Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 154197 |
| ensemblid | ENSG00000146453.13 |
| hgncid | 21185 |
| symbol | PNLDC1 |
| name | PARN like ribonuclease domain containing exonuclease 1 |
| refseq_nuc | NM_001271862.2 |
| refseq_prot | NP_001258791.1 |
| ensembl_nuc | ENST00000392167.4 |
| ensembl_prot | ENSP00000376007.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 159800276 |
| end | 159820704 |
| strand | + |
| ver | v1.2 |
| region | chr6:159800276-159820704 |
| region5000 | chr6:159795276-159825704 |
| regionname0 | PNLDC1_chr6_159800276_159820704 |
| regionname5000 | PNLDC1_chr6_159795276_159825704 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 531 | 397 | 91 | 74 | 171 | 16 | 43 | 125 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | MDVGA others(526): Show |
chr6 | 159795276 | 159825704 |
| a0002 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | MDVGA others(526): Show |
chr6 | 159795276 | 159825704 |
| a0003 | 0/0 | 536 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | MDVGA others(531): Show |
chr6 | 159795276 | 159825704 |
| a0004 | 0/0 | 531 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | MDVGA others(526): Show |
chr6 | 159795276 | 159825704 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1593 | 250 | 59 | 28 | 135 | 5 | 22 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0002 | 0/1 | 1593 | 128 | 28 | 43 | 31 | 10 | 15 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0003 | 0/0 | 1593 | 6 | 0 | 2 | 0 | 1 | 3 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0004 | 0/0 | 1593 | 4 | 3 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0005 | 0/0 | 1593 | 2 | 0 | 0 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0006 | 0/0 | 1593 | 2 | 0 | 0 | 0 | 0 | 2 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0007 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0008 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0009 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0012 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0001c0014 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0002c0010 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 | ||
| a0003c0013 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1603): Show |
chr6 | 159795276 | 159825704 | ||
| a0004c0011 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | ATGGA others(1588): Show |
chr6 | 159795276 | 159825704 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1815 | 237 | 46 | 28 | 135 | 5 | 22 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0001t0002 | 0/0 | 1815 | 10 | 10 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0001t0003 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0001t0005 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0002t0001 | 0/1 | 1815 | 123 | 25 | 42 | 30 | 10 | 15 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0002t0002 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0002t0004 | 0/0 | 1815 | 2 | 1 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0002t0006 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0003t0001 | 0/0 | 1815 | 6 | 0 | 2 | 0 | 1 | 3 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0004t0001 | 0/0 | 1815 | 4 | 3 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0005t0001 | 0/0 | 1815 | 2 | 0 | 0 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0006t0001 | 0/0 | 1815 | 2 | 0 | 0 | 0 | 0 | 2 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0007t0001 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0008t0001 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0009t0001 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0012t0001 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0001c0014t0001 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0002c0010t0001 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| a0003c0013t0001 | 0/0 | 1830 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1825): Show |
chr6 | 159795276 | 159825704 |
| a0004c0011t0001 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | AGCGC others(1810): Show |
chr6 | 159795276 | 159825704 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 1 | 4 | 22 | 1 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0002 | 0/0 | 25 | 0 | 0 | 24 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0002g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0005 | 0/0 | 5 | 1 | 1 | 2 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0006 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0002t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0008t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0009t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0012t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0001c0014t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0002c0010t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0003c0013t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| a0004c0011t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0235 | EUR | GBR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0237 | EUR | GBR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0019 | EUR | GBR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0194 | EUR | GBR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0250 | EUR | FIN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0176 | EUR | FIN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00544 | hp2 | a0001 | c0005 | t0001 | g0025 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0191 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0173 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0172 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0168 | AMR | PUR | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0227 | EUR | IBS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0234 | EUR | IBS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0236 | EUR | IBS | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02083 | hp1 | a0001 | c0008 | t0001 | g0005 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02135 | hp2 | a0001 | c0005 | t0001 | g0054 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | CDX | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0212 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02523 | hp2 | a0001 | c0007 | t0001 | g0108 | EAS | KHV | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02647 | hp2 | a0002 | c0010 | t0001 | g0183 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0174 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02738 | hp1 | a0003 | c0013 | t0001 | g0134 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0177 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0238 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0192 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0175 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0167 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0257 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03834 | hp1 | a0001 | c0009 | t0001 | g0233 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0148 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG04184 | hp1 | a0001 | c0006 | t0001 | g0251 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | BEB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | STU | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | STU | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG04228 | hp2 | a0001 | c0006 | t0001 | g0239 | SAS | STU | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | YRI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18968 | hp2 | a0004 | c0011 | t0001 | g0077 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18980 | hp2 | a0001 | c0014 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | LWK | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19043 | hp1 | a0001 | c0012 | t0001 | g0166 | AFR | LWK | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | LWK | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19059 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19077 | hp1 | a0001 | c0002 | t0006 | g0262 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0240 | AFR | YRI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ASW | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | TSI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0253 | EUR | TSI | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | GIH | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0258 | SAS | GIH | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | CLM | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0170 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | MSL | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | USA | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0169 | AFR | USA | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | USA | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0206 | REF | REF | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0063 | REF | REF | PNLDC1_chr6_159795276_159825704 | PNLDC1 | chr6 | 159795276 | 159825704 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159810051 | T | C | 1 | a0002 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.809T>C | p.Met270Thr | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/19 | 841/1815 | 809/1596 | 270/531 | chr6 | 159810051 | |||
| chr6:159811737 | T | TCAATAGC others(8): Show |
1 | a0003 | 1 | HG02738.hp1 | disruptive_inframe_insertion | MODERATE | c.890_891insCAATAGCC others(7): Show |
p.Leu297_Phe298insAs others(13): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/19 | 923/1815 | 891/1596 | 297/531 | chr6 | 159811737 | |||
| chr6:159811746 | T | A | 1 | a0003 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.899T>A | p.Val300Asp | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/19 | 931/1815 | 899/1596 | 300/531 | chr6 | 159811746 | |||
| chr6:159811748 | C | A | 1 | a0003 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.901C>A | p.Leu301Ile | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/19 | 933/1815 | 901/1596 | 301/531 | chr6 | 159811748 | |||
