | 1 | 11 | 25 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1131 | 109 | 54 | 7 | 34 | 1 | 13 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| c0002 | 0/0 | 1131 | 91 | 29 | 14 | 36 | 1 | 11 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| c0003 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| c0004 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2392 | 153 | 72 | 19 | 45 | 1 | 16 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0002 | 0/0 | 2392 | 34 | 1 | 1 | 24 | 1 | 7 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0003 | 0/0 | 2392 | 4 | 3 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0004 | 0/0 | 2391 | 3 | 3 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0005 | 0/0 | 2392 | 2 | 2 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0006 | 0/0 | 2392 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0007 | 0/0 | 2392 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0008 | 0/0 | 2392 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0009 | 0/0 | 2392 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0010 | 0/0 | 2392 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| t0011 | 0/0 | 2392 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1131 | 109 | 54 | 7 | 34 | 1 | 13 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0003 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0002c0002 | 0/0 | 1131 | 91 | 29 | 14 | 36 | 1 | 11 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0002c0004 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3522 | 63 | 44 | 4 | 10 | 0 | 5 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0001t0002 | 0/0 | 3522 | 34 | 1 | 1 | 24 | 1 | 7 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0001t0003 | 0/0 | 3522 | 4 | 3 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0001t0004 | 0/0 | 3521 | 3 | 3 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0001t0005 | 0/0 | 3522 | 2 | 2 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0001t0007 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0001t0009 | 0/0 | 3522 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0001t0011 | 0/0 | 3522 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0001c0003t0001 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0002c0002t0001 | 0/0 | 3522 | 88 | 27 | 14 | 35 | 1 | 11 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0002c0002t0006 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0002c0002t0008 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0002c0002t0010 | 0/0 | 3522 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| a0002c0004t0001 | 0/0 | 3522 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | copy fasta | chr10 | 59171643 | 59252770 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0001t0011g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0002t0010g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| a0002c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00597 | hp2 | a0002 | c0002 | t0010 | g0161 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | CHS | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01071 | hp1 | a0002 | c0004 | t0001 | g0137 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0177 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0122 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PEL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02622 | hp2 | a0002 | c0002 | t0008 | g0100 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0039 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0140 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03516 | hp1 | a0002 | c0002 | t0006 | g0113 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | STU | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | STU | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | YRI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ASW | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0186 | AFR | ASW | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | TSI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0128 | EUR | TSI | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0165 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG01123 | hp2 | a0001 | c0001 | t0011 | g0021 | AMR | CLM | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | ACB | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | MSL | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | USA | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | USA | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | USA | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | PHYHIPL_chr10_59171643_59252770 | PHYHIPL | chr10 | 59171643 | 59252770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59245484
|
G | C | 1 | a0002 | 92 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(89): Show |
missense_variant | MODERATE | c.1024G>C | p.Val342Leu | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1235/3521 | 1024/1131 | 342/376 | chr10 | 59245484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59245303
|
G | A | 1 | a0001c0003 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.843G>A | p.Val281Val | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1054/3521 | 843/1131 | 281/376 | chr10 | 59245303 | ||
| chr10:59245444
|
C | T | 1 | a0002c0004 | 1 | HG01071.hp1 | synonymous_variant | LOW | c.984C>T | p.Val328Val | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1195/3521 | 984/1131 | 328/376 | chr10 | 59245444 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59176707
|
C | T | 1 | a0001c0001t0011 | 1 | HG01123.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/5 | 147 | chr10 | 59176707 | |||||
| chr10:59176796
|
C | T | 1 | a0002c0002t0010 | 1 | HG00597.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/5 | 58 | chr10 | 59176796 | |||||
| chr10:59245720
|
C | T | 1 | a0001c0001t0009 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 129 | chr10 | 59245720 | |||||
| chr10:59245795
|
T | C | 1 | a0001c0001t0003 | 4 | HG00639.hp2 HG02486.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*204T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 204 | chr10 | 59245795 | |||||
| chr10:59245856
|
T | C | 1 | a0001c0001t0005 | 2 | HG03453.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*265T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 265 | chr10 | 59245856 | |||||
| chr10:59246005
|
G | A | 1 | a0002c0002t0006 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 414 | chr10 | 59246005 | |||||
| chr10:59246501
|
C | T | 1 | a0002c0002t0008 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 910 | chr10 | 59246501 | |||||
| chr10:59246650
|
G | A | 2 | a0001c0001t0002a0001c0001t0009 | 35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1059G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1059 | chr10 | 59246650 | |||||
| chr10:59246776
|
A | G | 1 | a0001c0001t0007 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1185A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1185 | chr10 | 59246776 | |||||
| chr10:59247009
|
C | T | 1 | a0001c0001t0011 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1418C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1418 | chr10 | 59247009 | |||||
| chr10:59247042
|
G | GA | 13 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1458dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 5/5 | 1459 | INFO_REALIGN_3_PRIME | chr10 | 59247042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:59177071
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+112C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177071 | ||||||
| chr10:59177147
|
G | A | 1 | a0001c0001t0003g0002 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.106+188G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177147 | ||||||
| chr10:59177305
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+346T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177305 | ||||||
| chr10:59177449
|
T | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+490T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177449 | ||||||
| chr10:59177453
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.106+494T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177453 | ||||||
| chr10:59177495
|
G | C | 1 | a0002c0002t0001g0023 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106+536G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177495 | ||||||
| chr10:59177550
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106+591C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177550 | ||||||
| chr10:59177696
|
T | C | 4 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(1): Show | 4 | HG02572.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+737T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177696 | ||||||
| chr10:59177730
|
A | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+771A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59177730 | ||||||
| chr10:59177785
|
G | GAGTCTGC others(12): Show |
1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+827_106+845dup others(19): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59177785 | |||||
| chr10:59178013
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+1054A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178013 | ||||||
| chr10:59178241
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG01167.hp1 HG02622.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+1282A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178241 | ||||||
| chr10:59178259
|
A | G | 1 | a0002c0002t0001g0197 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.106+1300A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178259 | ||||||
| chr10:59178364
|
G | A | 1 | a0002c0002t0001g0023 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.106+1405G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178364 | ||||||
| chr10:59178655
|
C | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+1696C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178655 | ||||||
| chr10:59178679
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+1720C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178679 | ||||||
| chr10:59178689
|
A | C | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+1730A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178689 | ||||||
| chr10:59178770
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.106+1811A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178770 | ||||||
| chr10:59178851
|
C | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+1892C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178851 | ||||||
| chr10:59178898
|
A | G | 1 | a0002c0002t0001g0190 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.106+1939A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59178898 | ||||||
| chr10:59179246
|
G | A | 113 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 115 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.106+2287G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179246 | ||||||
| chr10:59179302
|
A | G | 113 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 115 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.106+2343A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179302 | ||||||
| chr10:59179458
|
C | T | 2 | a0002c0002t0001g0188a0002c0002t0001g0189 | 2 | HG01255.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.106+2499C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179458 | ||||||
| chr10:59179462
|
C | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+2503C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179462 | ||||||
| chr10:59179540
|
A | G | 1 | a0002c0002t0001g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.106+2581A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179540 | ||||||
| chr10:59179743
|
A | G | 1 | a0002c0002t0001g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.106+2784A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179743 | ||||||
| chr10:59179754
|
A | T | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | HG02135.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.106+2795A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59179754 | ||||||
| chr10:59179765
|
ATATT | A | 33 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0030others(30): Show | 35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+2809_106+2812d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179765 | |||||
| chr10:59179842
|
T | TAC | 33 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0076others(30): Show | 33 | HG00738.hp2 HG01071.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.106+2926_106+2927d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59179842
|
T | TACAC | 16 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(13): Show | 16 | HG00738.hp1 HG02015.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.106+2924_106+2927d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59179842
|
T | TACACAC | 12 | a0001c0001t0001g0022a0001c0001t0001g0063a0001c0001t0001g0064others(9): Show | 12 | HG01106.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.106+2922_106+2927d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59179842
|
T | TACACACA others(1): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02647.hp1 NA18947.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.106+2920_106+2927d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59179842
|
TAC | T | 19 | a0001c0001t0001g0103a0001c0001t0002g0047a0001c0001t0002g0048others(16): Show | 19 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+2926_106+2927d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59179842
|
TACAC | T | 33 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(30): Show | 33 | HG00558.hp1 HG00597.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.106+2924_106+2927d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59179842
|
TACACAC | T | 21 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.106+2922_106+2927d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59179842
|
TACACACA others(1): Show |
T | 11 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0111others(8): Show | 11 | HG00639.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+2920_106+2927d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59179842
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0112 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.106+2914_106+2927d others(16): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59179842 | |||||
| chr10:59180101
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.106+3142A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180101 | ||||||
| chr10:59180249
|
C | CAT | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+3298_106+3299d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180249 | |||||
| chr10:59180255
|
T | TACAC | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+3297_106+3298i others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180255 | |||||
| chr10:59180257
|
T | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+3298T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180257 | ||||||
| chr10:59180257
|
T | TAC | 50 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(47): Show | 50 | HG00639.hp1 HG00639.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.106+3318_106+3319d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | |||||
| chr10:59180257
|
T | TACAC | 2 | a0001c0001t0001g0094a0002c0002t0001g0192 | 2 | HG02258.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.106+3316_106+3319d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | |||||
| chr10:59180257
|
T | TACACAC | 47 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0063others(44): Show | 49 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.106+3314_106+3319d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | |||||
| chr10:59180257
|
T | TACACACA others(1): Show |
2 | a0001c0001t0002g0041a0001c0001t0002g0191 | 2 | NA18982.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.106+3312_106+3319d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | |||||
| chr10:59180257
|
T | TATAC | 5 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009others(2): Show | 5 | HG02145.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+3299_106+3300i others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180257 | |||||
| chr10:59180259
|
C | T | 6 | a0002c0002t0001g0114a0002c0002t0001g0118a0002c0002t0001g0119others(3): Show | 6 | HG02630.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+3300C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180259 | ||||||
| chr10:59180279
|
T | C | 4 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0040others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+3320T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180279 | ||||||
| chr10:59180294
|
A | AAT | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+3347_106+3348d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180294 | |||||
| chr10:59180294
|
AATATATA others(30): Show |
