Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3131 |
| ensemblid | ENSG00000108924.14 |
| hgncid | 4977 |
| symbol | HLF |
| name | HLF transcription factor, PAR bZIP family member |
| refseq_nuc | NM_002126.5 |
| refseq_prot | NP_002117.1 |
| ensembl_nuc | ENST00000226067.10 |
| ensembl_prot | ENSP00000226067.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 55264960 |
| end | 55325187 |
| strand | + |
| ver | v1.2 |
| region | chr17:55264960-55325187 |
| region5000 | chr17:55259960-55330187 |
| regionname0 | HLF_chr17_55264960_55325187 |
| regionname5000 | HLF_chr17_55259960_55330187 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 885 | 399 | 90 | 74 | 171 | 16 | 46 | HLF_chr17_55259960_55330187 | HLF | ATGGA others(880): Show |
chr17 | 55259960 | 55330187 | ||
| a0001c0002 | 0/0 | 885 | 3 | 3 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ATGGA others(880): Show |
chr17 | 55259960 | 55330187 | ||
| a0001c0003 | 0/0 | 885 | 3 | 3 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ATGGA others(880): Show |
chr17 | 55259960 | 55330187 | ||
| a0001c0004 | 0/0 | 885 | 2 | 0 | 2 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ATGGA others(880): Show |
chr17 | 55259960 | 55330187 | ||
| a0001c0005 | 0/0 | 885 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ATGGA others(880): Show |
chr17 | 55259960 | 55330187 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5725 | 153 | 24 | 31 | 67 | 6 | 25 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0002 | 0/0 | 5724 | 58 | 11 | 5 | 39 | 2 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5719): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0003 | 1/0 | 5721 | 45 | 6 | 12 | 26 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0004 | 0/1 | 5731 | 22 | 0 | 7 | 6 | 1 | 7 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5726): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0005 | 0/0 | 5720 | 16 | 4 | 1 | 8 | 2 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5715): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0006 | 0/0 | 5727 | 7 | 0 | 0 | 6 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0007 | 0/0 | 5727 | 7 | 1 | 3 | 1 | 2 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0008 | 0/0 | 5735 | 5 | 4 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5730): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0009 | 0/0 | 5725 | 5 | 5 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0010 | 0/0 | 5725 | 4 | 0 | 2 | 0 | 0 | 2 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0011 | 0/0 | 5729 | 4 | 4 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5724): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0012 | 0/0 | 5725 | 3 | 3 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0013 | 0/0 | 5728 | 3 | 0 | 1 | 0 | 0 | 2 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5723): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0014 | 0/0 | 5733 | 3 | 3 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5728): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0015 | 0/0 | 5731 | 3 | 0 | 2 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5726): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0016 | 0/0 | 5727 | 2 | 2 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0017 | 0/0 | 5721 | 2 | 2 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0018 | 0/0 | 5724 | 2 | 0 | 2 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5719): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0019 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0021 | 0/0 | 5727 | 2 | 0 | 0 | 1 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0022 | 0/0 | 5725 | 2 | 2 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0023 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0024 | 0/0 | 5725 | 2 | 2 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0025 | 0/0 | 5721 | 2 | 0 | 2 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0026 | 0/0 | 5720 | 2 | 0 | 0 | 2 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5715): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0027 | 0/0 | 5724 | 2 | 0 | 0 | 2 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5719): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0028 | 0/0 | 5725 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0029 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0030 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0031 | 0/0 | 5727 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0032 | 0/0 | 5721 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0033 | 0/0 | 5720 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5715): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0034 | 0/0 | 5722 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5717): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0035 | 0/0 | 5726 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5721): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0036 | 0/0 | 5721 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0037 | 0/0 | 5723 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5718): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0038 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0039 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0040 | 0/0 | 5729 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5724): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0041 | 0/0 | 5729 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5724): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0042 | 0/0 | 5731 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5726): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0043 | 0/0 | 5721 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0044 | 0/0 | 5723 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5718): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0045 | 0/0 | 5721 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0046 | 0/0 | 5721 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0047 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0048 | 0/0 | 5721 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0049 | 0/0 | 5721 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0050 | 0/0 | 5721 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0051 | 0/0 | 5720 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5715): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0052 | 0/0 | 5721 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5716): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0053 | 0/0 | 5725 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0054 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0055 | 0/0 | 5731 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5726): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0056 | 0/0 | 5724 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5719): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0057 | 0/0 | 5724 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5719): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0058 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0059 | 0/0 | 5737 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5732): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0060 | 0/0 | 5731 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5726): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0061 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5722): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0062 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0063 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0064 | 0/0 | 5731 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5726): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0065 | 0/0 | 5724 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5719): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0066 | 0/0 | 5728 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5723): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0067 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0001t0068 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0002t0019 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0002t0020 | 0/0 | 5729 | 2 | 2 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5724): Show |
chr17 | 55259960 | 55330187 |
| a0001c0003t0001 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0003t0012 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0003t0023 | 0/0 | 5725 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0004t0001 | 0/0 | 5725 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| a0001c0004t0002 | 0/0 | 5724 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5719): Show |
chr17 | 55259960 | 55330187 |
| a0001c0005t0001 | 0/0 | 5725 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | ACTCT others(5720): Show |
chr17 | 55259960 | 55330187 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0001g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0002g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0345 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0003g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0011 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0004g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0005g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0006g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0006g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0006g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0007g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0007g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0008g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0008g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0008g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0009g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0009g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0010g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0011g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0011g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0011g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0011g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0012g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0013g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0013g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0014g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0014g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0015g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0015g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0016g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0016g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0017g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0017g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0018g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0018g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0019g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0021g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0021g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0022g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0022g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0023g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0024g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0024g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0025g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0025g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0026g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0026g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0027g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0027g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0028g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0029g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0030g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0031g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0032g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0033g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0034g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0035g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0036g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0037g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0038g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0039g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0040g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0041g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0042g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0043g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0044g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0045g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0046g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0047g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0048g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0049g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0050g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0051g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0052g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0053g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0054g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0055g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0056g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0057g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0058g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0059g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0060g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0061g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0062g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0063g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0064g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0065g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0066g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0067g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0001t0068g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0002t0019g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0002t0020g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0002t0020g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0003t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0003t0023g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0004t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0004t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| a0001c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0113 | EUR | GBR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | GBR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | GBR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0214 | EUR | FIN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0350 | EUR | FIN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0063 | EUR | FIN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00408 | hp2 | a0001 | c0001 | t0049 | g0161 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0288 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0292 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0106 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0381 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0200 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00735 | hp2 | a0001 | c0001 | t0059 | g0114 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0395 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG00741 | hp2 | a0001 | c0004 | t0002 | g0117 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01070 | hp1 | a0001 | c0001 | t0015 | g0002 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01071 | hp2 | a0001 | c0001 | t0015 | g0002 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01074 | hp2 | a0001 | c0001 | t0018 | g0188 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0259 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0326 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01192 | hp1 | a0001 | c0001 | t0031 | g0314 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0364 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0353 | AMR | PUR | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0303 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01256 | hp1 | a0001 | c0001 | t0018 | g0195 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01258 | hp2 | a0001 | c0001 | t0035 | g0315 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0116 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0377 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01358 | hp1 | a0001 | c0001 | t0025 | g0321 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0201 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0378 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0204 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0380 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0394 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01516 | hp1 | a0001 | c0001 | t0057 | g0171 | EUR | IBS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01517 | hp1 | a0001 | c0001 | t0015 | g0149 | EUR | IBS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01884 | hp1 | a0001 | c0001 | t0060 | g0376 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0366 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0371 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0115 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0379 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01952 | hp1 | a0001 | c0001 | t0025 | g0323 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0306 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01978 | hp1 | a0001 | c0001 | t0030 | g0342 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01981 | hp2 | a0001 | c0001 | t0010 | g0101 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02004 | hp2 | a0001 | c0001 | t0056 | g0001 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0352 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0388 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0293 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02145 | hp1 | a0001 | c0003 | t0023 | g0092 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CDX | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | CDX | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0391 | EAS | CDX | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0386 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0221 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0372 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02602 | hp2 | a0001 | c0001 | t0013 | g0082 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0090 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0337 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0390 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02683 | hp1 | a0001 | c0001 | t0066 | g0150 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0368 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02717 | hp2 | a0001 | c0001 | t0064 | g0085 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02738 | hp2 | a0001 | c0001 | t0010 | g0216 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0362 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0289 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02818 | hp1 | a0001 | c0001 | t0039 | g0334 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0336 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0291 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0060 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0232 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02895 | hp2 | a0001 | c0001 | t0058 | g0385 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0190 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02922 | hp2 | a0001 | c0002 | t0020 | g0107 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0344 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02965 | hp2 | a0001 | c0001 | t0023 | g0086 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0370 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02970 | hp2 | a0001 | c0001 | t0047 | g0338 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0373 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0375 