| chr6:159811761 | A | T | 1 | a0003 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.914A>T | p.Lys305Met | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/19 | 946/1815 | 914/1596 | 305/531 | chr6 | 159811761 | |||
| chr6:159811764 | G | A | 1 | a0003 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.917G>A | p.Ser306Asn | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/19 | 949/1815 | 917/1596 | 306/531 | chr6 | 159811764 | |||
| chr6:159819291 | A | T | 1 | a0004 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1471A>T | p.Thr491Ser | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/19 | 1503/1815 | 1471/1596 | 491/531 | chr6 | 159819291 | |||
| chr6:159820702 | G | A | 1 | a0001 | 12 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
splice_region_variant | LOW | c.*185G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 19/19 | chr6 | 159820702 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159800361 | C | G | 1 | a0001c0014 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.54C>G | p.Leu18Leu | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/19 | 86/1815 | 54/1596 | 18/531 | chr6 | 159800361 | |||
| chr6:159800791 | G | A | 1 | a0001c0005 | 2 | HG00544.hp2 HG02135.hp2 |
synonymous_variant | LOW | c.96G>A | p.Thr32Thr | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 2/19 | 128/1815 | 96/1596 | 32/531 | chr6 | 159800791 | |||
| chr6:159803968 | T | C | 1 | a0001c0007 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.252T>C | p.Tyr84Tyr | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/19 | 284/1815 | 252/1596 | 84/531 | chr6 | 159803968 | |||
| chr6:159803980 | T | G | 4 | a0001c0002 a0001c0006 a0001c0008 others(1): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
synonymous_variant | LOW | c.264T>G | p.Ser88Ser | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/19 | 296/1815 | 264/1596 | 88/531 | chr6 | 159803980 | |||
| chr6:159804025 | A | G | 1 | a0001c0009 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.309A>G | p.Ser103Ser | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/19 | 341/1815 | 309/1596 | 103/531 | chr6 | 159804025 | |||
| chr6:159806019 | C | T | 1 | a0001c0004 | 4 | HG01243.hp2 HG02559.hp1 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.498C>T | p.Asp166Asp | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/19 | 530/1815 | 498/1596 | 166/531 | chr6 | 159806019 | |||
| chr6:159809020 | A | G | 2 | a0001c0003 a0001c0004 |
10 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
synonymous_variant | LOW | c.645A>G | p.Val215Val | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/19 | 677/1815 | 645/1596 | 215/531 | chr6 | 159809020 | |||
| chr6:159811738 | A | T | 1 | a0003c0013 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.891A>T | p.Leu297Leu | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/19 | 923/1815 | 891/1596 | 297/531 | chr6 | 159811738 | |||
| chr6:159811759 | C | A | 1 | a0003c0013 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.912C>A | p.Thr304Thr | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/19 | 944/1815 | 912/1596 | 304/531 | chr6 | 159811759 | |||
| chr6:159818558 | C | T | 1 | a0001c0012 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1161C>T | p.Ile387Ile | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 16/19 | 1193/1815 | 1161/1596 | 387/531 | chr6 | 159818558 | |||
| chr6:159818612 | C | T | 1 | a0001c0006 | 2 | HG04184.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.1215C>T | p.Tyr405Tyr | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 16/19 | 1247/1815 | 1215/1596 | 405/531 | chr6 | 159818612 | |||
| chr6:159819335 | C | T | 1 | a0001c0008 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1515C>T | p.Asn505Asn | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/19 | 1547/1815 | 1515/1596 | 505/531 | chr6 | 159819335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159800286 | G | A | 1 | a0001c0001t0003 | 2 | HG02572.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-22G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/19 | 22 | chr6 | 159800286 | ||||||
| chr6:159800306 | C | A | 1 | a0001c0001t0005 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/19 | 2 | chr6 | 159800306 | ||||||
| chr6:159820625 | C | T | 1 | a0001c0002t0006 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*108C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 19/19 | 108 | chr6 | 159820625 | ||||||
| chr6:159820657 | G | A | 1 | a0001c0002t0004 | 2 | HG01109.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*140G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 19/19 | 140 | chr6 | 159820657 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:159800410 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.76+27G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/18 | chr6 | 159800410 | |||||||
| chr6:159800411 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.76+28C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/18 | chr6 | 159800411 | |||||||
| chr6:159800443 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(200): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.76+60A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/18 | chr6 | 159800443 | |||||||
| chr6:159800446 | A | AG | 6 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(3): Show |
6 | HG00621.hp2 HG01934.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.76+68dupG | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 159800446 | ||||||
| chr6:159800482 | CAGAG | C | 3 | a0001c0002t0001g0044 a0001c0002t0001g0261 a0001c0002t0006g0262 |
4 | HG02165.hp1 NA19012.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.76+102_76+105delAG others(2): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 159800482 | ||||||
| chr6:159800528 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(65): Show |
115 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.76+145G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/18 | chr6 | 159800528 | |||||||
| chr6:159800658 | GCTT | G | 86 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(83): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.77-110_77-108delCT others(1): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr6 | 159800658 | ||||||
| chr6:159800754 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA19005.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.77-18T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 1/18 | chr6 | 159800754 | |||||||
| chr6:159800960 | CTTT | C | 104 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0254 others(101): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.134+135_134+137del others(3): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr6 | 159800960 | ||||||
| chr6:159800981 | A | T | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.135-132A>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 2/18 | chr6 | 159800981 | |||||||
| chr6:159801025 | C | T | 1 | a0001c0002t0001g0260 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.135-88C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 2/18 | chr6 | 159801025 | |||||||
| chr6:159801218 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.208+32A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801218 | |||||||
| chr6:159801320 | C | T | 1 | a0001c0002t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.208+134C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801320 | |||||||
| chr6:159801445 | C | T | 102 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(99): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.208+259C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801445 | |||||||
| chr6:159801492 | A | G | 103 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.208+306A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801492 | |||||||
| chr6:159801652 | G | C | 103 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.208+466G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801652 | |||||||
| chr6:159801661 | T | G | 103 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.208+475T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801661 | |||||||
| chr6:159801725 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.208+539C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801725 | |||||||
| chr6:159801726 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0160 others(3): Show |
10 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.208+540G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801726 | |||||||
| chr6:159801750 | A | AT | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0146 others(10): Show |
13 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.208+573dupT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 159801750 | ||||||
| chr6:159801786 | AT | A | 103 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.208+608delT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 159801786 | ||||||
| chr6:159801817 | CT | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0160 others(6): Show |
13 | HG01109.hp2 HG02145.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.208+642delT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 159801817 | ||||||
| chr6:159801827 | T | C | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.208+641T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801827 | |||||||
| chr6:159801828 | T | C | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.208+642T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159801828 | |||||||
| chr6:159802114 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.208+928G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802114 | |||||||
| chr6:159802122 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.208+936C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802122 | |||||||
| chr6:159802136 | T | G | 103 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.208+950T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802136 | |||||||