A | 1 | a0002c0002t0001g0117 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.106+3349_106+3385d others(39): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180294 | |||||
| chr10:59180313
|
A | AGTAT | 2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG01433.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.106+3355_106+3358d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180313 | |||||
| chr10:59180313
|
A | AGTATGTG others(3): Show |
1 | a0001c0001t0004g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.106+3358_106+3359i others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180313 | |||||
| chr10:59180314
|
G | GTA | 4 | a0001c0001t0002g0040a0001c0001t0002g0056a0002c0002t0001g0144others(1): Show | 4 | HG02027.hp1 HG03831.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+3402_106+3403d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
G | GTATA | 5 | a0001c0001t0002g0031a0001c0001t0002g0032a0002c0002t0001g0145others(2): Show | 5 | HG02015.hp1 HG02698.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+3400_106+3403d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
G | GTATATA | 2 | a0002c0002t0001g0147a0002c0002t0001g0190 | 2 | HG00673.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.106+3398_106+3403d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
G | GTATATAT others(1): Show |
2 | a0002c0002t0001g0148a0002c0002t0001g0149 | 2 | HG01884.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.106+3396_106+3403d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0002g0038 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.106+3392_106+3403d others(14): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
G | GTATGTGT others(7): Show |
1 | a0001c0001t0004g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.106+3358_106+3359i others(16): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTA | G | 8 | a0001c0001t0001g0198a0001c0001t0002g0030a0001c0001t0002g0051others(5): Show | 8 | HG00558.hp2 HG01433.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+3402_106+3403d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATA | G | 16 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0002g0050others(13): Show | 16 | HG00738.hp2 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.106+3400_106+3403d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATA | G | 10 | a0001c0001t0001g0099a0001c0001t0001g0195a0001c0001t0001g0196others(7): Show | 10 | HG00733.hp1 HG01071.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+3398_106+3403d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(1): Show |
G | 17 | a0001c0001t0001g0016a0001c0001t0001g0108a0001c0001t0002g0034others(14): Show | 17 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.106+3396_106+3403d others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(3): Show |
G | 19 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0074others(16): Show | 19 | HG02258.hp2 HG02280.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+3394_106+3403d others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(5): Show |
G | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 24 | HG00639.hp2 HG01167.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.106+3392_106+3403d others(14): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(7): Show |
G | 11 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0083others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+3390_106+3403d others(16): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(9): Show |
G | 18 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0066others(15): Show | 18 | HG02622.hp2 HG03041.hp1 HG03225.hp1 others(15): Show |
intron_variant | MODIFIER | c.106+3388_106+3403d others(18): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(11): Show |
G | 6 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(3): Show | 6 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+3386_106+3403d others(20): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(13): Show |
G | 2 | a0001c0001t0001g0091a0001c0003t0001g0090 | 2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106+3384_106+3403d others(22): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+3378_106+3403d others(28): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(21): Show |
G | 33 | a0002c0002t0001g0023a0002c0002t0001g0129a0002c0002t0001g0130others(30): Show | 33 | HG00558.hp1 HG00597.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.106+3376_106+3403d others(30): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180314
|
GTATATAT others(23): Show |
G | 1 | a0002c0002t0001g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.106+3374_106+3403d others(32): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180314 | |||||
| chr10:59180316
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0004g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.106+3358_106+3359i others(14): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180316 | |||||
| chr10:59180318
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0019 | 2 | HG03704.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.106+3359A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180318 | ||||||
| chr10:59180322
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0011g0021 | 2 | HG01123.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.106+3363A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180322 | ||||||
| chr10:59180324
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.106+3365A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180324 | ||||||
| chr10:59180326
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG02027.hp2 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.106+3367A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180326 | ||||||
| chr10:59180328
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.106+3379_106+3380i others(19): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59180328 | |||||
| chr10:59180328
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0003g0010others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+3369A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180328 | ||||||
| chr10:59180330
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.106+3371A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180330 | ||||||
| chr10:59180342
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+3383A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180342 | ||||||
| chr10:59180346
|
A | T | 1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+3387A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180346 | ||||||
| chr10:59180359
|
T | C | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+3400T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180359 | ||||||
| chr10:59180375
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG01167.hp1 HG02622.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+3416C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180375 | ||||||
| chr10:59180383
|
A | C | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+3424A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180383 | ||||||
| chr10:59180535
|
C | G | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 117 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.106+3576C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180535 | ||||||
| chr10:59180559
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+3600C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180559 | ||||||
| chr10:59180752
|
T | C | 2 | a0001c0001t0002g0031a0001c0001t0002g0032 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.106+3793T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180752 | ||||||
| chr10:59180798
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | HG02258.hp2 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.106+3839G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59180798 | ||||||
| chr10:59181315
|
A | G | 35 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(32): Show | 35 | HG01884.hp1 HG01891.hp1 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.106+4356A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181315 | ||||||
| chr10:59181567
|
G | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+4608G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181567 | ||||||
| chr10:59181616
|
C | T | 1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+4657C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181616 | ||||||
| chr10:59181618
|
A | C | 1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+4659A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181618 | ||||||
| chr10:59181642
|
G | A | 1 | a0002c0002t0001g0155 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.106+4683G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59181642 | ||||||
| chr10:59181831
|
C | CAA | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 117 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.106+4873_106+4874d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59181831 | |||||
| chr10:59182200
|
G | T | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+5241G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182200 | ||||||
| chr10:59182347
|
G | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+5388G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182347 | ||||||
| chr10:59182725
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.106+5766A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182725 | ||||||
| chr10:59182735
|
G | A | 1 | a0002c0002t0001g0181 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.106+5776G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182735 | ||||||
| chr10:59182757
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+5798G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182757 | ||||||
| chr10:59182774
|
G | T | 130 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(127): Show | 132 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(129): Show |
intron_variant | MODIFIER | c.106+5815G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182774 | ||||||
| chr10:59182794
|
G | T | 1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+5835G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59182794 | ||||||
| chr10:59183043
|
G | T | 1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+6084G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183043 | ||||||
| chr10:59183135
|
G | A | 112 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 114 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.106+6176G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183135 | ||||||
| chr10:59183145
|
T | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+6186T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183145 | ||||||
| chr10:59183270
|
A | G | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+6311A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183270 | ||||||
| chr10:59183374
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+6415A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183374 | ||||||
| chr10:59183512
|
G | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+6553G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183512 | ||||||
| chr10:59183516
|
C | T | 6 | a0002c0002t0001g0114a0002c0002t0001g0118a0002c0002t0001g0119others(3): Show | 6 | HG02630.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+6557C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183516 | ||||||
| chr10:59183634
|
A | G | 2 | a0001c0001t0001g0091a0001c0003t0001g0090 | 2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106+6675A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183634 | ||||||
| chr10:59183678
|
A | C | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+6719A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183678 | ||||||
| chr10:59183692
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+6733C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183692 | ||||||
| chr10:59183710
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.106+6751C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183710 | ||||||
| chr10:59183729
|
G | T | 1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+6770G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59183729 | ||||||
| chr10:59183806
|
TGTA | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+6850_106+6852d others(5): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59183806 | |||||
| chr10:59184012
|
T | G | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+7053T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184012 | ||||||
| chr10:59184060
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0059 | 2 | HG03927.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.106+7101A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184060 | ||||||
| chr10:59184174
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.106+7215C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184174 | ||||||
| chr10:59184262
|
A | G | 2 | a0002c0002t0001g0117a0002c0002t0001g0128 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.106+7303A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184262 | ||||||
| chr10:59184342
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.106+7383C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184342 | ||||||
| chr10:59184402
|
C | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+7443C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184402 | ||||||
| chr10:59184495
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0108 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.106+7536C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184495 | ||||||
| chr10:59184540
|
A | G | 2 | a0002c0002t0001g0172a0002c0002t0001g0183 | 2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.106+7581A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184540 | ||||||
| chr10:59184564
|
A | G | 2 | a0001c0001t0001g0091a0001c0003t0001g0090 | 2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.106+7605A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184564 | ||||||
| chr10:59184569
|
G | A | 112 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 114 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.106+7610G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184569 | ||||||
| chr10:59184612
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.106+7653C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184612 | ||||||
| chr10:59184613
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+7654G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184613 | ||||||
| chr10:59184627
|
GT | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+7680delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59184627 | |||||
| chr10:59184785
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.106+7826C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184785 | ||||||
| chr10:59184803
|
C | T | 1 | a0002c0002t0001g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.106+7844C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184803 | ||||||
| chr10:59184843
|
T | C | 196 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(193): Show | 198 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.106+7884T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59184843 | ||||||
| chr10:59184984
|
A | AT | 5 | a0001c0001t0001g0077a0002c0002t0001g0130a0002c0002t0001g0147others(2): Show | 5 | HG00673.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+8049dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59184984 | |||||
| chr10:59184984
|
AT | A | 73 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(70): Show | 75 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.106+8049delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59184984 | |||||
| chr10:59184984
|
ATT | A | 26 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(23): Show | 26 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.106+8048_106+8049d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59184984 | |||||
| chr10:59185057
|
C | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+8098C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185057 | ||||||
| chr10:59185084
|
A | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+8125A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185084 | ||||||
| chr10:59185151
|
C | T | 2 | a0002c0002t0001g0123a0002c0002t0001g0124 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.106+8192C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185151 | ||||||
| chr10:59185200
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0004g0005a0001c0001t0004g0008others(1): Show | 4 | HG02145.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+8241C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185200 | ||||||
| chr10:59185201
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+8242G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185201 | ||||||
| chr10:59185219
|