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0369 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03130 | hp2 | a0001 | c0001 | t0054 | g0183 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0282 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03195 | hp1 | a0001 | c0001 | t0024 | g0089 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0339 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03209 | hp1 | a0001 | c0001 | t0063 | g0236 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03225 | hp2 | a0001 | c0001 | t0038 | g0348 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03239 | hp2 | a0001 | c0001 | t0037 | g0317 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03453 | hp2 | a0001 | c0001 | t0048 | g0351 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03486 | hp1 | a0001 | c0002 | t0020 | g0374 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0059 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0202 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03516 | hp2 | a0001 | c0001 | t0017 | g0346 | AFR | ESN | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03540 | hp2 | a0001 | c0001 | t0016 | g0347 | AFR | GWD | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03579 | hp1 | a0001 | c0001 | t0024 | g0088 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03654 | hp1 | a0001 | c0001 | t0053 | g0199 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03654 | hp2 | a0001 | c0001 | t0028 | g0272 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0325 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0049 | SAS | STU | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0075 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0080 | SAS | PJL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03831 | hp2 | a0001 | c0001 | t0065 | g0152 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03834 | hp1 | a0001 | c0001 | t0013 | g0097 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0278 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG04115 | hp2 | a0001 | c0001 | t0043 | g0285 | SAS | STU | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0215 | SAS | STU | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG04228 | hp2 | a0001 | c0001 | t0021 | g0163 | SAS | STU | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0383 | AFR | YRI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0327 | AFR | YRI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0280 | EAS | CHB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | YRI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0229 | AFR | YRI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18939 | hp1 | a0001 | c0001 | t0027 | g0045 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18940 | hp2 | a0001 | c0001 | t0027 | g0053 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18953 | hp1 | a0001 | c0001 | t0068 | g0029 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18962 | hp1 | a0001 | c0001 | t0029 | g0174 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18962 | hp2 | a0001 | c0001 | t0034 | g0006 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18964 | hp2 | a0001 | c0001 | t0045 | g0318 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18966 | hp2 | a0001 | c0001 | t0046 | g0329 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18967 | hp1 | a0001 | c0001 | t0067 | g0022 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18967 | hp2 | a0001 | c0001 | t0021 | g0268 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18974 | hp1 | a0001 | c0001 | t0036 | g0320 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18975 | hp1 | a0001 | c0001 | t0026 | g0208 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18977 | hp1 | a0001 | c0005 | t0001 | g0271 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0392 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19002 | hp1 | a0001 | c0001 | t0026 | g0206 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0294 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19010 | hp1 | a0001 | c0001 | t0032 | g0008 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19030 | hp1 | a0001 | c0001 | t0022 | g0039 | AFR | LWK | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0384 | AFR | LWK | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0217 | AFR | LWK | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0226 | AFR | LWK | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19057 | hp2 | a0001 | c0001 | t0052 | g0312 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0387 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0389 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19070 | hp2 | a0001 | c0001 | t0051 | g0006 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0300 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19077 | hp2 | a0001 | c0001 | t0019 | g0104 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0340 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19085 | hp1 | a0001 | c0001 | t0062 | g0166 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0393 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19240 | hp1 | a0001 | c0001 | t0050 | g0332 | AFR | YRI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA19240 | hp2 | a0001 | c0001 | t0044 | g0335 | AFR | YRI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ASW | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20129 | hp2 | a0001 | c0001 | t0040 | g0328 | AFR | ASW | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0076 | EUR | TSI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20805 | hp1 | a0001 | c0001 | t0033 | g0324 | EUR | TSI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0297 | EUR | TSI | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0071 | SAS | GIH | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | GIH | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02109 | hp1 | a0001 | c0003 | t0012 | g0091 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02486 | hp1 | a0001 | c0001 | t0042 | g0349 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0365 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02559 | hp1 | a0001 | c0002 | t0019 | g0087 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0359 | AFR | ACB | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0205 | AFR | MSL | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG06807 | hp1 | a0001 | c0001 | t0061 | g0363 | AFR | USA | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0333 | AFR | USA | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0382 | AFR | USA | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA20300 | hp2 | a0001 | c0001 | t0041 | g0084 | AFR | USA | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA21309 | hp1 | a0001 | c0001 | t0055 | g0094 | AFR | LWK | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0011 | REF | REF | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0345 | REF | REF | HLF_chr17_55259960_55330187 | HLF | chr17 | 55259960 | 55330187 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:55265559 | G | A | 1 | a0001c0004 | 2 | HG00741.hp2 HG01261.hp1 |
synonymous_variant | LOW | c.75G>A | p.Leu25Leu | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | 600/5721 | 75/888 | 25/295 | chr17 | 55265559 | |||
| chr17:55265572 | C | T | 1 | a0001c0003 | 3 | HG02109.hp1 HG02145.hp1 HG02615.hp1 |
synonymous_variant | LOW | c.88C>T | p.Leu30Leu | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | 613/5721 | 88/888 | 30/295 | chr17 | 55265572 | |||
| chr17:55315435 | T | C | 1 | a0001c0002 | 3 | HG02559.hp1 HG02922.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.660T>C | p.Pro220Pro | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/4 | 1185/5721 | 660/888 | 220/295 | chr17 | 55315435 | |||
| chr17:55320675 | C | T | 1 | a0001c0005 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.684C>T | p.Tyr228Tyr | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1209/5721 | 684/888 | 228/295 | chr17 | 55320675 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:55264968 | C | G | 1 | a0001c0001t0027 | 2 | NA18939.hp1 NA18940.hp2 |
5_prime_UTR_variant | MODIFIER | c.-517C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | 517 | chr17 | 55264968 | ||||||
| chr17:55265032 | G | T | 1 | a0001c0001t0026 | 2 | NA18975.hp1 NA19002.hp1 |
5_prime_UTR_variant | MODIFIER | c.-453G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | 453 | chr17 | 55265032 | ||||||
| chr17:55265106 | C | T | 2 | a0001c0001t0067 a0001c0001t0068 |
2 | NA18953.hp1 NA18967.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-379C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | chr17 | 55265106 | |||||||
| chr17:55265121 | T | G | 1 | a0001c0001t0028 | 1 | HG03654.hp2 | 5_prime_UTR_variant | MODIFIER | c.-364T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | 364 | chr17 | 55265121 | ||||||
| chr17:55265221 | C | T | 1 | a0001c0001t0025 | 2 | HG01358.hp1 HG01952.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-264C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | chr17 | 55265221 | |||||||
| chr17:55265305 | A | G | 1 | a0001c0001t0024 | 2 | HG03195.hp1 HG03579.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-180A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | chr17 | 55265305 | |||||||
| chr17:55265336 | T | C | 1 | a0001c0001t0029 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-149T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | 149 | chr17 | 55265336 | ||||||
| chr17:55265419 | A | G | 3 | a0001c0001t0015 a0001c0001t0065 a0001c0001t0066 |
5 | HG01070.hp1 HG01071.hp2 HG01517.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-66A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | 66 | chr17 | 55265419 | ||||||
| chr17:55265435 | G | GTTTC | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(42): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
5_prime_UTR_variant | MODIFIER | c.-43_-40dupTCTT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/4 | 39 | INFO_REALIGN_3_PRIME | chr17 | 55265435 | |||||
| chr17:55321052 | C | T | 3 | a0001c0001t0012 a0001c0001t0024 a0001c0003t0012 |
6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*173C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 173 | chr17 | 55321052 | ||||||
| chr17:55321098 | T | G | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0015 others(4): Show |
35 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*219T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 219 | chr17 | 55321098 | ||||||
| chr17:55321137 | A | G | 1 | a0001c0001t0052 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*258A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 258 | chr17 | 55321137 | ||||||
| chr17:55321191 | C | G | 1 | a0001c0001t0064 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 312 | chr17 | 55321191 | ||||||
| chr17:55321405 | A | T | 1 | a0001c0001t0051 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*526A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 526 | chr17 | 55321405 | ||||||
| chr17:55321533 | A | G | 3 | a0001c0001t0023 a0001c0001t0050 a0001c0003t0023 |
3 | HG02145.hp1 HG02965.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*654A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 654 | chr17 | 55321533 | ||||||
| chr17:55321671 | A | G | 1 | a0001c0001t0049 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 792 | chr17 | 55321671 | ||||||
| chr17:55321775 | T | C | 1 | a0001c0001t0054 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*896T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 896 | chr17 | 55321775 | ||||||
| chr17:55321839 | A | G | 3 | a0001c0001t0009 a0001c0001t0048 a0001c0001t0063 |
7 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*960A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 960 | chr17 | 55321839 | ||||||
| chr17:55321886 | G | T | 2 | a0001c0001t0062 a0001c0001t0068 |
2 | NA18953.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1007G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1007 | chr17 | 55321886 | ||||||
| chr17:55321927 | C | T | 4 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0022 others(1): Show |
9 | HG01884.hp2 HG02257.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1048C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1048 | chr17 | 55321927 | ||||||
| chr17:55322080 | T | C | 1 | a0001c0001t0055 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1201T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1201 | chr17 | 55322080 | ||||||
| chr17:55322144 | G | A | 1 | a0001c0001t0010 | 4 | HG01361.hp2 HG01981.hp2 HG02738.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1265G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1265 | chr17 | 55322144 | ||||||
| chr17:55322567 | G | A | 2 | a0001c0001t0018 a0001c0001t0033 |
3 | HG01074.hp2 HG01256.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1688G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1688 | chr17 | 55322567 | ||||||
| chr17:55322678 | A | G | 1 | a0001c0001t0046 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1799A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1799 | chr17 | 55322678 | ||||||
| chr17:55322744 | C | T | 1 | a0001c0001t0045 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1865C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1865 | chr17 | 55322744 | ||||||
| chr17:55322749 | T | C | 19 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(16): Show |
97 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1870T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 1870 | chr17 | 55322749 | ||||||
| chr17:55322958 | C | T | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0011 others(7): Show |
43 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2079C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 2079 | chr17 | 55322958 | ||||||
| chr17:55323014 | T | G | 1 | a0001c0001t0031 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2135T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 2135 | chr17 | 55323014 | ||||||
| chr17:55323165 | G | T | 1 | a0001c0001t0044 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2286G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 2286 | chr17 | 55323165 | ||||||
| chr17:55323249 | G | T | 4 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0022 others(1): Show |
9 | HG01884.hp2 HG02257.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2370G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 2370 | chr17 | 55323249 | ||||||
| chr17:55323339 | A | T | 2 | a0001c0001t0009 a0001c0001t0063 |
6 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2460A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 2460 | chr17 | 55323339 | ||||||
| chr17:55323557 | GT | G | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(12): Show |
92 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2681delT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 2681 | INFO_REALIGN_3_PRIME | chr17 | 55323557 | |||||
| chr17:55323648 | C | G | 1 | a0001c0001t0057 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2769C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 2769 | chr17 | 55323648 | ||||||
| chr17:55323726 | G | A | 1 | a0001c0001t0056 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2847G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 2847 | chr17 | 55323726 | ||||||
| chr17:55323920 | A | C | 1 | a0001c0001t0061 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3041A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3041 | chr17 | 55323920 | ||||||
| chr17:55323980 | A | G | 5 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0022 others(2): Show |
10 | HG01884.hp2 HG02257.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3101A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3101 | chr17 | 55323980 | ||||||
| chr17:55324276 | C | T | 1 | a0001c0001t0043 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3397C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3397 | chr17 | 55324276 | ||||||
| chr17:55324319 | A | T | 6 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0022 others(3): Show |
11 | HG01884.hp2 HG02257.hp1 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3440A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3440 | chr17 | 55324319 | ||||||
| chr17:55324342 | C | T | 3 | a0001c0001t0016 a0001c0001t0060 a0001c0001t0064 |
4 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3463C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3463 | chr17 | 55324342 | ||||||
| chr17:55324443 | G | A | 2 | a0001c0001t0009 a0001c0001t0063 |
6 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3564G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3564 | chr17 | 55324443 | ||||||
| chr17:55324634 | A | T | 1 | a0001c0001t0063 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3755A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3755 | chr17 | 55324634 | ||||||
| chr17:55324783 | G | A | 1 | a0001c0001t0058 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3904G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3904 | chr17 | 55324783 | ||||||
| chr17:55324790 | A | AGT | 5 | a0001c0001t0007 a0001c0001t0034 a0001c0001t0037 others(2): Show |
11 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3929_*3930dupTG | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3931 | INFO_REALIGN_3_PRIME | chr17 | 55324790 | |||||
| chr17:55324790 | A | AGTGT | 5 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0047 others(2): Show |
11 | HG01167.hp2 HG02257.hp1 HG02602.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3927_*3930dupTGTG | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3931 | INFO_REALIGN_3_PRIME | chr17 | 55324790 | |||||
| chr17:55324790 | A | AGTGTGT | 5 | a0001c0001t0016 a0001c0001t0039 a0001c0001t0040 others(2): Show |
6 | HG02717.hp2 HG02818.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3925_*3930dupTGTG others(2): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3931 | INFO_REALIGN_3_PRIME | chr17 | 55324790 | |||||
| chr17:55324790 | A | AGTGTGTG others(1): Show |
2 | a0001c0001t0014 a0001c0001t0041 |
4 | HG02647.hp2 HG02723.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3923_*3930dupTGTG others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3931 | INFO_REALIGN_3_PRIME | chr17 | 55324790 | |||||
| chr17:55324790 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0008 a0001c0001t0042 |
6 | HG01243.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3921_*3930dupTGTG others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3931 | INFO_REALIGN_3_PRIME | chr17 | 55324790 | |||||
| chr17:55324790 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0059 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3919_*3930dupTGTG others(8): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3931 | INFO_REALIGN_3_PRIME | chr17 | 55324790 | |||||
| chr17:55324808 | T | TGTGTGC | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0015 others(4): Show |
35 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3930_*3931insTGTG others(2): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3931 | INFO_REALIGN_3_PRIME | chr17 | 55324808 | |||||
| chr17:55324815 | A | ATG | 5 | a0001c0001t0021 a0001c0001t0038 a0001c0001t0040 others(2): Show |
6 | HG03225.hp2 HG04228.hp2 HG06807.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3950_*3951dupGT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 4/4 | 3952 | INFO_REALIGN_3_PRIME | chr17 | 55324815 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:55265602 | G | A | 1 | a0001c0001t0002g0013 | 1 | NA18992.hp2 | splice_region_variant&intron_variant | LOW | c.115+3G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55265602 | |||||||
| chr17:55265683 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(59): Show |
63 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.115+84C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55265683 | |||||||
| chr17:55265870 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.115+271G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55265870 | |||||||
| chr17:55266065 | T | A | 1 | a0001c0001t0005g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.115+466T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266065 | |||||||
