Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57475 |
| ensemblid | ENSG00000054690.14 |
| hgncid | 17733 |
| symbol | PLEKHH1 |
| name | pleckstrin homology, MyTH4 and FERM domain containing H1 |
| refseq_nuc | NM_020715.3 |
| refseq_prot | NP_065766.1 |
| ensembl_nuc | ENST00000329153.10 |
| ensembl_prot | ENSP00000330278.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 67533290 |
| end | 67589612 |
| strand | + |
| ver | v1.2 |
| region | chr14:67533290-67589612 |
| region5000 | chr14:67528290-67594612 |
| regionname0 | PLEKHH1_chr14_67533290_67589612 |
| regionname5000 | PLEKHH1_chr14_67528290_67594612 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1364 | 92 | 40 | 16 | 26 | 2 | 7 | 17 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0002 | 0/0 | 1364 | 66 | 13 | 8 | 29 | 2 | 14 | 23 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0003 | 0/0 | 1364 | 57 | 5 | 15 | 27 | 4 | 6 | 25 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0004 | 0/0 | 1364 | 42 | 0 | 3 | 32 | 3 | 4 | 26 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0005 | 0/0 | 1364 | 22 | 2 | 4 | 7 | 2 | 7 | 3 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0006 | 0/0 | 1364 | 20 | 0 | 2 | 18 | 0 | 0 | 13 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0007 | 0/0 | 1364 | 15 | 2 | 10 | 2 | 0 | 1 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0008 | 0/1 | 1364 | 14 | 0 | 0 | 13 | 0 | 0 | 6 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0009 | 0/0 | 1364 | 13 | 0 | 1 | 12 | 0 | 0 | 11 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0010 | 0/0 | 1364 | 11 | 7 | 2 | 1 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0011 | 0/0 | 1364 | 9 | 1 | 4 | 2 | 1 | 1 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0012 | 0/0 | 1364 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0013 | 0/0 | 1364 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0014 | 0/0 | 1364 | 6 | 4 | 0 | 2 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0015 | 0/0 | 1364 | 5 | 0 | 4 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0016 | 0/0 | 1364 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0017 | 0/0 | 1364 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0018 | 0/0 | 1364 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0019 | 0/0 | 1364 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0020 | 0/0 | 1364 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0021 | 0/0 | 1364 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0022 | 0/0 | 1364 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0023 | 0/0 | 1364 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0024 | 0/0 | 1364 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0025 | 0/0 | 1364 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0026 | 0/0 | 1364 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0027 | 0/0 | 1364 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0028 | 0/0 | 1364 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0029 | 0/0 | 1364 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0030 | 0/0 | 1364 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0031 | 0/0 | 1364 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0032 | 0/0 | 1364 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0033 | 0/0 | 1364 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0034 | 0/0 | 1364 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0035 | 0/0 | 1364 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1359): Show |
chr14 | 67528290 | 67594612 |
| a0036 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | MAELK others(1342): Show |
chr14 | 67528290 | 67594612 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 4092 | 34 | 3 | 9 | 19 | 2 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0003 | 1/0 | 4092 | 30 | 22 | 4 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0010 | 0/0 | 4092 | 10 | 2 | 1 | 4 | 0 | 3 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0019 | 0/0 | 4092 | 5 | 4 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0022 | 0/0 | 4092 | 4 | 1 | 1 | 0 | 0 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0023 | 0/0 | 4092 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0034 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0068 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0069 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0001c0086 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0004 | 0/0 | 4092 | 29 | 2 | 2 | 19 | 1 | 5 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0011 | 0/0 | 4092 | 10 | 0 | 2 | 5 | 0 | 3 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0013 | 0/0 | 4092 | 8 | 0 | 2 | 4 | 0 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0025 | 0/0 | 4092 | 4 | 0 | 0 | 1 | 0 | 3 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0028 | 0/0 | 4092 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0036 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0037 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0038 | 0/0 | 4092 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0047 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0054 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0056 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0067 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0002c0070 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0003c0001 | 0/0 | 4092 | 49 | 1 | 12 | 26 | 4 | 6 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0003c0040 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0003c0041 | 0/0 | 4092 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0003c0042 | 0/0 | 4092 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0003c0075 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0003c0077 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0004c0006 | 0/0 | 4092 | 20 | 0 | 2 | 13 | 3 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0004c0007 | 0/0 | 4092 | 14 | 0 | 0 | 14 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0004c0018 | 0/0 | 4092 | 6 | 0 | 1 | 4 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0004c0079 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0004c0080 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0005c0005 | 0/0 | 4092 | 20 | 2 | 4 | 7 | 0 | 7 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0005c0044 | 0/0 | 4092 | 2 | 0 | 0 | 0 | 2 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0006c0014 | 0/0 | 4092 | 8 | 0 | 2 | 6 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0006c0015 | 0/0 | 4092 | 8 | 0 | 0 | 8 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0006c0032 | 0/0 | 4092 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0006c0081 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0007c0008 | 0/0 | 4092 | 13 | 1 | 9 | 2 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0007c0035 | 0/0 | 4092 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0008c0012 | 0/0 | 4092 | 8 | 0 | 0 | 8 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0008c0017 | 0/1 | 4092 | 6 | 0 | 0 | 5 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0009c0009 | 0/0 | 4092 | 11 | 0 | 0 | 11 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0009c0049 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0009c0050 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0010c0026 | 0/0 | 4092 | 4 | 1 | 1 | 1 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0010c0031 | 0/0 | 4092 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0010c0039 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0010c0058 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0010c0072 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0011c0027 | 0/0 | 4092 | 4 | 0 | 3 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0011c0030 | 0/0 | 4092 | 3 | 0 | 1 | 1 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0011c0059 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0011c0078 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0012c0020 | 