T | G | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+8260T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185219 | ||||||
| chr10:59185285
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG00639.hp2 HG00673.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+8326C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185285 | ||||||
| chr10:59185453
|
G | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+8494G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185453 | ||||||
| chr10:59185578
|
G | C | 1 | a0002c0002t0001g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.106+8619G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185578 | ||||||
| chr10:59185579
|
C | T | 1 | a0002c0002t0001g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.106+8620C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185579 | ||||||
| chr10:59185598
|
A | C | 114 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 116 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.106+8639A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185598 | ||||||
| chr10:59185629
|
G | A | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+8670G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59185629 | ||||||
| chr10:59186064
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+9105G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186064 | ||||||
| chr10:59186122
|
C | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+9163C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186122 | ||||||
| chr10:59186133
|
A | G | 1 | a0002c0002t0001g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.106+9174A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186133 | ||||||
| chr10:59186264
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106+9305T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186264 | ||||||
| chr10:59186328
|
T | C | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+9369T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186328 | ||||||
| chr10:59186438
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+9479C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186438 | ||||||
| chr10:59186710
|
A | C | 2 | a0001c0001t0002g0048a0001c0001t0002g0056 | 2 | HG00673.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.106+9751A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186710 | ||||||
| chr10:59186872
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+9913A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186872 | ||||||
| chr10:59186888
|
A | G | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154 | 3 | NA18997.hp1 NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.106+9929A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59186888 | ||||||
| chr10:59187128
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+10169G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187128 | ||||||
| chr10:59187142
|
A | G | 10 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0071others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+10183A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187142 | ||||||
| chr10:59187222
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+10263C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187222 | ||||||
| chr10:59187264
|
G | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+10305G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187264 | ||||||
| chr10:59187265
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+10306T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187265 | ||||||
| chr10:59187320
|
G | A | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+10361G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187320 | ||||||
| chr10:59187358
|
C | T | 1 | a0002c0002t0001g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.106+10399C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187358 | ||||||
| chr10:59187364
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+10405G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187364 | ||||||
| chr10:59187556
|
G | T | 1 | a0002c0002t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106+10597G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187556 | ||||||
| chr10:59187600
|
C | T | 113 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 115 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.106+10641C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187600 | ||||||
| chr10:59187696
|
G | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+10737G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187696 | ||||||
| chr10:59187709
|
G | A | 1 | a0002c0002t0001g0131 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.106+10750G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187709 | ||||||
| chr10:59187853
|
T | C | 3 | a0002c0002t0001g0152a0002c0002t0001g0153a0002c0002t0001g0154 | 3 | NA18997.hp1 NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.106+10894T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187853 | ||||||
| chr10:59187916
|
C | G | 1 | a0002c0002t0001g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.106+10957C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187916 | ||||||
| chr10:59187938
|
T | C | 2 | a0001c0001t0002g0030a0002c0002t0001g0116 | 2 | HG02602.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.106+10979T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187938 | ||||||
| chr10:59187984
|
T | C | 1 | a0002c0002t0001g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.106+11025T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59187984 | ||||||
| chr10:59188084
|
C | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.106+11125C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188084 | ||||||
| chr10:59188402
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.106+11443G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188402 | ||||||
| chr10:59188446
|
A | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+11487A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188446 | ||||||
| chr10:59188525
|
A | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+11566A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188525 | ||||||
| chr10:59188538
|
A | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+11579A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188538 | ||||||
| chr10:59188727
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+11768T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188727 | ||||||
| chr10:59188748
|
G | GT | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+11791dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59188748 | |||||
| chr10:59188779
|
A | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+11820A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59188779 | ||||||
| chr10:59189105
|
C | A | 4 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(1): Show | 4 | HG02572.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+12146C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189105 | ||||||
| chr10:59189141
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+12182T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189141 | ||||||
| chr10:59189719
|
A | G | 1 | a0002c0002t0001g0121 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106+12760A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189719 | ||||||
| chr10:59189818
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.106+12859A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189818 | ||||||
| chr10:59189982
|
A | G | 2 | a0001c0001t0002g0050a0001c0001t0002g0055 | 2 | NA18954.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.106+13023A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59189982 | ||||||
| chr10:59190068
|
A | G | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+13109A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190068 | ||||||
| chr10:59190426
|
A | G | 1 | a0001c0001t0002g0029 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.106+13467A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190426 | ||||||
| chr10:59190550
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.106+13591G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190550 | ||||||
| chr10:59190638
|
T | C | 2 | a0002c0002t0001g0136a0002c0002t0001g0174 | 2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.106+13679T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190638 | ||||||
| chr10:59190934
|
T | C | 2 | a0002c0002t0001g0136a0002c0002t0001g0174 | 2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.106+13975T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59190934 | ||||||
| chr10:59191027
|
T | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+14068T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59191027 | ||||||
| chr10:59191277
|
C | T | 114 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 116 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.106+14318C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59191277 | ||||||
| chr10:59191403
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG02027.hp2 HG03704.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+14444T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59191403 | ||||||
| chr10:59191902
|
G | GA | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 117 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.106+14945dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59191902 | |||||
| chr10:59192033
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.106+15074T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192033 | ||||||
| chr10:59192052
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.106+15093G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192052 | ||||||
| chr10:59192053
|
C | T | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+15094C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192053 | ||||||
| chr10:59192130
|
T | G | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+15171T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192130 | ||||||
| chr10:59192257
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106+15298G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192257 | ||||||
| chr10:59192390
|
T | C | 1 | a0001c0001t0003g0006 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.106+15431T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192390 | ||||||
| chr10:59192394
|
T | C | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+15435T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192394 | ||||||
| chr10:59192534
|
T | C | 1 | a0002c0002t0001g0181 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.106+15575T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192534 | ||||||
| chr10:59192536
|
G | A | 1 | a0002c0004t0001g0137 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.106+15577G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192536 | ||||||
| chr10:59192586
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+15627C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192586 | ||||||
| chr10:59192601
|
CAA | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+15643_106+1564 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192601 | ||||||
| chr10:59192837
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.106+15878G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192837 | ||||||
| chr10:59192899
|
A | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.106+15940A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59192899 | ||||||
| chr10:59193152
|
C | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+16193C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193152 | ||||||
| chr10:59193153
|
A | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+16194A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193153 | ||||||
| chr10:59193307
|
A | G | 1 | a0002c0002t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.106+16348A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193307 | ||||||
| chr10:59193343
|
G | T | 1 | a0002c0002t0001g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+16384G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193343 | ||||||
| chr10:59193359
|
A | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+16400A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193359 | ||||||
| chr10:59193409
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+16450G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193409 | ||||||
| chr10:59193660
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+16701G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193660 | ||||||
| chr10:59193697
|
T | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+16738T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193697 | ||||||
| chr10:59193836
|
G | C | 1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+16877G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59193836 | ||||||
| chr10:59194004
|
C | A | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+17045C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194004 | ||||||
| chr10:59194039
|
G | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+17080G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194039 | ||||||
| chr10:59194079
|
TG | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG02622.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.106+17121delG | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194079 | ||||||
| chr10:59194080
|
G | GT | 45 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(42): Show | 45 | HG00639.hp1 HG00733.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.106+17142dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59194080 | |||||
| chr10:59194080
|
G | GTT | 7 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0001g0107others(4): Show | 7 | HG02257.hp2 HG03098.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+17141_106+1714 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59194080 | |||||
| chr10:59194080
|
GT | G | 6 | a0001c0001t0001g0091a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG00673.hp2 HG02698.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+17142delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59194080 | |||||
| chr10:59194084
|
T | G | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+17125T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194084 | ||||||
| chr10:59194105
|
G | A | 56 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(53): Show | 58 | HG00558.hp2 HG00597.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.106+17146G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194105 | ||||||
| chr10:59194482
|
G | A | 6 | a0002c0002t0001g0114a0002c0002t0001g0118a0002c0002t0001g0119others(3): Show | 6 | HG02630.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+17523G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194482 | ||||||
| chr10:59194651
|
G | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+17692G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194651 | ||||||
| chr10:59194659
|
T | C | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 117 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.106+17700T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194659 | ||||||
| chr10:59194850
|
G | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+17891G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59194850 | ||||||
| chr10:59195080
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+18121A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195080 | ||||||
| chr10:59195180
|
TTAA | T | 34 | a0001c0001t0001g0091a0001c0001t0002g0001a0001c0001t0002g0029others(31): Show | 36 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.106+18222_106+1822 others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195180 | ||||||
| chr10:59195627
|
T | C | 1 | a0001c0001t0002g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.106+18668T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195627 | ||||||
| chr10:59195670
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+18711T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195670 | ||||||
| chr10:59195706
|
G | A | 1 | a0002c0002t0001g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.106+18747G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59195706 | ||||||
| chr10:59196335
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.106+19376A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196335 | ||||||
| chr10:59196344
|
A | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+19385A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196344 | ||||||
| chr10:59196415
|
A | AT | 5 | a0001c0001t0001g0076a0001c0001t0001g0092a0002c0002t0001g0095others(2): Show | 5 | HG02723.hp2 HG02965.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+19473dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59196415 | |||||
| chr10:59196415
|