| chr17:55266080 | T | G | 1 | a0001c0001t0002g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.115+481T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266080 | |||||||
| chr17:55266142 | C | A | 1 | a0001c0001t0003g0077 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.115+543C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266142 | |||||||
| chr17:55266157 | G | C | 1 | a0001c0001t0003g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.115+558G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266157 | |||||||
| chr17:55266159 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.115+560G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266159 | |||||||
| chr17:55266258 | G | C | 4 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0004g0080 others(1): Show |
4 | HG02602.hp2 HG03017.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+659G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266258 | |||||||
| chr17:55266282 | C | T | 2 | a0001c0001t0001g0395 a0001c0001t0002g0394 |
2 | HG00741.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.115+683C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266282 | |||||||
| chr17:55266285 | A | T | 3 | a0001c0001t0003g0391 a0001c0001t0003g0392 a0001c0001t0003g0393 |
3 | HG02165.hp2 NA18980.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.115+686A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266285 | |||||||
| chr17:55266293 | C | T | 1 | a0001c0001t0014g0390 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.115+694C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266293 | |||||||
| chr17:55266389 | C | T | 1 | a0001c0001t0003g0389 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.115+790C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266389 | |||||||
| chr17:55266423 | C | G | 1 | a0001c0001t0006g0388 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.115+824C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266423 | |||||||
| chr17:55266533 | T | C | 1 | a0001c0001t0041g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.115+934T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266533 | |||||||
| chr17:55266571 | G | A | 3 | a0001c0001t0023g0086 a0001c0001t0064g0085 a0001c0002t0019g0087 |
3 | HG02559.hp1 HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.115+972G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266571 | |||||||
| chr17:55266718 | G | A | 5 | a0001c0001t0024g0088 a0001c0001t0024g0089 a0001c0003t0001g0090 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-1033G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55266718 | |||||||
| chr17:55267228 | G | A | 1 | a0001c0001t0003g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.116-523G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55267228 | |||||||
| chr17:55267247 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0055g0094 |
2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.116-504T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55267247 | |||||||
| chr17:55267505 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0013g0097 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.116-246G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55267505 | |||||||
| chr17:55267597 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.116-154T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55267597 | |||||||
| chr17:55267690 | G | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18966.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.116-61G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 1/3 | chr17 | 55267690 | |||||||
| chr17:55268430 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.451+344A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55268430 | |||||||
| chr17:55268433 | A | G | 1 | a0001c0001t0003g0387 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.451+347A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55268433 | |||||||
| chr17:55268512 | C | A | 1 | a0001c0001t0010g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.451+426C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55268512 | |||||||
| chr17:55268577 | A | T | 1 | a0001c0001t0001g0012 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.451+491A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55268577 | |||||||
| chr17:55268590 | A | AT | 14 | a0001c0001t0001g0096 a0001c0001t0001g0378 a0001c0001t0001g0380 others(11): Show |
14 | HG00733.hp1 HG01346.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.451+513dupT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55268590 | ||||||
| chr17:55268691 | A | T | 23 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0001g0358 others(20): Show |
24 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.451+605A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55268691 | |||||||
| chr17:55268704 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0010g0071 |
3 | HG03669.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.451+618C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55268704 | |||||||
| chr17:55268705 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.451+619G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55268705 | |||||||
| chr17:55268737 | CT | C | 46 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0099 others(43): Show |
46 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.451+664delT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55268737 | ||||||
| chr17:55268761 | T | C | 2 | a0001c0001t0024g0088 a0001c0001t0024g0089 |
2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.451+675T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55268761 | |||||||
| chr17:55269262 | A | G | 1 | a0001c0001t0003g0357 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.451+1176A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269262 | |||||||
| chr17:55269357 | C | T | 41 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0105 others(38): Show |
41 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.451+1271C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269357 | |||||||
| chr17:55269359 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(241): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.451+1273T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269359 | |||||||
| chr17:55269360 | G | A | 18 | a0001c0001t0001g0012 a0001c0001t0001g0102 a0001c0001t0001g0103 others(15): Show |
20 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.451+1274G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269360 | |||||||
| chr17:55269387 | A | G | 1 | a0001c0001t0060g0376 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.451+1301A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269387 | |||||||
| chr17:55269396 | G | A | 41 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0105 others(38): Show |
41 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.451+1310G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269396 | |||||||
| chr17:55269399 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0242 a0001c0001t0001g0244 others(38): Show |
42 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.451+1313C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269399 | |||||||
| chr17:55269409 | A | G | 10 | a0001c0001t0001g0235 a0001c0001t0001g0237 a0001c0001t0001g0238 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+1323A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269409 | |||||||
| chr17:55269431 | C | G | 1 | a0001c0001t0001g0375 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451+1345C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269431 | |||||||
| chr17:55269518 | C | T | 21 | a0001c0001t0001g0098 a0001c0001t0001g0358 a0001c0001t0001g0360 others(18): Show |
22 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.451+1432C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269518 | |||||||
| chr17:55269617 | A | G | 40 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0108 others(37): Show |
40 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.451+1531A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269617 | |||||||
| chr17:55269721 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18955.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.451+1635A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269721 | |||||||
| chr17:55269724 | ATTG | A | 6 | a0001c0001t0001g0098 a0001c0001t0001g0358 a0001c0001t0001g0360 others(3): Show |
6 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+1643_451+1645d others(5): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55269724 | ||||||
| chr17:55269782 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0242 others(39): Show |
43 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.451+1696C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269782 | |||||||
| chr17:55269876 | A | C | 1 | a0001c0001t0003g0353 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451+1790A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269876 | |||||||
| chr17:55269890 | C | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(69): Show |
73 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.451+1804C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55269890 | |||||||
| chr17:55270100 | C | T | 2 | a0001c0001t0002g0373 a0001c0002t0020g0374 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.451+2014C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270100 | |||||||
| chr17:55270480 | G | A | 2 | a0001c0001t0003g0391 a0001c0001t0003g0392 |
2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.451+2394G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270480 | |||||||
| chr17:55270502 | G | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0004g0080 others(1): Show |
4 | HG02602.hp2 HG03017.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+2416G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270502 | |||||||
| chr17:55270552 | A | C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0138 a0001c0001t0005g0350 others(1): Show |
4 | HG00280.hp2 HG00738.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+2466A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270552 | |||||||
| chr17:55270592 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(118): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.451+2506G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270592 | |||||||
| chr17:55270609 | T | G | 1 | a0001c0001t0043g0285 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.451+2523T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270609 | |||||||
| chr17:55270656 | C | CT | 12 | a0001c0001t0001g0196 a0001c0001t0001g0230 a0001c0001t0002g0010 others(9): Show |
13 | HG01891.hp2 HG02056.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.451+2592dupT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55270656 | ||||||
| chr17:55270656 | CT | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(268): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.451+2592delT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55270656 | ||||||
| chr17:55270656 | CTT | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0099 others(12): Show |
15 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.451+2591_451+2592d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55270656 | ||||||
| chr17:55270683 | C | CGGAGTCT others(23): Show |
1 | a0001c0001t0001g0225 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.451+2599_451+2628d others(32): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55270683 | ||||||
| chr17:55270684 | G | A | 1 | a0001c0001t0016g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.451+2598G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270684 | |||||||
| chr17:55270691 | C | T | 2 | a0001c0001t0009g0226 a0001c0001t0009g0227 |
2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.451+2605C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270691 | |||||||
| chr17:55270721 | C | T | 2 | a0001c0001t0003g0290 a0001c0001t0003g0326 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.451+2635C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270721 | |||||||
| chr17:55270724 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0358 a0001c0001t0001g0360 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+2638G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270724 | |||||||
| chr17:55270724 | G | C | 1 | a0001c0001t0041g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.451+2638G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270724 | |||||||
| chr17:55270774 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0162 |
2 | HG00609.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.451+2688T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270774 | |||||||
| chr17:55270786 | G | A | 1 | a0001c0001t0041g0084 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.451+2700G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270786 | |||||||
| chr17:55270787 | T | A | 3 | a0001c0001t0001g0162 a0001c0001t0005g0327 a0001c0001t0040g0328 |
3 | HG00609.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.451+2701T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270787 | |||||||
| chr17:55270799 | A | G | 6 | a0001c0001t0001g0098 a0001c0001t0001g0358 a0001c0001t0001g0360 others(3): Show |
6 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+2713A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270799 | |||||||
| chr17:55270852 | C | T | 1 | a0001c0001t0049g0161 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.451+2766C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270852 | |||||||
| chr17:55270877 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0006g0325 |
2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.451+2791C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270877 | |||||||
| chr17:55270889 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(46): Show |
51 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.451+2803G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270889 | |||||||
| chr17:55270912 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0040g0328 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.451+2826A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270912 | |||||||
| chr17:55270916 | A | GCAGGCGT others(882): Show |
1 | a0001c0001t0033g0324 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.451+2829_451+2830i others(891): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270916 | |||||||
| chr17:55270932 | G | A | 1 | a0001c0001t0009g0369 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.451+2846G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270932 | |||||||
| chr17:55270933 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.451+2847C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270933 | |||||||
| chr17:55270991 | G | T | 20 | a0001c0001t0001g0096 a0001c0001t0001g0237 a0001c0001t0001g0238 others(17): Show |
20 | HG00741.hp1 HG01081.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.451+2905G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55270991 | |||||||
| chr17:55271009 | G | A | 24 | a0001c0001t0001g0072 a0001c0001t0001g0203 a0001c0001t0001g0270 others(21): Show |
24 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.451+2923G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271009 | |||||||
| chr17:55271033 | G | C | 3 | a0001c0001t0001g0034 a0001c0001t0004g0032 a0001c0001t0004g0033 |
3 | NA18953.hp2 NA18963.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.451+2947G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271033 | |||||||
| chr17:55271224 | G | A | 1 | a0001c0001t0003g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.451+3138G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271224 | |||||||
| chr17:55271513 | T | G | 6 | a0001c0001t0001g0035 a0001c0001t0002g0373 a0001c0001t0009g0226 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+3427T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271513 | |||||||
| chr17:55271552 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0002g0373 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+3466T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271552 | |||||||
| chr17:55271582 | T | A | 6 | a0001c0001t0002g0076 a0001c0001t0005g0297 a0001c0001t0005g0350 others(3): Show |
6 | HG00280.hp2 HG00735.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+3496T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271582 | |||||||
| chr17:55271691 | G | A | 2 | a0001c0001t0003g0292 a0001c0001t0028g0272 |
2 | HG00642.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.451+3605G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271691 | |||||||
| chr17:55271731 | T | C | 3 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0016g0347 |
3 | HG01081.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.451+3645T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271731 | |||||||
| chr17:55271811 | G | A | 25 | a0001c0001t0001g0378 a0001c0001t0002g0037 a0001c0001t0002g0062 others(22): Show |
26 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.451+3725G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271811 | |||||||
| chr17:55271833 | A | G | 1 | a0001c0001t0060g0376 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.451+3747A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271833 | |||||||
| chr17:55271915 | T | G | 16 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0002g0010 others(13): Show |
17 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+3829T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55271915 | |||||||
| chr17:55272009 | G | A | 1 | a0001c0001t0026g0206 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.451+3923G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272009 | |||||||
| chr17:55272056 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18960.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.451+3970G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272056 | |||||||
| chr17:55272165 | C | T | 1 | a0001c0001t0025g0323 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.451+4079C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272165 | |||||||
| chr17:55272354 | A | T | 34 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0058 others(31): Show |
35 | HG00597.hp2 HG00673.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.451+4268A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272354 | |||||||
| chr17:55272358 | T | C | 1 | a0001c0001t0003g0298 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.451+4272T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272358 | |||||||
| chr17:55272373 | T | C | 1 | a0001c0001t0005g0009 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.451+4287T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272373 | |||||||
| chr17:55272445 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.451+4359G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272445 | |||||||
| chr17:55272736 | T | C | 1 | a0001c0001t0010g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.451+4650T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272736 | |||||||
| chr17:55272737 | C | T | 16 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0132 others(13): Show |
16 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+4651C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272737 | |||||||
| chr17:55272760 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18960.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.451+4674A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272760 | |||||||
| chr17:55272796 | C | T | 16 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0132 others(13): Show |
16 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+4710C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272796 | |||||||
| chr17:55272798 | G | A | 1 | a0001c0001t0001g0380 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.451+4712G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272798 | |||||||
| chr17:55272805 | G | A | 2 | a0001c0001t0003g0282 a0001c0001t0061g0363 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.451+4719G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55272805 | |||||||