0/0 | 4092 | 5 | 5 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0012c0029 | 0/0 | 4092 | 3 | 2 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0013c0016 | 0/0 | 4092 | 7 | 7 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0014c0033 | 0/0 | 4092 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0014c0045 | 0/0 | 4092 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0014c0083 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0015c0021 | 0/0 | 4092 | 4 | 0 | 3 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0015c0053 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0016c0024 | 0/0 | 4092 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0016c0065 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0017c0043 | 0/0 | 4092 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0018c0046 | 0/0 | 4092 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0019c0073 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0020c0066 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0021c0052 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0022c0048 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0023c0071 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0024c0061 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0025c0060 | 0/0 | 4092 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0026c0084 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0027c0057 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0028c0076 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0029c0085 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0030c0051 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0031c0082 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0032c0074 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0033c0055 | 0/0 | 4092 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0034c0063 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0035c0062 | 0/0 | 4092 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 | ||
| a0036c0064 | 0/0 | 4092 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | ATGGC others(4087): Show |
chr14 | 67528290 | 67594612 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 6615 | 2 | 0 | 0 | 1 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0002t0002 | 0/0 | 6615 | 31 | 3 | 9 | 17 | 1 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0002t0009 | 0/0 | 6616 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0001c0003t0002 | 0/0 | 6615 | 27 | 21 | 3 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0003t0007 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0003t0009 | 0/0 | 6616 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0001c0003t0011 | 1/0 | 6615 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0010t0001 | 0/0 | 6615 | 7 | 0 | 1 | 4 | 0 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0010t0004 | 0/0 | 6616 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0001c0010t0006 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0019t0001 | 0/0 | 6615 | 5 | 4 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0022t0002 | 0/0 | 6615 | 4 | 1 | 1 | 0 | 0 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0023t0002 | 0/0 | 6615 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0034t0002 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0068t0002 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0069t0008 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0001c0086t0002 | 0/0 | 6615 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0004t0001 | 0/0 | 6615 | 20 | 1 | 1 | 14 | 1 | 3 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0004t0003 | 0/0 | 6615 | 4 | 0 | 1 | 2 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0004t0004 | 0/0 | 6616 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0002c0004t0010 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0004t0013 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0004t0015 | 0/0 | 6616 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0002c0011t0001 | 0/0 | 6615 | 6 | 0 | 2 | 4 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0011t0005 | 0/0 | 6615 | 4 | 0 | 0 | 1 | 0 | 3 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0013t0001 | 0/0 | 6615 | 7 | 0 | 1 | 4 | 0 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0013t0003 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0025t0001 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0025t0005 | 0/0 | 6615 | 3 | 0 | 0 | 0 | 0 | 3 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0028t0001 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0028t0007 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0036t0001 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0036t0002 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0037t0002 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0038t0001 | 0/0 | 6615 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0047t0012 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0054t0001 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0056t0001 | 0/0 | 6615 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0067t0005 | 0/0 | 6615 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0002c0070t0008 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0003c0001t0001 | 0/0 | 6615 | 44 | 1 | 11 | 23 | 3 | 6 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0003c0001t0004 | 0/0 | 6616 | 5 | 0 | 1 | 3 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0003c0040t0001 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0003c0041t0002 | 0/0 | 6615 | 2 | 0 | 1 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0003c0042t0008 | 0/0 | 6615 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0003c0075t0002 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0003c0077t0002 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0004c0006t0001 | 0/0 | 6615 | 17 | 0 | 2 | 11 | 3 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0004c0006t0004 | 0/0 | 6616 | 3 | 0 | 0 | 2 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0004c0007t0001 | 0/0 | 6615 | 14 | 0 | 0 | 14 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0004c0018t0001 | 0/0 | 6615 | 2 | 0 | 0 | 1 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0004c0018t0003 | 0/0 | 6615 | 4 | 0 | 1 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0004c0079t0003 | 0/0 | 6615 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0004c0080t0001 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0005c0005t0001 | 0/0 | 6615 | 15 | 2 | 4 | 3 | 0 | 6 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0005c0005t0002 | 0/0 | 6615 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0005c0005t0004 | 0/0 | 6616 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0005c0044t0005 | 0/0 | 6615 | 2 | 0 | 0 | 0 | 2 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0006c0014t0001 | 0/0 | 6615 | 7 | 0 | 2 | 5 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0006c0014t0004 | 0/0 | 6616 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0006c0015t0001 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0006c0015t0002 | 0/0 | 6615 | 7 | 0 | 0 | 7 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0006c0032t0002 | 0/0 | 6615 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0006c0081t0002 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0007c0008t0001 | 0/0 | 6615 | 12 | 1 | 8 | 2 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0007c0008t0004 | 0/0 | 6616 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0007c0035t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0007c0035t0002 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0008c0012t0002 | 0/0 | 6615 | 8 | 0 | 0 | 8 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0008c0017t0002 | 0/1 | 6615 | 4 | 0 | 0 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0008c0017t0009 | 0/0 | 6616 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0009c0009t0001 | 0/0 | 6615 | 10 | 0 | 0 | 10 