AT | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(25): Show | 28 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.106+19473delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59196415 | |||||
| chr10:59196518
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+19559C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196518 | ||||||
| chr10:59196576
|
G | A | 1 | a0002c0002t0001g0185 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.106+19617G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196576 | ||||||
| chr10:59196610
|
G | A | 1 | a0001c0001t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.106+19651G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196610 | ||||||
| chr10:59196661
|
G | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+19702G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196661 | ||||||
| chr10:59196695
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.106+19736G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196695 | ||||||
| chr10:59196815
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+19856C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196815 | ||||||
| chr10:59196927
|
C | T | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+19968C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59196927 | ||||||
| chr10:59197144
|
T | C | 48 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(45): Show | 48 | HG00639.hp1 HG01106.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.106+20185T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59197144 | ||||||
| chr10:59197442
|
G | T | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+20483G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59197442 | ||||||
| chr10:59197758
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+20799A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59197758 | ||||||
| chr10:59197844
|
C | T | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+20885C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59197844 | ||||||
| chr10:59198053
|
CT | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+21101delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59198053 | |||||
| chr10:59198153
|
G | A | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.106+21194G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198153 | ||||||
| chr10:59198332
|
C | T | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+21373C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198332 | ||||||
| chr10:59198339
|
T | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+21380T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198339 | ||||||
| chr10:59198385
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+21426A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198385 | ||||||
| chr10:59198431
|
AT | A | 5 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+21480delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59198431 | |||||
| chr10:59198566
|
A | G | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+21607A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198566 | ||||||
| chr10:59198666
|
C | T | 1 | a0002c0004t0001g0137 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.106+21707C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198666 | ||||||
| chr10:59198668
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106+21709C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198668 | ||||||
| chr10:59198669
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106+21710T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198669 | ||||||
| chr10:59198747
|
CT | C | 109 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 111 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.106+21789delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198747 | ||||||
| chr10:59198818
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.106+21859T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59198818 | ||||||
| chr10:59199000
|
G | C | 1 | a0002c0002t0001g0028 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.106+22041G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199000 | ||||||
| chr10:59199003
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0107others(1): Show | 4 | HG02257.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+22044C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199003 | ||||||
| chr10:59199269
|
A | G | 1 | a0002c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.106+22310A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199269 | ||||||
| chr10:59199273
|
A | T | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+22314A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199273 | ||||||
| chr10:59199417
|
T | G | 1 | a0001c0001t0002g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.106+22458T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199417 | ||||||
| chr10:59199455
|
C | T | 108 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 110 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.106+22496C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199455 | ||||||
| chr10:59199469
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.106+22510A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199469 | ||||||
| chr10:59199599
|
G | A | 5 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+22640G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199599 | ||||||
| chr10:59199763
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG02970.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+22804G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199763 | ||||||
| chr10:59199786
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+22827G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59199786 | ||||||
| chr10:59200089
|
T | C | 1 | a0002c0002t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.106+23130T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200089 | ||||||
| chr10:59200163
|
T | A | 1 | a0002c0002t0001g0153 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.106+23204T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200163 | ||||||
| chr10:59200269
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+23310G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200269 | ||||||
| chr10:59200584
|
G | T | 1 | a0002c0002t0001g0167 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.106+23625G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200584 | ||||||
| chr10:59200622
|
A | T | 1 | a0001c0001t0002g0037 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.106+23663A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200622 | ||||||
| chr10:59200626
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+23667G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200626 | ||||||
| chr10:59200814
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.106+23855A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200814 | ||||||
| chr10:59200830
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0063others(8): Show | 11 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+23871C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200830 | ||||||
| chr10:59200873
|
AG | A | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+23915delG | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200873 | ||||||
| chr10:59200972
|
C | T | 109 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 111 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.106+24013C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200972 | ||||||
| chr10:59200973
|
G | A | 2 | a0002c0002t0001g0176a0002c0002t0001g0184 | 2 | HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.106+24014G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59200973 | ||||||
| chr10:59201076
|
C | T | 1 | a0002c0002t0001g0155 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.106+24117C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201076 | ||||||
| chr10:59201166
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106+24207A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201166 | ||||||
| chr10:59201219
|
A | G | 1 | a0002c0002t0001g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.106+24260A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201219 | ||||||
| chr10:59201344
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+24385C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201344 | ||||||
| chr10:59201460
|
A | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+24501A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201460 | ||||||
| chr10:59201464
|
A | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+24505A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201464 | ||||||
| chr10:59201489
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0111 | 3 | HG03041.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.106+24530A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201489 | ||||||
| chr10:59201550
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+24591G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201550 | ||||||
| chr10:59201580
|
G | A | 1 | a0001c0001t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.106+24621G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201580 | ||||||
| chr10:59201728
|
A | G | 36 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(33): Show | 36 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.106+24769A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201728 | ||||||
| chr10:59201927
|
G | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+24968G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59201927 | ||||||
| chr10:59202073
|
G | A | 1 | a0002c0002t0001g0174 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.106+25114G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202073 | ||||||
| chr10:59202155
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+25196T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202155 | ||||||
| chr10:59202178
|
G | T | 1 | a0002c0002t0001g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.106+25219G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202178 | ||||||
| chr10:59202284
|
C | T | 5 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+25325C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202284 | ||||||
| chr10:59202377
|
C | G | 1 | a0001c0001t0011g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.106+25418C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202377 | ||||||
| chr10:59202496
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+25537C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202496 | ||||||
| chr10:59202505
|
T | G | 35 | a0001c0001t0001g0091a0001c0001t0002g0001a0001c0001t0002g0029others(32): Show | 37 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.106+25546T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202505 | ||||||
| chr10:59202511
|
G | GAATGAC | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+25553_106+2555 others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59202511 | |||||
| chr10:59202520
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+25561G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202520 | ||||||
| chr10:59202580
|
T | C | 4 | a0002c0002t0001g0095a0002c0002t0001g0101a0002c0002t0001g0102others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+25621T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202580 | ||||||
| chr10:59202946
|
G | A | 1 | a0002c0002t0001g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.106+25987G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59202946 | ||||||
| chr10:59203103
|
A | G | 13 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.106+26144A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203103 | ||||||
| chr10:59203184
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.106+26225C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203184 | ||||||
| chr10:59203212
|
A | G | 1 | a0002c0002t0001g0172 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.106+26253A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203212 | ||||||
| chr10:59203215
|
A | G | 1 | a0001c0001t0001g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.106+26256A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203215 | ||||||
| chr10:59203450
|
T | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+26491T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203450 | ||||||
| chr10:59203462
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+26503G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203462 | ||||||
| chr10:59203487
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+26528A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203487 | ||||||
| chr10:59203607
|
G | T | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.106+26648G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203607 | ||||||
| chr10:59203649
|
G | C | 1 | a0002c0002t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.106+26690G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203649 | ||||||
| chr10:59203652
|
C | A | 1 | a0002c0002t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.106+26693C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203652 | ||||||
| chr10:59203660
|
C | T | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106+26701C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203660 | ||||||
| chr10:59203932
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0063others(8): Show | 11 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+26973C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203932 | ||||||
| chr10:59203997
|
G | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.106+27038G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59203997 | ||||||
| chr10:59204022
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+27063C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204022 | ||||||
| chr10:59204152
|
A | G | 1 | a0002c0002t0001g0136 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.106+27193A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204152 | ||||||
| chr10:59204204
|
T | G | 1 | a0002c0002t0001g0157 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.106+27245T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204204 | ||||||
| chr10:59204230
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+27271A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204230 | ||||||
| chr10:59204328
|
A | ATAAT | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 113 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.106+27370_106+2737 others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59204328 | |||||
| chr10:59204473
|
G | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.106+27514G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204473 | ||||||
| chr10:59204506
|
G | A | 32 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0030others(29): Show | 34 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.106+27547G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204506 | ||||||
| chr10:59204660
|
G | T | 110 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 112 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.106+27701G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204660 | ||||||
| chr10:59204729
|
A | G | 1 | a0002c0002t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.106+27770A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204729 | ||||||
| chr10:59204745
|
C | A | 110 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 112 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.106+27786C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59204745 | ||||||
| chr10:59204863
|
G | GT | 11 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0002g0041others(8): Show | 11 | HG00673.hp2 HG01106.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+27923dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59204863 | |||||
| chr10:59204863
|
GT | G | 13 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0018others(10): Show | 13 | HG00639.hp2 HG01123.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.106+27923delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59204863 | |||||
| chr10:59204863
|
GTT | G | 5 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009others(2): Show | 5 | HG02145.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+27922_106+2792 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59204863 | |||||
| chr10:59205114
|
C | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+28155C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205114 | ||||||
| chr10:59205175
|
C | T | 1 | a0002c0002t0001g0167 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.106+28216C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205175 | ||||||
| chr10:59205262
|
G | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+28303G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205262 | ||||||
| chr10:59205301
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.106+28342G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205301 | ||||||