| chr17:55273234 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.451+5148C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55273234 | |||||||
| chr17:55273235 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.451+5149G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55273235 | |||||||
| chr17:55273283 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.451+5197C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55273283 | |||||||
| chr17:55273607 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0002g0179 a0001c0001t0002g0234 others(1): Show |
4 | HG02615.hp2 HG02818.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+5521T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55273607 | |||||||
| chr17:55273701 | GC | G | 3 | a0001c0001t0025g0323 a0001c0004t0001g0116 a0001c0004t0002g0117 |
3 | HG00741.hp2 HG01261.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.451+5616delC | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55273701 | |||||||
| chr17:55273755 | C | CT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0159 a0001c0001t0002g0179 others(4): Show |
7 | HG02486.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+5685dupT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55273755 | ||||||
| chr17:55273755 | CT | C | 211 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.451+5685delT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55273755 | ||||||
| chr17:55273847 | A | C | 11 | a0001c0001t0001g0035 a0001c0001t0002g0010 a0001c0001t0002g0179 others(8): Show |
12 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.451+5761A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55273847 | |||||||
| chr17:55273894 | G | A | 8 | a0001c0001t0002g0010 a0001c0001t0002g0231 a0001c0001t0002g0370 others(5): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+5808G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55273894 | |||||||
| chr17:55273985 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.451+5899G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55273985 | |||||||
| chr17:55274082 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0057 |
2 | NA18747.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.451+5996A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55274082 | |||||||
| chr17:55274184 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(86): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.451+6098G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55274184 | |||||||
| chr17:55274225 | A | G | 1 | a0001c0001t0008g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.451+6139A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55274225 | |||||||
| chr17:55274249 | A | G | 375 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(372): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.451+6163A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55274249 | |||||||
| chr17:55274339 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.451+6253G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55274339 | |||||||
| chr17:55274351 | G | A | 1 | a0001c0001t0003g0295 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.451+6265G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55274351 | |||||||
| chr17:55274517 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0003g0330 others(1): Show |
4 | HG00597.hp1 NA18960.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+6431T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55274517 | |||||||
| chr17:55274642 | C | T | 2 | a0001c0001t0003g0292 a0001c0001t0028g0272 |
2 | HG00642.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.451+6556C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55274642 | |||||||
| chr17:55275157 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.451+7071G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55275157 | |||||||
| chr17:55275242 | T | A | 2 | a0001c0001t0005g0009 a0001c0001t0060g0376 |
3 | HG01884.hp1 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.451+7156T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55275242 | |||||||
| chr17:55275341 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.451+7255C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55275341 | |||||||
| chr17:55275804 | G | C | 1 | a0001c0001t0014g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.451+7718G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55275804 | |||||||
| chr17:55275978 | C | T | 1 | a0001c0001t0003g0219 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.451+7892C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55275978 | |||||||
| chr17:55276078 | A | G | 1 | a0001c0001t0001g0375 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451+7992A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55276078 | |||||||
| chr17:55276176 | C | T | 2 | a0001c0004t0001g0116 a0001c0004t0002g0117 |
2 | HG00741.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.451+8090C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55276176 | |||||||
| chr17:55276615 | A | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0002g0233 others(6): Show |
9 | HG01081.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+8529A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55276615 | |||||||
| chr17:55276813 | CA | C | 5 | a0001c0001t0012g0229 a0001c0001t0016g0291 a0001c0001t0063g0236 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+8728delA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55276813 | |||||||
| chr17:55276819 | CACT | C | 5 | a0001c0001t0012g0229 a0001c0001t0016g0291 a0001c0001t0063g0236 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+8734_451+8736d others(5): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55276819 | |||||||
| chr17:55276913 | A | G | 239 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(236): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.451+8827A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55276913 | |||||||
| chr17:55277061 | A | G | 1 | a0001c0001t0004g0202 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.451+8975A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277061 | |||||||
| chr17:55277233 | T | TTGTG | 88 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0023 others(85): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.451+9148_451+9149i others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277233 | ||||||
| chr17:55277233 | TTA | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0132 a0001c0001t0001g0238 others(8): Show |
11 | HG01070.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+9149_451+9150d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277233 | ||||||
| chr17:55277233 | TTATG | T | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0237 others(5): Show |
8 | HG01074.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.451+9149_451+9152d others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277233 | ||||||
| chr17:55277233 | TTATGTG | T | 9 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0137 others(6): Show |
9 | HG00673.hp1 HG03491.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+9155_451+9160d others(8): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277233 | ||||||
| chr17:55277233 | TTATGTGT others(1): Show |
T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0066 others(24): Show |
28 | HG00597.hp2 HG01168.hp1 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.451+9149_451+9156d others(10): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277233 | ||||||
| chr17:55277233 | TTATGTGT others(3): Show |
T | 23 | a0001c0001t0001g0378 a0001c0001t0002g0177 a0001c0001t0002g0213 others(20): Show |
24 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.451+9149_451+9158d others(12): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277233 | ||||||
| chr17:55277233 | TTATGTGT others(5): Show |
T | 10 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0003g0331 others(7): Show |
10 | HG00558.hp2 HG00621.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.451+9149_451+9160d others(14): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277233 | ||||||
| chr17:55277234 | TATGTGTA others(8): Show |
T | 1 | a0001c0001t0002g0037 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.451+9149_451+9163d others(17): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277234 | |||||||
| chr17:55277235 | A | G | 63 | a0001c0001t0001g0028 a0001c0001t0001g0044 a0001c0001t0001g0054 others(60): Show |
63 | HG00639.hp2 HG01099.hp1 HG01192.hp2 others(60): Show |
intron_variant | MODIFIER | c.451+9149A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277235 | |||||||
| chr17:55277237 | G | GTA | 50 | a0001c0001t0001g0028 a0001c0001t0001g0044 a0001c0001t0001g0054 others(47): Show |
50 | HG00639.hp2 HG01099.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.451+9152_451+9153i others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277237 | ||||||
| chr17:55277239 | G | A | 3 | a0001c0001t0001g0246 a0001c0001t0003g0074 a0001c0001t0042g0349 |
3 | HG01192.hp2 HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.451+9153G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277239 | |||||||
| chr17:55277241 | A | G | 178 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0023 others(175): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.451+9155A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277241 | |||||||
| chr17:55277241 | ATGTG | A | 10 | a0001c0001t0001g0153 a0001c0001t0001g0225 a0001c0001t0001g0355 others(7): Show |
10 | HG01496.hp2 HG02056.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.451+9186_451+9189d others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277241 | ||||||
| chr17:55277241 | ATGTGTG | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(117): Show |
123 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.451+9184_451+9189d others(8): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277241 | ||||||
| chr17:55277241 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.451+9180_451+9189d others(12): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277241 | ||||||
| chr17:55277249 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.451+9163G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277249 | |||||||
| chr17:55277256 | T | G | 1 | a0001c0001t0003g0283 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.451+9170T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277256 | |||||||
| chr17:55277261 | G | C | 15 | a0001c0001t0001g0035 a0001c0001t0002g0010 a0001c0001t0002g0179 others(12): Show |
16 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.451+9175G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277261 | |||||||
| chr17:55277270 | T | C | 2 | a0001c0001t0002g0373 a0001c0001t0014g0205 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.451+9184T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277270 | |||||||
| chr17:55277272 | T | C | 2 | a0001c0001t0002g0373 a0001c0001t0014g0205 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.451+9186T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277272 | |||||||
| chr17:55277274 | T | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0026 others(165): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.451+9188T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277274 | |||||||
| chr17:55277274 | T | TGC | 16 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0055 others(13): Show |
16 | HG00323.hp2 HG00597.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.451+9195_451+9196d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277274 | ||||||
| chr17:55277274 | T | TGTGC | 4 | a0001c0001t0001g0056 a0001c0001t0001g0380 a0001c0001t0003g0313 others(1): Show |
4 | HG01123.hp1 HG01496.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+9189_451+9190i others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277274 | ||||||
| chr17:55277274 | T | TGTGTGC | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0002g0062 |
3 | HG01978.hp2 HG02004.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.451+9189_451+9190i others(8): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277274 | ||||||
| chr17:55277434 | C | A | 375 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(372): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.451+9348C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277434 | |||||||
| chr17:55277489 | C | T | 1 | a0001c0001t0017g0289 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.451+9403C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277489 | |||||||
| chr17:55277621 | G | A | 1 | a0001c0001t0061g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.451+9535G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277621 | |||||||
| chr17:55277625 | T | TG | 85 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0066 others(82): Show |
87 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.451+9547dupG | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55277625 | ||||||
| chr17:55277973 | CT | C | 15 | a0001c0001t0001g0035 a0001c0001t0002g0010 a0001c0001t0002g0179 others(12): Show |
16 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.451+9888delT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55277973 | |||||||
| chr17:55278540 | G | GGGAAAA | 282 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(279): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.451+10455_451+1045 others(10): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55278540 | ||||||
| chr17:55278626 | A | C | 1 | a0001c0001t0008g0364 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.451+10540A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55278626 | |||||||
| chr17:55278717 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.451+10631G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55278717 | |||||||
| chr17:55278765 | G | T | 148 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(145): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.451+10679G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55278765 | |||||||
| chr17:55278776 | A | T | 5 | a0001c0001t0005g0009 a0001c0001t0009g0365 a0001c0001t0055g0094 others(2): Show |
6 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+10690A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55278776 | |||||||
| chr17:55279009 | A | G | 1 | a0001c0001t0008g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.451+10923A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279009 | |||||||
| chr17:55279275 | G | A | 1 | a0001c0001t0014g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.451+11189G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279275 | |||||||
| chr17:55279559 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
92 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.451+11473C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279559 | |||||||
| chr17:55279571 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0262 a0001c0001t0001g0395 |
3 | HG00741.hp1 HG01175.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.451+11485A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279571 | |||||||
| chr17:55279582 | A | G | 5 | a0001c0001t0005g0009 a0001c0001t0009g0365 a0001c0001t0055g0094 others(2): Show |
6 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+11496A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279582 | |||||||
| chr17:55279670 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.451+11584A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279670 | |||||||
| chr17:55279808 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.451+11722G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279808 | |||||||
| chr17:55279844 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.451+11758C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279844 | |||||||
| chr17:55279944 | G | A | 34 | a0001c0001t0001g0378 a0001c0001t0002g0037 a0001c0001t0002g0177 others(31): Show |
35 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.451+11858G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279944 | |||||||
| chr17:55279947 | C | CA | 22 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0367 others(19): Show |
22 | HG01081.hp2 HG02145.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.451+11863dupA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55279947 | ||||||
| chr17:55279948 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0267 |
2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.451+11862A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279948 | |||||||
| chr17:55279964 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.451+11878G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55279964 | |||||||
| chr17:55280037 | G | T | 1 | a0001c0001t0046g0329 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.451+11951G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55280037 | |||||||
| chr17:55280214 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0132 |
3 | HG01074.hp1 HG02602.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.451+12128C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55280214 | |||||||
| chr17:55280301 | C | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0253 a0001c0001t0003g0074 |
3 | HG01934.hp2 HG01975.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.451+12215C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55280301 | |||||||
| chr17:55280449 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.451+12363T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55280449 | |||||||
| chr17:55280652 | C | T | 1 | a0001c0001t0042g0349 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.451+12566C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55280652 | |||||||
| chr17:55280656 | AGTT | A | 70 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0066 others(67): Show |
72 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.451+12578_451+1258 others(7): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55280656 | ||||||
| chr17:55280897 | G | A | 1 | a0001c0001t0003g0306 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.451+12811G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55280897 | |||||||
| chr17:55281096 | G | A | 4 | a0001c0001t0016g0291 a0001c0001t0063g0236 a0001c0001t0064g0085 others(1): Show |
4 | HG02109.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+13010G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55281096 | |||||||
| chr17:55281162 | GAGGGATG others(9): Show |
G | 1 | a0001c0001t0002g0160 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.451+13079_451+1309 others(20): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55281162 | ||||||
| chr17:55281531 | C | G | 4 | a0001c0001t0004g0033 a0001c0001t0005g0305 a0001c0001t0006g0008 others(1): Show |
4 | NA18963.hp1 NA18970.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+13445C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55281531 | |||||||
| chr17:55281531 | C | T | 1 | a0001c0001t0005g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.451+13445C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55281531 | |||||||
| chr17:55281665 | T | A | 6 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0001g0137 others(3): Show |
6 | HG03491.hp1 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+13579T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55281665 | |||||||
| chr17:55281815 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.451+13729G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55281815 | |||||||
| chr17:55281944 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.451+13858C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55281944 | |||||||
| chr17:55282295 | T | C | 4 | a0001c0001t0011g0383 a0001c0001t0011g0384 a0001c0001t0011g0386 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+14209T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282295 | |||||||
| chr17:55282299 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.451+14213T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282299 | |||||||
| chr17:55282379 | A | G | 5 | a0001c0001t0005g0009 a0001c0001t0009g0365 a0001c0001t0055g0094 others(2): Show |
6 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+14293A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282379 | |||||||
