Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5470 |
| ensemblid | ENSG00000156194.19 |
| hgncid | 9244 |
| symbol | PPEF2 |
| name | protein phosphatase with EF-hand domain 2 |
| refseq_nuc | NM_006239.3 |
| refseq_prot | NP_006230.2 |
| ensembl_nuc | ENST00000286719.12 |
| ensembl_prot | ENSP00000286719.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 75859867 |
| end | 75902452 |
| strand | - |
| ver | v1.2 |
| region | chr4:75859867-75902452 |
| region5000 | chr4:75854867-75907452 |
| regionname0 | PPEF2_chr4_75859867_75902452 |
| regionname5000 | PPEF2_chr4_75854867_75907452 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 753 | 212 | 48 | 51 | 72 | 16 | 24 | 45 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0002 | 0/0 | 753 | 15 | 13 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0003 | 0/0 | 753 | 12 | 3 | 4 | 0 | 0 | 5 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0004 | 0/0 | 753 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0005 | 0/0 | 753 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0006 | 0/0 | 447 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(442): Show |
chr4 | 75854867 | 75907452 |
| a0007 | 0/0 | 753 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0008 | 0/0 | 753 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0009 | 0/0 | 653 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(648): Show |
chr4 | 75854867 | 75907452 |
| a0010 | 0/0 | 753 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0011 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0012 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0013 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0014 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| a0015 | 0/0 | 747 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(742): Show |
chr4 | 75854867 | 75907452 |
| a0016 | 0/1 | 753 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | MGSGT others(748): Show |
chr4 | 75854867 | 75907452 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2259 | 195 | 36 | 48 | 71 | 16 | 24 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0001c0002 | 0/0 | 2259 | 13 | 10 | 3 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0001c0016 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0001c0017 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0001c0021 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0001c0025 | 1/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0002c0004 | 0/0 | 2259 | 10 | 8 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0002c0008 | 0/0 | 2259 | 3 | 3 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0002c0011 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0003c0003 | 0/0 | 2259 | 12 | 3 | 4 | 0 | 0 | 5 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0004c0005 | 0/0 | 2259 | 7 | 7 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0005c0006 | 0/0 | 2259 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0005c0018 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0005c0019 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0006c0007 | 0/0 | 2260 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2255): Show |
chr4 | 75854867 | 75907452 | ||
| a0007c0009 | 0/0 | 2259 | 3 | 1 | 1 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0008c0010 | 0/0 | 2259 | 2 | 1 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0008c0020 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0009c0024 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0010c0023 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0011c0012 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0012c0015 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0013c0013 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0014c0026 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 | ||
| a0015c0022 | 0/0 | 2275 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2270): Show |
chr4 | 75854867 | 75907452 | ||
| a0016c0014 | 0/1 | 2259 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | ATGGG others(2254): Show |
chr4 | 75854867 | 75907452 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3343 | 152 | 27 | 35 | 66 | 7 | 17 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0001t0002 | 0/0 | 3343 | 37 | 5 | 12 | 4 | 9 | 7 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0001t0003 | 0/0 | 3343 | 3 | 3 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0001t0004 | 0/0 | 3343 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0001t0005 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0001t0007 | 0/0 | 3343 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0002t0001 | 0/0 | 3343 | 6 | 4 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0002t0002 | 0/0 | 3343 | 7 | 6 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0016t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0017t0008 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0021t0001 | 0/0 | 3343 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0001c0025t0001 | 1/0 | 3343 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0002c0004t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0002c0004t0003 | 0/0 | 3343 | 7 | 6 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0002c0004t0006 | 0/0 | 3343 | 2 | 1 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0002c0008t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0002c0008t0003 | 0/0 | 3343 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0002c0011t0001 | 0/0 | 3343 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0003c0003t0001 | 0/0 | 3343 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0003c0003t0002 | 0/0 | 3343 | 8 | 0 | 4 | 0 | 0 | 4 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0003c0003t0004 | 0/0 | 3343 | 2 | 1 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0004c0005t0003 | 0/0 | 3343 | 7 | 7 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0005c0006t0001 | 0/0 | 3343 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0005c0018t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0005c0019t0005 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0006c0007t0003 | 0/0 | 3344 | 4 | 4 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3339): Show |
chr4 | 75854867 | 75907452 |
| a0007c0009t0001 | 0/0 | 3343 | 2 | 0 | 1 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0007c0009t0002 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0008c0010t0001 | 0/0 | 3343 | 2 | 1 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0008c0020t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0009c0024t0002 | 0/0 | 3343 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0010c0023t0001 | 0/0 | 3343 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0011c0012t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0012c0015t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0013c0013t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0014c0026t0001 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| a0015c0022t0001 | 0/0 | 3359 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3354): Show |
chr4 | 75854867 | 75907452 |
| a0016c0014t0001 | 0/1 | 3343 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | GTGAA others(3338): Show |
chr4 | 75854867 | 75907452 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0016t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0017t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0021t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0001c0025t0001g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0004t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0008t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0008t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0008t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0011t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0002c0011t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0003c0003t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0004c0005t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0004c0005t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0004c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0004c0005t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0004c0005t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0004c0005t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0004c0005t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0005c0006t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0005c0006t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0005c0006t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0005c0006t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0005c0018t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0005c0019t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0006c0007t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0006c0007t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0006c0007t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0006c0007t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0007c0009t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0007c0009t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0007c0009t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0008c0010t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0008c0010t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0008c0020t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0009c0024t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0010c0023t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0011c0012t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0012c0015t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0013c0013t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0014c0026t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0015c0022t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| a0016c0014t0001g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | GBR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | FIN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | FIN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01081 | hp2 | a0003 | c0003 | t0002 | g0251 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0256 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01175 | hp2 | a0002 | c0004 | t0006 | g0263 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01192 | hp2 | a0007 | c0009 | t0001 | g0215 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01243 | hp1 | a0002 | c0004 | t0003 | g0261 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01243 | hp2 | a0008 | c0010 | t0001 | g0206 | AMR | PUR | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0230 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01496 | hp2 | a0009 | c0024 | t0002 | g0232 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01891 | hp2 | a0005 | c0006 | t0001 | g0219 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02055 | hp2 | a0003 | c0003 | t0004 | g0249 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0157 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02132 | hp1 | a0010 | c0023 | t0001 | g0183 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02145 | hp2 | a0006 | c0007 | t0003 | g0202 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02258 | hp1 | a0002 | c0004 | t0003 | g0260 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02258 | hp2 | a0002 | c0011 | t0001 | g0055 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02451 | hp2 | a0011 | c0012 | t0001 | g0085 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02572 | hp1 | a0008 | c0020 | t0001 | g0032 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02572 | hp2 | a0004 | c0005 | t0003 | g0247 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02615 | hp1 | a0005 | c0006 | t0001 | g0235 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02615 | hp2 | a0002 | c0008 | t0003 | g0240 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02630 | hp2 | a0004 | c0005 | t0003 | g0245 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02647 | hp2 | a0002 | c0004 | t0003 | g0041 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02723 | hp1 | a0002 | c0008 | t0003 | g0241 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02809 | hp1 | a0004 | c0005 | t0003 | g0252 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02809 | hp2 | a0006 | c0007 | t0003 | g0203 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02818 | hp1 | a0004 | c0005 | t0003 | g0016 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0233 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02922 | hp2 | a0005 | c0019 | t0005 | g0228 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02965 | hp1 | a0002 | c0004 | t0003 | g0225 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02970 | hp1 | a0006 | c0007 | t0003 | g0205 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02976 | hp1 | a0012 | c0015 | t0001 | g0216 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02976 | hp2 | a0006 | c0007 | t0003 | g0207 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03017 | hp2 | a0003 | c0003 | t0004 | g0250 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03098 | hp1 | a0013 | c0013 | t0001 | g0243 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03098 | hp2 | a0004 | c0005 | t0003 | g0258 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03139 | hp2 | a0002 | c0004 | t0003 | g0208 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0265 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0253 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03209 | hp2 | a0008 | c0010 | t0001 | g0264 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03225 | hp2 | a0001 | c0017 | t0008 | g0259 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03239 | hp2 | a0003 | c0003 | t0002 | g0255 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03453 | hp2 | a0002 | c0008 | t0001 | g0212 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03486 | hp1 | a0002 | c0004 | t0001 | g0094 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03486 | hp2 | a0005 | c0006 | t0001 | g0237 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03516 | hp2 | a0005 | c0006 | t0001 | g0229 | AFR | ESN | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03540 | hp2 | a0002 | c0004 | t0006 | g0262 | AFR | GWD | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03669 | hp1 | a0003 | c0003 | t0002 | g0254 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03688 | hp1 | a0003 | c0003 | t0002 | g0244 | SAS | STU | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03710 | hp1 | a0007 | c0009 | t0001 | g0213 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG04199 | hp2 | a0003 | c0003 | t0002 | g0257 | SAS | STU | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18522 | hp2 | a0002 | c0011 | t0001 | g0053 | AFR | YRI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18960 | hp1 | a0015 | c0022 | t0001 | g0056 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18971 | hp2 | a0001 | c0021 | t0001 | g0114 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | YRI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA20129 | hp1 | a0002 | c0004 | t0003 | g0052 | AFR | ASW | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | ASW | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02109 | hp1 | a0007 | c0009 | t0002 | g0214 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02486 | hp1 | a0004 | c0005 | t0003 | g0246 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02559 | hp1 | a0005 | c0018 | t0001 | g0187 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03471 | hp1 | a0001 | c0016 | t0001 | g0054 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG06807 | hp1 | a0014 | c0026 | t0001 | g0204 | AFR | USA | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| HG06807 | hp2 | a0002 | c0004 | t0003 | g0049 | AFR | USA | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA21309 | hp1 | a0004 | c0005 | t0003 | g0248 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| homoSapiens | chm13v2 | a0016 | c0014 | t0001 | g0266 | REF | REF | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| homoSapiens | grch38p0 | a0001 | c0025 | t0001 | g0209 | REF | REF | PPEF2_chr4_75854867_75907452 | PPEF2 | chr4 | 75854867 | 75907452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75860716 | T | TGTGGGCA others(9): Show |
1 | a0015 | 1 | NA18960.hp1 | frameshift_variant | HIGH | c.2197_2212dupGCCTCA others(10): Show |
p.Gln738fs | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 2493/3343 | 2212/2262 | 738/753 | chr4 | 75860716 | |||
| chr4:75864488 | G | A | 1 | a0009 | 1 | HG01496.hp2 | stop_gained | HIGH | c.1960C>T | p.Arg654* | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/17 | 2241/3343 | 1960/2262 | 654/753 | chr4 | 75864488 | |||