| chr6:159802149 | G | A | 105 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0254 others(102): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.208+963G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802149 | |||||||
| chr6:159802421 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.209-850A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802421 | |||||||
| chr6:159802501 | CGTTT | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG00280.hp2 HG02602.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-761_209-758del others(4): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 159802501 | ||||||
| chr6:159802586 | T | G | 103 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(100): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.209-685T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802586 | |||||||
| chr6:159802687 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.209-584A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802687 | |||||||
| chr6:159802731 | C | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG01884.hp1 HG03209.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-540C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802731 | |||||||
| chr6:159802802 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(65): Show |
115 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.209-469C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802802 | |||||||
| chr6:159802868 | C | G | 102 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(99): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.209-403C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802868 | |||||||
| chr6:159802872 | C | T | 3 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 |
3 | HG01255.hp1 HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.209-399C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802872 | |||||||
| chr6:159802889 | C | CT | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0160 others(8): Show |
15 | HG01069.hp1 HG02145.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.209-370dupT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr6 | 159802889 | ||||||
| chr6:159802995 | A | C | 14 | a0001c0001t0001g0171 a0001c0001t0001g0178 a0001c0001t0001g0179 others(11): Show |
14 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.209-276A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159802995 | |||||||
| chr6:159803019 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.209-252C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159803019 | |||||||
| chr6:159803171 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0088 a0001c0001t0001g0089 |
4 | HG01069.hp2 HG01071.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-100A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159803171 | |||||||
| chr6:159803195 | G | T | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.209-76G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 3/18 | chr6 | 159803195 | |||||||
| chr6:159803314 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(199): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
splice_region_variant&intron_variant | LOW | c.248+4T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803314 | |||||||
| chr6:159803419 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.248+109C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803419 | |||||||
| chr6:159803420 | G | A | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.248+110G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803420 | |||||||
| chr6:159803472 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.248+162G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803472 | |||||||
| chr6:159803511 | G | A | 99 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0008 others(96): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.248+201G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803511 | |||||||
| chr6:159803680 | C | A | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.249-285C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803680 | |||||||
| chr6:159803682 | C | G | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(6): Show |
9 | HG02615.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.249-283C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803682 | |||||||
| chr6:159803721 | C | T | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(6): Show |
9 | HG02615.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.249-244C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803721 | |||||||
| chr6:159803760 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.249-205G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803760 | |||||||
| chr6:159803766 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(70): Show |
120 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.249-199C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803766 | |||||||
| chr6:159803792 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.249-173C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803792 | |||||||
| chr6:159803876 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.249-89A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803876 | |||||||
| chr6:159803886 | C | A | 1 | a0001c0002t0001g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.249-79C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 4/18 | chr6 | 159803886 | |||||||
| chr6:159804148 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.372+60G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/18 | chr6 | 159804148 | |||||||
| chr6:159804189 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.372+101C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/18 | chr6 | 159804189 | |||||||
| chr6:159804291 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.372+203A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/18 | chr6 | 159804291 | |||||||
| chr6:159804292 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.372+204C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/18 | chr6 | 159804292 | |||||||
| chr6:159804315 | G | A | 4 | a0001c0004t0001g0167 a0001c0004t0001g0168 a0001c0004t0001g0169 others(1): Show |
4 | HG01243.hp2 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+227G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/18 | chr6 | 159804315 | |||||||
| chr6:159804431 | G | T | 99 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0008 others(96): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.373-118G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/18 | chr6 | 159804431 | |||||||
| chr6:159804527 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(199): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.373-22G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/18 | chr6 | 159804527 | |||||||
| chr6:159804529 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.373-20T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 5/18 | chr6 | 159804529 | |||||||
| chr6:159804707 | G | A | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(6): Show |
9 | HG02615.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.461+70G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159804707 | |||||||
| chr6:159804732 | C | G | 2 | a0001c0002t0001g0035 a0001c0002t0001g0090 |
3 | HG02451.hp1 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.461+95C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159804732 | |||||||
| chr6:159804749 | G | T | 1 | a0001c0002t0001g0253 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.461+112G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159804749 | |||||||
| chr6:159804913 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01074.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.461+276G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159804913 | |||||||
| chr6:159804993 | T | G | 98 | a0001c0001t0005g0159 a0001c0002t0001g0005 a0001c0002t0001g0006 others(95): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.461+356T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159804993 | |||||||
| chr6:159805111 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.461+474C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805111 | |||||||
| chr6:159805197 | G | A | 2 | a0001c0002t0001g0036 a0001c0002t0001g0194 |
3 | HG00140.hp2 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.461+560G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805197 | |||||||
| chr6:159805305 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(201): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.461+668A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805305 | |||||||
| chr6:159805347 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.462-636C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805347 | |||||||
| chr6:159805389 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(68): Show |
118 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.462-594G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805389 | |||||||
| chr6:159805502 | A | G | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.462-481A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805502 | |||||||
| chr6:159805771 | G | T | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.462-212G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805771 | |||||||
| chr6:159805823 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.462-160A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805823 | |||||||
| chr6:159805846 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.462-137G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805846 | |||||||
| chr6:159805849 | T | G | 2 | a0001c0002t0001g0035 a0001c0002t0001g0090 |
3 | HG02451.hp1 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.462-134T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805849 | |||||||
| chr6:159805891 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(68): Show |
118 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.462-92A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805891 | |||||||
