Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10038 |
| ensemblid | ENSG00000129484.14 |
| hgncid | 272 |
| symbol | PARP2 |
| name | poly(ADP-ribose) polymerase 2 |
| refseq_nuc | NM_001042618.2 |
| refseq_prot | NP_001036083.1 |
| ensembl_nuc | ENST00000429687.8 |
| ensembl_prot | ENSP00000392972.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 20343635 |
| end | 20357904 |
| strand | + |
| ver | v1.2 |
| region | chr14:20343635-20357904 |
| region5000 | chr14:20338635-20362904 |
| regionname0 | PARP2_chr14_20343635_20357904 |
| regionname5000 | PARP2_chr14_20338635_20362904 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 570 | 393 | 89 | 67 | 185 | 10 | 41 | 139 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0002 | 0/1 | 570 | 9 | 2 | 4 | 0 | 1 | 1 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0003 | 0/0 | 570 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0004 | 0/0 | 570 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0005 | 0/0 | 570 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0006 | 0/0 | 570 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0007 | 0/0 | 570 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0008 | 0/0 | 570 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0009 | 0/0 | 570 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| a0010 | 0/0 | 570 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | MAARR others(565): Show |
chr14 | 20338635 | 20362904 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1710 | 203 | 25 | 42 | 112 | 5 | 19 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0001c0002 | 1/0 | 1710 | 173 | 51 | 23 | 72 | 5 | 21 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0001c0004 | 0/0 | 1710 | 9 | 8 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0001c0005 | 0/0 | 1710 | 4 | 3 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0001c0011 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0001c0013 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0001c0015 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0002c0003 | 0/1 | 1710 | 9 | 2 | 4 | 0 | 1 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0003c0006 | 0/0 | 1710 | 4 | 0 | 0 | 4 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0004c0008 | 0/0 | 1710 | 3 | 3 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0005c0007 | 0/0 | 1710 | 3 | 0 | 0 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0006c0009 | 0/0 | 1710 | 3 | 0 | 0 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0007c0010 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0008c0016 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 1 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0009c0014 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 | ||
| a0010c0012 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | ATGGC others(1705): Show |
chr14 | 20338635 | 20362904 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1827 | 174 | 23 | 39 | 92 | 5 | 15 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0001t0002 | 0/0 | 1827 | 27 | 2 | 3 | 18 | 0 | 4 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0001t0003 | 0/0 | 1827 | 2 | 0 | 0 | 2 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0002t0001 | 1/0 | 1827 | 112 | 51 | 11 | 38 | 1 | 10 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0002t0002 | 0/0 | 1827 | 61 | 0 | 12 | 34 | 4 | 11 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0004t0001 | 0/0 | 1827 | 9 | 8 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0005t0001 | 0/0 | 1827 | 4 | 3 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0011t0002 | 0/0 | 1827 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0013t0001 | 0/0 | 1827 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0001c0015t0002 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0002c0003t0001 | 0/1 | 1827 | 9 | 2 | 4 | 0 | 1 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0003c0006t0002 | 0/0 | 1827 | 4 | 0 | 0 | 4 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0004c0008t0001 | 0/0 | 1827 | 3 | 3 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0005c0007t0001 | 0/0 | 1827 | 3 | 0 | 0 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0006c0009t0002 | 0/0 | 1827 | 3 | 0 | 0 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0007c0010t0001 | 0/0 | 1827 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0008c0016t0002 | 0/0 | 1827 | 1 | 0 | 0 | 0 | 1 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0009c0014t0002 | 0/0 | 1827 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| a0010c0012t0002 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | GAATT others(1822): Show |
chr14 | 20338635 | 20362904 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 65 | 3 | 19 | 35 | 5 | 3 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0004 | 0/0 | 13 | 0 | 6 | 6 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0006 | 0/0 | 11 | 2 | 0 | 9 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0007 | 0/0 | 10 | 1 | 2 | 6 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0003 | 0/0 | 13 | 1 | 1 | 9 | 0 | 2 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0001 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0002 | 0/0 | 33 | 3 | 4 | 22 | 0 | 4 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0010 | 0/0 | 6 | 2 | 0 | 3 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0013 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0022 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0003 | 0/0 | 17 | 0 | 9 | 4 | 3 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0005 | 0/0 | 10 | 0 | 0 | 6 | 0 | 4 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0004t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0005t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0011t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0011t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0013t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0001c0015t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0002c0003t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0002c0003t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0002c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0002c0003t0001g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0003c0006t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0003c0006t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0004c0008t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0004c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0005c0007t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0006c0009t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0007c0010t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0007c0010t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0008c0016t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0009c0014t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| a0010c0012t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0057 | EUR | GBR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | FIN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00280 | hp2 | a0008 | c0016 | t0002 | g0005 | EUR | FIN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0152 | EUR | FIN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0158 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0042 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01255 | hp2 | a0001 | c0005 | t0001 | g0031 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01358 | hp1 | a0009 | c0014 | t0002 | g0003 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01496 | hp2 | a0001 | c0013 | t0001 | g0125 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01516 | hp1 | a0002 | c0003 | t0001 | g0160 | EUR | IBS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | CDX | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | CDX | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0029 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02809 | hp2 | a0007 | c0010 | t0001 | g0156 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02895 | hp1 | a0004 | c0008 | t0001 | g0146 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0030 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02970 | hp2 | a0001 | c0011 | t0002 | g0062 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0028 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0067 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0070 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03209 | hp2 | a0004 | c0008 | t0001 | g0040 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0068 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03486 | hp1 | a0007 | c0010 | t0001 | g0157 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03540 | hp2 | a0004 | c0008 | t0001 | g0040 | AFR | GWD | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0024 | SAS | BEB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0024 | SAS | BEB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04204 | hp2 | a0001 | c0004 | t0001 | g0069 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0145 | AFR | YRI | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | YRI | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CHB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | CHB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | YRI | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | YRI | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18947 | hp1 | a0005 | c0007 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18950 | hp2 | a0005 | c0007 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18963 | hp2 | a0003 | c0006 | t0002 | g0017 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18968 | hp1 | a0003 | c0006 | t0002 | g0017 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18970 | hp1 | a0003 | c0006 | t0002 | g0017 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18988 | hp2 | a0006 | c0009 | t0002 | g0005 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18993 | hp1 | a0010 | c0012 | t0002 | g0016 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18994 | hp1 | a0001 | c0015 | t0002 | g0008 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19009 | hp2 | a0006 | c0009 | t0002 | g0005 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19011 | hp2 | a0003 | c0006 | t0002 | g0060 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | LWK | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | LWK | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19054 | hp2 | a0005 | c0007 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19090 | hp2 | a0006 | c0009 | t0002 | g0005 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | YRI | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | YRI | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0159 | AFR | ASW | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0161 | SAS | GIH | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0031 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0029 | AFR | ACB | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03471 | hp1 | a0001 | c0011 | t0002 | g0063 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | USA | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0028 | AFR | USA | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | USA | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | USA | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0042 | AFR | LWK | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | LWK | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0162 | REF | REF | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0001 | REF | REF | PARP2_chr14_20338635_20362904 | PARP2 | chr14 | 20338635 | 20362904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:20351068 | G | A | 1 | a0007 | 2 | HG02809.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.443G>A | p.Ser148Asn | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/16 | 450/1827 | 443/1713 | 148/570 | chr14 | 20351068 | |||