| chr4:75866193 | C | T | 1 | a0013 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1916G>A | p.Arg639His | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/17 | 2197/3343 | 1916/2262 | 639/753 | chr4 | 75866193 | |||
| chr4:75867346 | T | A | 5 | a0002 a0004 a0005 others(2): Show |
33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
missense_variant | MODERATE | c.1723A>T | p.Ser575Cys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/17 | 2004/3343 | 1723/2262 | 575/753 | chr4 | 75867346 | |||
| chr4:75867411 | C | T | 5 | a0002 a0004 a0005 others(2): Show |
33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
missense_variant | MODERATE | c.1658G>A | p.Arg553Lys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/17 | 1939/3343 | 1658/2262 | 553/753 | chr4 | 75867411 | |||
| chr4:75873297 | A | AC | 1 | a0006 | 4 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(1): Show |
frameshift_variant | HIGH | c.1335dupG | p.Trp446fs | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/17 | 1616/3343 | 1335/2262 | 445/753 | chr4 | 75873297 | |||
| chr4:75876373 | C | T | 2 | a0008 a0014 |
4 | HG01243.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
missense_variant | MODERATE | c.1234G>A | p.Glu412Lys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/17 | 1515/3343 | 1234/2262 | 412/753 | chr4 | 75876373 | |||
| chr4:75876427 | C | G | 1 | a0005 | 6 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
missense_variant | MODERATE | c.1180G>C | p.Val394Leu | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/17 | 1461/3343 | 1180/2262 | 394/753 | chr4 | 75876427 | |||
| chr4:75882984 | T | C | 1 | a0010 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.875A>G | p.His292Arg | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/17 | 1156/3343 | 875/2262 | 292/753 | chr4 | 75882984 | |||
| chr4:75888232 | C | T | 1 | a0012 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.514G>A | p.Glu172Lys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/17 | 795/3343 | 514/2262 | 172/753 | chr4 | 75888232 | |||
| chr4:75888243 | G | A | 1 | a0007 | 3 | HG01192.hp2 HG02109.hp1 HG03710.hp1 |
missense_variant | MODERATE | c.503C>T | p.Thr168Ile | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/17 | 784/3343 | 503/2262 | 168/753 | chr4 | 75888243 | |||
| chr4:75890022 | G | A | 2 | a0006 a0014 |
5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.352C>T | p.Arg118Cys | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/17 | 633/3343 | 352/2262 | 118/753 | chr4 | 75890022 | |||
| chr4:75890022 | G | T | 3 | a0003 a0004 a0013 |
20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
missense_variant | MODERATE | c.352C>A | p.Arg118Ser | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/17 | 633/3343 | 352/2262 | 118/753 | chr4 | 75890022 | |||
| chr4:75891927 | C | T | 1 | a0011 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.107G>A | p.Arg36His | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 3/17 | 388/3343 | 107/2262 | 36/753 | chr4 | 75891927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75864441 | T | G | 3 | a0001c0017 a0005c0006 a0005c0019 |
6 | HG01891.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.2007A>C | p.Ser669Ser | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/17 | 2288/3343 | 2007/2262 | 669/753 | chr4 | 75864441 | |||
| chr4:75867398 | C | T | 1 | a0001c0021 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1671G>A | p.Ser557Ser | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/17 | 1952/3343 | 1671/2262 | 557/753 | chr4 | 75867398 | |||
| chr4:75872075 | A | G | 21 | a0001c0001 a0001c0002 a0001c0016 others(18): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
synonymous_variant | LOW | c.1599T>C | p.Ile533Ile | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/17 | 1880/3343 | 1599/2262 | 533/753 | chr4 | 75872075 | |||
| chr4:75884749 | C | T | 13 | a0001c0001 a0001c0021 a0002c0004 others(10): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
synonymous_variant | LOW | c.591G>A | p.Pro197Pro | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/17 | 872/3343 | 591/2262 | 197/753 | chr4 | 75884749 | |||
| chr4:75886872 | A | G | 4 | a0001c0016 a0001c0017 a0002c0011 others(1): Show |
6 | HG01243.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
synonymous_variant | LOW | c.559T>C | p.Leu187Leu | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/17 | 840/3343 | 559/2262 | 187/753 | chr4 | 75886872 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75859918 | T | C | 2 | a0001c0001t0005 a0005c0019t0005 |
2 | HG02486.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*749A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 749 | chr4 | 75859918 | ||||||
| chr4:75859952 | T | C | 1 | a0002c0004t0006 | 2 | HG01175.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*715A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 715 | chr4 | 75859952 | ||||||
| chr4:75860005 | T | A | 1 | a0001c0017t0008 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 662 | chr4 | 75860005 | ||||||
| chr4:75860018 | C | G | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(5): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*649G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 649 | chr4 | 75860018 | ||||||
| chr4:75860033 | A | G | 1 | a0001c0001t0007 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*634T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 634 | chr4 | 75860033 | ||||||
| chr4:75860202 | G | T | 2 | a0001c0001t0004 a0003c0003t0004 |
3 | HG01167.hp1 HG02055.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*465C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 465 | chr4 | 75860202 | ||||||
| chr4:75860524 | C | A | 6 | a0001c0001t0003 a0002c0004t0003 a0002c0004t0006 others(3): Show |
25 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 17/17 | 143 | chr4 | 75860524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75861090 | A | G | 1 | a0012c0015t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2009-170T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861090 | |||||||
| chr4:75861171 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2009-251C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861171 | |||||||
| chr4:75861179 | T | C | 1 | a0003c0003t0001g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2009-259A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861179 | |||||||
| chr4:75861202 | C | T | 34 | a0001c0017t0008g0259 a0002c0004t0001g0094 a0002c0004t0003g0041 others(31): Show |
34 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.2009-282G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861202 | |||||||
| chr4:75861441 | T | TG | 131 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2009-522dupC | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861441 | |||||||
| chr4:75861479 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-559C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861479 | |||||||
| chr4:75861491 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2009-571G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861491 | |||||||
| chr4:75861500 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2009-580T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861500 | |||||||
| chr4:75861522 | A | G | 8 | a0001c0017t0008g0259 a0002c0004t0006g0262 a0002c0004t0006g0263 others(5): Show |
8 | HG01175.hp2 HG01891.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009-602T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861522 | |||||||
| chr4:75861614 | G | GT | 33 | a0001c0017t0008g0259 a0002c0004t0001g0094 a0002c0004t0003g0041 others(30): Show |
33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.2009-695dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTT | 66 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.2009-696_2009-695d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(298): Show |
4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG02895.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(307): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(303): Show |
1 | a0001c0001t0001g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(312): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(306): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0140 |
2 | HG02056.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(315): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(309): Show |
1 | a0001c0001t0001g0159 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(318): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(310): Show |
3 | a0001c0001t0001g0103 a0001c0001t0001g0175 a0001c0001t0001g0188 |
3 | NA18952.hp1 NA19068.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(319): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(310): Show |
19 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0060 others(16): Show |
20 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(319): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(311): Show |
1 | a0001c0001t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(320): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(311): Show |
21 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0001t0001g0064 others(18): Show |
21 | HG00099.hp1 HG00741.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(320): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(312): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0171 |
2 | HG01123.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(321): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(311): Show |
1 | a0001c0001t0001g0123 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2009-695_2009-694i others(320): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(312): Show |
9 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0075 others(6): Show |
9 | HG01168.hp1 HG02155.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(321): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(313): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0127 a0001c0001t0001g0144 |
3 | HG01496.hp1 HG01934.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(322): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(314): Show |
1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(323): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(316): Show |
1 | a0001c0001t0001g0200 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(325): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(317): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0173 |
2 | HG01934.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(326): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(318): Show |
2 | a0001c0001t0001g0161 a0001c0002t0001g0211 |
2 | HG01975.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(327): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(319): Show |
3 | a0001c0001t0001g0068 a0001c0001t0001g0096 a0010c0023t0001g0183 |
3 | HG02132.hp1 NA18973.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(328): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(320): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0196 |
2 | HG02155.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(329): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(321): Show |
2 | a0001c0001t0001g0097 a0001c0001t0001g0190 |
2 | NA18951.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(330): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(322): Show |
4 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0001g0120 others(1): Show |
4 | HG00423.hp1 HG00423.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(331): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(323): Show |
1 | a0001c0001t0001g0137 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2009-695_2009-694i others(332): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(322): Show |
1 | a0001c0021t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(331): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(323): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0130 |
2 | HG03669.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(332): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(324): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0138 |
2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(333): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(325): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0069 |
2 | HG02622.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(334): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(326): Show |
1 | a0001c0001t0001g0030 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(335): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(328): Show |
3 | a0001c0001t0001g0058 a0001c0001t0001g0162 a0001c0002t0001g0210 |
3 | HG01261.hp1 HG02129.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(337): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(328): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0152 |
2 | NA18998.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(337): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(329): Show |
16 | a0001c0001t0001g0057 a0001c0001t0001g0088 a0001c0001t0001g0093 others(13): Show |
17 | HG00140.hp2 HG00280.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(338): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(330): Show |
1 | a0001c0001t0001g0132 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(339): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(329): Show |
1 | a0001c0001t0001g0139 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2009-695_2009-694i others(338): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(329): Show |
1 | a0001c0001t0001g0029 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2009-695_2009-694i others(338): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(330): Show |
17 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0087 others(14): Show |
17 | HG01192.hp2 HG01255.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(339): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(331): Show |
8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0077 others(5): Show |
8 | HG01358.hp1 HG03710.hp2 NA18992.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(340): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(332): Show |
4 | a0001c0001t0001g0065 a0001c0001t0001g0107 a0001c0001t0001g0142 others(1): Show |
4 | HG00438.hp2 HG01175.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(341): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(333): Show |
4 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0001g0113 others(1): Show |
4 | HG02165.hp1 HG02165.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(342): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(334): Show |
6 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0134 others(3): Show |
6 | HG02083.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009-695_2009-694i others(343): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(335): Show |
3 | a0001c0001t0001g0109 a0001c0001t0001g0135 a0001c0001t0001g0192 |
3 | HG00673.hp1 HG02071.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2009-695_2009-694i others(344): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861614 | G | GTTTTTTT others(339): Show |
1 | a0001c0001t0001g0112 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2009-695_2009-694i others(348): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861614 | |||||||
| chr4:75861640 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2009-720G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861640 | |||||||
| chr4:75861687 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2009-767T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861687 | |||||||
| chr4:75861692 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00099.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2009-772G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861692 | |||||||
| chr4:75861702 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2009-782A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861702 | |||||||
| chr4:75861755 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-835T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861755 | |||||||
| chr4:75861767 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-847A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861767 | |||||||
| chr4:75861898 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-978G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861898 | |||||||
| chr4:75861904 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-984A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861904 | |||||||
| chr4:75861905 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-985T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861905 | |||||||