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0009c0009t0004 | 0/0 | 6616 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0009c0049t0003 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0009c0050t0001 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0010c0026t0001 | 0/0 | 6615 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0010c0026t0002 | 0/0 | 6615 | 2 | 1 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0010c0031t0002 | 0/0 | 6615 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0010c0039t0002 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0010c0058t0002 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0010c0072t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0011c0027t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0011c0027t0003 | 0/0 | 6615 | 3 | 0 | 2 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0011c0030t0001 | 0/0 | 6615 | 3 | 0 | 1 | 1 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0011c0059t0001 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0011c0078t0001 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0012c0020t0001 | 0/0 | 6615 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0012c0020t0003 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0012c0029t0001 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0012c0029t0014 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0013c0016t0001 | 0/0 | 6615 | 4 | 4 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0013c0016t0004 | 0/0 | 6616 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0013c0016t0010 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0014c0033t0006 | 0/0 | 6615 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0014c0045t0002 | 0/0 | 6615 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0014c0083t0001 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0015c0021t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0015c0021t0003 | 0/0 | 6615 | 2 | 0 | 2 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0015c0021t0004 | 0/0 | 6616 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0015c0053t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0016c0024t0003 | 0/0 | 6615 | 4 | 3 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0016c0065t0003 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0017c0043t0007 | 0/0 | 6615 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0018c0046t0001 | 0/0 | 6615 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0019c0073t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0020c0066t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0021c0052t0004 | 0/0 | 6616 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0022c0048t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0023c0071t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0024c0061t0002 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0025c0060t0001 | 0/0 | 6615 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0026c0084t0002 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0027c0057t0001 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0028c0076t0001 | 0/0 | 6615 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0029c0085t0001 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0030c0051t0001 | 0/0 | 6615 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0031c0082t0001 | 0/0 | 6615 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0032c0074t0004 | 0/0 | 6616 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6611): Show |
chr14 | 67528290 | 67594612 |
| a0033c0055t0011 | 0/0 | 6615 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0034c0063t0001 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0035c0062t0002 | 0/0 | 6615 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| a0036c0064t0001 | 0/0 | 6615 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | GGCGG others(6610): Show |
chr14 | 67528290 | 67594612 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0002t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0003t0011g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0010t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0019t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0019t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0019t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0019t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0019t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0022t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0022t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0022t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0022t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0023t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0023t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0023t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0023t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0034t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0068t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0069t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0001c0086t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0013g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0004t0015g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0005g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0011t0005g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0013t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0013t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0013t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0013t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0013t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0013t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0013t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0013t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0025t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0025t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0025t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0025t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0028t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0028t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0028t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0036t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0036t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0037t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0038t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0038t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0047t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0047t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0054t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0056t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0067t0005g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0002c0070t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0040t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0040t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0041t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0041t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0042t0008g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0042t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0075t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0003c0077t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0004g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0006t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0007t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0018t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0018t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0018t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0018t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0018t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0018t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0079t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0004c0080t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0005t