| chr14:20351109 | A | G | 1 | a0006 | 3 | NA18988.hp2 NA19009.hp2 NA19090.hp2 |
missense_variant | MODERATE | c.484A>G | p.Ile162Val | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/16 | 491/1827 | 484/1713 | 162/570 | chr14 | 20351109 | |||
| chr14:20354097 | A | G | 1 | a0004 | 3 | HG02895.hp1 HG03209.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.613A>G | p.Thr205Ala | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/16 | 620/1827 | 613/1713 | 205/570 | chr14 | 20354097 | |||
| chr14:20354149 | A | G | 1 | a0008 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.665A>G | p.Asp222Gly | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/16 | 672/1827 | 665/1713 | 222/570 | chr14 | 20354149 | |||
| chr14:20354874 | C | T | 1 | a0005 | 3 | NA18947.hp1 NA18950.hp2 NA19054.hp2 |
missense_variant | MODERATE | c.829C>T | p.Arg277Trp | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/16 | 836/1827 | 829/1713 | 277/570 | chr14 | 20354874 | |||
| chr14:20354893 | G | A | 1 | a0002 | 8 | HG01070.hp2 HG01081.hp1 HG01168.hp1 others(5): Show |
missense_variant | MODERATE | c.848G>A | p.Arg283Gln | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/16 | 855/1827 | 848/1713 | 283/570 | chr14 | 20354893 | |||
| chr14:20355802 | T | C | 1 | a0010 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.953T>C | p.Ile318Thr | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 10/16 | 960/1827 | 953/1713 | 318/570 | chr14 | 20355802 | |||
| chr14:20357123 | A | C | 1 | a0003 | 4 | NA18963.hp2 NA18968.hp1 NA18970.hp1 others(1): Show |
missense_variant | MODERATE | c.1402A>C | p.Asn468His | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 14/16 | 1409/1827 | 1402/1713 | 468/570 | chr14 | 20357123 | |||
| chr14:20357430 | C | T | 1 | a0009 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1463C>T | p.Ala488Val | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 15/16 | 1470/1827 | 1463/1713 | 488/570 | chr14 | 20357430 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:20354936 | G | A | 2 | a0001c0004 a0001c0005 |
13 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
synonymous_variant | LOW | c.891G>A | p.Pro297Pro | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/16 | 898/1827 | 891/1713 | 297/570 | chr14 | 20354936 | |||
| chr14:20355963 | T | C | 1 | a0001c0013 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1033T>C | p.Leu345Leu | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 11/16 | 1040/1827 | 1033/1713 | 345/570 | chr14 | 20355963 | |||
| chr14:20356022 | T | C | 3 | a0001c0001 a0001c0005 a0005c0007 |
210 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(207): Show |
synonymous_variant | LOW | c.1092T>C | p.Tyr364Tyr | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 11/16 | 1099/1827 | 1092/1713 | 364/570 | chr14 | 20356022 | |||
| chr14:20357135 | C | T | 1 | a0001c0015 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.1414C>T | p.Leu472Leu | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 14/16 | 1421/1827 | 1414/1713 | 472/570 | chr14 | 20357135 | |||
| chr14:20357716 | T | C | 1 | a0001c0011 | 2 | HG02970.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.1632T>C | p.Asn544Asn | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 16/16 | 1639/1827 | 1632/1713 | 544/570 | chr14 | 20357716 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:20357806 | A | C | 9 | a0001c0001t0002 a0001c0002t0002 a0001c0011t0002 others(6): Show |
101 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*9A>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 16/16 | 9 | chr14 | 20357806 | ||||||
| chr14:20357807 | T | C | 1 | a0001c0001t0003 | 2 | HG00558.hp1 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 16/16 | 10 | chr14 | 20357807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:20343691 | C | A | 1 | a0001c0001t0001g0044 | 1 | HG02071.hp1 | splice_region_variant&intron_variant | LOW | c.46+4C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20343691 | |||||||
| chr14:20343700 | A | G | 1 | a0001c0002t0001g0164 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46+13A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20343700 | |||||||
| chr14:20343752 | C | G | 1 | a0001c0002t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.46+65C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20343752 | |||||||
| chr14:20343767 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.46+80T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20343767 | |||||||
| chr14:20343800 | T | A | 1 | a0001c0002t0001g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.46+113T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20343800 | |||||||
| chr14:20344308 | C | A | 32 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(29): Show |
80 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.46+621C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344308 | |||||||
| chr14:20344313 | C | T | 6 | a0002c0003t0001g0042 a0002c0003t0001g0043 a0002c0003t0001g0158 others(3): Show |
8 | HG01070.hp2 HG01081.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.47-619C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344313 | |||||||
| chr14:20344333 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.47-599G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344333 | |||||||
| chr14:20344444 | T | C | 1 | a0001c0002t0001g0027 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.47-488T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344444 | |||||||
| chr14:20344507 | C | T | 2 | a0007c0010t0001g0156 a0007c0010t0001g0157 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.47-425C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344507 | |||||||
| chr14:20344604 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.47-328C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344604 | |||||||
| chr14:20344611 | G | T | 2 | a0001c0011t0002g0062 a0001c0011t0002g0063 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.47-321G>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344611 | |||||||
| chr14:20344748 | G | A | 14 | a0001c0002t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0029 others(11): Show |
17 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.47-184G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344748 | |||||||
| chr14:20344792 | G | A | 13 | a0001c0001t0002g0005 a0001c0002t0002g0005 a0001c0002t0002g0023 others(10): Show |
26 | HG00280.hp2 HG01928.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.47-140G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 1/15 | chr14 | 20344792 | |||||||
| chr14:20345130 | G | A | 32 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(29): Show |
80 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.202+43G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 2/15 | chr14 | 20345130 | |||||||
| chr14:20345483 | G | A | 8 | a0001c0004t0001g0028 a0001c0004t0001g0029 a0001c0004t0001g0030 others(5): Show |
10 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+19G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20345483 | |||||||
| chr14:20345513 | A | G | 32 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(29): Show |
80 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.273+49A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20345513 | |||||||
| chr14:20345566 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.273+102A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20345566 | |||||||
| chr14:20345724 | A | AAAGAGGT others(4): Show |
1 | a0001c0011t0002g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.273+262_273+272dup others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 20345724 | ||||||
| chr14:20345788 | A | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(71): Show |
137 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.273+324A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20345788 | |||||||
| chr14:20345846 | G | A | 11 | a0001c0004t0001g0028 a0001c0004t0001g0029 a0001c0004t0001g0030 others(8): Show |
13 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+382G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20345846 | |||||||
| chr14:20345910 | AAG | A | 11 | a0001c0004t0001g0028 a0001c0004t0001g0029 a0001c0004t0001g0030 others(8): Show |
13 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+452_273+453del others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 20345910 | ||||||
| chr14:20345932 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(57): Show |
116 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.273+468C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20345932 | |||||||
| chr14:20346030 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.273+566A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346030 | |||||||
| chr14:20346080 | A | G | 1 | a0001c0002t0001g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.273+616A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346080 | |||||||
| chr14:20346119 | A | G | 6 | a0002c0003t0001g0042 a0002c0003t0001g0043 a0002c0003t0001g0158 others(3): Show |
8 | HG01070.hp2 HG01081.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.273+655A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346119 | |||||||
| chr14:20346209 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(30): Show |
81 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.274-654A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346209 | |||||||
| chr14:20346221 | T | C | 8 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0046 others(5): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-642T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346221 | |||||||
| chr14:20346269 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(65): Show |
129 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.274-594G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346269 | |||||||
| chr14:20346321 | C | CT | 13 | a0001c0001t0001g0045 a0001c0001t0001g0111 a0001c0001t0001g0112 others(10): Show |
15 | HG00741.hp2 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.274-518dupT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 20346321 | ||||||
| chr14:20346321 | C | CTTT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(21): Show |