| chr17:55282483 | A | G | 220 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0016 others(217): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.451+14397A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282483 | |||||||
| chr17:55282494 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(69): Show |
73 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.451+14408T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282494 | |||||||
| chr17:55282534 | G | A | 63 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(60): Show |
65 | HG01074.hp1 HG01081.hp2 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.451+14448G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282534 | |||||||
| chr17:55282592 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.451+14506A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282592 | |||||||
| chr17:55282634 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.451+14548G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282634 | |||||||
| chr17:55282745 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451+14659C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282745 | |||||||
| chr17:55282745 | C | T | 1 | a0001c0001t0006g0288 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.451+14659C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282745 | |||||||
| chr17:55282903 | A | G | 214 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(211): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.451+14817A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282903 | |||||||
| chr17:55282980 | G | A | 11 | a0001c0001t0001g0035 a0001c0001t0002g0010 a0001c0001t0002g0179 others(8): Show |
12 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.451+14894G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55282980 | |||||||
| chr17:55283072 | G | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0108 a0001c0001t0001g0110 others(1): Show |
4 | HG00558.hp1 HG02132.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+14986G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55283072 | |||||||
| chr17:55283162 | C | T | 72 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(69): Show |
73 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.451+15076C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55283162 | |||||||
| chr17:55283326 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(152): Show |
158 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.451+15240G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55283326 | |||||||
| chr17:55283438 | G | T | 69 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0066 others(66): Show |
71 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.451+15352G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55283438 | |||||||
| chr17:55283461 | G | A | 1 | a0001c0001t0006g0388 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.451+15375G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55283461 | |||||||
| chr17:55283515 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.451+15429G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55283515 | |||||||
| chr17:55283614 | T | A | 63 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(60): Show |
65 | HG01074.hp1 HG01081.hp2 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.451+15528T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55283614 | |||||||
| chr17:55283923 | G | A | 58 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(55): Show |
59 | HG01074.hp1 HG01081.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.451+15837G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55283923 | |||||||
| chr17:55284420 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.451+16334C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284420 | |||||||
| chr17:55284427 | C | T | 21 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0367 others(18): Show |
21 | HG01081.hp2 HG02145.hp1 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.451+16341C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284427 | |||||||
| chr17:55284460 | A | G | 2 | a0001c0001t0002g0373 a0001c0001t0014g0205 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.451+16374A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284460 | |||||||
| chr17:55284477 | T | G | 170 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(167): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.451+16391T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284477 | |||||||
| chr17:55284599 | G | A | 8 | a0001c0001t0002g0010 a0001c0001t0002g0231 a0001c0001t0002g0370 others(5): Show |
9 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+16513G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284599 | |||||||
| chr17:55284739 | G | T | 58 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(55): Show |
59 | HG01074.hp1 HG01081.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.451+16653G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284739 | |||||||
| chr17:55284811 | A | G | 1 | a0001c0001t0005g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451+16725A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284811 | |||||||
| chr17:55284840 | G | A | 4 | a0001c0001t0016g0291 a0001c0001t0063g0236 a0001c0001t0064g0085 others(1): Show |
4 | HG02109.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+16754G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284840 | |||||||
| chr17:55284841 | G | T | 1 | a0001c0001t0009g0365 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.451+16755G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284841 | |||||||
| chr17:55284849 | G | A | 4 | a0001c0001t0016g0291 a0001c0001t0063g0236 a0001c0001t0064g0085 others(1): Show |
4 | HG02109.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+16763G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55284849 | |||||||
| chr17:55285108 | G | A | 1 | a0001c0003t0012g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.451+17022G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55285108 | |||||||
| chr17:55285886 | C | T | 1 | a0001c0001t0004g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.451+17800C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55285886 | |||||||
| chr17:55285907 | C | T | 1 | a0001c0002t0019g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.451+17821C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55285907 | |||||||
| chr17:55286425 | G | A | 9 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0132 others(6): Show |
9 | HG01074.hp1 HG01243.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.451+18339G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286425 | |||||||
| chr17:55286447 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(231): Show |
238 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.451+18361A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286447 | |||||||
| chr17:55286477 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(178): Show |
184 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.451+18391C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286477 | |||||||
| chr17:55286665 | T | C | 15 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0132 others(12): Show |
16 | HG01074.hp1 HG01243.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+18579T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286665 | |||||||
| chr17:55286677 | T | C | 1 | a0001c0001t0031g0314 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.451+18591T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286677 | |||||||
| chr17:55286785 | A | G | 46 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0058 others(43): Show |
48 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.451+18699A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286785 | |||||||
| chr17:55286913 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.451+18827G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286913 | |||||||
| chr17:55286939 | T | C | 84 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0054 others(81): Show |
84 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.451+18853T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286939 | |||||||
| chr17:55286996 | T | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(95): Show |
100 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.451+18910T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55286996 | |||||||
| chr17:55287030 | A | G | 2 | a0001c0001t0012g0229 a0001c0001t0016g0291 |
2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.451+18944A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287030 | |||||||
| chr17:55287238 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.451+19152T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287238 | |||||||
| chr17:55287388 | CAT | C | 70 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0072 others(67): Show |
73 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.451+19303_451+1930 others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287388 | |||||||
| chr17:55287427 | C | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(314): Show |
323 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.451+19341C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287427 | |||||||
| chr17:55287554 | C | T | 2 | a0001c0001t0063g0236 a0001c0001t0064g0085 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.451+19468C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287554 | |||||||
| chr17:55287693 | C | T | 1 | a0001c0002t0020g0374 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.451+19607C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287693 | |||||||
| chr17:55287744 | T | C | 10 | a0001c0001t0002g0010 a0001c0001t0002g0231 a0001c0001t0002g0370 others(7): Show |
11 | HG00323.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+19658T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287744 | |||||||
| chr17:55287811 | A | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(314): Show |
323 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.451+19725A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287811 | |||||||
| chr17:55287852 | A | G | 1 | a0001c0001t0061g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.451+19766A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55287852 | |||||||
| chr17:55288209 | G | A | 1 | a0001c0001t0021g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.451+20123G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288209 | |||||||
| chr17:55288368 | T | A | 20 | a0001c0001t0001g0018 a0001c0001t0002g0030 a0001c0001t0002g0050 others(17): Show |
20 | HG00673.hp2 HG02040.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.451+20282T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288368 | |||||||
| chr17:55288441 | C | G | 1 | a0001c0001t0001g0355 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.451+20355C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288441 | |||||||
| chr17:55288500 | C | T | 63 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0072 others(60): Show |
65 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.451+20414C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288500 | |||||||
| chr17:55288512 | C | T | 1 | a0001c0002t0019g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.451+20426C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288512 | |||||||
| chr17:55288528 | C | T | 5 | a0001c0001t0007g0063 a0001c0001t0017g0289 a0001c0001t0044g0335 others(2): Show |
5 | HG00323.hp2 HG01884.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+20442C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288528 | |||||||
| chr17:55288605 | A | G | 1 | a0001c0001t0007g0106 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.451+20519A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288605 | |||||||
| chr17:55288671 | G | A | 4 | a0001c0001t0005g0303 a0001c0001t0018g0188 a0001c0001t0018g0195 others(1): Show |
4 | HG01074.hp2 HG01255.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+20585G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288671 | |||||||
| chr17:55288755 | C | CA | 301 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(298): Show |
306 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.451+20682dupA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55288755 | ||||||
| chr17:55288785 | T | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(315): Show |
324 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.451+20699T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288785 | |||||||
| chr17:55288859 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.451+20773A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55288859 | |||||||
| chr17:55289154 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(239): Show |
246 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.451+21068A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55289154 | |||||||
| chr17:55289205 | G | T | 94 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0054 others(91): Show |
95 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.451+21119G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55289205 | |||||||
| chr17:55289248 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0240 |
2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.451+21162G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55289248 | |||||||
| chr17:55289383 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.451+21297C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55289383 | |||||||
| chr17:55289843 | C | G | 1 | a0001c0001t0002g0184 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.451+21757C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55289843 | |||||||
| chr17:55289862 | G | A | 63 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0072 others(60): Show |
65 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.451+21776G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55289862 | |||||||
| chr17:55289939 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(233): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.451+21853A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55289939 | |||||||
| chr17:55290013 | C | T | 1 | a0001c0001t0061g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.451+21927C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290013 | |||||||
| chr17:55290090 | TG | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(308): Show |
317 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.451+22006delG | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55290090 | ||||||
| chr17:55290097 | T | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(308): Show |
317 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.451+22011T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290097 | |||||||
| chr17:55290103 | C | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(233): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.451+22017C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290103 | |||||||
| chr17:55290249 | G | A | 2 | a0001c0001t0063g0236 a0001c0001t0064g0085 |
2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.451+22163G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290249 | |||||||
| chr17:55290280 | C | T | 63 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0072 others(60): Show |
65 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.451+22194C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290280 | |||||||
| chr17:55290299 | G | A | 1 | a0001c0001t0008g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.451+22213G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290299 | |||||||
| chr17:55290427 | T | A | 107 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0040 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.451+22341T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290427 | |||||||
| chr17:55290513 | A | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0240 |
2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.451+22427A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290513 | |||||||
| chr17:55290863 | C | G | 4 | a0001c0001t0003g0333 a0001c0001t0012g0190 a0001c0001t0024g0088 others(1): Show |
4 | HG02922.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+22777C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290863 | |||||||
| chr17:55290904 | C | T | 1 | a0001c0001t0007g0106 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.451+22818C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55290904 | |||||||
| chr17:55291198 | G | A | 1 | a0001c0001t0011g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451+23112G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291198 | |||||||
| chr17:55291203 | T | C | 1 | a0001c0001t0053g0199 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.451+23117T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291203 | |||||||
| chr17:55291204 | A | G | 1 | a0001c0001t0001g0382 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.451+23118A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291204 | |||||||
| chr17:55291582 | A | T | 1 | a0001c0002t0019g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.451+23496A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291582 | |||||||
| chr17:55291608 | TA | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(233): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.451+23524delA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55291608 | ||||||
| chr17:55291651 | A | G | 11 | a0001c0001t0001g0035 a0001c0001t0001g0066 a0001c0001t0001g0098 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+23565A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291651 | |||||||
| chr17:55291688 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.452-23539A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291688 | |||||||
| chr17:55291706 | T | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(234): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.452-23521T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291706 | |||||||
| chr17:55291799 | C | T | 6 | a0001c0001t0009g0222 a0001c0001t0009g0226 a0001c0001t0009g0227 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-23428C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291799 | |||||||
| chr17:55291884 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.452-23343A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55291884 | |||||||
| chr17:55292233 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(313): Show |
322 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.452-22994A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292233 | |||||||
| chr17:55292250 | A | G | 1 | a0001c0001t0002g0194 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.452-22977A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292250 | |||||||
| chr17:55292400 | A | G | 64 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0072 others(61): Show |
66 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.452-22827A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292400 | |||||||
| chr17:55292413 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.452-22814A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292413 | |||||||
| chr17:55292511 | C | T | 1 | a0001c0001t0002g0373 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.452-22716C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292511 | |||||||
| chr17:55292613 | C | A | 1 | a0001c0001t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.452-22614C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292613 | |||||||
| chr17:55292700 | T | C | 7 | a0001c0001t0001g0043 a0001c0001t0003g0336 a0001c0001t0003g0337 others(4): Show |
7 | HG02145.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-22527T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292700 | |||||||
| chr17:55292917 | A | T | 1 | a0001c0001t0001g0270 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.452-22310A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292917 | |||||||
| chr17:55292957 | G | A | 11 | a0001c0001t0001g0038 a0001c0001t0002g0233 a0001c0001t0003g0283 others(8): Show |