| chr10:59205503
|
A | T | 1 | a0002c0002t0001g0185 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.106+28544A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205503 | ||||||
| chr10:59205700
|
C | T | 1 | a0002c0002t0001g0155 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.107-28604C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205700 | ||||||
| chr10:59205778
|
A | G | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-28526A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205778 | ||||||
| chr10:59205958
|
T | G | 2 | a0002c0002t0001g0177a0002c0002t0001g0179 | 2 | HG00733.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.107-28346T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59205958 | ||||||
| chr10:59206493
|
G | A | 51 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(48): Show | 51 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.107-27811G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59206493 | ||||||
| chr10:59206596
|
A | G | 1 | a0002c0002t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.107-27708A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59206596 | ||||||
| chr10:59206714
|
A | G | 1 | a0002c0002t0001g0166 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.107-27590A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59206714 | ||||||
| chr10:59206946
|
G | A | 87 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(84): Show | 89 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.107-27358G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59206946 | ||||||
| chr10:59207092
|
C | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-27212C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207092 | ||||||
| chr10:59207432
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0107others(2): Show | 5 | HG02257.hp2 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-26872G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207432 | ||||||
| chr10:59207755
|
G | A | 4 | a0002c0002t0001g0095a0002c0002t0001g0101a0002c0002t0001g0102others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-26549G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207755 | ||||||
| chr10:59207788
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.107-26516G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207788 | ||||||
| chr10:59207890
|
C | CA | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 15 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.107-26398dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59207890 | |||||
| chr10:59207890
|
C | CAA | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-26399_107-2639 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59207890 | |||||
| chr10:59207952
|
C | A | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-26352C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59207952 | ||||||
| chr10:59208244
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107-26060C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208244 | ||||||
| chr10:59208339
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-25965G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208339 | ||||||
| chr10:59208412
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG00639.hp2 HG01167.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-25892A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208412 | ||||||
| chr10:59208427
|
A | G | 1 | a0002c0002t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.107-25877A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208427 | ||||||
| chr10:59208797
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-25507C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208797 | ||||||
| chr10:59208862
|
A | T | 87 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(84): Show | 89 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.107-25442A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208862 | ||||||
| chr10:59208951
|
T | C | 2 | a0002c0002t0001g0188a0002c0002t0001g0189 | 2 | HG01255.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.107-25353T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59208951 | ||||||
| chr10:59209078
|
C | T | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-25226C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209078 | ||||||
| chr10:59209203
|
A | G | 24 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(21): Show | 24 | HG01884.hp1 HG02015.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.107-25101A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209203 | ||||||
| chr10:59209232
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.107-25072A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209232 | ||||||
| chr10:59209413
|
A | G | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.107-24891A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209413 | ||||||
| chr10:59209496
|
G | A | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-24808G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209496 | ||||||
| chr10:59209503
|
T | C | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 113 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.107-24801T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209503 | ||||||
| chr10:59209749
|
C | T | 1 | a0002c0002t0001g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.107-24555C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209749 | ||||||
| chr10:59209796
|
C | A | 39 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(36): Show | 41 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.107-24508C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59209796 | ||||||
| chr10:59210121
|
C | G | 3 | a0001c0001t0004g0005a0001c0001t0004g0008a0001c0001t0004g0009 | 3 | HG02145.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.107-24183C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59210121 | ||||||
| chr10:59210169
|
C | T | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0107others(2): Show | 5 | HG02257.hp2 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-24135C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59210169 | ||||||
| chr10:59210694
|
A | G | 6 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG02257.hp2 HG03041.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-23610A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59210694 | ||||||
| chr10:59210944
|
A | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-23360A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59210944 | ||||||
| chr10:59211026
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-23278A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211026 | ||||||
| chr10:59211041
|
C | CT | 6 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0063others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-23262dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211041 | |||||
| chr10:59211062
|
A | T | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-23242A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211062 | ||||||
| chr10:59211373
|
T | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-22931T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211373 | ||||||
| chr10:59211664
|
T | TAAA | 50 | a0002c0002t0001g0023a0002c0002t0001g0095a0002c0002t0001g0101others(47): Show | 50 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.107-22616_107-2261 others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | |||||
| chr10:59211664
|
T | TAAAA | 32 | a0001c0001t0002g0191a0002c0002t0001g0026a0002c0002t0001g0027others(29): Show | 32 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.107-22617_107-2261 others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | |||||
| chr10:59211664
|
T | TAAAAA | 5 | a0001c0001t0001g0022a0002c0002t0001g0024a0002c0002t0001g0025others(2): Show | 5 | HG01106.hp1 HG01106.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-22618_107-2261 others(9): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | |||||
| chr10:59211664
|
TA | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-22614delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | |||||
| chr10:59211664
|
TAA | T | 53 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(50): Show | 55 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.107-22615_107-2261 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | |||||
| chr10:59211664
|
TAAA | T | 27 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0076others(24): Show | 27 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.107-22616_107-2261 others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | |||||
| chr10:59211664
|
TAAAA | T | 5 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0002g0057others(2): Show | 5 | HG03453.hp2 HG03491.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-22617_107-2261 others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59211664 | |||||
| chr10:59211665
|
A | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-22639A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211665 | ||||||
| chr10:59211666
|
A | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0096 | 2 | HG02145.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.107-22638A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211666 | ||||||
| chr10:59211667
|
A | T | 53 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(50): Show | 55 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.107-22637A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211667 | ||||||
| chr10:59211668
|
A | T | 27 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0076others(24): Show | 27 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.107-22636A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211668 | ||||||
| chr10:59211669
|
A | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0038a0001c0001t0002g0057 | 3 | HG03491.hp1 NA18946.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.107-22635A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211669 | ||||||
| chr10:59211747
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107-22557A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211747 | ||||||
| chr10:59211900
|
G | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-22404G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211900 | ||||||
| chr10:59211949
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-22355A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59211949 | ||||||
| chr10:59212270
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-22034G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59212270 | ||||||
| chr10:59212625
|
A | G | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-21679A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59212625 | ||||||
| chr10:59212875
|
G | A | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-21429G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59212875 | ||||||
| chr10:59213136
|
T | C | 186 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(183): Show | 188 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.107-21168T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213136 | ||||||
| chr10:59213167
|
T | TA | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-21126dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59213167 | |||||
| chr10:59213327
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-20977C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213327 | ||||||
| chr10:59213591
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.107-20713C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213591 | ||||||
| chr10:59213616
|
A | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-20688A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213616 | ||||||
| chr10:59213712
|
T | C | 40 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(37): Show | 42 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.107-20592T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59213712 | ||||||
| chr10:59214313
|
CA | C | 178 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(175): Show | 180 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(177): Show |
intron_variant | MODIFIER | c.107-19983delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59214313 | |||||
| chr10:59214619
|
A | G | 1 | a0002c0002t0001g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.107-19685A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59214619 | ||||||
| chr10:59214668
|
C | T | 86 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(83): Show | 88 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.107-19636C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59214668 | ||||||
| chr10:59214916
|
A | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-19388A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59214916 | ||||||
| chr10:59215044
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.107-19260A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215044 | ||||||
| chr10:59215082
|
C | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-19222C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215082 | ||||||
| chr10:59215244
|
A | G | 1 | a0002c0002t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.107-19060A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215244 | ||||||
| chr10:59215264
|
A | G | 92 | a0001c0001t0001g0022a0001c0001t0002g0191a0002c0002t0001g0023others(89): Show | 92 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.107-19040A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215264 | ||||||
| chr10:59215410
|
T | A | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-18894T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215410 | ||||||
| chr10:59215583
|
T | G | 2 | a0001c0001t0001g0091a0001c0003t0001g0090 | 2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.107-18721T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215583 | ||||||
| chr10:59215638
|
T | C | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.107-18666T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215638 | ||||||
| chr10:59215710
|
A | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-18594A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215710 | ||||||
| chr10:59215733
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-18571C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215733 | ||||||
| chr10:59215835
|
GA | G | 93 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0002g0191others(90): Show | 93 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.107-18457delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59215835 | |||||
| chr10:59215835
|
GAA | G | 89 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(86): Show | 91 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.107-18458_107-1845 others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59215835 | |||||
| chr10:59215963
|
T | A | 1 | a0002c0002t0001g0142 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.107-18341T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59215963 | ||||||
| chr10:59216018
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.107-18286T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216018 | ||||||
| chr10:59216269
|
C | A | 1 | a0001c0001t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107-18035C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216269 | ||||||
| chr10:59216337
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-17967A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216337 | ||||||
| chr10:59216508
|
C | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-17796C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216508 | ||||||
| chr10:59216512
|
G | A | 86 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(83): Show | 88 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.107-17792G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216512 | ||||||
| chr10:59216892
|
A | G | 1 | a0002c0002t0001g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.107-17412A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59216892 | ||||||
| chr10:59217003
|
ATACTT | A | 3 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0178 | 3 | HG02965.hp2 HG03041.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.107-17291_107-1728 others(9): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59217003 | |||||
| chr10:59217352
|
A | G | 92 | a0001c0001t0001g0022a0001c0001t0002g0191a0002c0002t0001g0023others(89): Show | 92 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.107-16952A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217352 | ||||||
| chr10:59217417
|
T | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-16887T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217417 | ||||||
| chr10:59217460
|
C | T | 2 | a0002c0002t0001g0131a0002c0002t0001g0144 | 2 | NA18965.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.107-16844C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217460 | ||||||
| chr10:59217655
|