| chr6:159805967 | A | C | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.462-16A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 6/18 | chr6 | 159805967 | |||||||
| chr6:159806094 | C | G | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.562+11C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806094 | |||||||
| chr6:159806330 | G | A | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.562+247G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806330 | |||||||
| chr6:159806344 | T | C | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.562+261T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806344 | |||||||
| chr6:159806403 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(199): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.562+320G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806403 | |||||||
| chr6:159806431 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18944.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.562+348G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806431 | |||||||
| chr6:159806498 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(201): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.562+415A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806498 | |||||||
| chr6:159806671 | C | T | 2 | a0001c0001t0003g0085 a0001c0001t0003g0086 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.562+588C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806671 | |||||||
| chr6:159806752 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.562+669T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806752 | |||||||
| chr6:159806888 | C | CT | 5 | a0001c0001t0001g0082 a0001c0001t0001g0187 a0001c0001t0001g0188 others(2): Show |
6 | HG03098.hp1 HG03516.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.562+825dupT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 159806888 | ||||||
| chr6:159806888 | CT | C | 95 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0048 others(92): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.562+825delT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 159806888 | ||||||
| chr6:159806888 | CTT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(83): Show |
136 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.562+824_562+825del others(2): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 159806888 | ||||||
| chr6:159806956 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.562+873G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806956 | |||||||
| chr6:159806986 | G | A | 3 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 |
3 | NA18995.hp1 NA19056.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.562+903G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159806986 | |||||||
| chr6:159807053 | C | T | 3 | a0001c0001t0005g0159 a0001c0002t0004g0191 a0001c0002t0004g0192 |
3 | HG01109.hp2 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.562+970C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807053 | |||||||
| chr6:159807102 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.562+1019A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807102 | |||||||
| chr6:159807331 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.562+1248A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807331 | |||||||
| chr6:159807371 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.562+1288G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807371 | |||||||
| chr6:159807381 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0160 others(3): Show |
10 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.562+1298G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807381 | |||||||
| chr6:159807398 | G | GA | 93 | a0001c0001t0001g0045 a0001c0002t0001g0005 a0001c0002t0001g0006 others(90): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.562+1325dupA | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 159807398 | ||||||
| chr6:159807521 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.563-1219C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807521 | |||||||
| chr6:159807733 | G | A | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0002t0001g0035 others(1): Show |
5 | HG01069.hp1 HG02451.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-1007G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807733 | |||||||
| chr6:159807749 | A | G | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.563-991A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807749 | |||||||
| chr6:159807799 | A | C | 1 | a0001c0002t0002g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.563-941A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807799 | |||||||
| chr6:159807870 | C | T | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.563-870C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807870 | |||||||
| chr6:159807891 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(199): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.563-849C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807891 | |||||||
| chr6:159807918 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.563-822T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807918 | |||||||
| chr6:159807919 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0002t0004g0191 others(1): Show |
4 | HG01069.hp1 HG01109.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-821C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159807919 | |||||||
| chr6:159807919 | CT | C | 8 | a0001c0001t0001g0048 a0001c0001t0001g0104 a0001c0001t0001g0138 others(5): Show |
9 | HG01192.hp1 HG01884.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.563-809delT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 159807919 | ||||||
| chr6:159808067 | C | G | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.563-673C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808067 | |||||||
| chr6:159808113 | C | T | 1 | a0001c0001t0001g0007 | 5 | HG02109.hp1 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-627C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808113 | |||||||
| chr6:159808193 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.563-547C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808193 | |||||||
| chr6:159808205 | C | T | 2 | a0001c0006t0001g0239 a0001c0006t0001g0251 |
2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.563-535C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808205 | |||||||
| chr6:159808225 | T | C | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.563-515T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808225 | |||||||
| chr6:159808277 | G | A | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | NA18977.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.563-463G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808277 | |||||||
| chr6:159808298 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(199): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.563-442A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808298 | |||||||
| chr6:159808433 | G | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(68): Show |
118 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.563-307G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808433 | |||||||
| chr6:159808457 | T | A | 1 | a0001c0002t0001g0035 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.563-283T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808457 | |||||||
| chr6:159808489 | C | T | 1 | a0001c0002t0001g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.563-251C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808489 | |||||||
| chr6:159808529 | T | TA | 19 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
21 | HG02055.hp1 HG02135.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.563-193dupA | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 159808529 | ||||||
| chr6:159808529 | T | TAA | 95 | a0001c0001t0001g0171 a0001c0001t0001g0178 a0001c0001t0001g0179 others(92): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.563-194_563-193dup others(2): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 159808529 | ||||||
| chr6:159808529 | T | TAAA | 12 | a0001c0002t0001g0037 a0001c0002t0001g0042 a0001c0002t0001g0149 others(9): Show |
14 | HG01346.hp2 HG01981.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.563-195_563-193dup others(3): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr6 | 159808529 | ||||||
| chr6:159808616 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.563-124C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808616 | |||||||
| chr6:159808629 | C | G | 5 | a0001c0001t0005g0159 a0001c0002t0001g0154 a0001c0002t0001g0155 others(2): Show |
5 | HG01109.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.563-111C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808629 | |||||||
| chr6:159808670 | A | G | 3 | a0001c0001t0005g0159 a0001c0002t0001g0154 a0001c0002t0001g0155 |
3 | HG02717.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.563-70A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808670 | |||||||
| chr6:159808672 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
6 | HG02071.hp2 HG02129.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.563-68G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808672 | |||||||
| chr6:159808680 | T | C | 3 | a0001c0001t0005g0159 a0001c0002t0001g0154 a0001c0002t0001g0155 |
3 | HG02717.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.563-60T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 7/18 | chr6 | 159808680 | |||||||
| chr6:159808835 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0092 others(8): Show |
16 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.639+19C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 8/18 | chr6 | 159808835 | |||||||
| chr6:159808857 | T | C | 93 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0008 others(90): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.639+41T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 8/18 | chr6 | 159808857 | |||||||
| chr6:159808907 | CACGCTGC others(6): Show |
C | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.639+92_640-95delAC others(11): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 8/18 | chr6 | 159808907 | |||||||
| chr6:159809227 | G | C | 13 | a0001c0001t0001g0171 a0001c0001t0001g0178 a0001c0001t0001g0179 others(10): Show |
13 | HG01884.hp1 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.783+69G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | chr6 | 159809227 | |||||||
| chr6:159809354 | G | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(9): Show |
23 | HG00544.hp2 HG00609.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.783+196G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | chr6 | 159809354 | |||||||
| chr6:159809415 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.783+257G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | chr6 | 159809415 | |||||||
| chr6:159809451 | A | AT | 36 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(33): Show |
41 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.783+315dupT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 159809451 | ||||||
| chr6:159809451 | A | ATT | 7 | a0001c0001t0001g0080 a0001c0001t0001g0171 a0001c0001t0001g0178 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+314_783+315dup others(2): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 159809451 | ||||||
| chr6:159809451 | AT | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0049 others(5): Show |
11 | HG02155.hp2 HG02523.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+315delT | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 159809451 | ||||||
| chr6:159809451 | ATTTTTTT others(2): Show |
A | 88 | a0001c0001t0001g0104 a0001c0002t0001g0005 a0001c0002t0001g0006 others(85): Show |
119 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.783+307_783+315del others(9): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr6 | 159809451 | ||||||
| chr6:159809455 | T | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.783+297T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | chr6 | 159809455 | |||||||
| chr6:159809459 | T | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.783+301T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | chr6 | 159809459 | |||||||
| chr6:159809829 | G | T | 13 | a0001c0001t0001g0171 a0001c0001t0001g0178 a0001c0001t0001g0179 others(10): Show |
13 | HG01884.hp1 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.784-197G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | chr6 | 159809829 | |||||||
| chr6:159809879 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.784-147A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 9/18 | chr6 | 159809879 | |||||||
| chr6:159810128 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
6 | HG02071.hp2 HG02129.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+33C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159810128 | |||||||
| chr6:159810130 | C | A | 3 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0158 |
3 | HG01255.hp1 HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.853+35C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159810130 | |||||||
| chr6:159810183 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.853+88T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159810183 | |||||||
| chr6:159810302 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0065 |
5 | HG02015.hp1 HG02683.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.853+207G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159810302 | |||||||
| chr6:159810569 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.853+474G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159810569 | |||||||
| chr6:159810569 | G | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0109 |
3 | HG01106.hp2 HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.853+474G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159810569 | |||||||
| chr6:159811250 | G | A | 1 | a0001c0009t0001g0233 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.854-451G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159811250 | |||||||
| chr6:159811285 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.854-416A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159811285 | |||||||
| chr6:159811403 | A | G | 2 | a0001c0002t0001g0232 a0001c0002t0001g0238 |
2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.854-298A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159811403 | |||||||
| chr6:159811543 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.854-158A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159811543 | |||||||
| chr6:159811548 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.854-153C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159811548 | |||||||
| chr6:159811664 | C | G | 2 | a0001c0002t0001g0230 a0001c0002t0001g0231 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.854-37C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 10/18 | chr6 | 159811664 | |||||||
| chr6:159811839 | A | T | 1 | a0003c0013t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.939+53A>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159811839 | |||||||
| chr6:159811859 | G | T | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.939+73G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159811859 | |||||||
| chr6:159811880 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.939+94G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159811880 | |||||||
| chr6:159811884 | T | TTTTTG | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(6): Show |
9 | HG02615.hp2 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.939+127_939+131dup others(5): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 159811884 | ||||||
| chr6:159811884 | TTTTTG | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(72): Show |
127 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.939+127_939+131del others(5): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 159811884 | ||||||
| chr6:159811884 | TTTTTGTT others(3): Show |
T | 1 | a0001c0001t0001g0140 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.939+122_939+131del others(10): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 159811884 | ||||||
| chr6:159811885 | T | G | 1 | a0003c0013t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.939+99T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159811885 | |||||||
| chr6:159811889 | G | T | 1 | a0003c0013t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.939+103G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159811889 | |||||||
| chr6:159811889 | GTTTTGT | G | 99 | a0001c0001t0001g0104 a0001c0001t0001g0164 a0001c0001t0001g0165 others(96): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.939+107_939+112del others(6): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 159811889 | ||||||
| chr6:159811961 | G | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0160 others(5): Show |
13 | HG02145.hp2 HG02451.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+175G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159811961 | |||||||
| chr6:159812076 | A | G | 1 | a0001c0002t0001g0229 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.939+290A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812076 | |||||||
| chr6:159812092 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.939+306G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812092 | |||||||
| chr6:159812108 | G | A | 3 | a0001c0001t0001g0080 a0001c0002t0001g0154 a0001c0002t0001g0155 |
3 | HG02280.hp2 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.939+322G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812108 | |||||||
| chr6:159812117 | G | T | 2 | a0001c0002t0001g0036 a0001c0002t0001g0194 |
3 | HG00140.hp2 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.939+331G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812117 | |||||||
| chr6:159812144 | C | A | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.939+358C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812144 | |||||||
| chr6:159812190 | G | A | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.939+404G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812190 | |||||||
| chr6:159812288 | A | G | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.939+502A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812288 | |||||||
| chr6:159812359 | G | A | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.939+573G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812359 | |||||||
| chr6:159812456 | TG | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(192): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.939+677delG | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 159812456 | ||||||
| chr6:159812459 | G | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG01074.hp2 HG01261.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.939+673G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812459 | |||||||
| chr6:159812573 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.939+787G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812573 | |||||||
| chr6:159812728 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.940-873G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812728 | |||||||
| chr6:159812816 | A | G | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.940-785A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159812816 | |||||||
| chr6:159813035 | AAAC | A | 112 | a0001c0001t0001g0029 a0001c0001t0001g0088 a0001c0001t0001g0089 others(109): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.940-559_940-557del others(3): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr6 | 159813035 | ||||||
| chr6:159813076 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.940-525C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159813076 | |||||||
| chr6:159813129 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.940-472G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159813129 | |||||||
| chr6:159813275 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.940-326C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159813275 | |||||||