11 | HG01081.hp2 HG02895.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.452-22270G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55292957 | |||||||
| chr17:55293041 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0052g0312 |
2 | NA18612.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.452-22186A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293041 | |||||||
| chr17:55293255 | T | TA | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(236): Show |
243 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.452-21970dupA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55293255 | ||||||
| chr17:55293266 | T | G | 1 | a0001c0001t0002g0373 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.452-21961T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293266 | |||||||
| chr17:55293344 | C | T | 5 | a0001c0001t0001g0065 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
5 | NA18747.hp2 NA18966.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-21883C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293344 | |||||||
| chr17:55293408 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0240 |
2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.452-21819G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293408 | |||||||
| chr17:55293556 | A | G | 1 | a0001c0001t0016g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.452-21671A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293556 | |||||||
| chr17:55293592 | C | T | 64 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0070 others(61): Show |
66 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.452-21635C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293592 | |||||||
| chr17:55293686 | G | A | 107 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0040 others(104): Show |
109 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.452-21541G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293686 | |||||||
| chr17:55293720 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.452-21507C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293720 | |||||||
| chr17:55293751 | C | T | 1 | a0001c0001t0054g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.452-21476C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55293751 | |||||||
| chr17:55294052 | TA | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(311): Show |
320 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.452-21173delA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55294052 | ||||||
| chr17:55294310 | A | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0052 others(35): Show |
39 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.452-20917A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55294310 | |||||||
| chr17:55294482 | T | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(204): Show |
211 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.452-20745T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55294482 | |||||||
| chr17:55294536 | A | G | 1 | a0001c0001t0047g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.452-20691A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55294536 | |||||||
| chr17:55294889 | A | G | 1 | a0001c0001t0061g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.452-20338A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55294889 | |||||||
| chr17:55295033 | GC | G | 5 | a0001c0001t0007g0063 a0001c0001t0017g0289 a0001c0001t0044g0335 others(2): Show |
5 | HG00323.hp2 HG01884.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-20193delC | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295033 | |||||||
| chr17:55295082 | T | C | 2 | a0001c0001t0004g0215 a0001c0001t0006g0325 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.452-20145T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295082 | |||||||
| chr17:55295093 | G | A | 1 | a0001c0001t0005g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.452-20134G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295093 | |||||||
| chr17:55295205 | G | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(315): Show |
324 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.452-20022G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295205 | |||||||
| chr17:55295219 | G | C | 1 | a0001c0001t0022g0366 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.452-20008G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295219 | |||||||
| chr17:55295336 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.452-19891C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295336 | |||||||
| chr17:55295464 | C | G | 1 | a0001c0001t0061g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.452-19763C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295464 | |||||||
| chr17:55295511 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.452-19716C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295511 | |||||||
| chr17:55295715 | C | G | 1 | a0001c0001t0003g0330 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.452-19512C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295715 | |||||||
| chr17:55295968 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.452-19259G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55295968 | |||||||
| chr17:55296189 | A | T | 109 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0040 others(106): Show |
111 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.452-19038A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55296189 | |||||||
| chr17:55296250 | C | T | 2 | a0001c0001t0015g0002 a0001c0001t0015g0149 |
3 | HG01070.hp1 HG01071.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.452-18977C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55296250 | |||||||
| chr17:55296326 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.452-18901C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55296326 | |||||||
| chr17:55296495 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.452-18732A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55296495 | |||||||
| chr17:55296708 | T | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(89): Show |
94 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.452-18519T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55296708 | |||||||
| chr17:55296837 | A | T | 20 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
21 | HG01243.hp1 HG02257.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.452-18390A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55296837 | |||||||
| chr17:55296838 | T | A | 1 | a0001c0001t0001g0382 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.452-18389T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55296838 | |||||||
| chr17:55296896 | A | C | 2 | a0001c0001t0004g0080 a0001c0001t0004g0202 |
2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.452-18331A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55296896 | |||||||
| chr17:55297249 | T | C | 116 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0040 others(113): Show |
118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.452-17978T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55297249 | |||||||
| chr17:55297715 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.452-17512C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55297715 | |||||||
| chr17:55297738 | C | CT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(213): Show |
219 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.452-17464dupT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55297738 | ||||||
| chr17:55297738 | C | CTT | 17 | a0001c0001t0001g0123 a0001c0001t0001g0378 a0001c0001t0002g0037 others(14): Show |
18 | HG00438.hp1 HG00621.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.452-17465_452-1746 others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55297738 | ||||||
| chr17:55297813 | G | A | 1 | a0001c0001t0007g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.452-17414G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55297813 | |||||||
| chr17:55297828 | C | T | 1 | a0001c0001t0013g0259 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.452-17399C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55297828 | |||||||
| chr17:55297843 | G | A | 1 | a0001c0001t0017g0346 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.452-17384G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55297843 | |||||||
| chr17:55297956 | G | A | 1 | a0001c0001t0044g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.452-17271G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55297956 | |||||||
| chr17:55298211 | C | T | 1 | a0001c0001t0014g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.452-17016C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55298211 | |||||||
| chr17:55298759 | C | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0001g0358 others(6): Show |
9 | HG01109.hp1 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-16468C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55298759 | |||||||
| chr17:55298792 | C | A | 1 | a0001c0001t0018g0195 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.452-16435C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55298792 | |||||||
| chr17:55299143 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(226): Show |
233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.452-16084C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299143 | |||||||
| chr17:55299163 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(247): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.452-16064A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299163 | |||||||
| chr17:55299340 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.452-15887C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299340 | |||||||
| chr17:55299368 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0003g0319 |
2 | NA18954.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.452-15859C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299368 | |||||||
| chr17:55299387 | T | C | 1 | a0001c0001t0004g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.452-15840T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299387 | |||||||
| chr17:55299581 | C | T | 102 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0054 others(99): Show |
104 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.452-15646C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299581 | |||||||
| chr17:55299647 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.452-15580G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299647 | |||||||
| chr17:55299722 | G | A | 1 | a0001c0001t0007g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.452-15505G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299722 | |||||||
| chr17:55299835 | TC | T | 13 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0002g0179 others(10): Show |
14 | HG01243.hp1 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.452-15390delC | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55299835 | ||||||
| chr17:55299857 | A | G | 1 | a0001c0001t0044g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.452-15370A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55299857 | |||||||
| chr17:55300138 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.452-15089C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300138 | |||||||
| chr17:55300177 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.452-15050G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300177 | |||||||
| chr17:55300244 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.452-14983G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300244 | |||||||
| chr17:55300446 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.452-14781A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300446 | |||||||
| chr17:55300519 | G | A | 1 | a0001c0001t0054g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.452-14708G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300519 | |||||||
| chr17:55300811 | A | G | 16 | a0001c0001t0001g0038 a0001c0001t0003g0282 a0001c0001t0003g0283 others(13): Show |
16 | HG01081.hp2 HG02809.hp2 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.452-14416A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300811 | |||||||
| chr17:55300853 | C | T | 11 | a0001c0001t0002g0013 a0001c0001t0002g0112 a0001c0001t0002g0147 others(8): Show |
11 | NA18943.hp2 NA18944.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-14374C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300853 | |||||||
| chr17:55300870 | C | T | 1 | a0001c0001t0001g0367 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.452-14357C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300870 | |||||||
| chr17:55300910 | T | C | 1 | a0001c0001t0060g0376 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.452-14317T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300910 | |||||||
| chr17:55300941 | C | T | 1 | a0001c0001t0021g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.452-14286C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55300941 | |||||||
| chr17:55301277 | G | A | 1 | a0001c0002t0020g0374 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.452-13950G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55301277 | |||||||
| chr17:55301410 | T | G | 1 | a0001c0003t0012g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.452-13817T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55301410 | |||||||
| chr17:55301433 | G | A | 8 | a0001c0001t0009g0222 a0001c0001t0009g0226 a0001c0001t0009g0227 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-13794G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55301433 | |||||||
| chr17:55301508 | G | A | 1 | a0001c0001t0004g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.452-13719G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55301508 | |||||||
| chr17:55301516 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.452-13711G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55301516 | |||||||
| chr17:55301540 | C | T | 1 | a0001c0001t0006g0293 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.452-13687C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55301540 | |||||||
| chr17:55301582 | T | C | 1 | a0001c0001t0002g0356 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.452-13645T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55301582 | |||||||
| chr17:55302045 | C | A | 1 | a0001c0001t0061g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.452-13182C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302045 | |||||||
| chr17:55302133 | A | G | 13 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0001g0238 others(10): Show |
13 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.452-13094A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302133 | |||||||
| chr17:55302143 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.452-13084C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302143 | |||||||
| chr17:55302367 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.452-12860C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302367 | |||||||
| chr17:55302371 | C | T | 33 | a0001c0001t0002g0037 a0001c0001t0003g0295 a0001c0001t0003g0331 others(30): Show |
34 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.452-12856C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302371 | |||||||
| chr17:55302398 | G | C | 1 | a0001c0001t0044g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.452-12829G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302398 | |||||||
| chr17:55302450 | C | T | 101 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0054 others(98): Show |
103 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.452-12777C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302450 | |||||||
| chr17:55302495 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(103): Show |
108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.452-12732G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302495 | |||||||
| chr17:55302528 | G | T | 3 | a0001c0001t0017g0289 a0001c0001t0017g0346 a0001c0001t0055g0094 |
3 | HG02809.hp2 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.452-12699G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302528 | |||||||
| chr17:55302529 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(109): Show |
114 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.452-12698T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302529 | |||||||
| chr17:55302603 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.452-12624G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302603 | |||||||
| chr17:55302801 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.452-12426G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302801 | |||||||
| chr17:55302934 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.452-12293A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55302934 | |||||||
| chr17:55303323 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.452-11904C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55303323 | |||||||
| chr17:55303416 | A | C | 4 | a0001c0001t0012g0190 a0001c0001t0012g0232 a0001c0001t0024g0088 others(1): Show |
4 | HG02895.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-11811A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55303416 | |||||||
| chr17:55303610 | C | CT | 4 | a0001c0001t0012g0190 a0001c0001t0012g0232 a0001c0001t0024g0088 others(1): Show |
4 | HG02895.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-11616dupT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55303610 | ||||||
| chr17:55303736 | C | T | 2 | a0001c0001t0004g0080 a0001c0001t0004g0202 |
2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.452-11491C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55303736 | |||||||
| chr17:55303787 | G | C | 11 | a0001c0001t0001g0038 a0001c0001t0003g0283 a0001c0001t0003g0284 others(8): Show |
11 | HG01081.hp2 HG02895.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.452-11440G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55303787 | |||||||
| chr17:55303802 | C | T | 1 | a0001c0001t0064g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.452-11425C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55303802 | |||||||
| chr17:55303827 | C | T | 1 | a0001c0001t0061g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.452-11400C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55303827 | |||||||
| chr17:55303860 | G | C | 19 | a0001c0001t0001g0109 a0001c0001t0001g0124 a0001c0001t0001g0125 others(16): Show |
19 | HG00408.hp1 HG01070.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-11367G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55303860 | |||||||
| chr17:55304094 | G | C | 36 | a0001c0001t0002g0037 a0001c0001t0003g0295 a0001c0001t0003g0331 others(33): Show |
37 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.452-11133G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304094 | |||||||
| chr17:55304149 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(292): Show |
300 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.452-11078T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304149 | |||||||
| chr17:55304208 | A | G | 1 | a0001c0001t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.452-11019A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304208 | |||||||
| chr17:55304270 | C | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(109): Show |
114 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.452-10957C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304270 | |||||||
| chr17:55304278 | C | A | 2 | a0001c0001t0004g0080 a0001c0001t0004g0202 |
2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.452-10949C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304278 | |||||||
| chr17:55304286 | C | T | 1 | a0001c0001t0043g0285 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.452-10941C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304286 | |||||||
| chr17:55304301 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0052g0312 |
2 | NA18612.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.452-10926C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304301 | |||||||
| chr17:55304360 | G | A | 1 | a0001c0001t0011g0386 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.452-10867G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304360 | |||||||