64 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.274-520_274-518dup others(3): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 20346321 | ||||||
| chr14:20346321 | C | CTTTT | 5 | a0001c0002t0001g0010 a0001c0002t0001g0151 a0001c0002t0001g0152 others(2): Show |
10 | HG00323.hp1 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-521_274-518dup others(4): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 20346321 | ||||||
| chr14:20346321 | CT | C | 31 | a0001c0001t0001g0071 a0001c0001t0002g0018 a0001c0002t0001g0013 others(28): Show |
41 | HG00639.hp1 HG01255.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.274-518delT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 20346321 | ||||||
| chr14:20346321 | CTT | C | 34 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0026 others(31): Show |
84 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.274-519_274-518del others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 20346321 | ||||||
| chr14:20346344 | T | G | 11 | a0001c0004t0001g0028 a0001c0004t0001g0029 a0001c0004t0001g0030 others(8): Show |
13 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-519T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346344 | |||||||
| chr14:20346370 | C | G | 2 | a0003c0006t0002g0017 a0003c0006t0002g0060 |
4 | NA18963.hp2 NA18968.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-493C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346370 | |||||||
| chr14:20346594 | G | A | 6 | a0002c0003t0001g0042 a0002c0003t0001g0043 a0002c0003t0001g0158 others(3): Show |
8 | HG01070.hp2 HG01081.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-269G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346594 | |||||||
| chr14:20346657 | T | TA | 12 | a0001c0002t0001g0013 a0001c0002t0001g0039 a0001c0002t0001g0123 others(9): Show |
17 | HG00639.hp1 HG01496.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.274-198dupA | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 20346657 | ||||||
| chr14:20346706 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0002g0004 others(13): Show |
38 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-157A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346706 | |||||||
| chr14:20346716 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.274-147C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346716 | |||||||
| chr14:20346781 | C | G | 7 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0064 others(4): Show |
12 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-82C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346781 | |||||||
| chr14:20346854 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.274-9C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 3/15 | chr14 | 20346854 | |||||||
| chr14:20347010 | C | CT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(46): Show |
108 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.324+113dupT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347010 | ||||||
| chr14:20347010 | CT | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0032 others(12): Show |
24 | HG00609.hp1 HG01070.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.324+113delT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347010 | ||||||
| chr14:20347027 | A | T | 8 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0002t0001g0027 others(5): Show |
9 | HG01109.hp2 HG01255.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+114A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347027 | |||||||
| chr14:20347055 | G | A | 1 | a0002c0003t0001g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.324+142G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347055 | |||||||
| chr14:20347074 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(65): Show |
129 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.324+161G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347074 | |||||||
| chr14:20347123 | G | A | 5 | a0001c0002t0001g0021 a0001c0002t0001g0119 a0001c0002t0001g0120 others(2): Show |
7 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.324+210G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347123 | |||||||
| chr14:20347154 | A | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.324+241A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347154 | |||||||
| chr14:20347156 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.324+243G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347156 | |||||||
| chr14:20347226 | C | T | 1 | a0001c0002t0001g0150 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.324+313C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347226 | |||||||
| chr14:20347235 | A | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.324+322A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347235 | |||||||
| chr14:20347313 | G | T | 2 | a0007c0010t0001g0156 a0007c0010t0001g0157 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.324+400G>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347313 | |||||||
| chr14:20347324 | C | T | 9 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0046 others(6): Show |
14 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.324+411C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347324 | |||||||
| chr14:20347343 | CAT | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0002t0001g0137 others(2): Show |
5 | HG01891.hp1 HG02451.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+433_324+434del others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347343 | ||||||
| chr14:20347344 | ATATGTG | A | 18 | a0001c0002t0001g0013 a0001c0002t0001g0027 a0001c0002t0001g0039 others(15): Show |
26 | HG00639.hp1 HG01109.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.324+433_324+438del others(6): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347344 | ||||||
| chr14:20347344 | ATATGTGT others(1): Show |
A | 6 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0064 others(3): Show |
11 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.324+433_324+440del others(8): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347344 | ||||||
| chr14:20347344 | ATATGTGT others(3): Show |
A | 1 | a0001c0002t0001g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324+433_324+442del others(10): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347344 | ||||||
| chr14:20347346 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(34): Show |
85 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.324+433A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347346 | |||||||
| chr14:20347348 | GTGTGTGT others(27): Show |
G | 1 | a0001c0002t0001g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.324+437_324+470del others(34): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347348 | ||||||
| chr14:20347350 | GTGTGTGT others(7): Show |
G | 3 | a0001c0004t0001g0066 a0001c0004t0001g0068 a0001c0005t0001g0067 |
3 | HG02055.hp2 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.324+439_324+452del others(14): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347350 | ||||||
| chr14:20347350 | GTGTGTGT others(11): Show |
G | 1 | a0001c0002t0001g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+439_324+456del others(18): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347350 | ||||||
| chr14:20347350 | GTGTGTGT others(23): Show |
G | 1 | a0001c0002t0001g0164 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.324+439_324+468del others(30): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347350 | ||||||
| chr14:20347352 | G | A | 4 | a0001c0002t0001g0123 a0001c0002t0001g0130 a0001c0002t0001g0131 others(1): Show |
4 | HG02280.hp1 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+439G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347352 | |||||||
| chr14:20347354 | G | A | 3 | a0001c0002t0001g0130 a0001c0002t0001g0131 a0001c0002t0001g0132 |
3 | HG02818.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.324+441G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347354 | |||||||
| chr14:20347354 | G | GTATATAT others(3): Show |
1 | a0001c0002t0001g0123 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.324+442_324+443ins others(10): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347354 | ||||||
| chr14:20347354 | GTGTATAT others(3): Show |
G | 2 | a0004c0008t0001g0040 a0004c0008t0001g0146 |
3 | HG02895.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.324+443_324+452del others(10): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347354 | ||||||
| chr14:20347356 | G | A | 21 | a0001c0001t0001g0036 a0001c0001t0001g0075 a0001c0001t0001g0100 others(18): Show |
34 | HG00280.hp2 HG00621.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.324+443G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347356 | |||||||
| chr14:20347356 | G | GTA | 5 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0020 others(2): Show |
6 | HG00408.hp2 HG00673.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+485_324+486dup others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTATA | 1 | a0001c0001t0001g0007 | 4 | HG04115.hp1 NA18943.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+483_324+486dup others(4): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTA | 3 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 |
3 | HG02615.hp2 NA18943.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.324+444_324+445ins others(4): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTATAT others(5): Show |
1 | a0001c0002t0002g0110 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.324+444_324+445ins others(12): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTATAT others(15): Show |
1 | a0001c0002t0002g0008 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.324+444_324+445ins others(22): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTATGT others(17): Show |
1 | a0001c0001t0001g0004 | 2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.324+444_324+445ins others(24): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTAT others(5): Show |
2 | a0001c0002t0002g0105 a0001c0002t0002g0108 |
2 | NA18992.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.324+444_324+445ins others(12): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTAT others(9): Show |
2 | a0001c0001t0002g0008 a0001c0002t0001g0004 |
2 | HG04199.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.324+444_324+445ins others(16): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTAT others(11): Show |
1 | a0001c0001t0001g0004 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.324+444_324+445ins others(18): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTAT others(13): Show |
1 | a0001c0002t0002g0109 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.324+444_324+445ins others(20): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTAT others(15): Show |
1 | a0001c0001t0001g0004 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.324+444_324+445ins others(22): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTAT others(9): Show |
1 | a0001c0002t0001g0004 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.324+444_324+445ins others(16): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTAT others(11): Show |