| chr6:159813315 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.940-286T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159813315 | |||||||
| chr6:159813593 | G | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(164): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
splice_region_variant&intron_variant | LOW | c.940-8G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 11/18 | chr6 | 159813593 | |||||||
| chr6:159813739 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0145 |
2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.995+83C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159813739 | |||||||
| chr6:159813764 | T | G | 21 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0088 others(18): Show |
22 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.995+108T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159813764 | |||||||
| chr6:159813995 | G | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0160 others(9): Show |
16 | HG02145.hp2 HG02615.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.995+339G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159813995 | |||||||
| chr6:159813995 | G | T | 2 | a0001c0001t0001g0012 a0004c0011t0001g0077 |
4 | NA18959.hp1 NA18968.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.995+339G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159813995 | |||||||
| chr6:159814007 | C | G | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.995+351C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814007 | |||||||
| chr6:159814039 | C | G | 2 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.995+383C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814039 | |||||||
| chr6:159814044 | C | T | 3 | a0001c0002t0001g0207 a0001c0002t0001g0219 a0001c0002t0001g0247 |
3 | HG01106.hp1 HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.995+388C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814044 | |||||||
| chr6:159814196 | G | A | 3 | a0001c0001t0001g0080 a0001c0002t0001g0154 a0001c0002t0001g0155 |
3 | HG02280.hp2 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.995+540G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814196 | |||||||
| chr6:159814223 | T | C | 1 | a0001c0004t0001g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.995+567T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814223 | |||||||
| chr6:159814254 | G | A | 2 | a0001c0001t0003g0085 a0001c0001t0003g0086 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.995+598G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814254 | |||||||
| chr6:159814283 | G | A | 1 | a0001c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.995+627G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814283 | |||||||
| chr6:159814304 | A | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.995+648A>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814304 | |||||||
| chr6:159814326 | T | A | 1 | a0001c0006t0001g0251 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.995+670T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814326 | |||||||
| chr6:159814472 | C | A | 2 | a0001c0001t0002g0081 a0001c0001t0002g0186 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.995+816C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814472 | |||||||
| chr6:159814790 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.995+1134A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814790 | |||||||
| chr6:159814798 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.995+1142A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814798 | |||||||
| chr6:159814909 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.996-1060T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159814909 | |||||||
| chr6:159815006 | A | T | 1 | a0001c0005t0001g0054 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.996-963A>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815006 | |||||||
| chr6:159815008 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0113 |
5 | HG00609.hp1 NA18959.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.996-961G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815008 | |||||||
| chr6:159815102 | A | G | 1 | a0001c0002t0001g0218 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.996-867A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815102 | |||||||
| chr6:159815272 | C | T | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(5): Show |
8 | HG02615.hp2 HG02647.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.996-697C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815272 | |||||||
| chr6:159815400 | C | T | 1 | a0001c0002t0001g0227 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.996-569C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815400 | |||||||
| chr6:159815402 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.996-567C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815402 | |||||||
| chr6:159815536 | T | C | 4 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0114 others(1): Show |
4 | NA18967.hp1 NA18981.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.996-433T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815536 | |||||||
| chr6:159815570 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0160 others(4): Show |
11 | HG02145.hp2 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.996-399T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815570 | |||||||
| chr6:159815589 | G | T | 1 | a0001c0001t0001g0030 | 2 | HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.996-380G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815589 | |||||||
| chr6:159815638 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(192): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.996-331G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815638 | |||||||
| chr6:159815655 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(110): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.996-314C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815655 | |||||||
| chr6:159815730 | A | C | 1 | a0001c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.996-239A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815730 | |||||||
| chr6:159815757 | G | C | 3 | a0001c0001t0001g0080 a0001c0002t0001g0154 a0001c0002t0001g0155 |
3 | HG02280.hp2 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.996-212G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815757 | |||||||
| chr6:159815832 | C | G | 1 | a0001c0002t0001g0217 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.996-137C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815832 | |||||||
| chr6:159815875 | A | T | 1 | a0001c0002t0001g0252 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.996-94A>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815875 | |||||||
| chr6:159815881 | T | A | 1 | a0001c0002t0001g0252 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.996-88T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815881 | |||||||
| chr6:159815944 | T | C | 87 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0062 others(84): Show |
105 | HG00323.hp1 HG00639.hp1 HG01069.hp1 others(102): Show |
intron_variant | MODIFIER | c.996-25T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 12/18 | chr6 | 159815944 | |||||||
| chr6:159816111 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1060+78G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816111 | |||||||
| chr6:159816119 | C | G | 2 | a0001c0002t0001g0213 a0001c0002t0001g0214 |
2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1060+86C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816119 | |||||||
| chr6:159816122 | A | C | 1 | a0001c0002t0006g0262 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1060+89A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816122 | |||||||
| chr6:159816126 | C | G | 1 | a0003c0013t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1060+93C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816126 | |||||||
| chr6:159816126 | C | T | 1 | a0001c0002t0006g0262 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1060+93C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816126 | |||||||
| chr6:159816127 | T | C | 1 | a0001c0002t0006g0262 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1060+94T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816127 | |||||||
| chr6:159816135 | C | A | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1060+102C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816135 | |||||||
| chr6:159816136 | A | C | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1060+103A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816136 | |||||||
| chr6:159816140 | G | GCACACAC others(95): Show |
1 | a0001c0001t0001g0083 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1060+108_1060+109i others(104): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(96): Show |
1 | a0001c0001t0002g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060+116_1060+117i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(95): Show |
1 | a0001c0001t0001g0031 | 2 | HG01496.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1060+116_1060+117i others(104): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(96): Show |
1 | a0001c0001t0001g0135 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1060+116_1060+117i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(97): Show |
1 | a0001c0002t0001g0148 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1060+116_1060+117i others(106): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(78): Show |
1 | a0001c0002t0001g0199 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1060+116_1060+117i others(87): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(95): Show |
1 | a0001c0001t0001g0115 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(104): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(98): Show |
1 | a0001c0012t0001g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(107): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(117): Show |