| chr17:55304435 | C | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(305): Show |
314 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.452-10792C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304435 | |||||||
| chr17:55304524 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(251): Show |
258 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.452-10703G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55304524 | |||||||
| chr17:55305033 | G | A | 1 | a0001c0001t0060g0376 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.452-10194G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305033 | |||||||
| chr17:55305124 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(106): Show |
111 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.452-10103C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305124 | |||||||
| chr17:55305290 | C | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0241 |
2 | NA19007.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.452-9937C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305290 | |||||||
| chr17:55305332 | C | T | 11 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0002g0179 others(8): Show |
12 | HG01243.hp1 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.452-9895C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305332 | |||||||
| chr17:55305343 | G | A | 4 | a0001c0001t0002g0373 a0001c0001t0012g0229 a0001c0001t0016g0291 others(1): Show |
4 | HG02109.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-9884G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305343 | |||||||
| chr17:55305384 | G | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0240 |
2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.452-9843G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305384 | |||||||
| chr17:55305468 | T | C | 96 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0054 others(93): Show |
98 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.452-9759T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305468 | |||||||
| chr17:55305494 | G | A | 1 | a0001c0001t0013g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.452-9733G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305494 | |||||||
| chr17:55305556 | G | T | 1 | a0001c0001t0054g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.452-9671G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305556 | |||||||
| chr17:55305699 | C | T | 1 | a0001c0001t0007g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.452-9528C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305699 | |||||||
| chr17:55305855 | T | C | 1 | a0001c0001t0006g0293 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.452-9372T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55305855 | |||||||
| chr17:55306034 | A | G | 11 | a0001c0001t0001g0038 a0001c0001t0003g0283 a0001c0001t0003g0284 others(8): Show |
11 | HG01081.hp2 HG02895.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.452-9193A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306034 | |||||||
| chr17:55306064 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.452-9163A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306064 | |||||||
| chr17:55306143 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0238 a0001c0001t0001g0358 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-9084C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306143 | |||||||
| chr17:55306156 | G | A | 2 | a0001c0001t0001g0367 a0001c0001t0003g0333 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.452-9071G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306156 | |||||||
| chr17:55306203 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.452-9024G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306203 | |||||||
| chr17:55306266 | G | A | 1 | a0001c0001t0017g0346 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.452-8961G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306266 | |||||||
| chr17:55306408 | G | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0064 others(40): Show |
45 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.452-8819G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306408 | |||||||
| chr17:55306425 | A | T | 1 | a0001c0002t0019g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.452-8802A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306425 | |||||||
| chr17:55306537 | A | AGT | 27 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0069 others(24): Show |
28 | HG00639.hp1 HG00735.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.452-8653_452-8652d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | A | AGTGT | 35 | a0001c0001t0001g0018 a0001c0001t0001g0081 a0001c0001t0001g0102 others(32): Show |
36 | HG00621.hp1 HG00673.hp1 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.452-8655_452-8652d others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | A | AGTGTGT | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(47): Show |
51 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.452-8657_452-8652d others(8): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | A | AGTGTGTG others(1): Show |
36 | a0001c0001t0001g0019 a0001c0001t0001g0058 a0001c0001t0001g0131 others(33): Show |
36 | HG00597.hp2 HG01074.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.452-8659_452-8652d others(10): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | A | AGTGTGTG others(3): Show |
47 | a0001c0001t0001g0040 a0001c0001t0001g0054 a0001c0001t0001g0061 others(44): Show |
47 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.452-8661_452-8652d others(12): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | A | AGTGTGTG others(5): Show |
18 | a0001c0001t0001g0267 a0001c0001t0002g0030 a0001c0001t0002g0112 others(15): Show |
18 | HG00438.hp2 HG01255.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.452-8663_452-8652d others(14): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | A | AGTGTGTG others(7): Show |
11 | a0001c0001t0001g0162 a0001c0001t0001g0257 a0001c0001t0002g0047 others(8): Show |
12 | HG00609.hp2 HG00741.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-8665_452-8652d others(16): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | A | AGTGTGTG others(9): Show |
7 | a0001c0001t0002g0130 a0001c0001t0002g0177 a0001c0001t0002g0277 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-8667_452-8652d others(18): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | AGT | A | 29 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0070 others(26): Show |
29 | HG00099.hp2 HG00140.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.452-8653_452-8652d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | AGTGT | A | 6 | a0001c0001t0001g0247 a0001c0001t0003g0306 a0001c0001t0003g0307 others(3): Show |
6 | HG01081.hp1 HG01975.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-8655_452-8652d others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | AGTGTGT | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0064 others(42): Show |
47 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.452-8657_452-8652d others(8): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | AGTGTGTG others(1): Show |
A | 3 | a0001c0001t0014g0036 a0001c0001t0041g0084 a0001c0001t0061g0363 |
3 | HG02723.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.452-8659_452-8652d others(10): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306537 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0173 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.452-8661_452-8652d others(12): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55306537 | ||||||
| chr17:55306631 | C | A | 1 | a0001c0001t0007g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.452-8596C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306631 | |||||||
| chr17:55306632 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.452-8595G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306632 | |||||||
| chr17:55306667 | T | C | 28 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0098 others(25): Show |
28 | HG01081.hp2 HG02258.hp2 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.452-8560T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306667 | |||||||
| chr17:55306777 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.452-8450C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55306777 | |||||||
| chr17:55307111 | C | T | 1 | a0001c0001t0043g0285 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.452-8116C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55307111 | |||||||
| chr17:55307147 | C | CT | 135 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(132): Show |
136 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.452-8056dupT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55307147 | ||||||
| chr17:55307147 | C | CTT | 12 | a0001c0001t0001g0182 a0001c0001t0001g0276 a0001c0001t0001g0279 others(9): Show |
12 | HG01243.hp2 HG01928.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.452-8057_452-8056d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55307147 | ||||||
| chr17:55307147 | CT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0061 others(46): Show |
51 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.452-8056delT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55307147 | ||||||
| chr17:55307171 | T | C | 6 | a0001c0001t0002g0145 a0001c0001t0002g0156 a0001c0001t0002g0169 others(3): Show |
6 | NA18983.hp2 NA19004.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-8056T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55307171 | |||||||
| chr17:55307218 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.452-8009A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55307218 | |||||||
| chr17:55307342 | A | T | 3 | a0001c0001t0003g0290 a0001c0001t0003g0326 a0001c0001t0060g0376 |
3 | HG01167.hp1 HG01169.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.452-7885A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55307342 | |||||||
| chr17:55307693 | G | A | 1 | a0001c0001t0040g0328 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.452-7534G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55307693 | |||||||
| chr17:55307830 | T | TA | 113 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0054 others(110): Show |
115 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.452-7381dupA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55307830 | ||||||
| chr17:55307830 | TA | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(103): Show |
108 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.452-7381delA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55307830 | ||||||
| chr17:55307923 | C | G | 1 | a0001c0001t0061g0363 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.452-7304C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55307923 | |||||||
| chr17:55307963 | GCAGAGGA others(15): Show |
G | 1 | a0001c0001t0021g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.452-7263_452-7242d others(24): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55307963 | |||||||
| chr17:55307990 | G | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0003g0336 others(5): Show |
8 | HG02145.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-7237G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55307990 | |||||||
| chr17:55308033 | C | T | 1 | a0001c0003t0001g0090 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.452-7194C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308033 | |||||||
| chr17:55308117 | C | T | 1 | a0001c0001t0003g0307 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.452-7110C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308117 | |||||||
| chr17:55308138 | A | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(259): Show |
266 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.452-7089A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308138 | |||||||
| chr17:55308236 | A | G | 5 | a0001c0001t0001g0162 a0001c0001t0002g0051 a0001c0001t0002g0136 others(2): Show |
5 | HG00438.hp2 HG00609.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-6991A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308236 | |||||||
| chr17:55308331 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.452-6896A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308331 | |||||||
| chr17:55308379 | A | C | 1 | a0001c0001t0048g0351 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.452-6848A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308379 | |||||||
| chr17:55308453 | A | G | 41 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0098 others(38): Show |
42 | HG01081.hp2 HG01243.hp1 HG02257.hp2 others(39): Show |
intron_variant | MODIFIER | c.452-6774A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308453 | |||||||
| chr17:55308518 | C | G | 3 | a0001c0001t0017g0289 a0001c0001t0017g0346 a0001c0001t0055g0094 |
3 | HG02809.hp2 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.452-6709C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308518 | |||||||
| chr17:55308715 | C | A | 1 | a0001c0001t0003g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.452-6512C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308715 | |||||||
| chr17:55308745 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.452-6482G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308745 | |||||||
| chr17:55308756 | A | C | 45 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0098 others(42): Show |
46 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(43): Show |
intron_variant | MODIFIER | c.452-6471A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308756 | |||||||
| chr17:55308770 | C | T | 1 | a0001c0001t0039g0334 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.452-6457C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308770 | |||||||
| chr17:55308875 | A | T | 1 | a0001c0001t0052g0312 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.452-6352A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55308875 | |||||||
| chr17:55309060 | C | T | 3 | a0001c0001t0017g0289 a0001c0001t0017g0346 a0001c0001t0055g0094 |
3 | HG02809.hp2 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.452-6167C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55309060 | |||||||
| chr17:55309131 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0257 |
2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.452-6096T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55309131 | |||||||
| chr17:55309143 | T | C | 12 | a0001c0001t0001g0133 a0001c0001t0002g0179 a0001c0001t0002g0234 others(9): Show |
13 | HG01243.hp1 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.452-6084T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55309143 | |||||||
| chr17:55309178 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0001g0238 others(7): Show |
10 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-6049C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55309178 | |||||||
| chr17:55309253 | A | G | 24 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0002g0179 others(21): Show |
25 | HG01081.hp2 HG01243.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.452-5974A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55309253 | |||||||
| chr17:55309465 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(290): Show |
298 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.452-5762G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55309465 | |||||||
| chr17:55309545 | C | T | 1 | a0001c0001t0009g0369 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.452-5682C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55309545 | |||||||
| chr17:55309703 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.452-5524A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55309703 | |||||||
| chr17:55310353 | G | T | 1 | a0001c0001t0001g0378 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.452-4874G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310353 | |||||||
| chr17:55310390 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.452-4837A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310390 | |||||||
| chr17:55310489 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.452-4738A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310489 | |||||||
| chr17:55310515 | T | TA | 93 | a0001c0001t0001g0131 a0001c0001t0001g0162 a0001c0001t0001g0196 others(90): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.452-4712_452-4711i others(3): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310515 | |||||||
| chr17:55310516 | T | A | 93 | a0001c0001t0001g0131 a0001c0001t0001g0162 a0001c0001t0001g0196 others(90): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.452-4711T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310516 | |||||||
| chr17:55310521 | T | C | 3 | a0001c0002t0019g0087 a0001c0002t0020g0107 a0001c0002t0020g0374 |
3 | HG02559.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-4706T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310521 | |||||||
| chr17:55310841 | C | T | 3 | a0001c0002t0019g0087 a0001c0002t0020g0107 a0001c0002t0020g0374 |
3 | HG02559.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.452-4386C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310841 | |||||||
| chr17:55310847 | G | A | 11 | a0001c0001t0002g0013 a0001c0001t0002g0112 a0001c0001t0002g0147 others(8): Show |
11 | NA18943.hp2 NA18944.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-4380G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310847 | |||||||
| chr17:55310972 | C | T | 1 | a0001c0001t0014g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.452-4255C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310972 | |||||||
| chr17:55310998 | T | C | 1 | a0001c0001t0039g0334 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.452-4229T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55310998 | |||||||
| chr17:55311073 | A | G | 15 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0001g0238 others(12): Show |
15 | HG02258.hp2 HG02451.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-4154A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55311073 | |||||||
| chr17:55311074 | ATAT | A | 93 | a0001c0001t0001g0131 a0001c0001t0001g0162 a0001c0001t0001g0196 others(90): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.452-4146_452-4144d others(5): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55311074 | ||||||
| chr17:55311092 | C | T | 1 | a0001c0001t0005g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.452-4135C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55311092 | |||||||
| chr17:55311277 | G | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0151 |
3 | NA18950.hp1 NA18952.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.452-3950G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55311277 | |||||||
| chr17:55311396 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(112): Show |
117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.452-3831C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55311396 | |||||||
| chr17:55311626 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.452-3601A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55311626 | |||||||
| chr17:55311961 | C | T | 1 | a0001c0001t0017g0346 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.452-3266C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55311961 | |||||||
| chr17:55312114 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(106): Show |
111 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.452-3113G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55312114 | |||||||
| chr17:55312190 | C | T | 2 | a0001c0001t0003g0344 a0001c0001t0007g0221 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.452-3037C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55312190 | |||||||
| chr17:55312283 | A | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0137 |
2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.452-2944A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55312283 | |||||||
| chr17:55312398 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.452-2829G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55312398 | |||||||