1 | a0001c0001t0002g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.324+444_324+445ins others(18): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTGT others(3): Show |
1 | a0001c0002t0001g0002 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.324+444_324+445ins others(10): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTGT others(11): Show |
2 | a0001c0001t0001g0004 a0001c0002t0001g0004 |
3 | HG01256.hp1 HG01258.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.324+444_324+445ins others(18): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0004 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.324+444_324+445ins others(20): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTGT others(19): Show |
1 | a0001c0001t0002g0107 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.324+444_324+445ins others(26): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | G | GTGTGTGT others(21): Show |
1 | a0001c0001t0001g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.324+444_324+445ins others(28): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | GTA | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0004 |
4 | HG02015.hp1 HG02056.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+485_324+486del others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | GTATA | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0071 |
4 | HG01192.hp2 HG01928.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+483_324+486del others(4): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | GTATATA | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0037 |
3 | HG02257.hp1 HG02735.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.324+481_324+486del others(6): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | GTATATAT others(1): Show |
G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0099 |
5 | HG02818.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+479_324+486del others(8): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | GTATATAT others(3): Show |
G | 1 | a0001c0002t0002g0008 | 2 | NA18954.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.324+477_324+486del others(10): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | GTATATAT others(9): Show |
G | 1 | a0001c0002t0001g0002 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.324+471_324+486del others(16): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347356 | GTATATAT others(17): Show |
G | 1 | a0001c0002t0001g0002 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.324+463_324+486del others(24): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347356 | ||||||
| chr14:20347358 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0138 others(17): Show |
33 | HG00609.hp2 HG01070.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.324+445A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347358 | |||||||
| chr14:20347360 | A | G | 8 | a0001c0001t0001g0004 a0001c0002t0001g0004 a0001c0002t0001g0038 others(5): Show |
11 | HG01070.hp2 HG01081.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+447A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347360 | |||||||
| chr14:20347362 | A | G | 4 | a0001c0002t0001g0038 a0002c0003t0001g0042 a0002c0003t0001g0043 others(1): Show |
7 | HG01070.hp2 HG01081.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+449A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347362 | |||||||
| chr14:20347364 | A | G | 1 | a0001c0002t0001g0038 | 2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.324+451A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347364 | |||||||
| chr14:20347364 | ATATATAT others(31): Show |
A | 1 | a0001c0001t0001g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.324+453_324+490del others(38): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347364 | ||||||
| chr14:20347365 | TATATATA others(18): Show |
T | 1 | a0001c0002t0001g0022 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.324+453_324+477del others(25): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347365 | |||||||
| chr14:20347368 | A | G | 1 | a0001c0002t0002g0008 | 2 | NA18954.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.324+455A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347368 | |||||||
| chr14:20347370 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.324+459_324+488del others(30): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347370 | ||||||
| chr14:20347370 | ATATATAT others(28): Show |
A | 1 | a0001c0001t0002g0003 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.324+459_324+493del others(35): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347370 | ||||||
| chr14:20347372 | ATATATAT others(26): Show |
A | 1 | a0001c0002t0002g0024 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.324+461_324+493del others(33): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347372 | ||||||
| chr14:20347372 | ATATATAT others(27): Show |
A | 14 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(11): Show |
26 | HG00280.hp2 HG01928.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.324+461_324+494del others(34): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347372 | ||||||
| chr14:20347372 | ATATATAT others(28): Show |
A | 17 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0026 others(14): Show |
44 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.324+461_324+495del others(35): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347372 | ||||||
| chr14:20347372 | ATATATAT others(29): Show |
A | 3 | a0001c0001t0002g0003 a0001c0001t0002g0056 a0003c0006t0002g0017 |
4 | NA18946.hp1 NA18970.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+461_324+496del others(36): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347372 | ||||||
| chr14:20347374 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.324+463_324+489del others(27): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347374 | ||||||
| chr14:20347374 | ATATATAT others(26): Show |
A | 2 | a0001c0011t0002g0062 a0001c0011t0002g0063 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.324+463_324+495del others(33): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347374 | ||||||
| chr14:20347374 | ATATATAT others(28): Show |
A | 1 | a0001c0001t0002g0003 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.324+463_324+497del others(35): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347374 | ||||||
| chr14:20347378 | ATATATAT others(16): Show |
A | 1 | a0001c0002t0001g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.324+467_324+489del others(23): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347378 | ||||||
| chr14:20347379 | TATATATA others(8): Show |
T | 1 | a0001c0002t0001g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.324+467_324+481del others(15): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347379 | |||||||
| chr14:20347380 | ATATATAT others(13): Show |
A | 1 | a0001c0002t0001g0001 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.324+469_324+488del others(20): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347380 | ||||||
| chr14:20347381 | TATATATA others(4): Show |
T | 1 | a0001c0002t0001g0002 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.324+469_324+479del others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347381 | |||||||
| chr14:20347382 | ATATATAT others(18): Show |
A | 1 | a0001c0002t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+471_324+495del others(25): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347382 | ||||||
| chr14:20347384 | ATATATAT others(8): Show |
A | 1 | a0001c0002t0001g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.324+473_324+487del others(15): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347384 | ||||||
| chr14:20347384 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0001g0096 a0001c0002t0001g0038 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.324+473_324+489del others(17): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347384 | ||||||
| chr14:20347384 | ATATATAT others(11): Show |
A | 1 | a0001c0002t0001g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.324+473_324+490del others(18): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347384 | ||||||
| chr14:20347384 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0001 a0001c0002t0001g0014 |
4 | HG02257.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+473_324+491del others(19): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347384 | ||||||
| chr14:20347385 | TATATATA others(4): Show |
T | 1 | a0001c0004t0001g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.324+473_324+483del others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347385 | |||||||
| chr14:20347387 | TATATATA others(4): Show |
T | 1 | a0001c0004t0001g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324+475_324+485del others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347387 | |||||||
| chr14:20347388 | A | T | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.324+475A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347388 | |||||||
| chr14:20347388 | ATATATAT others(4): Show |
A | 1 | a0001c0004t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.324+477_324+487del others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347388 | ||||||
| chr14:20347390 | A | T | 3 | a0001c0001t0001g0006 a0001c0002t0001g0002 a0001c0002t0001g0027 |
3 | HG01109.hp2 HG03453.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.324+477A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347390 | |||||||
| chr14:20347390 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0076 |
5 | HG02083.hp1 NA18951.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+479_324+488del others(10): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347390 | ||||||
| chr14:20347391 | TA | T | 3 | a0001c0002t0001g0002 a0001c0002t0001g0145 a0001c0002t0001g0153 |
3 | HG02109.hp1 HG03710.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.324+479delA | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347391 | |||||||
| chr14:20347392 | A | ATT | 1 | a0001c0002t0001g0002 | 4 | HG00438.hp2 HG01978.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+480_324+481ins others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347392 | ||||||
| chr14:20347392 | A | ATTTTTTT others(6): Show |
1 | a0001c0002t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.324+480_324+481ins others(13): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347392 | ||||||
| chr14:20347392 | A | G | 2 | a0004c0008t0001g0040 a0004c0008t0001g0146 |
3 | HG02895.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.324+479A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347392 | |||||||
| chr14:20347392 | A | T | 7 | a0001c0001t0001g0006 a0001c0002t0001g0002 a0001c0002t0001g0010 others(4): Show |
11 | HG01109.hp2 HG02886.hp2 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.324+479A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347392 | |||||||
| chr14:20347392 | ATATATAT others(1): Show |
A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0090 a0001c0001t0001g0114 others(4): Show |