T | C | 2 | a0001c0001t0001g0091a0001c0003t0001g0090 | 2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.107-16649T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217655 | ||||||
| chr10:59217748
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.107-16556C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59217748 | ||||||
| chr10:59218055
|
G | A | 1 | a0002c0002t0001g0181 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.107-16249G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218055 | ||||||
| chr10:59218138
|
A | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.107-16166A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218138 | ||||||
| chr10:59218311
|
C | A | 88 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(85): Show | 90 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-15993C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218311 | ||||||
| chr10:59218674
|
TTTGAGTG others(61): Show |
T | 33 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0030others(30): Show | 35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-15561_107-1549 others(72): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59218674 | |||||
| chr10:59218677
|
G | C | 145 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(142): Show | 145 | HG00558.hp1 HG00597.hp2 HG00639.hp1 others(142): Show |
intron_variant | MODIFIER | c.107-15627G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218677 | ||||||
| chr10:59218745
|
G | C | 33 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0030others(30): Show | 35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-15559G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218745 | ||||||
| chr10:59218905
|
A | G | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-15399A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218905 | ||||||
| chr10:59218920
|
A | T | 2 | a0002c0002t0001g0116a0002c0002t0001g0134 | 2 | NA18970.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.107-15384A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218920 | ||||||
| chr10:59218947
|
TC | T | 2 | a0002c0002t0001g0156a0002c0002t0001g0183 | 2 | HG02300.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.107-15356delC | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59218947 | ||||||
| chr10:59219000
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107-15304G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59219000 | ||||||
| chr10:59219201
|
A | C | 178 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(175): Show | 180 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(177): Show |
intron_variant | MODIFIER | c.107-15103A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59219201 | ||||||
| chr10:59219346
|
GA | G | 47 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(44): Show | 47 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-14956delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59219346 | |||||
| chr10:59219833
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-14471G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59219833 | ||||||
| chr10:59219838
|
G | A | 180 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(177): Show | 182 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.107-14466G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59219838 | ||||||
| chr10:59220831
|
T | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-13473T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59220831 | ||||||
| chr10:59220843
|
A | G | 36 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(33): Show | 36 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-13461A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59220843 | ||||||
| chr10:59221041
|
A | G | 6 | a0002c0002t0001g0114a0002c0002t0001g0118a0002c0002t0001g0119others(3): Show | 6 | HG02630.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-13263A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221041 | ||||||
| chr10:59221194
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.107-13110T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221194 | ||||||
| chr10:59221381
|
C | T | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-12923C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221381 | ||||||
| chr10:59221493
|
G | A | 7 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0042others(4): Show | 9 | NA18950.hp1 NA18956.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-12811G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221493 | ||||||
| chr10:59221564
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.107-12740G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221564 | ||||||
| chr10:59221663
|
T | C | 90 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(87): Show | 92 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.107-12641T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221663 | ||||||
| chr10:59221749
|
T | A | 90 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(87): Show | 92 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.107-12555T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59221749 | ||||||
| chr10:59222168
|
C | T | 10 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0071others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.107-12136C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222168 | ||||||
| chr10:59222194
|
A | G | 35 | a0001c0001t0001g0091a0001c0001t0002g0001a0001c0001t0002g0029others(32): Show | 37 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-12110A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222194 | ||||||
| chr10:59222330
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.107-11974G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222330 | ||||||
| chr10:59222402
|
C | A | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-11902C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222402 | ||||||
| chr10:59222473
|
A | G | 36 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(33): Show | 36 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-11831A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222473 | ||||||
| chr10:59222574
|
G | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | NA18941.hp1 NA18947.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-11730G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222574 | ||||||
| chr10:59222716
|
TG | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-11580delG | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59222716 | |||||
| chr10:59222717
|
G | T | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.107-11587G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222717 | ||||||
| chr10:59222733
|
G | GA | 200 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(197): Show | 202 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(199): Show |
intron_variant | MODIFIER | c.107-11564dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59222733 | |||||
| chr10:59222839
|
A | G | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-11465A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222839 | ||||||
| chr10:59222935
|
A | G | 1 | a0002c0002t0001g0147 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.107-11369A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59222935 | ||||||
| chr10:59223095
|
T | C | 88 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(85): Show | 90 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.107-11209T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223095 | ||||||
| chr10:59223230
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.107-11074G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223230 | ||||||
| chr10:59223235
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.107-11069A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223235 | ||||||
| chr10:59223453
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.107-10851G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223453 | ||||||
| chr10:59223455
|
CTGTT | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-10847_107-1084 others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59223455 | |||||
| chr10:59223498
|
A | T | 180 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(177): Show | 182 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.107-10806A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223498 | ||||||
| chr10:59223603
|
G | A | 2 | a0002c0002t0001g0126a0002c0002t0001g0128 | 2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.107-10701G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223603 | ||||||
| chr10:59223670
|
A | AT | 91 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(88): Show | 93 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.107-10624dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59223670 | |||||
| chr10:59223686
|
A | C | 1 | a0002c0002t0001g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.107-10618A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223686 | ||||||
| chr10:59223734
|
C | T | 33 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0030others(30): Show | 35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-10570C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223734 | ||||||
| chr10:59223948
|
C | T | 1 | a0002c0002t0001g0142 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.107-10356C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59223948 | ||||||
| chr10:59224356
|
T | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-9948T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224356 | ||||||
| chr10:59224456
|
G | GAAACA | 27 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0011g0021others(24): Show | 27 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.107-9809_107-9805d others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224456 | |||||
| chr10:59224456
|
G | GAAACAAA others(3): Show |
50 | a0002c0002t0001g0023a0002c0002t0001g0025a0002c0002t0001g0114others(47): Show | 50 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.107-9814_107-9805d others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224456 | |||||
| chr10:59224456
|
G | GAAACAAA others(8): Show |
11 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0126others(8): Show | 11 | HG00738.hp2 HG01123.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-9819_107-9805d others(17): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224456 | |||||
| chr10:59224456
|
GAAACA | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 17 | HG00639.hp2 HG01167.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.107-9809_107-9805d others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224456 | |||||
| chr10:59224497
|
A | AAACAAAA others(11): Show |
1 | a0002c0002t0001g0172 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.107-9805_107-9804i others(20): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224497 | |||||
| chr10:59224497
|
A | AAACAAAA others(8): Show |
2 | a0001c0001t0002g0040a0001c0001t0002g0051 | 2 | HG03831.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.107-9805_107-9804i others(17): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224497 | |||||
| chr10:59224497
|
A | AAACAAAA others(3): Show |
24 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0081others(21): Show | 24 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.107-9805_107-9804i others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224497 | |||||
| chr10:59224497
|
A | AAACAC | 35 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0064others(32): Show | 35 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-9805_107-9804i others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59224497 | |||||
| chr10:59224497
|
A | C | 25 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0067others(22): Show | 27 | HG02257.hp2 HG02451.hp1 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.107-9807A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224497 | ||||||
| chr10:59224509
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.107-9795A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224509 | ||||||
| chr10:59224712
|
A | G | 4 | a0002c0002t0001g0095a0002c0002t0001g0101a0002c0002t0001g0102others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-9592A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224712 | ||||||
| chr10:59224900
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0108 | 3 | HG01891.hp1 HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.107-9404A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59224900 | ||||||
| chr10:59225143
|
T | TAAGAAAT others(304): Show |
1 | a0002c0002t0001g0138 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.107-9143_107-9142i others(313): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(308): Show |
1 | a0002c0002t0001g0179 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.107-9143_107-9142i others(317): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(309): Show |
2 | a0002c0002t0001g0177a0002c0002t0001g0189 | 2 | HG01255.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.107-9143_107-9142i others(318): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(315): Show |
1 | a0002c0002t0001g0162 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.107-9143_107-9142i others(324): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(317): Show |
1 | a0002c0002t0010g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.107-9143_107-9142i others(326): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(321): Show |
2 | a0002c0002t0001g0131a0002c0002t0001g0181 | 2 | NA18965.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.107-9143_107-9142i others(330): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(322): Show |
44 | a0002c0002t0001g0024a0002c0002t0001g0026a0002c0002t0001g0027others(41): Show | 44 | HG00738.hp1 HG01071.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.107-9143_107-9142i others(331): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(323): Show |
28 | a0002c0002t0001g0023a0002c0002t0001g0025a0002c0002t0001g0028others(25): Show | 28 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.107-9143_107-9142i others(332): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(324): Show |
4 | a0002c0002t0001g0147a0002c0002t0001g0170a0002c0002t0001g0184others(1): Show | 4 | HG00673.hp2 HG02602.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-9143_107-9142i others(333): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(325): Show |
3 | a0002c0002t0001g0123a0002c0002t0001g0124a0002c0002t0001g0127 | 3 | HG01433.hp1 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107-9143_107-9142i others(334): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(326): Show |
1 | a0002c0002t0001g0185 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.107-9143_107-9142i others(335): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225143
|
T | TAAGAAAT others(328): Show |
1 | a0002c0002t0001g0180 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.107-9143_107-9142i others(337): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59225143 | |||||
| chr10:59225377
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.107-8927C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225377 | ||||||
| chr10:59225390
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-8914C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225390 | ||||||
| chr10:59225511
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-8793A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225511 | ||||||
| chr10:59225714
|
GA | G | 90 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(87): Show | 92 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.107-8589delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225714 | ||||||
| chr10:59225751
|
G | A | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-8553G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225751 | ||||||
| chr10:59225873
|
G | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-8431G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59225873 | ||||||
| chr10:59226145
|
CAGGAG | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0063others(8): Show | 11 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-8156_107-8152d others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59226145 | |||||
| chr10:59226148
|
G | A | 79 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(76): Show | 81 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.107-8156G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226148 | ||||||
| chr10:59226185
|
T | C | 47 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(44): Show | 47 | HG00639.hp1 HG01106.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.107-8119T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226185 | ||||||
| chr10:59226365
|
C | T | 35 | a0001c0001t0001g0091a0001c0001t0002g0001a0001c0001t0002g0029others(32): Show | 37 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-7939C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226365 | ||||||