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0044t0005g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0005c0044t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0014t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0014t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0014t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0014t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0014t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0014t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0014t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0015t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0015t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0015t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0015t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0015t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0032t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0032t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0032t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0006c0081t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0008t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0035t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0007c0035t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0012t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0012t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0012t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0012t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0012t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0012t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0012t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0012t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0017t0002g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0017t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0017t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0017t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0008c0017t0009g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0009t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0049t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0009c0050t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0026t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0026t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0026t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0026t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0031t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0031t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0031t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0039t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0039t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0058t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0010c0072t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0027t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0027t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0027t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0027t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0030t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0030t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0030t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0059t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0011c0078t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0012c0020t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0012c0020t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0012c0020t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0012c0020t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0012c0020t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0012c0029t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0012c0029t0014g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0013c0016t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0013c0016t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0013c0016t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0013c0016t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0013c0016t0010g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0013c0016t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0014c0033t0006g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0014c0045t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0014c0045t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0014c0083t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0015c0021t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0015c0021t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0015c0021t0003g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0015c0021t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0015c0053t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0016c0024t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0016c0024t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0016c0024t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0016c0024t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0016c0065t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0017c0043t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0017c0043t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0018c0046t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0018c0046t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0019c0073t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0020c0066t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0021c0052t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0022c0048t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0023c0071t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0024c0061t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0025c0060t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0026c0084t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0027c0057t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0028c0076t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0029c0085t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0030c0051t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0031c0082t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0032c0074t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0033c0055t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0034c0063t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0035c0062t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| a0036c0064t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0004 | c0006 | t0001 | g0299 | EUR | GBR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00140 | hp2 | a0003 | c0001 | t0001 | g0060 | EUR | GBR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00280 | hp1 | a0011 | c0027 | t0003 | g0070 | EUR | FIN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00280 | hp2 | a0004 | c0006 | t0001 | g0034 | EUR | FIN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00323 | hp1 | a0004 | c0006 | t0001 | g0293 | EUR | FIN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0030 | EUR | FIN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00408 | hp1 | a0008 | c0017 | t0009 | g0028 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00408 | hp2 | a0006 | c0014 | t0001 | g0284 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00423 | hp1 | a0010 | c0026 | t0002 | g0113 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00423 | hp2 | a0008 | c0012 | t0002 | g0191 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00438 | hp1 | a0001 | c0010 | t0001 | g0349 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00438 | hp2 | a0014 | c0045 | t0002 | g0158 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00544 | hp2 | a0002 | c0004 | t0001 | g0018 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00558 | hp1 | a0002 | c0004 | t0001 | g0320 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00558 | hp2 | a0001 | c0002 | t0009 | g0120 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00609 | hp1 | a0001 | c0010 | t0001 | g0036 