8 | HG00639.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+481_324+488del others(8): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347392 | ||||||
| chr14:20347392 | ATATATAT others(7): Show |
A | 1 | a0001c0002t0002g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.324+481_324+494del others(14): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347392 | ||||||
| chr14:20347392 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.324+481_324+499del others(19): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347392 | ||||||
| chr14:20347393 | TA | T | 3 | a0001c0002t0001g0002 a0001c0002t0001g0022 a0001c0002t0001g0129 |
4 | HG02258.hp1 HG02897.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+481delA | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347393 | |||||||
| chr14:20347394 | A | ATT | 2 | a0001c0001t0001g0002 a0001c0002t0001g0002 |
3 | HG01106.hp2 NA18987.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.324+482_324+483ins others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347394 | ||||||
| chr14:20347394 | A | ATTTT | 2 | a0001c0002t0001g0002 a0001c0002t0001g0139 |
3 | HG01952.hp2 HG02293.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.324+482_324+483ins others(4): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347394 | ||||||
| chr14:20347394 | A | ATTTTTTT others(9): Show |
1 | a0001c0002t0001g0002 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.324+482_324+483ins others(16): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347394 | ||||||
| chr14:20347394 | A | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0144 others(14): Show |
31 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.324+481A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347394 | |||||||
| chr14:20347394 | ATATAT | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0089 |
6 | HG01261.hp1 HG02004.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+483_324+487del others(5): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347394 | ||||||
| chr14:20347394 | ATATATT | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(4): Show |
10 | HG00738.hp1 HG01123.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.324+483_324+488del others(6): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347394 | ||||||
| chr14:20347394 | ATATATTT others(4): Show |
A | 1 | a0002c0003t0001g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.324+483_324+493del others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347394 | ||||||
| chr14:20347395 | TATA | T | 2 | a0001c0001t0001g0011 a0001c0002t0002g0008 |
3 | HG01070.hp1 NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.324+483_324+485del others(3): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347395 | |||||||
| chr14:20347396 | A | ATTTT | 2 | a0001c0002t0001g0002 a0001c0002t0001g0133 |
3 | HG00544.hp2 HG06807.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.324+484_324+485ins others(4): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347396 | ||||||
| chr14:20347396 | A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0149 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.324+484_324+485ins others(14): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347396 | ||||||
| chr14:20347396 | A | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(23): Show |
52 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.324+483A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347396 | |||||||
| chr14:20347396 | ATAT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0097 others(3): Show |
15 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.324+485_324+487del others(3): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347396 | ||||||
| chr14:20347396 | ATATT | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(6): Show |
20 | HG00609.hp1 HG01074.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.324+485_324+488del others(4): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347396 | ||||||
| chr14:20347396 | ATATTT | A | 5 | a0001c0001t0001g0001 a0001c0002t0001g0021 a0001c0002t0001g0119 others(2): Show |
7 | HG02145.hp2 HG02280.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+485_324+489del others(5): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347396 | ||||||
| chr14:20347396 | ATATTTTT others(14): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.324+485_324+505del others(21): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347396 | ||||||
| chr14:20347398 | A | AT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0075 others(3): Show |
10 | HG00140.hp1 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+520dupT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.324+486_324+487ins others(29): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0002 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.324+486_324+487ins others(17): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | ATATATAT others(7): Show |
1 | a0001c0002t0001g0002 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.324+486_324+487ins others(14): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.324+486_324+487ins others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0142 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.324+486_324+487ins others(17): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | ATATATTT others(11): Show |
1 | a0001c0002t0001g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.324+486_324+487ins others(18): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | ATATATTT others(23): Show |
1 | a0001c0002t0001g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.324+486_324+487ins others(30): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | ATATTTTT others(3): Show |
3 | a0001c0001t0001g0009 a0001c0002t0001g0002 a0001c0002t0001g0010 |
4 | HG02922.hp2 NA18972.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+486_324+487ins others(10): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | A | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(37): Show |
78 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.324+485A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347398 | |||||||
| chr14:20347398 | AT | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0083 others(5): Show |
9 | HG02809.hp2 HG02818.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+520delT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | ATT | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0032 others(7): Show |
16 | HG00558.hp1 HG01975.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.324+519_324+520del others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | ATTT | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0074 others(4): Show |
9 | HG01516.hp1 HG02965.hp1 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+518_324+520del others(3): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347398 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0001 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.324+505_324+520del others(16): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347398 | ||||||
| chr14:20347399 | T | TA | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0077 others(1): Show |
7 | HG01081.hp1 HG01169.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+486_324+487ins others(1): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347399 | |||||||
| chr14:20347399 | T | TATA | 5 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG01258.hp1 HG02148.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+486_324+487ins others(3): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347399 | |||||||
| chr14:20347399 | T | TATATATA others(6): Show |
1 | a0001c0002t0002g0104 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.324+486_324+487ins others(13): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347399 | |||||||
| chr14:20347400 | T | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0033 others(9): Show |
25 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.324+487T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347400 | |||||||
| chr14:20347401 | T | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0077 others(8): Show |
13 | HG01081.hp1 HG01169.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+488T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347401 | |||||||
| chr14:20347402 | T | A | 11 | a0001c0001t0001g0033 a0001c0001t0001g0080 a0001c0001t0001g0085 others(8): Show |
13 | HG00639.hp2 HG01070.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+489T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347402 | |||||||
| chr14:20347403 | T | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0002t0001g0124 others(3): Show |
7 | HG01081.hp1 HG01169.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+490T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347403 | |||||||
| chr14:20347404 | T | A | 4 | a0001c0002t0001g0039 a0001c0002t0001g0130 a0002c0003t0001g0042 others(1): Show |
6 | HG01070.hp2 HG01168.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+491T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347404 | |||||||
| chr14:20347405 | T | A | 4 | a0001c0002t0001g0064 a0001c0002t0001g0124 a0002c0003t0001g0160 others(1): Show |
4 | HG01516.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+492T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347405 | |||||||
| chr14:20347406 | T | A | 1 | a0001c0002t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.324+493T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347406 | |||||||
| chr14:20347407 | T | A | 3 | a0001c0002t0001g0064 a0002c0003t0001g0160 a0002c0003t0001g0161 |
3 | HG01516.hp1 HG02723.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.324+494T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347407 | |||||||
| chr14:20347549 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.324+636G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347549 | |||||||
| chr14:20347553 | C | A | 1 | a0001c0002t0001g0027 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.324+640C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347553 | |||||||
| chr14:20347594 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(66): Show |
130 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.324+681A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347594 | |||||||
| chr14:20347661 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.324+748T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347661 | |||||||
| chr14:20347708 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(30): Show |
81 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.324+795G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347708 | |||||||
| chr14:20347871 | AT | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(69): Show |
134 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.324+974delT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20347871 | ||||||
| chr14:20347872 | T | C | 16 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0026 others(13): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.324+959T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347872 | |||||||