| chr4:75861951 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2009-1031C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861951 | |||||||
| chr4:75861966 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-1046T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861966 | |||||||
| chr4:75861982 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-1062G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75861982 | |||||||
| chr4:75862020 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-1100G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862020 | |||||||
| chr4:75862118 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-1198G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862118 | |||||||
| chr4:75862248 | G | A | 1 | a0002c0008t0001g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2009-1328C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862248 | |||||||
| chr4:75862292 | CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0150 a0001c0001t0001g0185 a0002c0004t0006g0263 others(2): Show |
5 | HG00741.hp2 HG01175.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009-1383_2009-137 others(15): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862292 | |||||||
| chr4:75862292 | CAAAAAAA others(5): Show |
C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2009-1384_2009-137 others(16): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862292 | |||||||
| chr4:75862292 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG02895.hp2 HG02896.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2009-1385_2009-137 others(17): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862292 | |||||||
| chr4:75862589 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2009-1669G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862589 | |||||||
| chr4:75862622 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0152 |
2 | NA18950.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2009-1702G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75862622 | |||||||
| chr4:75863076 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2008+1364A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863076 | |||||||
| chr4:75863192 | G | A | 1 | a0001c0001t0002g0010 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2008+1248C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863192 | |||||||
| chr4:75863208 | TA | T | 4 | a0002c0004t0001g0094 a0002c0011t0001g0053 a0002c0011t0001g0055 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2008+1231delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863208 | |||||||
| chr4:75863210 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2008+1230C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863210 | |||||||
| chr4:75863335 | CA | C | 35 | a0001c0001t0001g0146 a0001c0001t0001g0163 a0001c0001t0001g0171 others(32): Show |
35 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.2008+1104delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863335 | |||||||
| chr4:75863335 | CAA | C | 219 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(216): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2008+1103_2008+110 others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863335 | |||||||
| chr4:75863448 | C | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 others(1): Show |
4 | HG02165.hp1 NA18973.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2008+992G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863448 | |||||||
| chr4:75863449 | G | A | 34 | a0001c0017t0008g0259 a0002c0004t0001g0094 a0002c0004t0003g0041 others(31): Show |
34 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.2008+991C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863449 | |||||||
| chr4:75863499 | CAA | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.2008+939_2008+940d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863499 | |||||||
| chr4:75863499 | CAAA | C | 23 | a0001c0001t0001g0093 a0001c0001t0001g0221 a0001c0001t0001g0222 others(20): Show |
23 | HG01070.hp1 HG01243.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.2008+938_2008+940d others(5): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863499 | |||||||
| chr4:75863504 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2008+936T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863504 | |||||||
| chr4:75863672 | C | T | 1 | a0002c0004t0001g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2008+768G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863672 | |||||||
| chr4:75863851 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2008+589T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863851 | |||||||
| chr4:75863915 | G | A | 1 | a0001c0017t0008g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2008+525C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863915 | |||||||
| chr4:75863941 | C | T | 1 | a0008c0010t0001g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2008+499G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863941 | |||||||
| chr4:75863971 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2008+469G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75863971 | |||||||
| chr4:75864031 | C | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0201 |
2 | HG01361.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2008+409G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75864031 | |||||||
| chr4:75864034 | G | A | 28 | a0002c0004t0001g0094 a0002c0004t0003g0041 a0002c0004t0003g0049 others(25): Show |
28 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.2008+406C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75864034 | |||||||
| chr4:75864151 | C | T | 5 | a0002c0004t0003g0208 a0004c0005t0003g0245 a0004c0005t0003g0246 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2008+289G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 16/16 | chr4 | 75864151 | |||||||
| chr4:75864563 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1921-36G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864563 | |||||||
| chr4:75864570 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1921-43T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864570 | |||||||
| chr4:75864583 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1921-56A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864583 | |||||||
| chr4:75864617 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1921-90G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864617 | |||||||
| chr4:75864624 | G | GA | 4 | a0002c0004t0003g0225 a0002c0004t0003g0260 a0002c0004t0006g0262 others(1): Show |
4 | HG01175.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1921-98dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75864624 | |||||||
| chr4:75865053 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1921-526G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75865053 | |||||||
| chr4:75865227 | G | A | 1 | a0004c0005t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1921-700C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75865227 | |||||||
| chr4:75865544 | G | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1920+645C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 15/16 | chr4 | 75865544 | |||||||
| chr4:75866520 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(224): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1757-168A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866520 | |||||||
| chr4:75866692 | C | T | 1 | a0001c0017t0008g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1757-340G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866692 | |||||||
| chr4:75866761 | T | C | 33 | a0002c0004t0001g0094 a0002c0004t0003g0041 a0002c0004t0003g0049 others(30): Show |
33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1757-409A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866761 | |||||||
| chr4:75866804 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
5 | HG02165.hp1 NA18973.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757-452C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866804 | |||||||
| chr4:75866970 | A | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1756+343T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75866970 | |||||||
| chr4:75867086 | G | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1756+227C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75867086 | |||||||
| chr4:75867115 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(157): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1756+198T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75867115 | |||||||
| chr4:75867259 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1756+54T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75867259 | |||||||
| chr4:75867299 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1756+14A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 14/16 | chr4 | 75867299 | |||||||
| chr4:75867424 | G | A | 1 | a0007c0009t0001g0213 | 1 | HG03710.hp1 | splice_region_variant&intron_variant | LOW | c.1650-5C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867424 | |||||||
| chr4:75867539 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-120G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867539 | |||||||
| chr4:75867623 | G | A | 33 | a0002c0004t0001g0094 a0002c0004t0003g0041 a0002c0004t0003g0049 others(30): Show |
33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1650-204C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867623 | |||||||
| chr4:75867704 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-285C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867704 | |||||||
| chr4:75867927 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(157): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1650-508A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867927 | |||||||
| chr4:75867985 | C | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-566G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75867985 | |||||||
| chr4:75868062 | C | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-643G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868062 | |||||||
| chr4:75868156 | C | CAA | 255 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(252): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1650-739_1650-738d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868156 | |||||||
| chr4:75868185 | G | A | 1 | a0005c0019t0005g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1650-766C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868185 | |||||||
| chr4:75868240 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-821G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868240 | |||||||
| chr4:75868258 | G | C | 2 | a0004c0005t0003g0246 a0004c0005t0003g0247 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1650-839C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868258 | |||||||
| chr4:75868309 | C | T | 1 | a0001c0001t0002g0009 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1650-890G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868309 | |||||||
| chr4:75868315 | C | CAA | 19 | a0002c0004t0003g0041 a0002c0004t0003g0049 a0002c0004t0003g0052 others(16): Show |
19 | HG01243.hp1 HG02145.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1650-898_1650-897d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | |||||||
| chr4:75868315 | C | CAAA | 8 | a0002c0004t0001g0094 a0002c0004t0003g0225 a0002c0004t0003g0260 others(5): Show |
8 | HG02258.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1650-899_1650-897d others(5): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | |||||||
| chr4:75868315 | C | CAAAAA | 13 | a0001c0001t0001g0123 a0001c0001t0001g0141 a0001c0001t0001g0164 others(10): Show |
13 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1650-901_1650-897d others(7): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | |||||||
| chr4:75868315 | C | CAAAAAA | 205 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(202): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1650-902_1650-897d others(8): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | |||||||
| chr4:75868315 | C | CAAAAAAA | 13 | a0001c0001t0001g0030 a0001c0001t0001g0069 a0001c0001t0001g0134 others(10): Show |
13 | HG02145.hp1 HG02486.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.1650-903_1650-897d others(9): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868315 | |||||||
| chr4:75868342 | A | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-923T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868342 | |||||||
| chr4:75868363 | C | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(224): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1650-944G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868363 | |||||||
| chr4:75868453 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-1034A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868453 | |||||||
| chr4:75868528 | T | G | 1 | a0001c0001t0002g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1650-1109A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868528 | |||||||
| chr4:75868563 | G | A | 1 | a0008c0010t0001g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1650-1144C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868563 | |||||||
| chr4:75868566 | C | T | 33 | a0002c0004t0001g0094 a0002c0004t0003g0041 a0002c0004t0003g0049 others(30): Show |
33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1650-1147G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868566 | |||||||
| chr4:75868652 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-1233A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868652 | |||||||
| chr4:75868738 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1650-1319G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868738 | |||||||
| chr4:75868745 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-1326T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868745 | |||||||
| chr4:75868851 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-1432A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868851 | |||||||
| chr4:75868883 | C | T | 5 | a0002c0004t0001g0094 a0002c0008t0001g0212 a0002c0011t0001g0053 others(2): Show |
5 | HG02258.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-1464G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75868883 | |||||||
| chr4:75869121 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1650-1702T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869121 | |||||||
| chr4:75869418 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(224): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1650-1999C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869418 | |||||||
| chr4:75869600 | A | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-2181T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869600 | |||||||
| chr4:75869611 | C | T | 5 | a0005c0006t0001g0219 a0005c0006t0001g0229 a0005c0006t0001g0235 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-2192G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869611 | |||||||
| chr4:75869627 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1650-2208T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869627 | |||||||
| chr4:75869674 | T | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-2255A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869674 | |||||||
| chr4:75869712 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650-2293T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869712 | |||||||
| chr4:75869838 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+2187G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869838 | |||||||
| chr4:75869854 | GA | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1649+2170delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869854 | |||||||
| chr4:75869868 | A | C | 4 | a0002c0004t0001g0094 a0002c0011t0001g0053 a0002c0011t0001g0055 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+2157T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869868 | |||||||
| chr4:75869868 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(253): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1649+2157T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75869868 | |||||||
| chr4:75870104 | A | G | 4 | a0002c0004t0003g0225 a0002c0004t0003g0260 a0002c0004t0006g0262 others(1): Show |
4 | HG01175.hp2 HG02258.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+1921T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870104 | |||||||
| chr4:75870153 | C | T | 33 | a0002c0004t0001g0094 a0002c0004t0003g0041 a0002c0004t0003g0049 others(30): Show |
33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1649+1872G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870153 | |||||||