3 | a0001c0001t0001g0020 a0001c0001t0001g0162 a0001c0009t0001g0233 |
5 | HG02145.hp2 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(126): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(117): Show |
1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(126): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(118): Show |
1 | a0001c0001t0001g0160 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(127): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(92): Show |
1 | a0001c0001t0001g0116 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(101): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(93): Show |
5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0187 others(2): Show |
5 | HG02647.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(102): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(94): Show |
1 | a0001c0001t0001g0188 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(103): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(92): Show |
1 | a0001c0001t0001g0055 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(101): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(94): Show |
1 | a0001c0001t0001g0117 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(103): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(94): Show |
110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(103): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(95): Show |
5 | a0001c0001t0001g0057 a0001c0001t0001g0087 a0001c0001t0001g0123 others(2): Show |
5 | HG01175.hp2 HG02074.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(104): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(95): Show |
1 | a0001c0001t0001g0133 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(104): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(95): Show |
9 | a0001c0001t0001g0027 a0001c0001t0001g0112 a0001c0001t0001g0124 others(6): Show |
10 | HG00140.hp2 HG00423.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(104): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(96): Show |
1 | a0001c0001t0001g0126 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(96): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0113 |
2 | HG00408.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(82): Show |
1 | a0001c0002t0001g0252 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1060+121_1060+122i others(91): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(78): Show |
1 | a0001c0002t0001g0196 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1060+121_1060+122i others(87): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GCCACACC others(71): Show |
1 | a0001c0002t0001g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1060+121_1060+122i others(80): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816140 | ||||||
| chr6:159816140 | G | GTCACACC others(94): Show |
1 | a0001c0002t0001g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1060+107_1060+108i others(103): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816140 | |||||||
| chr6:159816143 | A | ACACCCCT others(111): Show |
1 | a0001c0001t0001g0045 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(120): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816143 | ||||||
| chr6:159816147 | C | CCCTCCCC others(96): Show |
1 | a0001c0001t0001g0071 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816147 | ||||||
| chr6:159816154 | C | CCACCCAC others(97): Show |
1 | a0001c0001t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1060+121_1060+122i others(106): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816154 | |||||||
| chr6:159816154 | C | CCCACCCA others(100): Show |
1 | a0003c0013t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1060+121_1060+122i others(109): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816154 | |||||||
| chr6:159816155 | A | ACCCACCC others(96): Show |
1 | a0001c0002t0001g0244 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(101): Show |
1 | a0001c0001t0001g0104 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(110): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(118): Show |
1 | a0001c0002t0001g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(127): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(79): Show |
1 | a0001c0003t0001g0172 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(88): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(54): Show |
1 | a0001c0001t0001g0165 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(63): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(54): Show |
4 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0178 others(1): Show |
4 | HG02486.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(63): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(55): Show |
1 | a0001c0001t0001g0179 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(64): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(96): Show |
1 | a0001c0002t0006g0262 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(95): Show |
21 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0064 others(18): Show |
27 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(104): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(114): Show |
1 | a0001c0001t0001g0068 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(123): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(96): Show |
1 | a0001c0001t0001g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(76): Show |
1 | a0001c0001t0001g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(85): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(96): Show |
9 | a0001c0001t0001g0060 a0001c0001t0001g0091 a0001c0001t0001g0106 others(6): Show |
9 | HG00741.hp2 HG01433.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(105): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(79): Show |
1 | a0001c0006t0001g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1060+125_1060+126i others(88): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(78): Show |
2 | a0001c0001t0001g0061 a0001c0002t0001g0208 |
2 | HG01515.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(87): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(77): Show |
1 | a0001c0002t0001g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(86): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(79): Show |
2 | a0001c0002t0001g0209 a0001c0004t0001g0167 |
2 | HG03486.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(88): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(76): Show |
2 | a0001c0002t0001g0038 a0001c0002t0001g0230 |
3 | HG02109.hp2 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(85): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(78): Show |
9 | a0001c0001t0001g0088 a0001c0002t0001g0039 a0001c0002t0001g0197 others(6): Show |
10 | HG01071.hp1 HG01123.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(87): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(79): Show |
1 | a0001c0002t0001g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(88): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(77): Show |
29 | a0001c0001t0001g0029 a0001c0001t0001g0062 a0001c0001t0001g0089 others(26): Show |
42 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(86): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(76): Show |
5 | a0001c0002t0001g0037 a0001c0002t0001g0193 a0001c0002t0001g0211 others(2): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060+125_1060+126i others(85): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(78): Show |
1 | a0001c0002t0001g0040 | 2 | HG01168.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(87): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(77): Show |
3 | a0001c0002t0001g0205 a0001c0002t0001g0229 a0001c0002t0002g0212 |
3 | HG02280.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(86): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(79): Show |
1 | a0001c0006t0001g0251 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1060+125_1060+126i others(88): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(100): Show |
2 | a0001c0002t0001g0226 a0001c0002t0001g0248 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(109): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | ACCCACCC others(76): Show |
2 | a0001c0002t0001g0241 a0001c0002t0001g0249 |
2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(85): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816155 | ||||||
| chr6:159816155 | A | C | 2 | a0001c0001t0001g0163 a0003c0013t0001g0134 |
2 | HG02738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1060+122A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816155 | |||||||
| chr6:159816155 | A | G | 3 | a0001c0002t0001g0196 a0001c0002t0001g0199 a0001c0002t0001g0252 |
3 | NA18977.hp2 NA18997.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1060+122A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816155 | |||||||
| chr6:159816156 | C | CCCACCCG others(73): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1060+125_1060+126i others(82): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr6 | 159816156 | ||||||
| chr6:159816175 | T | G | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(5): Show |
8 | HG02615.hp2 HG02647.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1060+142T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816175 | |||||||
| chr6:159816182 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1060+149C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816182 | |||||||
| chr6:159816217 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1060+184A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816217 | |||||||
| chr6:159816322 | T | A | 1 | a0001c0002t0001g0244 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1061-221T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816322 | |||||||
| chr6:159816376 | C | T | 1 | a0001c0002t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1061-167C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816376 | |||||||
| chr6:159816457 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(191): Show |