| chr14:20347873 | T | C | 7 | a0001c0001t0002g0056 a0002c0003t0001g0042 a0002c0003t0001g0043 others(4): Show |
9 | HG01070.hp2 HG01081.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+960T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20347873 | |||||||
| chr14:20348019 | G | A | 11 | a0001c0004t0001g0028 a0001c0004t0001g0029 a0001c0004t0001g0030 others(8): Show |
13 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.324+1106G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348019 | |||||||
| chr14:20348021 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.324+1108A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348021 | |||||||
| chr14:20348048 | A | G | 1 | a0001c0002t0001g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.324+1135A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348048 | |||||||
| chr14:20348215 | G | A | 1 | a0001c0002t0002g0053 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.324+1302G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348215 | |||||||
| chr14:20348241 | A | C | 1 | a0001c0002t0001g0148 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.324+1328A>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348241 | |||||||
| chr14:20348302 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0035 others(3): Show |
11 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+1389T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348302 | |||||||
| chr14:20348319 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.324+1406C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348319 | |||||||
| chr14:20348396 | GT | G | 15 | a0001c0001t0001g0085 a0001c0002t0001g0079 a0001c0002t0001g0136 others(12): Show |
17 | HG01255.hp2 HG02055.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.324+1496delT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20348396 | ||||||
| chr14:20348409 | T | A | 7 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0064 others(4): Show |
12 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+1496T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348409 | |||||||
| chr14:20348530 | G | C | 1 | a0001c0002t0002g0105 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.324+1617G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348530 | |||||||
| chr14:20348547 | C | A | 4 | a0001c0002t0001g0039 a0001c0002t0001g0124 a0001c0002t0001g0130 others(1): Show |
5 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+1634C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348547 | |||||||
| chr14:20348757 | C | T | 1 | a0001c0004t0001g0068 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.325-1769C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348757 | |||||||
| chr14:20348811 | G | C | 11 | a0001c0004t0001g0028 a0001c0004t0001g0029 a0001c0004t0001g0030 others(8): Show |
13 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.325-1715G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348811 | |||||||
| chr14:20348974 | G | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(30): Show |
81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.325-1552G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348974 | |||||||
| chr14:20348983 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.325-1543T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20348983 | |||||||
| chr14:20349095 | T | A | 1 | a0001c0001t0001g0074 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.325-1431T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349095 | |||||||
| chr14:20349166 | T | C | 1 | a0001c0002t0001g0086 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.325-1360T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349166 | |||||||
| chr14:20349218 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.325-1308G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349218 | |||||||
| chr14:20349369 | A | G | 12 | a0001c0002t0001g0013 a0001c0002t0001g0039 a0001c0002t0001g0123 others(9): Show |
17 | HG00639.hp1 HG01496.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.325-1157A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349369 | |||||||
| chr14:20349470 | A | T | 1 | a0001c0002t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.325-1056A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349470 | |||||||
| chr14:20349514 | CA | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.325-1003delA | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr14 | 20349514 | ||||||
| chr14:20349564 | T | C | 2 | a0001c0001t0001g0009 a0001c0002t0001g0009 |
6 | NA18999.hp1 NA19064.hp2 NA19070.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-962T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349564 | |||||||
| chr14:20349622 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.325-904G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349622 | |||||||
| chr14:20349626 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.325-900G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349626 | |||||||
| chr14:20349628 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(103): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.325-898T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349628 | |||||||
| chr14:20349665 | C | G | 1 | a0002c0003t0001g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.325-861C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349665 | |||||||
| chr14:20349754 | C | T | 39 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(36): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.325-772C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349754 | |||||||
| chr14:20349757 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.325-769T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349757 | |||||||
| chr14:20349886 | C | G | 1 | a0001c0004t0001g0030 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.325-640C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349886 | |||||||
| chr14:20349972 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(63): Show |
126 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.325-554T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349972 | |||||||
| chr14:20349984 | G | A | 1 | a0001c0002t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-542G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20349984 | |||||||
| chr14:20350020 | C | A | 1 | a0001c0002t0002g0048 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.325-506C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20350020 | |||||||
| chr14:20350109 | T | A | 1 | a0001c0002t0002g0048 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.325-417T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20350109 | |||||||
| chr14:20350443 | C | G | 33 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(30): Show |
81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.325-83C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 4/15 | chr14 | 20350443 | |||||||
| chr14:20350823 | G | A | 1 | a0001c0002t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.421+201G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 5/15 | chr14 | 20350823 | |||||||
| chr14:20350824 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(63): Show |
126 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.421+202C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 5/15 | chr14 | 20350824 | |||||||
| chr14:20350953 | T | A | 33 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(30): Show |
81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.422-94T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 5/15 | chr14 | 20350953 | |||||||
| chr14:20351190 | T | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(63): Show |
126 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.497+68T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351190 | |||||||
| chr14:20351191 | T | A | 11 | a0001c0004t0001g0028 a0001c0004t0001g0029 a0001c0004t0001g0030 others(8): Show |
13 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.497+69T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351191 | |||||||
| chr14:20351395 | T | G | 1 | a0001c0002t0001g0127 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497+273T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351395 | |||||||
| chr14:20351460 | G | C | 1 | a0001c0002t0001g0014 | 4 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.497+338G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351460 | |||||||
| chr14:20351508 | A | G | 2 | a0007c0010t0001g0156 a0007c0010t0001g0157 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.497+386A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351508 | |||||||
| chr14:20351570 | C | T | 39 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(36): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.497+448C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351570 | |||||||
| chr14:20351682 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.497+560T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351682 | |||||||
| chr14:20351692 | G | A | 2 | a0007c0010t0001g0156 a0007c0010t0001g0157 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.498-553G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351692 | |||||||
| chr14:20351749 | G | GGCTC | 130 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(127): Show |
272 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.498-496_498-495ins others(4): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351749 | |||||||
| chr14:20351792 | T | C | 39 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(36): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.498-453T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351792 | |||||||
| chr14:20351871 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.498-374A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20351871 | |||||||
| chr14:20351874 | AAG | A | 39 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(36): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.498-367_498-366del others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 20351874 | ||||||
| chr14:20352166 | T | C | 1 | a0001c0002t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.498-79T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 6/15 | chr14 | 20352166 | |||||||
| chr14:20352378 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(102): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.600+31A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352378 | |||||||
| chr14:20352389 | T | C | 11 | a0001c0004t0001g0028 a0001c0004t0001g0029 a0001c0004t0001g0030 others(8): Show |
13 | HG01255.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.600+42T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352389 | |||||||
| chr14:20352503 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.600+156C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352503 | |||||||
| chr14:20352558 | C | CTCTTTTT others(5): Show |
1 | a0001c0002t0002g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.600+212_600+213ins others(12): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 20352558 | ||||||