| chr10:59226555
|
A | G | 90 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(87): Show | 92 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.107-7749A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226555 | ||||||
| chr10:59226827
|
C | T | 1 | a0002c0002t0001g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.107-7477C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226827 | ||||||
| chr10:59226946
|
A | G | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.107-7358A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59226946 | ||||||
| chr10:59227036
|
A | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-7268A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227036 | ||||||
| chr10:59227149
|
A | G | 1 | a0002c0002t0001g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.107-7155A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227149 | ||||||
| chr10:59227250
|
A | G | 180 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(177): Show | 182 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.107-7054A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227250 | ||||||
| chr10:59227535
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0111 | 3 | HG03041.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.107-6769A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227535 | ||||||
| chr10:59227621
|
A | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-6683A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227621 | ||||||
| chr10:59227855
|
T | C | 2 | a0002c0002t0001g0117a0002c0004t0001g0137 | 2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.107-6449T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227855 | ||||||
| chr10:59227879
|
G | A | 189 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 191 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(188): Show |
intron_variant | MODIFIER | c.107-6425G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59227879 | ||||||
| chr10:59227975
|
G | GAGAGATA others(11): Show |
1 | a0001c0001t0001g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107-6328_107-6327i others(20): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GAGAGATA others(17): Show |
1 | a0001c0001t0002g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.107-6328_107-6327i others(26): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GAGATATA others(13): Show |
5 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0043others(2): Show | 7 | NA18950.hp1 NA18956.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-6328_107-6327i others(22): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GAGATATA others(15): Show |
4 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0041others(1): Show | 4 | HG03491.hp1 HG03492.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-6328_107-6327i others(24): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GAGATATA others(17): Show |
15 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0034others(12): Show | 15 | HG00558.hp2 HG00597.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-6328_107-6327i others(26): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GAGATATA others(19): Show |
6 | a0001c0001t0002g0040a0001c0001t0002g0048a0001c0001t0002g0056others(3): Show | 6 | HG00673.hp1 HG02027.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-6328_107-6327i others(28): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GAGATATA others(21): Show |
2 | a0001c0001t0002g0035a0001c0001t0002g0045 | 2 | HG04228.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.107-6328_107-6327i others(30): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATAGATA others(15): Show |
2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.107-6326_107-6325i others(24): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATAT | 3 | a0001c0001t0001g0080a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | HG02258.hp2 HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.107-6320_107-6317d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATAT | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-6322_107-6317d others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(15): Show |
1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.107-6317_107-6316i others(24): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(7): Show |
1 | a0001c0001t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107-6317_107-6316i others(16): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(9): Show |
4 | a0001c0001t0001g0110a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG00639.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(18): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(11): Show |
1 | a0001c0001t0001g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.107-6317_107-6316i others(20): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(13): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0072a0001c0001t0001g0082others(2): Show | 5 | HG01106.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(22): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(15): Show |
23 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0071others(20): Show | 23 | HG01891.hp1 HG01891.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(24): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(17): Show |
6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0065others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(26): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(19): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0067others(3): Show | 6 | HG02886.hp2 NA18941.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-6317_107-6316i others(28): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(21): Show |
3 | a0001c0001t0001g0064a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02109.hp2 HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.107-6317_107-6316i others(30): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(25): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0014 | 2 | HG01167.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.107-6317_107-6316i others(34): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(27): Show |
1 | a0001c0001t0001g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.107-6317_107-6316i others(36): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(29): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0015 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.107-6317_107-6316i others(38): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59227975
|
G | GATATATA others(25): Show |
3 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0007 | 3 | HG00639.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.107-6317_107-6316i others(34): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59227975 | |||||
| chr10:59228333
|
T | C | 3 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0007 | 3 | HG00639.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.107-5971T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228333 | ||||||
| chr10:59228379
|
G | C | 1 | a0001c0001t0002g0057 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.107-5925G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228379 | ||||||
| chr10:59228795
|
C | T | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-5509C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228795 | ||||||
| chr10:59228823
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.107-5481C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228823 | ||||||
| chr10:59228899
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.107-5405C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228899 | ||||||
| chr10:59228952
|
A | G | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.107-5352A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59228952 | ||||||
| chr10:59229106
|
G | A | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-5198G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229106 | ||||||
| chr10:59229109
|
T | G | 31 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(28): Show | 31 | HG01884.hp1 HG01891.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.107-5195T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229109 | ||||||
| chr10:59229243
|
ATAGT | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-5055_107-5052d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59229243 | |||||
| chr10:59229330
|
C | A | 1 | a0002c0002t0001g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.107-4974C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229330 | ||||||
| chr10:59229392
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.107-4912G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229392 | ||||||
| chr10:59229392
|
G | T | 34 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0030others(31): Show | 36 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-4912G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229392 | ||||||
| chr10:59229465
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.107-4839G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229465 | ||||||
| chr10:59229506
|
T | C | 2 | a0002c0002t0001g0123a0002c0002t0001g0124 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107-4798T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229506 | ||||||
| chr10:59229609
|
T | C | 99 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(96): Show | 101 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.107-4695T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229609 | ||||||
| chr10:59229673
|
C | CA | 86 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(83): Show | 88 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.107-4623dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59229673 | |||||
| chr10:59229674
|
A | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-4630A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229674 | ||||||
| chr10:59229678
|
A | AT | 11 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0063others(8): Show | 11 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-4626_107-4625i others(3): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229678 | ||||||
| chr10:59229707
|
C | T | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-4597C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229707 | ||||||
| chr10:59229859
|
CTTAG | C | 41 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(38): Show | 43 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.107-4440_107-4437d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59229859 | |||||
| chr10:59229915
|
A | G | 1 | a0002c0002t0001g0157 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.107-4389A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229915 | ||||||
| chr10:59229997
|
A | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-4307A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59229997 | ||||||
| chr10:59230057
|
T | C | 3 | a0002c0002t0001g0136a0002c0002t0001g0174a0002c0002t0001g0175 | 3 | HG02083.hp2 HG02132.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.107-4247T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59230057 | ||||||
| chr10:59230117
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.107-4187G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59230117 | ||||||
| chr10:59230167
|
G | A | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-4137G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59230167 | ||||||
| chr10:59230212
|
C | CT | 174 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(171): Show | 176 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(173): Show |
intron_variant | MODIFIER | c.107-4073dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59230212 | |||||
| chr10:59230212
|
C | CTT | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG01106.hp2 HG01123.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.107-4074_107-4073d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59230212 | |||||
| chr10:59230373
|
C | A | 1 | a0002c0002t0001g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.107-3931C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59230373 | ||||||
| chr10:59231107
|
AT | A | 189 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 191 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(188): Show |
intron_variant | MODIFIER | c.107-3189delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59231107 | |||||
| chr10:59231127
|
A | T | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107-3177A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231127 | ||||||
| chr10:59231365
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.107-2939G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231365 | ||||||
| chr10:59231380
|
G | C | 1 | a0001c0001t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107-2924G>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231380 | ||||||
| chr10:59231719
|
C | T | 99 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(96): Show | 101 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.107-2585C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231719 | ||||||
| chr10:59231871
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-2433G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59231871 | ||||||
| chr10:59232006
|
T | C | 1 | a0001c0001t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.107-2298T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232006 | ||||||
| chr10:59232038
|
C | G | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-2266C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232038 | ||||||
| chr10:59232284
|
G | T | 36 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(33): Show | 36 | HG00639.hp1 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.107-2020G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232284 | ||||||
| chr10:59232326
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107-1978A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232326 | ||||||
| chr10:59232376
|
A | G | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-1928A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232376 | ||||||
| chr10:59232426
|
G | A | 2 | a0002c0002t0001g0123a0002c0002t0001g0124 | 2 | HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.107-1878G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232426 | ||||||
| chr10:59232474
|
T | C | 5 | a0001c0001t0001g0110a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG00639.hp1 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-1830T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232474 | ||||||
| chr10:59232561
|
T | C | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.107-1743T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232561 | ||||||
| chr10:59232754
|
TCTA | T | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.107-1546_107-1544d others(5): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr10 | 59232754 | |||||
| chr10:59232804
|
G | A | 1 | a0002c0002t0001g0120 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.107-1500G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232804 | ||||||
| chr10:59232941
|
T | C | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-1363T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59232941 | ||||||
| chr10:59233063
|
T | C | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1241T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233063 | ||||||
| chr10:59233205
|
C | A | 1 | a0001c0001t0005g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.107-1099C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233205 | ||||||
| chr10:59233209
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG01167.hp1 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-1095A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233209 | ||||||
| chr10:59233269
|
G | A | 3 | a0002c0002t0001g0136a0002c0002t0001g0174a0002c0002t0001g0175 | 3 | HG02083.hp2 HG02132.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.107-1035G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233269 | ||||||
| chr10:59233287
|
A | G | 1 | a0002c0002t0001g0138 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.107-1017A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233287 | ||||||
| chr10:59233336
|
A | G | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-968A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233336 | ||||||
| chr10:59233382
|
G | T | 7 | a0001c0001t0002g0001a0001c0001t0002g0033a0001c0001t0002g0042others(4): Show | 9 | NA18950.hp1 NA18956.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-922G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233382 | ||||||
| chr10:59233577
|
T | G | 90 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(87): Show | 90 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.107-727T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233577 | ||||||
| chr10:59233883
|