| chr4:75870325 | A | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG00621.hp2 NA18951.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+1700T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870325 | |||||||
| chr4:75870500 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+1525A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870500 | |||||||
| chr4:75870588 | A | G | 1 | a0008c0010t0001g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1649+1437T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870588 | |||||||
| chr4:75870643 | T | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(224): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1649+1382A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870643 | |||||||
| chr4:75870676 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1649+1349C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870676 | |||||||
| chr4:75870875 | T | C | 33 | a0002c0004t0001g0094 a0002c0004t0003g0041 a0002c0004t0003g0049 others(30): Show |
33 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1649+1150A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870875 | |||||||
| chr4:75870878 | C | CATTTATT others(1): Show |
12 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0153 others(9): Show |
13 | HG00323.hp1 HG01081.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1649+1139_1649+114 others(12): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | |||||||
| chr4:75870878 | C | CATTTATT others(5): Show |
207 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1649+1135_1649+114 others(16): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | |||||||
| chr4:75870878 | C | CATTTATT others(9): Show |
37 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0048 others(34): Show |
38 | HG00673.hp1 HG01099.hp1 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.1649+1131_1649+114 others(20): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | |||||||
| chr4:75870878 | C | CATTTATT others(13): Show |
2 | a0001c0001t0001g0132 a0001c0001t0002g0027 |
2 | HG01257.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1649+1127_1649+114 others(24): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | |||||||
| chr4:75870878 | C | CATTTATT others(17): Show |
1 | a0001c0001t0001g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1649+1123_1649+114 others(28): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75870878 | |||||||
| chr4:75871002 | CA | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+1022delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871002 | |||||||
| chr4:75871080 | G | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0123 |
2 | HG02015.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1649+945C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871080 | |||||||
| chr4:75871093 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+932A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871093 | |||||||
| chr4:75871111 | G | C | 1 | a0001c0001t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1649+914C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871111 | |||||||
| chr4:75871121 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1649+904A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871121 | |||||||
| chr4:75871158 | C | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+867G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871158 | |||||||
| chr4:75871166 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1649+859G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871166 | |||||||
| chr4:75871172 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1649+853T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871172 | |||||||
| chr4:75871210 | G | A | 1 | a0005c0019t0005g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1649+815C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871210 | |||||||
| chr4:75871236 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+789C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871236 | |||||||
| chr4:75871245 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+780A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871245 | |||||||
| chr4:75871463 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+562A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871463 | |||||||
| chr4:75871517 | C | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+508G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871517 | |||||||
| chr4:75871644 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1649+381T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871644 | |||||||
| chr4:75871723 | A | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1649+302T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871723 | |||||||
| chr4:75871746 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1649+279G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871746 | |||||||
| chr4:75871755 | G | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0186 others(1): Show |
4 | HG01255.hp1 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+270C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871755 | |||||||
| chr4:75871776 | T | A | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0186 others(1): Show |
4 | HG01255.hp1 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+249A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 13/16 | chr4 | 75871776 | |||||||
| chr4:75872429 | C | A | 1 | a0001c0001t0002g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1507-262G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/16 | chr4 | 75872429 | |||||||
| chr4:75872614 | G | A | 1 | a0005c0006t0001g0229 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1507-447C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/16 | chr4 | 75872614 | |||||||
| chr4:75872715 | C | T | 1 | a0005c0019t0005g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1506+412G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/16 | chr4 | 75872715 | |||||||
| chr4:75872905 | G | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0186 others(1): Show |
4 | HG01255.hp1 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+222C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 12/16 | chr4 | 75872905 | |||||||
| chr4:75873509 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1321-197A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75873509 | |||||||
| chr4:75873742 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0020 |
2 | HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1321-430G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75873742 | |||||||
| chr4:75873794 | A | AT | 8 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0050 others(5): Show |
9 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1321-483dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75873794 | |||||||
| chr4:75874056 | A | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1321-744T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874056 | |||||||
| chr4:75874062 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1321-750G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874062 | |||||||
| chr4:75874115 | CAAACAAA others(9): Show |
C | 1 | a0001c0001t0001g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1321-819_1321-804d others(18): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874115 | |||||||
| chr4:75874123 | CAAACAAA others(1): Show |
C | 4 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0184 others(1): Show |
4 | HG02083.hp1 HG02083.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1321-819_1321-812d others(10): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874123 | |||||||
| chr4:75874127 | CAAAT | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1321-819_1321-816d others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874127 | |||||||
| chr4:75874393 | T | C | 1 | a0001c0002t0002g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1321-1081A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874393 | |||||||
| chr4:75874396 | A | G | 1 | a0004c0005t0003g0258 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1321-1084T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874396 | |||||||
| chr4:75874505 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0153 others(2): Show |
5 | HG01109.hp2 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-1193G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874505 | |||||||
| chr4:75874548 | C | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0163 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1321-1236G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874548 | |||||||
| chr4:75874752 | T | C | 12 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(9): Show |
12 | HG00423.hp1 HG00621.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.1321-1440A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874752 | |||||||
| chr4:75874760 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG00099.hp1 HG00741.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1321-1448G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874760 | |||||||
| chr4:75874796 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0013 |
2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1321-1484G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874796 | |||||||
| chr4:75874902 | C | CT | 28 | a0001c0001t0001g0059 a0001c0001t0002g0066 a0002c0004t0001g0094 others(25): Show |
28 | HG00621.hp1 HG01243.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1320+1384dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874902 | |||||||
| chr4:75874902 | CT | C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0168 a0001c0001t0001g0174 others(3): Show |
6 | HG01175.hp2 HG02451.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320+1384delA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874902 | |||||||
| chr4:75874906 | T | C | 1 | a0001c0002t0002g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1320+1381A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874906 | |||||||
| chr4:75874961 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1320+1326C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75874961 | |||||||
| chr4:75875466 | A | G | 5 | a0005c0006t0001g0219 a0005c0006t0001g0229 a0005c0006t0001g0235 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1320+821T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75875466 | |||||||
| chr4:75875718 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1320+569G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75875718 | |||||||
| chr4:75875767 | T | C | 6 | a0005c0006t0001g0219 a0005c0006t0001g0229 a0005c0006t0001g0235 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1320+520A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75875767 | |||||||
| chr4:75876184 | A | AAGAG | 259 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1320+99_1320+102du others(5): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75876184 | |||||||
| chr4:75876237 | T | G | 4 | a0002c0004t0001g0094 a0002c0008t0001g0212 a0002c0011t0001g0053 others(1): Show |
4 | HG02258.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1320+50A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 11/16 | chr4 | 75876237 | |||||||
| chr4:75876797 | G | A | 68 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(65): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.934-124C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75876797 | |||||||
| chr4:75876991 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.934-318C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75876991 | |||||||
| chr4:75876995 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.934-322C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75876995 | |||||||
| chr4:75877006 | A | AAAAAGAA others(42): Show |
1 | a0001c0001t0001g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(49): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(43): Show |
1 | a0001c0001t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.934-334_934-333ins others(50): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(50): Show |
1 | a0001c0001t0002g0035 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.934-334_934-333ins others(57): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(58): Show |
1 | a0001c0001t0002g0036 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.934-334_934-333ins others(65): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(9): Show |
3 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0191 |
3 | HG01358.hp1 HG02040.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.934-349_934-334dup others(16): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(21): Show |
1 | a0001c0001t0001g0059 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.934-361_934-334dup others(28): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(25): Show |
3 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0131 |
3 | HG01070.hp1 HG03942.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.934-365_934-334dup others(32): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(29): Show |
16 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0129 others(13): Show |
16 | HG01069.hp1 HG01071.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(36): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(33): Show |
28 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0069 others(25): Show |
29 | HG00323.hp2 HG00738.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(40): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(37): Show |
34 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0088 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(44): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(41): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(42): Show |
46 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(48): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(45): Show |
38 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0031 others(35): Show |
39 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(52): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(49): Show |
16 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0095 others(13): Show |
16 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(56): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(53): Show |
11 | a0001c0001t0001g0030 a0001c0001t0001g0075 a0001c0001t0001g0132 others(8): Show |
11 | HG00423.hp2 HG01081.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(60): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(57): Show |
8 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0001t0001g0147 others(5): Show |
8 | HG01358.hp2 HG02155.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.934-334_934-333ins others(64): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAAGAAA others(61): Show |
2 | a0001c0001t0001g0029 a0001c0001t0001g0112 |
2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.934-334_934-333ins others(68): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAGAAAG others(28): Show |
1 | a0001c0001t0001g0144 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(35): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAAGAAAG others(40): Show |
1 | a0001c0001t0001g0096 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(47): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AAGAAAGA others(43): Show |
3 | a0001c0001t0001g0173 a0001c0001t0002g0099 a0001c0001t0003g0226 |
3 | HG01934.hp1 HG02280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.934-334_934-333ins others(50): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AGAAAGAA others(34): Show |
1 | a0001c0001t0001g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(41): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | A | AGAAAGAA others(42): Show |
1 | a0001c0001t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.934-334_934-333ins others(49): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877006 | AAAAGAAA others(1): Show |
A | 35 | a0001c0001t0001g0168 a0002c0004t0001g0094 a0002c0004t0003g0041 others(32): Show |
35 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.934-341_934-334del others(8): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877006 | |||||||
| chr4:75877013 | A | AAGAAAGA others(59): Show |
1 | a0001c0001t0002g0037 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.934-341_934-340ins others(66): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877013 | |||||||
| chr4:75877014 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.934-341C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877014 | |||||||
| chr4:75877028 | A | AAGAAAGA others(45): Show |
1 | a0001c0001t0001g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.934-356_934-355ins others(52): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877028 | |||||||