| chr14:20352558 | C | CTTTTTTT others(2): Show |
20 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0021 others(17): Show |
30 | HG00323.hp1 HG00639.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.600+213_600+221dup others(9): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 20352558 | ||||||
| chr14:20352558 | C | CTTTTTTT others(3): Show |
42 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(39): Show |
91 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.600+212_600+221dup others(10): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 20352558 | ||||||
| chr14:20352558 | C | CTTTTTTT others(4): Show |
6 | a0002c0003t0001g0042 a0002c0003t0001g0043 a0002c0003t0001g0158 others(3): Show |
8 | HG01070.hp2 HG01081.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+221_600+222ins others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 20352558 | ||||||
| chr14:20352567 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.600+220T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352567 | |||||||
| chr14:20352568 | T | G | 1 | a0001c0002t0002g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.600+221T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352568 | |||||||
| chr14:20352568 | T | TTTTTTTT others(4): Show |
2 | a0001c0002t0002g0047 a0001c0002t0002g0053 |
2 | HG02698.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.600+221_600+222ins others(11): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352568 | |||||||
| chr14:20352568 | T | TTTTTTTT others(5): Show |
25 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(22): Show |
71 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.600+221_600+222ins others(12): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352568 | |||||||
| chr14:20352568 | T | TTTTTTTT others(6): Show |
5 | a0001c0001t0002g0026 a0001c0001t0002g0059 a0001c0002t0002g0024 others(2): Show |
7 | HG02970.hp2 HG03239.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+221_600+222ins others(13): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352568 | |||||||
| chr14:20352569 | G | A | 1 | a0001c0002t0001g0027 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.600+222G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352569 | |||||||
| chr14:20352635 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.600+288G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352635 | |||||||
| chr14:20352735 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(102): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.600+388G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352735 | |||||||
| chr14:20352821 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18957.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.600+474A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352821 | |||||||
| chr14:20352856 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(102): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.600+509T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352856 | |||||||
| chr14:20352868 | T | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(28): Show |
78 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.600+521T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352868 | |||||||
| chr14:20352879 | CT | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(100): Show |
213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.600+546delT | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 20352879 | ||||||
| chr14:20352910 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.600+563C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352910 | |||||||
| chr14:20352951 | G | A | 1 | a0001c0002t0002g0058 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.600+604G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352951 | |||||||
| chr14:20352979 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.600+632C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20352979 | |||||||
| chr14:20353026 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(28): Show |
78 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.600+679G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353026 | |||||||
| chr14:20353123 | A | G | 1 | a0001c0002t0001g0148 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.600+776A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353123 | |||||||
| chr14:20353127 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(63): Show |
126 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.600+780G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353127 | |||||||
| chr14:20353181 | A | G | 2 | a0001c0002t0001g0136 a0001c0002t0001g0164 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.600+834A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353181 | |||||||
| chr14:20353227 | GTT | G | 39 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0018 others(36): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.601-852_601-851del others(2): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 20353227 | ||||||
| chr14:20353233 | T | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(22): Show |
71 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.601-852T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353233 | |||||||
| chr14:20353236 | G | A | 9 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0046 others(6): Show |
14 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-849G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353236 | |||||||
| chr14:20353250 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.601-835G>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353250 | |||||||
| chr14:20353327 | C | T | 8 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0046 others(5): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.601-758C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353327 | |||||||
| chr14:20353328 | G | A | 1 | a0001c0002t0002g0051 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.601-757G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353328 | |||||||
| chr14:20353341 | C | T | 1 | a0001c0002t0001g0038 | 2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.601-744C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353341 | |||||||
| chr14:20353364 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.601-721C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353364 | |||||||
| chr14:20353486 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.601-599G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353486 | |||||||
| chr14:20353522 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG02818.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.601-563C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353522 | |||||||
| chr14:20353535 | G | A | 8 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0046 others(5): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.601-550G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353535 | |||||||
| chr14:20353620 | T | G | 12 | a0001c0002t0001g0013 a0001c0002t0001g0039 a0001c0002t0001g0123 others(9): Show |
17 | HG00639.hp1 HG01496.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.601-465T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353620 | |||||||
| chr14:20353639 | C | A | 1 | a0002c0003t0001g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.601-446C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353639 | |||||||
| chr14:20353714 | C | T | 1 | a0001c0002t0002g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.601-371C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353714 | |||||||
| chr14:20353949 | C | T | 1 | a0001c0002t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.601-136C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353949 | |||||||
| chr14:20353956 | C | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(102): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.601-129C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353956 | |||||||
| chr14:20353991 | T | A | 1 | a0001c0002t0001g0163 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.601-94T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20353991 | |||||||
| chr14:20354060 | G | C | 2 | a0004c0008t0001g0040 a0004c0008t0001g0146 |
3 | HG02895.hp1 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.601-25G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20354060 | |||||||
| chr14:20354060 | G | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(61): Show |
123 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.601-25G>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 7/15 | chr14 | 20354060 | |||||||
| chr14:20354277 | C | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02074.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.763+30C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354277 | |||||||
| chr14:20354336 | G | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(64): Show |
127 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.763+89G>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354336 | |||||||
| chr14:20354419 | G | A | 2 | a0001c0011t0002g0062 a0001c0011t0002g0063 |
2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.763+172G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354419 | |||||||
| chr14:20354484 | C | G | 3 | a0001c0004t0001g0029 a0001c0005t0001g0029 a0001c0005t0001g0067 |
3 | HG02559.hp2 HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.763+237C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354484 | |||||||
| chr14:20354613 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(62): Show |
125 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.764-196C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354613 | |||||||
| chr14:20354667 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.764-142C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354667 | |||||||
| chr14:20354703 | GA | G | 20 | a0001c0001t0001g0085 a0001c0001t0002g0003 a0001c0001t0002g0018 others(17): Show |
55 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.764-96delA | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr14 | 20354703 | ||||||
| chr14:20354740 | G | A | 1 | a0001c0002t0002g0049 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.764-69G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354740 | |||||||
| chr14:20354742 | A | G | 1 | a0001c0002t0002g0049 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.764-67A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354742 | |||||||
| chr14:20354744 | G | A | 1 | a0001c0002t0002g0025 | 2 | HG00408.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.764-65G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 8/15 | chr14 | 20354744 | |||||||
| chr14:20355053 | A | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(29): Show |
79 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.902+106A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355053 | |||||||
| chr14:20355056 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.902+109G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355056 | |||||||