C | T | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.107-421C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233883 | ||||||
| chr10:59233911
|
T | C | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp1 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-393T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233911 | ||||||
| chr10:59233915
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.107-389C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233915 | ||||||
| chr10:59233997
|
T | G | 89 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(86): Show | 89 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.107-307T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59233997 | ||||||
| chr10:59234021
|
C | T | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.107-283C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59234021 | ||||||
| chr10:59234153
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.107-151G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 1/4 | chr10 | 59234153 | ||||||
| chr10:59234697
|
T | C | 2 | a0002c0002t0001g0177a0002c0002t0001g0179 | 2 | HG00733.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.303+197T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59234697 | ||||||
| chr10:59234797
|
C | T | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.303+297C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59234797 | ||||||
| chr10:59235246
|
A | G | 1 | a0002c0002t0001g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.303+746A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235246 | ||||||
| chr10:59235322
|
T | C | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.303+822T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235322 | ||||||
| chr10:59235558
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-925G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235558 | ||||||
| chr10:59235614
|
A | T | 90 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(87): Show | 90 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.304-869A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235614 | ||||||
| chr10:59235654
|
G | T | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.304-829G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235654 | ||||||
| chr10:59235713
|
G | T | 1 | a0001c0001t0002g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.304-770G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235713 | ||||||
| chr10:59235824
|
C | T | 1 | a0001c0001t0007g0073 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.304-659C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235824 | ||||||
| chr10:59235825
|
G | A | 31 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0064others(28): Show | 31 | HG01884.hp1 HG01891.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.304-658G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235825 | ||||||
| chr10:59235828
|
A | G | 1 | a0002c0002t0001g0185 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.304-655A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59235828 | ||||||
| chr10:59236250
|
A | G | 8 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0007others(5): Show | 8 | HG00639.hp2 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-233A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59236250 | ||||||
| chr10:59236320
|
A | G | 1 | a0002c0002t0001g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.304-163A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59236320 | ||||||
| chr10:59236355
|
TTCCCTTC others(15): Show |
T | 2 | a0002c0002t0001g0145a0002c0002t0001g0146 | 2 | HG02698.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.304-120_304-99delT others(21): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr10 | 59236355 | |||||
| chr10:59236465
|
T | C | 1 | a0002c0002t0001g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.304-18T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 2/4 | chr10 | 59236465 | ||||||
| chr10:59236693
|
G | A | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.478+36G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59236693 | ||||||
| chr10:59236998
|
CT | C | 83 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(80): Show | 85 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.478+355delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr10 | 59236998 | |||||
| chr10:59236998
|
CTT | C | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.478+354_478+355del others(2): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr10 | 59236998 | |||||
| chr10:59237039
|
A | G | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.478+382A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59237039 | ||||||
| chr10:59237806
|
T | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.479-782T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59237806 | ||||||
| chr10:59238034
|
G | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0067others(3): Show | 6 | NA18941.hp1 NA18947.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-554G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238034 | ||||||
| chr10:59238090
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.479-498T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238090 | ||||||
| chr10:59238320
|
A | T | 1 | a0002c0002t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.479-268A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238320 | ||||||
| chr10:59238492
|
C | T | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.479-96C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238492 | ||||||
| chr10:59238524
|
T | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.479-64T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 3/4 | chr10 | 59238524 | ||||||
| chr10:59238995
|
C | T | 4 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(1): Show | 4 | HG02572.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+290C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59238995 | ||||||
| chr10:59239033
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.596+328C>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239033 | ||||||
| chr10:59239042
|
A | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00639.hp2 HG01167.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.596+337A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239042 | ||||||
| chr10:59239086
|
CTGTT | C | 2 | a0002c0002t0001g0129a0002c0002t0001g0130 | 2 | NA18990.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.596+383_596+386del others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59239086 | |||||
| chr10:59239149
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.596+444T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239149 | ||||||
| chr10:59239344
|
G | A | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.596+639G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239344 | ||||||
| chr10:59239427
|
C | T | 2 | a0001c0001t0001g0091a0001c0003t0001g0090 | 2 | HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.596+722C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239427 | ||||||
| chr10:59239436
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.596+731A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239436 | ||||||
| chr10:59239440
|
A | G | 1 | a0002c0002t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.596+735A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239440 | ||||||
| chr10:59239448
|
T | C | 2 | a0002c0002t0001g0172a0002c0002t0001g0183 | 2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.596+743T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239448 | ||||||
| chr10:59239528
|
T | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0063others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+823T>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239528 | ||||||
| chr10:59239639
|
G | T | 1 | a0002c0002t0001g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.596+934G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239639 | ||||||
| chr10:59239768
|
C | T | 1 | a0002c0002t0001g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.596+1063C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59239768 | ||||||
| chr10:59239874
|
A | AT | 197 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(194): Show | 199 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.596+1170dupT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59239874 | |||||
| chr10:59240040
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.596+1335C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240040 | ||||||
| chr10:59240231
|
A | G | 2 | a0002c0002t0001g0126a0002c0002t0001g0128 | 2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.596+1526A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240231 | ||||||
| chr10:59240639
|
T | C | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.596+1934T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240639 | ||||||
| chr10:59240720
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.596+2015C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240720 | ||||||
| chr10:59240756
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.596+2051A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240756 | ||||||
| chr10:59240842
|
G | A | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.596+2137G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59240842 | ||||||
| chr10:59241274
|
T | C | 191 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(188): Show | 193 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(190): Show |
intron_variant | MODIFIER | c.596+2569T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241274 | ||||||
| chr10:59241335
|
AT | A | 33 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0030others(30): Show | 35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.596+2631delT | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241335 | ||||||
| chr10:59241424
|
A | G | 2 | a0001c0001t0005g0199a0001c0001t0005g0200 | 2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.596+2719A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241424 | ||||||
| chr10:59241443
|
T | C | 101 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(98): Show | 103 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.596+2738T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241443 | ||||||
| chr10:59241555
|
C | G | 99 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(96): Show | 101 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.596+2850C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241555 | ||||||
| chr10:59241926
|
C | G | 1 | a0001c0001t0002g0037 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.597-3131C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241926 | ||||||
| chr10:59241927
|
A | G | 1 | a0001c0001t0002g0037 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.597-3130A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59241927 | ||||||
| chr10:59242382
|
A | G | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-2675A>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242382 | ||||||
| chr10:59242420
|
TAGTC | T | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-2634_597-2631d others(6): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59242420 | |||||
| chr10:59242533
|
C | G | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-2524C>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242533 | ||||||
| chr10:59242650
|
A | C | 33 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0030others(30): Show | 35 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.597-2407A>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242650 | ||||||
| chr10:59242670
|
G | T | 1 | a0001c0001t0005g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.597-2387G>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242670 | ||||||
| chr10:59242671
|
A | T | 1 | a0001c0001t0005g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.597-2386A>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59242671 | ||||||
| chr10:59243128
|
G | GAA | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01123.hp2 HG01433.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-1918_597-1917d others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59243128 | |||||
| chr10:59243128
|
GA | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(86): Show | 91 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.597-1917delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59243128 | |||||
| chr10:59243261
|
C | T | 1 | a0002c0002t0010g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.597-1796C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243261 | ||||||
| chr10:59243301
|
T | G | 1 | a0001c0001t0002g0048 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.597-1756T>G | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243301 | ||||||
| chr10:59243429
|
C | T | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 99 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.597-1628C>T | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243429 | ||||||
| chr10:59243923
|
T | C | 93 | a0001c0001t0005g0200a0002c0002t0001g0003a0002c0002t0001g0004others(90): Show | 93 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.597-1134T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243923 | ||||||
| chr10:59243990
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.597-1067T>C | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59243990 | ||||||
| chr10:59244151
|
G | A | 90 | a0001c0001t0005g0200a0002c0002t0001g0023a0002c0002t0001g0024others(87): Show | 90 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.597-906G>A | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | chr10 | 59244151 | ||||||
| chr10:59244268
|
TA | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0107others(1): Show | 4 | HG02257.hp2 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-784delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244268 | |||||
| chr10:59244562
|
C | CA | 57 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(54): Show | 59 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.597-471dupA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
C | CAA | 20 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0076others(17): Show | 20 | HG00558.hp2 HG02135.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.597-472_597-471dup others(2): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
C | CAAAA | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01433.hp2 HG02027.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-474_597-471dup others(4): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
C | CAAAAAAA others(1): Show |
32 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0095others(29): Show | 32 | HG00733.hp2 HG01123.hp1 HG02135.hp1 others(29): Show |
intron_variant | MODIFIER | c.597-478_597-471dup others(8): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
C | CAAAAAAA others(2): Show |
28 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027others(25): Show | 28 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.597-479_597-471dup others(9): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
C | CAAAAAAA others(3): Show |
14 | a0002c0002t0001g0028a0002c0002t0001g0123a0002c0002t0001g0124others(11): Show | 14 | HG01071.hp1 HG02083.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.597-480_597-471dup others(10): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
C | CAAAAAAA others(4): Show |
2 | a0002c0002t0001g0117a0002c0002t0001g0148 | 2 | HG00738.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.597-481_597-471dup others(11): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
C | CAAAAAAA others(5): Show |
2 | a0002c0002t0001g0121a0002c0002t0010g0161 | 2 | HG00597.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.597-482_597-471dup others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
C | CAAAAAAA others(6): Show |
2 | a0002c0002t0001g0135a0002c0002t0001g0143 | 2 | HG01106.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.597-483_597-471dup others(13): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
CA | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0063others(5): Show | 8 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.597-471delA | PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
CAAAAAAA | C | 7 | a0002c0002t0001g0127a0002c0002t0001g0141a0002c0002t0001g0147others(4): Show | 7 | HG00673.hp2 HG01433.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.597-477_597-471del others(7): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 | |||||
| chr10:59244562
|
CAAAAAAA others(5): Show |
C | 3 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0192 | 3 | HG02965.hp2 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.597-482_597-471del others(12): Show |
PHYHIPL | ENSG00000165443.12 | transcript | ENST00000373880.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr10 | 59244562 |