| chr4:75877038 | G | GAAAGAAA others(46): Show |
1 | a0001c0001t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.934-366_934-365ins others(53): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877038 | |||||||
| chr4:75877039 | A | AAAGAAAG others(36): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG00673.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.934-367_934-366ins others(43): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877039 | |||||||
| chr4:75877039 | A | AAAGAAAG others(40): Show |
1 | a0001c0001t0004g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.934-367_934-366ins others(47): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877039 | |||||||
| chr4:75877039 | A | AAAGAAAG others(44): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0070 |
2 | NA18992.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.934-367_934-366ins others(51): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877039 | |||||||
| chr4:75877039 | A | AAAGAAAG others(48): Show |
1 | a0001c0002t0001g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.934-367_934-366ins others(55): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877039 | |||||||
| chr4:75877115 | A | G | 8 | a0002c0004t0003g0208 a0002c0008t0003g0240 a0002c0008t0003g0241 others(5): Show |
8 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-442T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877115 | |||||||
| chr4:75877135 | C | T | 1 | a0005c0019t0005g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.934-462G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877135 | |||||||
| chr4:75877173 | C | A | 6 | a0005c0006t0001g0219 a0005c0006t0001g0229 a0005c0006t0001g0235 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-500G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877173 | |||||||
| chr4:75877213 | T | C | 3 | a0001c0001t0003g0220 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG02055.hp1 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.934-540A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877213 | |||||||
| chr4:75877246 | G | A | 30 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(27): Show |
30 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.934-573C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877246 | |||||||
| chr4:75877268 | C | T | 1 | a0005c0019t0005g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.934-595G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877268 | |||||||
| chr4:75877376 | AAG | A | 9 | a0002c0004t0001g0094 a0002c0008t0001g0212 a0002c0011t0001g0053 others(6): Show |
9 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-705_934-704del others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877376 | |||||||
| chr4:75877378 | G | GAGAAAGA others(1): Show |
5 | a0005c0019t0005g0228 a0008c0010t0001g0206 a0008c0010t0001g0264 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-706_934-705ins others(8): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877378 | |||||||
| chr4:75877380 | G | GAA | 225 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(222): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.934-708_934-707ins others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877380 | |||||||
| chr4:75877382 | G | A | 25 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(22): Show |
25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-709C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877382 | |||||||
| chr4:75877384 | A | G | 25 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(22): Show |
25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-711T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877384 | |||||||
| chr4:75877386 | G | A | 25 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(22): Show |
25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-713C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877386 | |||||||
| chr4:75877386 | GA | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(222): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.934-714delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877386 | |||||||
| chr4:75877594 | T | C | 5 | a0001c0001t0001g0168 a0002c0004t0003g0225 a0002c0004t0003g0260 others(2): Show |
5 | HG01175.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-921A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877594 | |||||||
| chr4:75877670 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.934-997G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877670 | |||||||
| chr4:75877672 | CT | C | 71 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(68): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.934-1000delA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877672 | |||||||
| chr4:75877674 | T | G | 1 | a0001c0017t0008g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.934-1001A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877674 | |||||||
| chr4:75877741 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.934-1068A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877741 | |||||||
| chr4:75877791 | A | G | 4 | a0008c0010t0001g0206 a0008c0010t0001g0264 a0008c0020t0001g0032 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-1118T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877791 | |||||||
| chr4:75877916 | C | T | 25 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(22): Show |
25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-1243G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877916 | |||||||
| chr4:75877946 | T | C | 34 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(31): Show |
34 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.934-1273A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877946 | |||||||
| chr4:75877957 | C | A | 1 | a0001c0016t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.934-1284G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75877957 | |||||||
| chr4:75878022 | T | C | 1 | a0005c0006t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.934-1349A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878022 | |||||||
| chr4:75878204 | T | C | 10 | a0001c0001t0001g0057 a0002c0004t0001g0094 a0002c0008t0001g0212 others(7): Show |
10 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.934-1531A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878204 | |||||||
| chr4:75878214 | T | A | 29 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(26): Show |
29 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.934-1541A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878214 | |||||||
| chr4:75878450 | C | T | 38 | a0001c0001t0001g0168 a0002c0004t0001g0094 a0002c0004t0003g0041 others(35): Show |
38 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.934-1777G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878450 | |||||||
| chr4:75878784 | T | C | 4 | a0008c0010t0001g0206 a0008c0010t0001g0264 a0008c0020t0001g0032 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-2111A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878784 | |||||||
| chr4:75878802 | T | G | 1 | a0002c0004t0003g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.934-2129A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878802 | |||||||
| chr4:75878811 | G | T | 29 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(26): Show |
29 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.934-2138C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878811 | |||||||
| chr4:75878830 | G | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0074 |
2 | NA18965.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.934-2157C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878830 | |||||||
| chr4:75878903 | G | A | 41 | a0001c0001t0001g0168 a0001c0002t0002g0230 a0001c0002t0002g0231 others(38): Show |
41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2230C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75878903 | |||||||
| chr4:75879005 | G | T | 1 | a0014c0026t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.934-2332C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879005 | |||||||
| chr4:75879181 | C | T | 1 | a0002c0008t0003g0240 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.934-2508G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879181 | |||||||
| chr4:75879195 | A | G | 41 | a0001c0001t0001g0168 a0001c0002t0002g0230 a0001c0002t0002g0231 others(38): Show |
41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2522T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879195 | |||||||
| chr4:75879229 | T | G | 41 | a0001c0001t0001g0168 a0001c0002t0002g0230 a0001c0002t0002g0231 others(38): Show |
41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2556A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879229 | |||||||
| chr4:75879272 | A | G | 41 | a0001c0001t0001g0168 a0001c0002t0002g0230 a0001c0002t0002g0231 others(38): Show |
41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2599T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879272 | |||||||
| chr4:75879327 | T | C | 41 | a0001c0001t0001g0168 a0001c0002t0002g0230 a0001c0002t0002g0231 others(38): Show |
41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2654A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879327 | |||||||
| chr4:75879332 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.934-2659C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879332 | |||||||
| chr4:75879350 | C | T | 16 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0233 others(13): Show |
16 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.934-2677G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879350 | |||||||
| chr4:75879384 | T | G | 25 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(22): Show |
25 | HG01175.hp2 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-2711A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879384 | |||||||
| chr4:75879398 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.934-2725C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879398 | |||||||
| chr4:75879558 | T | C | 41 | a0001c0001t0001g0168 a0001c0002t0002g0230 a0001c0002t0002g0231 others(38): Show |
41 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.934-2885A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879558 | |||||||
| chr4:75879576 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.934-2903T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879576 | |||||||
| chr4:75879613 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.934-2940A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879613 | |||||||
| chr4:75879838 | A | AT | 215 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(212): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.933+3087dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879838 | |||||||
| chr4:75879954 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+2972C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879954 | |||||||
| chr4:75879964 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.933+2962C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879964 | |||||||
| chr4:75879986 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+2940T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75879986 | |||||||
| chr4:75880064 | G | A | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG01070.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.933+2862C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880064 | |||||||
| chr4:75880144 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+2782T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880144 | |||||||
| chr4:75880229 | C | T | 16 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0233 others(13): Show |
16 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.933+2697G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880229 | |||||||
| chr4:75880230 | G | A | 1 | a0001c0002t0001g0236 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.933+2696C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880230 | |||||||
| chr4:75880275 | C | G | 1 | a0001c0001t0002g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.933+2651G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880275 | |||||||
| chr4:75880595 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+2331G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880595 | |||||||
| chr4:75880625 | A | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+2301T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880625 | |||||||
| chr4:75880670 | T | C | 12 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0233 others(9): Show |
12 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+2256A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880670 | |||||||
| chr4:75880804 | C | CT | 17 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0233 others(14): Show |
17 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.933+2121dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880804 | |||||||
| chr4:75880804 | C | CTT | 29 | a0001c0001t0001g0168 a0002c0004t0003g0041 a0002c0004t0003g0049 others(26): Show |
29 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.933+2120_933+2121d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880804 | |||||||
| chr4:75880818 | T | TTTTG | 213 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(210): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.933+2107_933+2108i others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880818 | |||||||
| chr4:75880818 | T | TTTTTG | 5 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0140 others(2): Show |
5 | HG02056.hp1 HG02056.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+2107_933+2108i others(7): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880818 | |||||||
| chr4:75880907 | C | T | 4 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0033 others(1): Show |
4 | HG01257.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+2019G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880907 | |||||||
| chr4:75880945 | G | A | 12 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0233 others(9): Show |
12 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+1981C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880945 | |||||||
| chr4:75880948 | C | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+1978G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880948 | |||||||
| chr4:75880960 | C | T | 1 | a0004c0005t0003g0248 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.933+1966G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880960 | |||||||
| chr4:75880991 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(154): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.933+1935C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75880991 | |||||||
| chr4:75881047 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.933+1879T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881047 | |||||||
| chr4:75881102 | A | AT | 191 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(188): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.933+1823dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881102 | |||||||
| chr4:75881102 | A | ATT | 66 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.933+1822_933+1823d others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881102 | |||||||
| chr4:75881243 | A | G | 247 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(244): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.933+1683T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881243 | |||||||
| chr4:75881289 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+1637T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881289 | |||||||
| chr4:75881320 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+1606C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881320 | |||||||
| chr4:75881358 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.933+1568T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881358 | |||||||
| chr4:75881487 | C | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(150): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.933+1439G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881487 | |||||||
| chr4:75881628 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.933+1298C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881628 | |||||||
| chr4:75881668 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.933+1258C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881668 | |||||||
| chr4:75881807 | G | A | 1 | a0001c0002t0002g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.933+1119C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881807 | |||||||
| chr4:75881917 | T | C | 16 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0233 others(13): Show |