| chr14:20355133 | C | T | 2 | a0001c0002t0001g0145 a0001c0002t0001g0153 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.902+186C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355133 | |||||||
| chr14:20355152 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0088 |
3 | HG02735.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.902+205T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355152 | |||||||
| chr14:20355221 | C | G | 1 | a0001c0002t0001g0086 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.902+274C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355221 | |||||||
| chr14:20355305 | A | G | 1 | a0004c0008t0001g0040 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.902+358A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355305 | |||||||
| chr14:20355339 | G | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.902+392G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355339 | |||||||
| chr14:20355341 | T | C | 3 | a0001c0002t0001g0143 a0001c0002t0002g0016 a0010c0012t0002g0016 |
4 | HG01884.hp1 NA18993.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.902+394T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355341 | |||||||
| chr14:20355343 | T | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.902+396T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355343 | |||||||
| chr14:20355344 | C | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.902+397C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355344 | |||||||
| chr14:20355345 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.902+398T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355345 | |||||||
| chr14:20355346 | G | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.902+399G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355346 | |||||||
| chr14:20355347 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.902+400G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355347 | |||||||
| chr14:20355348 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.902+401T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355348 | |||||||
| chr14:20355349 | T | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.902+402T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355349 | |||||||
| chr14:20355350 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-402T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355350 | |||||||
| chr14:20355354 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-398T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355354 | |||||||
| chr14:20355356 | C | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-396C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355356 | |||||||
| chr14:20355359 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-393T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355359 | |||||||
| chr14:20355360 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-392T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355360 | |||||||
| chr14:20355361 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-391T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355361 | |||||||
| chr14:20355362 | C | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-390C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355362 | |||||||
| chr14:20355363 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-389T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355363 | |||||||
| chr14:20355370 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-382T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355370 | |||||||
| chr14:20355371 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-381T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355371 | |||||||
| chr14:20355372 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-380T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355372 | |||||||
| chr14:20355374 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-378T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355374 | |||||||
| chr14:20355375 | A | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(101): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.903-377A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355375 | |||||||
| chr14:20355379 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-373T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355379 | |||||||
| chr14:20355380 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-372T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355380 | |||||||
| chr14:20355382 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-370T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355382 | |||||||
| chr14:20355386 | G | T | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-366G>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355386 | |||||||
| chr14:20355388 | C | T | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-364C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355388 | |||||||
| chr14:20355390 | C | T | 3 | a0001c0002t0001g0143 a0001c0011t0002g0062 a0001c0011t0002g0063 |
3 | HG01884.hp1 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.903-362C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355390 | |||||||
| chr14:20355391 | G | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-361G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355391 | |||||||
| chr14:20355393 | G | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-359G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355393 | |||||||
| chr14:20355395 | C | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-357C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355395 | |||||||
| chr14:20355397 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-355T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355397 | |||||||
| chr14:20355399 | G | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-353G>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355399 | |||||||
| chr14:20355402 | A | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-350A>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355402 | |||||||
| chr14:20355403 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-349T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355403 | |||||||
| chr14:20355405 | A | C | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-347A>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355405 | |||||||
| chr14:20355406 | C | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-346C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355406 | |||||||
| chr14:20355407 | C | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-345C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355407 | |||||||
| chr14:20355408 | C | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-344C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355408 | |||||||
| chr14:20355409 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-343T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355409 | |||||||
| chr14:20355413 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-339T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355413 | |||||||
| chr14:20355416 | T | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-336T>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355416 | |||||||
| chr14:20355417 | C | A | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-335C>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355417 | |||||||
| chr14:20355420 | C | G | 1 | a0001c0002t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.903-332C>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355420 | |||||||
| chr14:20355652 | C | T | 1 | a0001c0002t0002g0023 | 2 | HG01928.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.903-100C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 9/15 | chr14 | 20355652 | |||||||
| chr14:20355830 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.966+15A>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 10/15 | chr14 | 20355830 | |||||||
| chr14:20356256 | G | T | 40 | a0001c0001t0001g0092 a0001c0001t0002g0003 a0001c0001t0002g0005 others(37): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1102-51G>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 11/15 | chr14 | 20356256 | |||||||
| chr14:20356462 | G | A | 1 | a0001c0004t0001g0030 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1229+28G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 12/15 | chr14 | 20356462 | |||||||
| chr14:20356535 | C | T | 2 | a0001c0001t0001g0015 a0001c0002t0001g0015 |
4 | HG02145.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1230-55C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 12/15 | chr14 | 20356535 | |||||||
| chr14:20356700 | T | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(38): Show |
94 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1329+11T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 13/15 | chr14 | 20356700 | |||||||
| chr14:20356743 | T | C | 2 | a0001c0002t0002g0054 a0001c0002t0002g0110 |
2 | HG00558.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1329+54T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 13/15 | chr14 | 20356743 | |||||||
| chr14:20356854 | C | T | 44 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(41): Show |
98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1329+165C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 13/15 | chr14 | 20356854 | |||||||
| chr14:20356868 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1329+179C>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 13/15 | chr14 | 20356868 | |||||||
| chr14:20356935 | A | G | 19 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0144 others(16): Show |
21 | HG01261.hp2 HG01891.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1330-116A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 13/15 | chr14 | 20356935 | |||||||
| chr14:20356954 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1330-97G>T | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 13/15 | chr14 | 20356954 | |||||||
| chr14:20357162 | T | TTTCAC | 52 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(49): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1428+13_1428+14ins others(5): Show |
PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 14/15 | chr14 | 20357162 | |||||||
| chr14:20357164 | T | G | 52 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(49): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1428+15T>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 14/15 | chr14 | 20357164 | |||||||
| chr14:20357203 | G | A | 45 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(42): Show |
99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1428+54G>A | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 14/15 | chr14 | 20357203 | |||||||
| chr14:20357326 | T | C | 1 | a0001c0002t0002g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1429-70T>C | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 14/15 | chr14 | 20357326 | |||||||
| chr14:20357636 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1554-2A>G | PARP2 | ENSG00000129484.14 | transcript | ENST00000429687.8 | protein_coding | 15/15 | chr14 | 20357636 |