283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1061-86T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 13/18 | chr6 | 159816457 | |||||||
| chr6:159816610 | T | A | 1 | a0001c0002t0001g0215 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1114+14T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 14/18 | chr6 | 159816610 | |||||||
| chr6:159816630 | CTT | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(186): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.1114+50_1114+51del others(2): Show |
PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr6 | 159816630 | ||||||
| chr6:159816642 | T | A | 1 | a0001c0002t0001g0244 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1114+46T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 14/18 | chr6 | 159816642 | |||||||
| chr6:159816995 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1115-114C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 14/18 | chr6 | 159816995 | |||||||
| chr6:159817023 | C | G | 2 | a0001c0002t0004g0191 a0001c0002t0004g0192 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1115-86C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 14/18 | chr6 | 159817023 | |||||||
| chr6:159817157 | T | C | 1 | a0001c0002t0001g0210 | 1 | HG02148.hp2 | splice_region_variant&intron_variant | LOW | c.1157+6T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817157 | |||||||
| chr6:159817193 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1157+42C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817193 | |||||||
| chr6:159817520 | G | T | 3 | a0001c0001t0001g0163 a0001c0002t0001g0035 a0001c0002t0001g0090 |
4 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1157+369G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817520 | |||||||
| chr6:159817564 | G | T | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1157+413G>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817564 | |||||||
| chr6:159817677 | C | T | 65 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
82 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.1157+526C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817677 | |||||||
| chr6:159817701 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0160 others(2): Show |
9 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1157+550G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817701 | |||||||
| chr6:159817727 | G | A | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0187 others(2): Show |
5 | HG02647.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+576G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817727 | |||||||
| chr6:159817755 | G | A | 11 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0002t0001g0156 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1157+604G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817755 | |||||||
| chr6:159817900 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1158-655G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817900 | |||||||
| chr6:159817951 | T | C | 3 | a0001c0001t0001g0163 a0001c0002t0001g0035 a0001c0002t0001g0090 |
4 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158-604T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159817951 | |||||||
| chr6:159818054 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0113 |
5 | HG00609.hp1 NA18959.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-501C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818054 | |||||||
| chr6:159818069 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(188): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1158-486G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818069 | |||||||
| chr6:159818232 | C | A | 2 | a0001c0002t0001g0223 a0001c0002t0001g0224 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1158-323C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818232 | |||||||
| chr6:159818236 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(191): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1158-319A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818236 | |||||||
| chr6:159818259 | C | G | 3 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG02970.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1158-296C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818259 | |||||||
| chr6:159818287 | T | C | 3 | a0001c0001t0001g0163 a0001c0002t0001g0035 a0001c0002t0001g0090 |
4 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158-268T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818287 | |||||||
| chr6:159818298 | A | G | 3 | a0001c0001t0001g0080 a0001c0002t0001g0154 a0001c0002t0001g0155 |
3 | HG02280.hp2 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1158-257A>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818298 | |||||||
| chr6:159818350 | T | C | 86 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0029 others(83): Show |
107 | HG00323.hp1 HG00639.hp1 HG01069.hp1 others(104): Show |
intron_variant | MODIFIER | c.1158-205T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818350 | |||||||
| chr6:159818423 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1158-132T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818423 | |||||||
| chr6:159818429 | G | A | 66 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0062 others(63): Show |
83 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.1158-126G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818429 | |||||||
| chr6:159818431 | C | T | 2 | a0001c0002t0004g0191 a0001c0002t0004g0192 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1158-124C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818431 | |||||||
| chr6:159818460 | T | A | 1 | a0004c0011t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1158-95T>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818460 | |||||||
| chr6:159818520 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1158-35G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818520 | |||||||
| chr6:159818525 | C | T | 2 | a0001c0002t0004g0191 a0001c0002t0004g0192 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1158-30C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 15/18 | chr6 | 159818525 | |||||||
| chr6:159818675 | C | G | 2 | a0001c0002t0004g0191 a0001c0002t0004g0192 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1257+21C>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 16/18 | chr6 | 159818675 | |||||||
| chr6:159818680 | C | T | 70 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0062 others(67): Show |
86 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.1257+26C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 16/18 | chr6 | 159818680 | |||||||
| chr6:159818779 | T | G | 1 | a0001c0002t0001g0150 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1257+125T>G | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 16/18 | chr6 | 159818779 | |||||||
| chr6:159818803 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(208): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1258-143T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 16/18 | chr6 | 159818803 | |||||||
| chr6:159819231 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1434-23C>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 17/18 | chr6 | 159819231 | |||||||
| chr6:159819403 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1532+51G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159819403 | |||||||
| chr6:159819666 | T | C | 8 | a0001c0001t0001g0163 a0001c0001t0001g0181 a0001c0001t0001g0184 others(5): Show |
9 | HG02451.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1532+314T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159819666 | |||||||
| chr6:159819731 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0005g0159 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1532+379G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159819731 | |||||||
| chr6:159819734 | T | C | 32 | a0001c0001t0001g0060 a0001c0001t0001g0080 a0001c0001t0001g0091 others(29): Show |
34 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1532+382T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159819734 | |||||||
| chr6:159819736 | T | C | 34 | a0001c0001t0001g0060 a0001c0001t0001g0080 a0001c0001t0001g0091 others(31): Show |
36 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.1532+384T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159819736 | |||||||
| chr6:159819766 | A | C | 1 | a0004c0011t0001g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1532+414A>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159819766 | |||||||
| chr6:159819815 | CG | C | 4 | a0001c0001t0001g0080 a0001c0001t0001g0099 a0001c0002t0001g0154 others(1): Show |
4 | HG02280.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1532+467delG | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr6 | 159819815 | ||||||
| chr6:159819945 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0073 |
2 | HG02155.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1533-509G>A | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159819945 | |||||||
| chr6:159819980 | C | T | 1 | a0001c0002t0001g0252 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1533-474C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159819980 | |||||||
| chr6:159820008 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1533-446C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159820008 | |||||||
| chr6:159820319 | T | C | 19 | a0001c0001t0001g0112 a0001c0001t0001g0119 a0001c0001t0001g0122 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1533-135T>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159820319 | |||||||
| chr6:159820408 | G | C | 28 | a0001c0001t0001g0112 a0001c0001t0001g0119 a0001c0001t0001g0122 others(25): Show |
28 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.1533-46G>C | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159820408 | |||||||
| chr6:159820424 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1533-30C>T | PNLDC1 | ENSG00000146453.13 | transcript | ENST00000392167.4 | protein_coding | 18/18 | chr6 | 159820424 |