16 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.933+1009A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881917 | |||||||
| chr4:75881974 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.933+952A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881974 | |||||||
| chr4:75881988 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.933+938C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75881988 | |||||||
| chr4:75882016 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+910T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882016 | |||||||
| chr4:75882033 | A | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+893T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882033 | |||||||
| chr4:75882172 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+754C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882172 | |||||||
| chr4:75882232 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+694A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882232 | |||||||
| chr4:75882304 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+622C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882304 | |||||||
| chr4:75882460 | C | T | 3 | a0002c0004t0001g0094 a0002c0011t0001g0053 a0002c0011t0001g0055 |
3 | HG02258.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.933+466G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882460 | |||||||
| chr4:75882476 | A | G | 1 | a0003c0003t0004g0250 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.933+450T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882476 | |||||||
| chr4:75882518 | G | T | 61 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(58): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.933+408C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882518 | |||||||
| chr4:75882530 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+396C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882530 | |||||||
| chr4:75882539 | C | CT | 7 | a0001c0001t0001g0073 a0001c0001t0001g0180 a0001c0001t0002g0007 others(4): Show |
7 | HG00323.hp2 HG01167.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+386dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882539 | |||||||
| chr4:75882539 | C | CTT | 211 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.933+385_933+386dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882539 | |||||||
| chr4:75882591 | G | T | 2 | a0004c0005t0003g0246 a0004c0005t0003g0247 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.933+335C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882591 | |||||||
| chr4:75882914 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.933+12T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 10/16 | chr4 | 75882914 | |||||||
| chr4:75883348 | A | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.747-146T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883348 | |||||||
| chr4:75883351 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.747-149G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883351 | |||||||
| chr4:75883355 | G | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.747-153C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883355 | |||||||
| chr4:75883532 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.747-330T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883532 | |||||||
| chr4:75883593 | C | T | 1 | a0001c0017t0008g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.747-391G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883593 | |||||||
| chr4:75883594 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.747-392C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883594 | |||||||
| chr4:75883601 | G | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.747-399C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883601 | |||||||
| chr4:75883767 | G | A | 225 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(222): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.747-565C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883767 | |||||||
| chr4:75883817 | C | CA | 23 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(20): Show |
23 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.747-616dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883817 | |||||||
| chr4:75883817 | C | CAA | 8 | a0001c0002t0002g0239 a0001c0016t0001g0054 a0002c0004t0003g0261 others(5): Show |
8 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.747-617_747-616dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883817 | |||||||
| chr4:75883817 | CA | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.747-616delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883817 | |||||||
| chr4:75883847 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(221): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.747-645C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883847 | |||||||
| chr4:75883852 | G | A | 15 | a0001c0002t0001g0003 a0001c0002t0001g0217 a0001c0002t0001g0236 others(12): Show |
16 | HG01255.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.747-650C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883852 | |||||||
| chr4:75883870 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0024 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.747-668C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883870 | |||||||
| chr4:75883889 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0024 others(152): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.747-687C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883889 | |||||||
| chr4:75883895 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.747-693A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883895 | |||||||
| chr4:75883938 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.746+656A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883938 | |||||||
| chr4:75883940 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(222): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.746+654T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75883940 | |||||||
| chr4:75884114 | G | C | 48 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(45): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.746+480C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884114 | |||||||
| chr4:75884312 | T | C | 232 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.746+282A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884312 | |||||||
| chr4:75884424 | C | CA | 150 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.746+169dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884424 | |||||||
| chr4:75884424 | C | CAA | 78 | a0001c0001t0001g0021 a0001c0001t0001g0057 a0001c0001t0001g0059 others(75): Show |
78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.746+168_746+169dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884424 | |||||||
| chr4:75884438 | AT | A | 5 | a0006c0007t0003g0202 a0006c0007t0003g0203 a0006c0007t0003g0205 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+155delA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884438 | |||||||
| chr4:75884439 | T | A | 3 | a0001c0002t0001g0003 a0001c0002t0001g0217 a0012c0015t0001g0216 |
4 | HG01891.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.746+155A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884439 | |||||||
| chr4:75884532 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG00673.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.746+62T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884532 | |||||||
| chr4:75884539 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.746+55T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884539 | |||||||
| chr4:75884566 | A | G | 3 | a0001c0016t0001g0054 a0002c0011t0001g0053 a0002c0011t0001g0055 |
3 | HG02258.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.746+28T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884566 | |||||||
| chr4:75884592 | A | G | 5 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
5 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(2): Show |
splice_donor_variant&intron_variant | HIGH | c.746+2T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 8/16 | chr4 | 75884592 | |||||||
| chr4:75884809 | G | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.580-49C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75884809 | |||||||
| chr4:75884825 | C | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.580-65G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75884825 | |||||||
| chr4:75885141 | G | A | 1 | a0001c0002t0002g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.580-381C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885141 | |||||||
| chr4:75885478 | T | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.580-718A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885478 | |||||||
| chr4:75885693 | G | A | 7 | a0001c0001t0001g0080 a0001c0001t0001g0178 a0001c0001t0001g0179 others(4): Show |
7 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-933C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885693 | |||||||
| chr4:75885701 | AAAAAATA others(32): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.580-980_580-942del others(39): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885701 | |||||||
| chr4:75885737 | G | A | 1 | a0005c0006t0001g0229 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.580-977C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885737 | |||||||
| chr4:75885739 | G | A | 231 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(228): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.580-979C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885739 | |||||||
| chr4:75885802 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.580-1042T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885802 | |||||||
| chr4:75885862 | A | G | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.579+990T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75885862 | |||||||
| chr4:75886009 | T | TA | 202 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(199): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.579+842dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886009 | |||||||
| chr4:75886009 | T | TAA | 14 | a0001c0001t0001g0140 a0001c0001t0001g0221 a0001c0001t0001g0222 others(11): Show |
14 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+841_579+842dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886009 | |||||||
| chr4:75886011 | A | AG | 20 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(17): Show |
21 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.579+840_579+841ins others(1): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886011 | |||||||
| chr4:75886054 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.579+798G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886054 | |||||||
| chr4:75886265 | A | G | 5 | a0006c0007t0003g0202 a0006c0007t0003g0203 a0006c0007t0003g0205 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+587T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886265 | |||||||
| chr4:75886308 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.579+544T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886308 | |||||||
| chr4:75886336 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.579+516G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886336 | |||||||
| chr4:75886389 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.579+463C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886389 | |||||||
| chr4:75886446 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.579+406A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886446 | |||||||
| chr4:75886557 | T | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0081 others(2): Show |
6 | HG00323.hp1 HG00741.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+295A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886557 | |||||||
| chr4:75886614 | G | A | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.579+238C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886614 | |||||||
| chr4:75886711 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.579+141G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886711 | |||||||
| chr4:75886715 | CA | C | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.579+136delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886715 | |||||||
| chr4:75886742 | A | T | 6 | a0001c0016t0001g0054 a0001c0017t0008g0259 a0002c0011t0001g0053 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+110T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 7/16 | chr4 | 75886742 | |||||||
| chr4:75886925 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.533-27T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75886925 | |||||||
| chr4:75886980 | C | G | 13 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(10): Show |
13 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.533-82G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75886980 | |||||||
| chr4:75887011 | G | T | 1 | a0002c0008t0001g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.533-113C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887011 | |||||||
| chr4:75887063 | T | C | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.533-165A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887063 | |||||||
| chr4:75887100 | G | T | 1 | a0004c0005t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.533-202C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887100 | |||||||
| chr4:75887149 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.533-251G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887149 | |||||||
| chr4:75887150 | G | A | 1 | a0010c0023t0001g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.533-252C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887150 | |||||||
| chr4:75887157 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.533-259A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887157 | |||||||
| chr4:75887234 | G | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.533-336C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887234 | |||||||
| chr4:75887351 | G | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG02895.hp2 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.533-453C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887351 | |||||||
| chr4:75887437 | C | T | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.533-539G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887437 | |||||||
| chr4:75887477 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.533-579G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887477 | |||||||
| chr4:75887516 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.533-618C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887516 | |||||||
| chr4:75887620 | CA | C | 66 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(63): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.532+593delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887620 | |||||||
| chr4:75887620 | CAA | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0024 others(144): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.532+592_532+593del others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887620 | |||||||
| chr4:75887620 | CAAA | C | 13 | a0001c0001t0001g0106 a0001c0001t0001g0145 a0001c0001t0001g0146 others(10): Show |
13 | HG01069.hp1 HG01175.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.532+591_532+593del others(3): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887620 | |||||||
| chr4:75887921 | T | C | 50 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(47): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.532+293A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887921 | |||||||
| chr4:75887926 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.532+288A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75887926 | |||||||
| chr4:75888067 | G | A | 5 | a0006c0007t0003g0202 a0006c0007t0003g0203 a0006c0007t0003g0205 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.532+147C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75888067 | |||||||
| chr4:75888089 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0194 |
2 | HG02015.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.532+125A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75888089 | |||||||
| chr4:75888166 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.532+48T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 6/16 | chr4 | 75888166 | |||||||
| chr4:75888416 | C | T | 72 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0060 others(69): Show |
72 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.418-88G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888416 | |||||||
| chr4:75888464 | A | G | 6 | a0001c0001t0001g0105 a0006c0007t0003g0202 a0006c0007t0003g0203 others(3): Show |