| chr17:55312420 | A | G | 4 | a0001c0001t0017g0289 a0001c0001t0017g0346 a0001c0001t0044g0335 others(1): Show |
4 | HG02809.hp2 HG03516.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-2807A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55312420 | |||||||
| chr17:55312533 | T | G | 1 | a0001c0001t0002g0169 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.452-2694T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55312533 | |||||||
| chr17:55312542 | C | T | 3 | a0001c0001t0002g0177 a0001c0001t0007g0004 a0001c0001t0007g0214 |
4 | HG00280.hp1 HG01109.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-2685C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55312542 | |||||||
| chr17:55312558 | T | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0239 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.452-2669T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55312558 | |||||||
| chr17:55313022 | G | A | 1 | a0001c0001t0055g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452-2205G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313022 | |||||||
| chr17:55313060 | G | A | 18 | a0001c0001t0004g0011 a0001c0001t0004g0049 a0001c0001t0004g0080 others(15): Show |
19 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.452-2167G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313060 | |||||||
| chr17:55313132 | A | T | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0127 others(1): Show |
4 | NA18966.hp1 NA18989.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-2095A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313132 | |||||||
| chr17:55313242 | G | A | 2 | a0001c0001t0002g0394 a0001c0004t0002g0117 |
2 | HG00741.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.452-1985G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313242 | |||||||
| chr17:55313320 | A | C | 10 | a0001c0001t0001g0038 a0001c0001t0003g0283 a0001c0001t0003g0284 others(7): Show |
10 | HG01081.hp2 HG02895.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.452-1907A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313320 | |||||||
| chr17:55313351 | G | GGT | 5 | a0001c0001t0012g0190 a0001c0001t0012g0232 a0001c0001t0016g0347 others(2): Show |
5 | HG02895.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-1870_452-1869d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313351 | ||||||
| chr17:55313351 | G | GGTGT | 13 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0002g0179 others(10): Show |
14 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.452-1872_452-1869d others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313351 | ||||||
| chr17:55313359 | C | CGT | 21 | a0001c0001t0001g0019 a0001c0001t0001g0098 a0001c0001t0001g0108 others(18): Show |
21 | HG00558.hp1 HG01884.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.452-1839_452-1838d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313359 | ||||||
| chr17:55313359 | C | CGTGT | 13 | a0001c0001t0001g0134 a0001c0001t0003g0286 a0001c0001t0003g0322 others(10): Show |
13 | HG00597.hp2 HG02055.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.452-1841_452-1838d others(6): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313359 | ||||||
| chr17:55313359 | C | CGTGTGT | 31 | a0001c0001t0004g0011 a0001c0001t0004g0015 a0001c0001t0004g0025 others(28): Show |
32 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.452-1843_452-1838d others(8): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313359 | ||||||
| chr17:55313359 | C | CGTGTGTG others(1): Show |
6 | a0001c0001t0004g0202 a0001c0001t0004g0215 a0001c0001t0004g0377 others(3): Show |
6 | HG01346.hp1 HG01943.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-1845_452-1838d others(10): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313359 | ||||||
| chr17:55313359 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0004g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.452-1847_452-1838d others(12): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313359 | ||||||
| chr17:55313359 | C | T | 26 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0002g0179 others(23): Show |
27 | HG01081.hp2 HG01243.hp1 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.452-1868C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313359 | |||||||
| chr17:55313359 | CGT | C | 85 | a0001c0001t0001g0122 a0001c0001t0001g0131 a0001c0001t0001g0162 others(82): Show |
86 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.452-1839_452-1838d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313359 | ||||||
| chr17:55313359 | CGTGTGT | C | 8 | a0001c0001t0002g0010 a0001c0001t0002g0231 a0001c0001t0002g0233 others(5): Show |
9 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-1843_452-1838d others(8): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313359 | ||||||
| chr17:55313359 | CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0173 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.452-1849_452-1838d others(14): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 55313359 | ||||||
| chr17:55313361 | T | C | 3 | a0001c0001t0011g0383 a0001c0001t0011g0384 a0001c0001t0011g0386 |
3 | HG02257.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.452-1866T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313361 | |||||||
| chr17:55313558 | G | T | 7 | a0001c0001t0009g0222 a0001c0001t0009g0226 a0001c0001t0009g0227 others(4): Show |
7 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-1669G>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313558 | |||||||
| chr17:55313712 | C | T | 19 | a0001c0001t0001g0109 a0001c0001t0001g0124 a0001c0001t0001g0125 others(16): Show |
19 | HG00408.hp1 HG01070.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-1515C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313712 | |||||||
| chr17:55313839 | C | T | 1 | a0001c0001t0005g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.452-1388C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313839 | |||||||
| chr17:55313860 | G | A | 8 | a0001c0001t0009g0222 a0001c0001t0009g0226 a0001c0001t0009g0227 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-1367G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55313860 | |||||||
| chr17:55314000 | A | G | 1 | a0001c0001t0005g0009 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.452-1227A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55314000 | |||||||
| chr17:55314476 | C | G | 13 | a0001c0001t0001g0133 a0001c0001t0002g0179 a0001c0001t0002g0234 others(10): Show |
14 | HG01243.hp1 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.452-751C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55314476 | |||||||
| chr17:55314540 | T | C | 5 | a0001c0001t0002g0145 a0001c0001t0002g0156 a0001c0001t0002g0169 others(2): Show |
5 | NA18983.hp2 NA19004.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.452-687T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55314540 | |||||||
| chr17:55314654 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.452-573C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55314654 | |||||||
| chr17:55314847 | A | T | 23 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0002g0179 others(20): Show |
24 | HG01081.hp2 HG01243.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-380A>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55314847 | |||||||
| chr17:55314915 | C | T | 19 | a0001c0001t0001g0109 a0001c0001t0001g0124 a0001c0001t0001g0125 others(16): Show |
19 | HG00408.hp1 HG01070.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-312C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55314915 | |||||||
| chr17:55315007 | T | C | 1 | a0001c0001t0003g0343 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.452-220T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55315007 | |||||||
| chr17:55315087 | C | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0003g0336 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-140C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55315087 | |||||||
| chr17:55315093 | A | C | 1 | a0001c0001t0002g0184 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.452-134A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55315093 | |||||||
| chr17:55315183 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(99): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.452-44T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 2/3 | chr17 | 55315183 | |||||||
| chr17:55315491 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(253): Show |
260 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.672+44G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55315491 | |||||||
| chr17:55315547 | GA | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(105): Show |
110 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+102delA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 55315547 | ||||||
| chr17:55315551 | G | A | 16 | a0001c0001t0004g0011 a0001c0001t0004g0049 a0001c0001t0004g0080 others(13): Show |
17 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.672+104G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55315551 | |||||||
| chr17:55315667 | G | A | 1 | a0001c0001t0002g0371 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.672+220G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55315667 | |||||||
| chr17:55315720 | A | G | 11 | a0001c0001t0009g0222 a0001c0001t0009g0226 a0001c0001t0009g0227 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.672+273A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55315720 | |||||||
| chr17:55315813 | A | G | 1 | a0001c0001t0025g0321 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.672+366A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55315813 | |||||||
| chr17:55316063 | G | A | 1 | a0001c0002t0020g0374 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.672+616G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55316063 | |||||||
| chr17:55316078 | C | G | 13 | a0001c0001t0001g0133 a0001c0001t0002g0179 a0001c0001t0002g0234 others(10): Show |
14 | HG01243.hp1 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+631C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55316078 | |||||||
| chr17:55316249 | C | T | 5 | a0001c0001t0014g0036 a0001c0001t0014g0205 a0001c0001t0014g0390 others(2): Show |
5 | HG02647.hp2 HG02723.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+802C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55316249 | |||||||
| chr17:55316340 | C | A | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | NA18946.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.672+893C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55316340 | |||||||
| chr17:55316344 | C | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0361 |
2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.672+897C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55316344 | |||||||
| chr17:55316558 | G | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | NA18946.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.672+1111G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55316558 | |||||||
| chr17:55316762 | C | G | 1 | a0001c0001t0021g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.672+1315C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55316762 | |||||||
| chr17:55316965 | G | GT | 157 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0038 others(154): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.672+1538dupT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 55316965 | ||||||
| chr17:55316965 | G | GTT | 14 | a0001c0001t0002g0169 a0001c0001t0002g0186 a0001c0001t0002g0372 others(11): Show |
14 | HG01358.hp2 HG01981.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+1537_672+1538d others(4): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 55316965 | ||||||
| chr17:55316965 | G | GTTT | 9 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0070 others(6): Show |
9 | HG00639.hp2 HG01099.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.672+1536_672+1538d others(5): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 55316965 | ||||||
| chr17:55316974 | T | TG | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(108): Show |
113 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.672+1527_672+1528i others(3): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55316974 | |||||||
| chr17:55317054 | G | A | 1 | a0001c0001t0005g0207 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.672+1607G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317054 | |||||||
| chr17:55317128 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.672+1681C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317128 | |||||||
| chr17:55317285 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.672+1838G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317285 | |||||||
| chr17:55317289 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0083 others(1): Show |
4 | HG03669.hp2 HG03704.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+1842C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317289 | |||||||
| chr17:55317493 | G | C | 2 | a0001c0001t0002g0233 a0001c0001t0002g0371 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.672+2046G>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317493 | |||||||
| chr17:55317657 | G | GT | 27 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0002g0179 others(24): Show |
28 | HG01081.hp2 HG01243.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.672+2211dupT | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 55317657 | ||||||
| chr17:55317729 | A | C | 27 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0002g0179 others(24): Show |
28 | HG01081.hp2 HG01243.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.672+2282A>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317729 | |||||||
| chr17:55317818 | CA | C | 8 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0001g0238 others(5): Show |
8 | HG02258.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.672+2372delA | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317818 | |||||||
| chr17:55317839 | G | A | 10 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0001g0238 others(7): Show |
10 | HG02258.hp2 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.672+2392G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317839 | |||||||
| chr17:55317916 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.672+2469T>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317916 | |||||||
| chr17:55317935 | A | G | 1 | a0001c0002t0020g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672+2488A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55317935 | |||||||
| chr17:55318011 | C | T | 1 | a0001c0001t0004g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.672+2564C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318011 | |||||||
| chr17:55318201 | C | G | 2 | a0001c0001t0014g0205 a0001c0001t0040g0328 |
2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.673-2463C>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318201 | |||||||
| chr17:55318344 | C | T | 4 | a0001c0001t0001g0131 a0001c0001t0002g0130 a0001c0001t0002g0394 others(1): Show |
4 | HG00741.hp2 HG01123.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-2320C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318344 | |||||||
| chr17:55318463 | T | C | 34 | a0001c0001t0004g0011 a0001c0001t0004g0015 a0001c0001t0004g0025 others(31): Show |
35 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.673-2201T>C | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318463 | |||||||
| chr17:55318521 | C | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0044 a0001c0001t0001g0118 others(3): Show |
6 | HG01943.hp2 HG01952.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-2143C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318521 | |||||||
| chr17:55318620 | G | A | 1 | a0001c0003t0012g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.673-2044G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318620 | |||||||
| chr17:55318683 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.673-1981C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318683 | |||||||
| chr17:55318773 | T | G | 3 | a0001c0002t0019g0087 a0001c0002t0020g0107 a0001c0002t0020g0374 |
3 | HG02559.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.673-1891T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318773 | |||||||
| chr17:55318815 | G | GAACTGGA others(18): Show |
1 | a0001c0001t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.673-1829_673-1805d others(27): Show |
HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 55318815 | ||||||
| chr17:55318901 | T | G | 4 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0006g0008 others(1): Show |
4 | NA18963.hp1 NA18970.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-1763T>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318901 | |||||||
| chr17:55318902 | C | A | 4 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0006g0008 others(1): Show |
4 | NA18963.hp1 NA18970.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-1762C>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55318902 | |||||||
| chr17:55319076 | G | A | 5 | a0001c0001t0009g0222 a0001c0001t0009g0226 a0001c0001t0009g0227 others(2): Show |
5 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-1588G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55319076 | |||||||
| chr17:55319237 | A | G | 34 | a0001c0001t0003g0306 a0001c0001t0004g0011 a0001c0001t0004g0015 others(31): Show |
35 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.673-1427A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55319237 | |||||||
| chr17:55319477 | G | A | 43 | a0001c0001t0001g0038 a0001c0001t0003g0283 a0001c0001t0003g0284 others(40): Show |
44 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.673-1187G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55319477 | |||||||
| chr17:55319552 | C | T | 1 | a0001c0001t0005g0009 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.673-1112C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55319552 | |||||||
| chr17:55319596 | C | T | 1 | a0001c0001t0009g0365 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.673-1068C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55319596 | |||||||
| chr17:55319609 | A | G | 43 | a0001c0001t0001g0038 a0001c0001t0003g0283 a0001c0001t0003g0284 others(40): Show |
44 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.673-1055A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55319609 | |||||||
| chr17:55319789 | A | G | 43 | a0001c0001t0001g0038 a0001c0001t0003g0283 a0001c0001t0003g0284 others(40): Show |
44 | HG00099.hp1 HG00558.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.673-875A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55319789 | |||||||
| chr17:55320106 | A | G | 1 | a0001c0001t0004g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.673-558A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55320106 | |||||||
| chr17:55320145 | G | A | 2 | a0001c0001t0002g0176 a0001c0001t0002g0197 |
2 | NA18944.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.673-519G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55320145 | |||||||
| chr17:55320149 | A | G | 1 | a0001c0001t0002g0373 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.673-515A>G | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55320149 | |||||||
| chr17:55320365 | G | A | 7 | a0001c0001t0012g0190 a0001c0001t0012g0229 a0001c0001t0012g0232 others(4): Show |
7 | HG02109.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-299G>A | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55320365 | |||||||
| chr17:55320382 | C | T | 1 | a0001c0001t0005g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.673-282C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55320382 | |||||||
| chr17:55320552 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0003g0283 a0001c0001t0003g0284 others(2): Show |
5 | HG01081.hp2 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.673-112C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55320552 | |||||||
| chr17:55320565 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.673-99C>T | HLF | ENSG00000108924.14 | transcript | ENST00000226067.10 | protein_coding | 3/3 | chr17 | 55320565 |