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00609 | hp2 | a0004 | c0007 | t0001 | g0010 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00621 | hp1 | a0003 | c0001 | t0001 | g0114 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00621 | hp2 | a0002 | c0013 | t0001 | g0244 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00639 | hp1 | a0003 | c0001 | t0004 | g0014 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00639 | hp2 | a0010 | c0072 | t0001 | g0066 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00642 | hp1 | a0011 | c0027 | t0001 | g0126 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00642 | hp2 | a0003 | c0001 | t0001 | g0008 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00673 | hp1 | a0006 | c0032 | t0002 | g0166 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00673 | hp2 | a0006 | c0015 | t0002 | g0291 | EAS | CHS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00733 | hp1 | a0019 | c0073 | t0001 | g0059 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00733 | hp2 | a0002 | c0011 | t0001 | g0262 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00735 | hp1 | a0005 | c0005 | t0001 | g0294 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0135 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00738 | hp1 | a0011 | c0030 | t0001 | g0096 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00738 | hp2 | a0002 | c0013 | t0003 | g0152 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00741 | hp1 | a0006 | c0014 | t0001 | g0328 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG00741 | hp2 | a0015 | c0021 | t0001 | g0332 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01071 | hp1 | a0003 | c0001 | t0001 | g0015 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01071 | hp2 | a0007 | c0008 | t0001 | g0260 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01074 | hp1 | a0003 | c0042 | t0008 | g0198 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01074 | hp2 | a0002 | c0038 | t0001 | g0064 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01081 | hp1 | a0005 | c0005 | t0001 | g0011 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0049 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01099 | hp1 | a0002 | c0038 | t0001 | g0062 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01099 | hp2 | a0001 | c0022 | t0002 | g0252 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01106 | hp1 | a0009 | c0049 | t0003 | g0183 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01106 | hp2 | a0005 | c0005 | t0001 | g0011 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01109 | hp1 | a0010 | c0026 | t0001 | g0069 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01109 | hp2 | a0001 | c0019 | t0001 | g0137 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01167 | hp1 | a0020 | c0066 | t0001 | g0207 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01167 | hp2 | a0001 | c0010 | t0001 | g0063 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01168 | hp1 | a0005 | c0005 | t0001 | g0289 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01168 | hp2 | a0007 | c0035 | t0001 | g0206 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01175 | hp1 | a0001 | c0003 | t0009 | g0211 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01175 | hp2 | a0006 | c0014 | t0001 | g0329 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0047 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01192 | hp2 | a0007 | c0008 | t0001 | g0078 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01243 | hp2 | a0016 | c0024 | t0003 | g0077 | AMR | PUR | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01255 | hp2 | a0002 | c0004 | t0003 | g0173 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01256 | hp1 | a0004 | c0006 | t0001 | g0248 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01256 | hp2 | a0011 | c0027 | t0003 | g0071 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01258 | hp1 | a0011 | c0027 | t0003 | g0072 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01258 | hp2 | a0003 | c0001 | t0001 | g0068 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01261 | hp2 | a0007 | c0008 | t0001 | g0235 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01346 | hp1 | a0003 | c0001 | t0001 | g0075 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01346 | hp2 | a0015 | c0053 | t0001 | g0330 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01358 | hp1 | a0007 | c0008 | t0001 | g0209 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01358 | hp2 | a0003 | c0001 | t0001 | g0145 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01361 | hp1 | a0003 | c0075 | t0002 | g0342 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01361 | hp2 | a0003 | c0001 | t0001 | g0109 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0153 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01433 | hp2 | a0012 | c0029 | t0014 | g0149 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01496 | hp1 | a0007 | c0008 | t0004 | g0202 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0208 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01515 | hp1 | a0021 | c0052 | t0004 | g0346 | EUR | IBS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01515 | hp2 | a0003 | c0001 | t0004 | g0042 | EUR | IBS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01516 | hp1 | a0005 | c0044 | t0005 | g0296 | EUR | IBS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01516 | hp2 | a0003 | c0001 | t0001 | g0014 | EUR | IBS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01517 | hp1 | a0003 | c0001 | t0001 | g0015 | EUR | IBS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01517 | hp2 | a0005 | c0044 | t0005 | g0295 | EUR | IBS | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01884 | hp1 | a0001 | c0010 | t0006 | g0159 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01884 | hp2 | a0002 | c0054 | t0001 | g0343 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01891 | hp1 | a0016 | c0024 | t0003 | g0240 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01891 | hp2 | a0014 | c0033 | t0006 | g0012 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01928 | hp1 | a0007 | c0008 | t0001 | g0009 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01928 | hp2 | a0003 | c0041 | t0002 | g0118 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01934 | hp1 | a0003 | c0001 | t0001 | g0061 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01943 | hp1 | a0003 | c0001 | t0001 | g0264 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01943 | hp2 | a0022 | c0048 | t0001 | g0184 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01975 | hp2 | a0003 | c0001 | t0001 | g0112 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01978 | hp1 | a0015 | c0021 | t0003 | g0331 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01978 | hp2 | a0007 | c0008 | t0001 | g0233 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01981 | hp1 | a0015 | c0021 | t0003 | g0356 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0090 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01993 | hp1 | a0002 | c0011 | t0001 | g0263 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01993 | hp2 | a0007 | c0008 | t0001 | g0224 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02004 | hp2 | a0023 | c0071 | t0001 | g0009 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02015 | hp2 | a0011 | c0078 | t0001 | g0087 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02027 | hp1 | a0008 | c0017 | t0002 | g0196 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02027 | hp2 | a0005 | c0005 | t0001 | g0327 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02040 | hp1 | a0002 | c0004 | t0001 | g0017 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02040 | hp2 | a0008 | c0017 | t0009 | g0028 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02055 | hp1 | a0003 | c0001 | t0001 | g0108 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02055 | hp2 | a0012 | c0020 | t0001 | g0095 