6 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-136T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888464 | |||||||
| chr4:75888724 | G | C | 1 | a0011c0012t0001g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.418-396C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888724 | |||||||
| chr4:75888726 | G | A | 1 | a0004c0005t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.418-398C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888726 | |||||||
| chr4:75888875 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.418-547G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888875 | |||||||
| chr4:75888961 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.418-633G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888961 | |||||||
| chr4:75888965 | A | G | 5 | a0006c0007t0003g0202 a0006c0007t0003g0203 a0006c0007t0003g0205 others(2): Show |
5 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-637T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888965 | |||||||
| chr4:75888977 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.418-649A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75888977 | |||||||
| chr4:75889046 | C | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(148): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.418-718G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889046 | |||||||
| chr4:75889068 | C | T | 2 | a0003c0003t0002g0004 a0003c0003t0002g0251 |
3 | HG01081.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.418-740G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889068 | |||||||
| chr4:75889111 | G | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(237): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.418-783C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889111 | |||||||
| chr4:75889161 | G | A | 52 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(49): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.417+796C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889161 | |||||||
| chr4:75889198 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.417+759G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889198 | |||||||
| chr4:75889428 | C | T | 10 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG00280.hp1 HG01070.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.417+529G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889428 | |||||||
| chr4:75889519 | A | C | 13 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(10): Show |
13 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.417+438T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889519 | |||||||
| chr4:75889553 | G | T | 15 | a0001c0002t0001g0236 a0001c0002t0002g0230 a0001c0002t0002g0231 others(12): Show |
15 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.417+404C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889553 | |||||||
| chr4:75889619 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.417+338A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889619 | |||||||
| chr4:75889621 | G | C | 15 | a0001c0002t0001g0236 a0001c0002t0002g0230 a0001c0002t0002g0231 others(12): Show |
15 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.417+336C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889621 | |||||||
| chr4:75889628 | A | G | 52 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(49): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.417+329T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889628 | |||||||
| chr4:75889672 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.417+285T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889672 | |||||||
| chr4:75889703 | C | A | 68 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(65): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.417+254G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889703 | |||||||
| chr4:75889732 | G | T | 1 | a0001c0001t0002g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.417+225C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889732 | |||||||
| chr4:75889787 | T | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(237): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.417+170A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889787 | |||||||
| chr4:75889874 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.417+83C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889874 | |||||||
| chr4:75889913 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.417+44A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 5/16 | chr4 | 75889913 | |||||||
| chr4:75890218 | C | T | 2 | a0001c0001t0002g0099 a0001c0001t0002g0100 |
2 | HG02735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.242-86G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890218 | |||||||
| chr4:75890470 | T | C | 32 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(29): Show |
33 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-338A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890470 | |||||||
| chr4:75890475 | T | C | 32 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(29): Show |
33 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-343A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890475 | |||||||
| chr4:75890481 | C | T | 32 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(29): Show |
33 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-349G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890481 | |||||||
| chr4:75890483 | T | C | 32 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(29): Show |
33 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.242-351A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890483 | |||||||
| chr4:75890488 | C | CAAAAAA | 10 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(7): Show |
10 | HG02055.hp1 HG02280.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.242-362_242-357dup others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890488 | |||||||
| chr4:75890488 | C | CAAAAAAA | 18 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(15): Show |
19 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.242-363_242-357dup others(7): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890488 | |||||||
| chr4:75890488 | CA | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.242-357delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890488 | |||||||
| chr4:75890608 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.242-476T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890608 | |||||||
| chr4:75890657 | A | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG00423.hp1 NA18971.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-525T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890657 | |||||||
| chr4:75890878 | T | C | 19 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(16): Show |
20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.242-746A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890878 | |||||||
| chr4:75890882 | A | G | 1 | a0001c0001t0002g0017 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.242-750T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75890882 | |||||||
| chr4:75891043 | G | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.241+605C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891043 | |||||||
| chr4:75891081 | A | G | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.241+567T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891081 | |||||||
| chr4:75891134 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.241+514A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891134 | |||||||
| chr4:75891152 | G | T | 6 | a0002c0004t0003g0208 a0006c0007t0003g0202 a0006c0007t0003g0203 others(3): Show |
6 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+496C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891152 | |||||||
| chr4:75891168 | G | A | 17 | a0001c0002t0001g0003 a0001c0002t0001g0217 a0001c0002t0001g0236 others(14): Show |
18 | HG01255.hp2 HG01496.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.241+480C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891168 | |||||||
| chr4:75891180 | C | CA | 44 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(41): Show |
45 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.241+467dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891180 | |||||||
| chr4:75891188 | AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.241+450_241+459del others(10): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891188 | |||||||
| chr4:75891222 | C | T | 1 | a0002c0004t0003g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.241+426G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891222 | |||||||
| chr4:75891250 | G | T | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.241+398C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891250 | |||||||
| chr4:75891279 | A | G | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.241+369T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891279 | |||||||
| chr4:75891331 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.241+317G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891331 | |||||||
| chr4:75891347 | C | T | 1 | a0004c0005t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.241+301G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891347 | |||||||
| chr4:75891520 | C | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.241+128G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891520 | |||||||
| chr4:75891526 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.241+122G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891526 | |||||||
| chr4:75891611 | C | T | 1 | a0002c0004t0001g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.241+37G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891611 | |||||||
| chr4:75891617 | GA | G | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG01070.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.241+30delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 4/16 | chr4 | 75891617 | |||||||
| chr4:75891711 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01975.hp2 | splice_region_variant&intron_variant | LOW | c.184-6C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 3/16 | chr4 | 75891711 | |||||||
| chr4:75891797 | G | A | 1 | a0005c0018t0001g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.183+54C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 3/16 | chr4 | 75891797 | |||||||
| chr4:75892087 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.56-109G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892087 | |||||||
| chr4:75892112 | T | C | 6 | a0002c0004t0003g0208 a0006c0007t0003g0202 a0006c0007t0003g0203 others(3): Show |
6 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-134A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892112 | |||||||
| chr4:75892353 | G | A | 1 | a0005c0019t0005g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.56-375C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892353 | |||||||
| chr4:75892503 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.56-525T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892503 | |||||||
| chr4:75892519 | G | A | 19 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(16): Show |
20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-541C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892519 | |||||||
| chr4:75892532 | GA | G | 6 | a0002c0004t0003g0208 a0006c0007t0003g0202 a0006c0007t0003g0203 others(3): Show |
6 | HG02145.hp2 HG02809.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-555delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892532 | |||||||
| chr4:75892641 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.56-663G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892641 | |||||||
| chr4:75892703 | T | C | 18 | a0001c0002t0001g0003 a0001c0002t0001g0217 a0001c0002t0001g0236 others(15): Show |
19 | HG01255.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.56-725A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892703 | |||||||
| chr4:75892742 | G | C | 2 | a0002c0004t0006g0262 a0002c0004t0006g0263 |
2 | HG01175.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.56-764C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892742 | |||||||
| chr4:75892894 | AGCTGGAT others(14): Show |
A | 1 | a0001c0001t0001g0188 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.56-937_56-917delCT others(19): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892894 | |||||||
| chr4:75892973 | T | G | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-995A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892973 | |||||||
| chr4:75892989 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.56-1011C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75892989 | |||||||
| chr4:75893001 | C | T | 15 | a0001c0002t0001g0236 a0001c0002t0002g0230 a0001c0002t0002g0231 others(12): Show |
15 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.56-1023G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893001 | |||||||
| chr4:75893078 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.56-1100A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893078 | |||||||
| chr4:75893223 | C | T | 1 | a0008c0010t0001g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.56-1245G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893223 | |||||||
| chr4:75893251 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.56-1273T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893251 | |||||||
| chr4:75893252 | C | T | 3 | a0001c0002t0001g0003 a0001c0002t0001g0217 a0012c0015t0001g0216 |
4 | HG01891.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.56-1274G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893252 | |||||||
| chr4:75893281 | T | C | 33 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(30): Show |
34 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.56-1303A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893281 | |||||||
| chr4:75893296 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.56-1318T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893296 | |||||||
| chr4:75893314 | A | G | 33 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(30): Show |
34 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.56-1336T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893314 | |||||||
| chr4:75893352 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | HG02622.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.56-1374C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893352 | |||||||
| chr4:75893433 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.56-1455C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893433 | |||||||
| chr4:75893487 | G | GAC | 170 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(167): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.56-1511_56-1510dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893487 | |||||||
| chr4:75893487 | G | GACACAC | 51 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(48): Show |
52 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.56-1515_56-1510dup others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893487 | |||||||
| chr4:75893487 | GAC | G | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-1511_56-1510del others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893487 | |||||||
| chr4:75893505 | C | CAT | 18 | a0001c0002t0001g0003 a0001c0002t0001g0217 a0001c0002t0001g0236 others(15): Show |
19 | HG01255.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.56-1528_56-1527ins others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893505 | |||||||
| chr4:75893510 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.56-1532A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893510 | |||||||
| chr4:75893512 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.56-1534T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893512 | |||||||
| chr4:75893540 | G | A | 3 | a0001c0016t0001g0054 a0002c0011t0001g0053 a0002c0011t0001g0055 |
3 | HG02258.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.56-1562C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893540 | |||||||
| chr4:75893684 | C | T | 19 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(16): Show |
20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.56-1706G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893684 | |||||||
| chr4:75893831 | G | GCAGCAGA others(12): Show |
5 | a0001c0016t0001g0054 a0002c0011t0001g0053 a0002c0011t0001g0055 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-1872_56-1854dup others(19): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893831 | |||||||
| chr4:75893861 | C | CTTTTTTT others(2): Show |
150 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.56-1884_56-1883ins others(9): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893861 | |||||||
| chr4:75893862 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.56-1884G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893862 | |||||||
| chr4:75893880 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0067 |
3 | HG01109.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.56-1902G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893880 | |||||||
| chr4:75893882 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.56-1904C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893882 | |||||||
| chr4:75893966 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.56-1988G>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75893966 | |||||||
| chr4:75894373 | TAGAG | T | 4 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(1): Show |
5 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1894_55+1897del others(4): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894373 | |||||||
| chr4:75894388 | C | T | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.55+1883G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894388 | |||||||
| chr4:75894641 | C | A | 1 | a0003c0003t0001g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.55+1630G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894641 | |||||||
| chr4:75894648 | G | A | 15 | a0001c0002t0001g0236 a0001c0002t0002g0230 a0001c0002t0002g0231 others(12): Show |
15 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.55+1623C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894648 | |||||||
| chr4:75894990 | G | A | 30 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.55+1281C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75894990 | |||||||
| chr4:75895127 | A | AT | 9 | a0001c0001t0002g0066 a0001c0001t0003g0220 a0002c0004t0003g0208 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.55+1143dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895127 | |||||||
| chr4:75895127 | A | ATT | 5 | a0004c0005t0003g0245 a0004c0005t0003g0246 a0004c0005t0003g0247 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+1142_55+1143dup others(2): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895127 | |||||||
| chr4:75895127 | A | ATTT | 44 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(41): Show |
45 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.55+1141_55+1143dup others(3): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895127 | |||||||
| chr4:75895127 | AT | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(140): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.55+1143delA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895127 | |||||||
| chr4:75895230 | C | T | 5 | a0001c0017t0008g0259 a0002c0004t0003g0260 a0002c0004t0003g0261 others(2): Show |
5 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1041G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895230 | |||||||
| chr4:75895257 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.55+1014C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895257 | |||||||
| chr4:75895301 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.55+970G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895301 | |||||||
| chr4:75895336 | G | A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+935C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895336 | |||||||
| chr4:75895343 | C | T | 17 | a0003c0003t0001g0253 a0003c0003t0002g0004 a0003c0003t0002g0244 others(14): Show |
18 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.55+928G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895343 | |||||||
| chr4:75895444 | T | A | 19 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(16): Show |
20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.55+827A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895444 | |||||||
| chr4:75895470 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.55+801G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895470 | |||||||
| chr4:75895485 | C | A | 3 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 |
3 | NA18951.hp1 NA18965.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.55+786G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895485 | |||||||
| chr4:75895498 | C | T | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.55+773G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895498 | |||||||
| chr4:75895601 | G | A | 6 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0002g0242 others(3): Show |
6 | HG01261.hp1 HG01975.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+670C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895601 | |||||||
| chr4:75895605 | G | T | 4 | a0002c0004t0003g0260 a0002c0004t0003g0261 a0002c0004t0006g0262 others(1): Show |
4 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+666C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895605 | |||||||
| chr4:75895728 | C | T | 106 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(103): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.55+543G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895728 | |||||||
| chr4:75895731 | C | CA | 39 | a0001c0001t0001g0193 a0001c0001t0001g0221 a0001c0001t0001g0222 others(36): Show |
40 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.55+539dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895731 | |||||||
| chr4:75895743 | A | AT | 19 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(16): Show |
20 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.55+527dupA | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895743 | |||||||
| chr4:75895743 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.55+528T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895743 | |||||||
| chr4:75895839 | G | T | 15 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(12): Show |
15 | HG01175.hp2 HG01243.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.55+432C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895839 | |||||||
| chr4:75895884 | T | TA | 23 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(20): Show |
24 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+386dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895884 | |||||||
| chr4:75895912 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.55+359T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895912 | |||||||
| chr4:75895918 | A | T | 1 | a0001c0001t0002g0017 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.55+353T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75895918 | |||||||
| chr4:75896068 | T | C | 57 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(54): Show |
59 | HG01081.hp2 HG01167.hp2 HG01175.hp2 others(56): Show |
intron_variant | MODIFIER | c.55+203A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75896068 | |||||||
| chr4:75896259 | G | A | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.55+12C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75896259 | |||||||
| chr4:75896267 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp2 | splice_region_variant&intron_variant | LOW | c.55+4C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 2/16 | chr4 | 75896267 | |||||||
| chr4:75896710 | A | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58-327T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896710 | |||||||
| chr4:75896868 | CA | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-58-486delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896868 | |||||||
| chr4:75896869 | A | T | 1 | a0001c0016t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58-486T>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896869 | |||||||
| chr4:75896870 | C | A | 1 | a0001c0016t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58-487G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896870 | |||||||
| chr4:75896870 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-58-487G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896870 | |||||||
| chr4:75896871 | A | C | 1 | a0001c0016t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58-488T>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896871 | |||||||
| chr4:75896875 | T | A | 1 | a0001c0001t0002g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-58-492A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896875 | |||||||
| chr4:75896876 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-58-493A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896876 | |||||||
| chr4:75896897 | T | C | 21 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 others(18): Show |
22 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.-58-514A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75896897 | |||||||
| chr4:75897010 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-58-627G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897010 | |||||||
| chr4:75897172 | A | G | 1 | a0005c0006t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58-789T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897172 | |||||||
| chr4:75897214 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-58-831T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897214 | |||||||
| chr4:75897293 | A | G | 1 | a0002c0011t0001g0053 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-58-910T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897293 | |||||||
| chr4:75897500 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-58-1117A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897500 | |||||||
| chr4:75897729 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-58-1346C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897729 | |||||||
| chr4:75897797 | A | G | 1 | a0013c0013t0001g0243 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-58-1414T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897797 | |||||||
| chr4:75897822 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-58-1439G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897822 | |||||||
| chr4:75897880 | A | G | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-58-1497T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897880 | |||||||
| chr4:75897887 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-58-1504C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897887 | |||||||
| chr4:75897946 | C | A | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-58-1563G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897946 | |||||||
| chr4:75897976 | C | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-58-1593G>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75897976 | |||||||
| chr4:75898015 | G | A | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-58-1632C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898015 | |||||||
| chr4:75898073 | G | A | 18 | a0003c0003t0001g0253 a0003c0003t0001g0265 a0003c0003t0002g0004 others(15): Show |
19 | HG01081.hp2 HG01167.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.-58-1690C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898073 | |||||||
| chr4:75898257 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-58-1874C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898257 | |||||||
| chr4:75898297 | T | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | NA19000.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-58-1914A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898297 | |||||||
| chr4:75898301 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-58-1918G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898301 | |||||||
| chr4:75898332 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(208): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-58-1949A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898332 | |||||||
| chr4:75898346 | C | T | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-58-1963G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898346 | |||||||
| chr4:75898534 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-58-2151C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898534 | |||||||
| chr4:75898664 | T | C | 5 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(2): Show |
5 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58-2281A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898664 | |||||||
| chr4:75898721 | T | A | 1 | a0003c0003t0001g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-58-2338A>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898721 | |||||||
| chr4:75898761 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-58-2378C>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898761 | |||||||
| chr4:75898857 | T | G | 1 | a0001c0017t0008g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-58-2474A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898857 | |||||||
| chr4:75898921 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-58-2538C>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75898921 | |||||||
| chr4:75899145 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-58-2762T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899145 | |||||||
| chr4:75899309 | A | G | 4 | a0001c0001t0002g0218 a0001c0002t0001g0003 a0001c0002t0001g0217 others(1): Show |
5 | HG01891.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+2921T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899309 | |||||||
| chr4:75899392 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG02129.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-59+2838G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899392 | |||||||
| chr4:75899499 | C | T | 1 | a0015c0022t0001g0056 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-59+2731G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899499 | |||||||
| chr4:75899512 | TC | T | 3 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0002c0008t0001g0212 |
3 | HG01261.hp1 HG01975.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-59+2717delG | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899512 | |||||||
| chr4:75899589 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-59+2641A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899589 | |||||||
| chr4:75899780 | C | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-59+2450G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899780 | |||||||
| chr4:75899781 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-59+2449T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899781 | |||||||
| chr4:75899782 | A | ATGGC | 156 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-59+2447_-59+2448i others(6): Show |
PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899782 | |||||||
| chr4:75899783 | C | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-59+2447G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75899783 | |||||||
| chr4:75900941 | G | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-59+1289C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75900941 | |||||||
| chr4:75901222 | A | G | 3 | a0001c0016t0001g0054 a0002c0011t0001g0053 a0002c0011t0001g0055 |
3 | HG02258.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-59+1008T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901222 | |||||||
| chr4:75901445 | T | C | 5 | a0002c0004t0003g0260 a0002c0004t0003g0261 a0002c0004t0006g0262 others(2): Show |
5 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+785A>G | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901445 | |||||||
| chr4:75901520 | C | CA | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(6): Show |
9 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-59+709dupT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901520 | |||||||
| chr4:75901520 | CA | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0058 others(153): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-59+709delT | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901520 | |||||||
| chr4:75901595 | T | G | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-59+635A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901595 | |||||||
| chr4:75901618 | C | T | 12 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(9): Show |
13 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-59+612G>A | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901618 | |||||||
| chr4:75901738 | G | A | 1 | a0003c0003t0001g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-59+492C>T | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901738 | |||||||
| chr4:75901970 | T | G | 2 | a0001c0001t0001g0051 a0002c0004t0003g0052 |
2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-59+260A>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75901970 | |||||||
| chr4:75902072 | A | G | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-59+158T>C | PPEF2 | ENSG00000156194.19 | transcript | ENST00000286719.12 | protein_coding | 1/16 | chr4 | 75902072 |