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02056 | hp1 | a0005 | c0005 | t0001 | g0259 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02056 | hp2 | a0001 | c0010 | t0001 | g0217 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02074 | hp1 | a0008 | c0017 | t0002 | g0195 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02074 | hp2 | a0006 | c0015 | t0002 | g0266 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02080 | hp1 | a0006 | c0015 | t0002 | g0002 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02080 | hp2 | a0009 | c0009 | t0001 | g0029 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02083 | hp1 | a0008 | c0012 | t0002 | g0168 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02083 | hp2 | a0003 | c0001 | t0001 | g0001 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02129 | hp1 | a0024 | c0061 | t0002 | g0243 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02129 | hp2 | a0002 | c0013 | t0001 | g0347 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02132 | hp1 | a0004 | c0006 | t0001 | g0305 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02132 | hp2 | a0014 | c0045 | t0002 | g0157 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02135 | hp1 | a0007 | c0008 | t0001 | g0232 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0236 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02145 | hp2 | a0012 | c0020 | t0001 | g0154 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02148 | hp1 | a0002 | c0013 | t0001 | g0134 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02148 | hp2 | a0003 | c0001 | t0001 | g0261 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02155 | hp1 | a0005 | c0005 | t0001 | g0167 | EAS | CDX | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | CDX | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02165 | hp1 | a0008 | c0017 | t0002 | g0177 | EAS | CDX | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02165 | hp2 | a0004 | c0018 | t0001 | g0283 | EAS | CDX | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02257 | hp1 | a0002 | c0004 | t0001 | g0203 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02257 | hp2 | a0013 | c0016 | t0001 | g0325 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02258 | hp1 | a0002 | c0036 | t0001 | g0170 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02258 | hp2 | a0014 | c0083 | t0001 | g0357 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02273 | hp1 | a0025 | c0060 | t0001 | g0205 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02273 | hp2 | a0003 | c0001 | t0001 | g0121 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02280 | hp1 | a0001 | c0019 | t0001 | g0151 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02280 | hp2 | a0016 | c0065 | t0003 | g0160 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02300 | hp1 | a0007 | c0008 | t0001 | g0093 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02300 | hp2 | a0004 | c0018 | t0003 | g0251 | AMR | PEL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02451 | hp1 | a0014 | c0033 | t0006 | g0012 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02451 | hp2 | a0002 | c0028 | t0001 | g0097 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02523 | hp1 | a0004 | c0006 | t0001 | g0003 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02523 | hp2 | a0002 | c0004 | t0013 | g0058 | EAS | KHV | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0026 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02572 | hp2 | a0002 | c0028 | t0007 | g0098 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02602 | hp1 | a0002 | c0011 | t0005 | g0065 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0300 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02615 | hp1 | a0013 | c0016 | t0004 | g0323 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02615 | hp2 | a0026 | c0084 | t0002 | g0164 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02622 | hp1 | a0010 | c0039 | t0002 | g0163 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02622 | hp2 | a0002 | c0037 | t0002 | g0022 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02630 | hp1 | a0003 | c0042 | t0008 | g0201 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02630 | hp2 | a0001 | c0010 | t0006 | g0123 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02647 | hp1 | a0027 | c0057 | t0001 | g0021 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0314 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02683 | hp1 | a0003 | c0001 | t0001 | g0019 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02683 | hp2 | a0004 | c0018 | t0001 | g0275 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02698 | hp1 | a0028 | c0076 | t0001 | g0073 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02698 | hp2 | a0002 | c0004 | t0003 | g0128 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0124 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02717 | hp2 | a0010 | c0031 | t0002 | g0043 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0204 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02723 | hp2 | a0013 | c0016 | t0001 | g0326 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02735 | hp1 | a0003 | c0001 | t0001 | g0186 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02735 | hp2 | a0005 | c0005 | t0001 | g0312 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02738 | hp1 | a0003 | c0001 | t0001 | g0146 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02738 | hp2 | a0004 | c0079 | t0003 | g0340 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02809 | hp1 | a0016 | c0024 | t0003 | g0044 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0309 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02818 | hp1 | a0013 | c0016 | t0010 | g0322 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02818 | hp2 | a0002 | c0070 | t0008 | g0055 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02886 | hp1 | a0017 | c0043 | t0007 | g0249 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02886 | hp2 | a0001 | c0019 | t0001 | g0225 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02895 | hp1 | a0003 | c0040 | t0001 | g0052 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02895 | hp2 | a0003 | c0077 | t0002 | g0125 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02896 | hp1 | a0010 | c0026 | t0002 | g0231 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02896 | hp2 | a0002 | c0047 | t0012 | g0045 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02897 | hp1 | a0002 | c0047 | t0012 | g0046 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02897 | hp2 | a0003 | c0040 | t0001 | g0051 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02922 | hp1 | a0013 | c0016 | t0010 | g0324 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02922 | hp2 | a0012 | c0029 | t0001 | g0020 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02965 | hp1 | a0001 | c0003 | t0002 | g0026 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02965 | hp2 | a0002 | c0036 | t0002 | g0210 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02970 | hp1 | a0029 | c0085 | t0001 | g0254 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0138 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0308 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02976 | hp2 | a0001 | c0003 | t0002 | g0161 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03017 | hp1 | a0002 | c0004 | t0001 | g0316 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03017 | hp2 | a0002 | c0011 | t0005 | g0350 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03041 | hp1 | a0001 | c0023 | t0002 | g0256 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03041 | hp2 | a0012 | c0020 | t0001 | g0228 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03098 | hp1 | a0002 | c0028 | t0001 | g0021 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0214 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0155 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03139 | hp1 | a0014 | c0033 | t0006 | g0012 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0310 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03195 | hp1 | a0001 | c0023 | t0002 | g0255 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03195 | hp2 | a0007 | c0035 | t0002 | g0239 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03209 | hp2 | a0010 | c0031 | t0002 | g0162 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03225 | hp1 | a0016 | c0024 | t0003 | g0230 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03225 | hp2 | a0002 | c0037 | t0002 | g0022 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03239 | hp1 | a0002 | c0004 | t0001 | g0129 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03239 | hp2 | a0030 | c0051 | t0001 | g0174 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03453 | hp1 | a0001 | c0022 | t0002 | g0257 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0100 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03486 | hp2 | a0001 | c0069 | t0008 | g0200 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03490 | hp1 | a0002 | c0067 | t0005 | g0351 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03490 | hp2 | a0001 | c0022 | t0002 | g0303 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03491 | hp1 | a0011 | c0030 | t0001 | g0057 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03491 | hp2 | a0018 | c0046 | t0001 | g0222 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03492 | hp1 | a0018 | c0046 | t0001 | g0213 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03492 | hp2 | a0001 | c0022 | t0002 | g0301 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03516 | hp2 | a0001 | c0019 | t0001 | g0238 | AFR | ESN | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03540 | hp1 | a0017 | c0043 | t0007 | g0250 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | GWD | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03579 | hp1 | a0001 | c0003 | t0007 | g0199 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03579 | hp2 | a0013 | c0016 | t0001 | g0038 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03654 | hp1 | a0003 | c0001 | t0001 | g0016 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03654 | hp2 | a0002 | c0025 | t0005 | g0223 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03688 | hp1 | a0005 | c0005 | t0001 | g0307 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03688 | hp2 | a0003 | c0001 | t0001 | g0001 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03704 | hp1 | a0002 | c0013 | t0001 | g0156 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03704 | hp2 | a0002 | c0025 | t0005 | g0221 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03710 | hp1 | a0002 | c0011 | t0005 | g0355 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03710 | hp2 | a0015 | c0021 | t0004 | g0333 | SAS | PJL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03831 | hp1 | a0001 | c0086 | t0002 | g0132 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03831 | hp2 | a0002 | c0004 | t0004 | g0081 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03834 | hp1 | a0007 | c0008 | t0001 | g0009 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03834 | hp2 | a0010 | c0026 | t0001 | g0106 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03927 | hp1 | a0005 | c0005 | t0001 | g0276 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03927 | hp2 | a0001 | c0010 | t0001 | g0142 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03942 | hp1 | a0005 | c0005 | t0001 | g0336 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03942 | hp2 | a0002 | c0025 | t0005 | g0220 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04115 | hp1 | a0002 | c0004 | t0001 | g0234 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04115 | hp2 | a0031 | c0082 | t0001 | g0306 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04184 | hp1 | a0001 | c0010 | t0004 | g0319 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04184 | hp2 | a0005 | c0005 | t0001 | g0334 | SAS | BEB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04199 | hp1 | a0005 | c0005 | t0004 | g0285 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04199 | hp2 | a0001 | c0010 | t0001 | g0082 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04204 | hp1 | a0002 | c0013 | t0001 | g0110 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04204 | hp2 | a0003 | c0001 | t0001 | g0019 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04228 | hp1 | a0004 | c0006 | t0004 | g0003 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG04228 | hp2 | a0032 | c0074 | t0004 | g0016 | SAS | STU | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18612 | hp1 | a0004 | c0007 | t0001 | g0268 | EAS | CHB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | CHB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18747 | hp1 | a0004 | c0018 | t0003 | g0272 | EAS | CHB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18747 | hp2 | a0005 | c0005 | t0002 | g0278 | EAS | CHB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18906 | hp1 | a0033 | c0055 | t0011 | g0311 | AFR | YRI | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0215 | AFR | YRI | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18939 | hp1 | a0009 | c0009 | t0001 | g0188 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18939 | hp2 | a0002 | c0025 | t0001 | g0089 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18942 | hp1 | a0008 | c0012 | t0002 | g0193 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18942 | hp2 | a0002 | c0004 | t0001 | g0018 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18943 | hp1 | a0005 | c0005 | t0002 | g0339 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18943 | hp2 | a0006 | c0015 | t0002 | g0337 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18945 | hp1 | a0003 | c0001 | t0001 | g0025 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18945 | hp2 | a0006 | c0015 | t0001 | g0287 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18947 | hp1 | a0004 | c0007 | t0001 | g0270 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18947 | hp2 | a0011 | c0030 | t0001 | g0076 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18948 | hp1 | a0003 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18948 | hp2 | a0006 | c0014 | t0001 | g0033 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18949 | hp1 | a0003 | c0001 | t0001 | g0140 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18949 | hp2 | a0001 | c0003 | t0002 | g0147 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18950 | hp1 | a0034 | c0063 | t0001 | g0037 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18950 | hp2 | a0003 | c0001 | t0001 | g0006 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18951 | hp1 | a0008 | c0012 | t0002 | g0171 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18951 | hp2 | a0002 | c0004 | t0001 | g0017 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18952 | hp1 | a0006 | c0032 | t0002 | g0348 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18952 | hp2 | a0003 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18954 | hp2 | a0004 | c0006 | t0001 | g0032 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18959 | hp1 | a0009 | c0009 | t0001 | g0181 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18959 | hp2 | a0003 | c0001 | t0001 | g0122 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18962 | hp1 | a0003 | c0001 | t0001 | g0025 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18962 | hp2 | a0009 | c0009 | t0001 | g0178 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18963 | hp1 | a0004 | c0006 | t0001 | g0338 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18963 | hp2 | a0002 | c0011 | t0001 | g0246 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18966 | hp1 | a0003 | c0001 | t0001 | g0144 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18966 | hp2 | a0009 | c0009 | t0001 | g0194 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18968 | hp1 | a0002 | c0011 | t0001 | g0185 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18968 | hp2 | a0004 | c0006 | t0004 | g0032 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0023 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18970 | hp1 | a0003 | c0001 | t0001 | g0008 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18970 | hp2 | a0004 | c0007 | t0001 | g0010 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18971 | hp1 | a0009 | c0009 | t0004 | g0179 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18971 | hp2 | a0003 | c0001 | t0001 | g0115 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18972 | hp1 | a0006 | c0014 | t0001 | g0274 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18973 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18977 | hp1 | a0002 | c0004 | t0003 | g0189 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18979 | hp1 | a0002 | c0004 | t0004 | g0352 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18979 | hp2 | a0003 | c0001 | t0001 | g0027 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18982 | hp1 | a0003 | c0001 | t0001 | g0143 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18982 | hp2 | a0004 | c0007 | t0001 | g0281 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18989 | hp1 | a0008 | c0012 | t0002 | g0169 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18989 | hp2 | a0002 | c0004 | t0001 | g0317 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18991 | hp1 | a0004 | c0007 | t0001 | g0315 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18992 | hp1 | a0003 | c0001 | t0004 | g0006 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18992 | hp2 | a0009 | c0009 | t0001 | g0180 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18993 | hp1 | a0003 | c0001 | t0004 | g0104 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18993 | hp2 | a0009 | c0009 | t0001 | g0182 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18994 | hp1 | a0004 | c0007 | t0001 | g0280 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18994 | hp2 | a0003 | c0001 | t0001 | g0092 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18995 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18995 | hp2 | a0004 | c0007 | t0001 | g0335 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18997 | hp1 | a0002 | c0004 | t0001 | g0037 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18997 | hp2 | a0002 | c0013 | t0001 | g0119 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18998 | hp1 | a0007 | c0008 | t0001 | g0216 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18998 | hp2 | a0004 | c0007 | t0001 | g0039 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18999 | hp1 | a0003 | c0001 | t0001 | g0088 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18999 | hp2 | a0002 | c0004 | t0001 | g0111 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19000 | hp1 | a0002 | c0011 | t0001 | g0245 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19001 | hp1 | a0005 | c0005 | t0002 | g0345 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19001 | hp2 | a0008 | c0012 | t0002 | g0172 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19002 | hp1 | a0006 | c0032 | t0002 | g0279 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19002 | hp2 | a0003 | c0001 | t0001 | g0008 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19004 | hp1 | a0006 | c0015 | t0002 | g0002 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19004 | hp2 | a0008 | c0012 | t0002 | g0192 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19005 | hp1 | a0005 | c0005 | t0002 | g0277 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19005 | hp2 | a0002 | c0004 | t0001 | g0023 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19007 | hp1 | a0009 | c0009 | t0001 | g0175 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19007 | hp2 | a0003 | c0001 | t0001 | g0067 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19010 | hp1 | a0006 | c0014 | t0001 | g0033 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19010 | hp2 | a0009 | c0009 | t0001 | g0187 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19011 | hp1 | a0035 | c0062 | t0002 | g0130 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19011 | hp2 | a0003 | c0001 | t0001 | g0148 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19012 | hp1 | a0006 | c0015 | t0002 | g0002 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19012 | hp2 | a0003 | c0001 | t0001 | g0099 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19030 | hp1 | a0001 | c0034 | t0002 | g0035 | AFR | LWK | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19030 | hp2 | a0001 | c0023 | t0002 | g0253 | AFR | LWK | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19043 | hp1 | a0012 | c0020 | t0001 | g0229 | AFR | LWK | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19043 | hp2 | a0001 | c0019 | t0001 | g0227 | AFR | LWK | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19054 | hp1 | a0003 | c0001 | t0004 | g0006 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19054 | hp2 | a0004 | c0007 | t0001 | g0039 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19057 | hp1 | a0004 | c0007 | t0001 | g0010 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19058 | hp1 | a0004 | c0007 | t0001 | g0267 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19058 | hp2 | a0002 | c0013 | t0001 | g0218 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19062 | hp1 | a0004 | c0006 | t0001 | g0003 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19062 | hp2 | a0002 | c0004 | t0015 | g0190 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19064 | hp1 | a0004 | c0018 | t0003 | g0273 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19064 | hp2 | a0004 | c0006 | t0001 | g0288 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19065 | hp1 | a0004 | c0006 | t0001 | g0003 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19065 | hp2 | a0006 | c0015 | t0002 | g0002 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19066 | hp1 | a0006 | c0014 | t0004 | g0271 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19066 | hp2 | a0004 | c0006 | t0001 | g0292 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19067 | hp1 | a0009 | c0009 | t0001 | g0197 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19067 | hp2 | a0004 | c0006 | t0001 | g0040 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19068 | hp1 | a0004 | c0006 | t0004 | g0282 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19068 | hp2 | a0006 | c0081 | t0002 | g0297 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19074 | hp1 | a0008 | c0012 | t0002 | g0176 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19074 | hp2 | a0003 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0354 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19076 | hp2 | a0001 | c0003 | t0002 | g0139 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19079 | hp1 | a0003 | c0001 | t0001 | g0027 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19079 | hp2 | a0004 | c0080 | t0001 | g0031 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19080 | hp1 | a0001 | c0010 | t0001 | g0036 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19080 | hp2 | a0004 | c0006 | t0001 | g0040 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19081 | hp1 | a0006 | c0014 | t0001 | g0321 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19085 | hp1 | a0004 | c0018 | t0003 | g0286 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19085 | hp2 | a0002 | c0004 | t0003 | g0247 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0116 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19086 | hp2 | a0003 | c0041 | t0002 | g0083 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19087 | hp1 | a0002 | c0011 | t0001 | g0141 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19087 | hp2 | a0002 | c0011 | t0005 | g0133 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19088 | hp1 | a0004 | c0007 | t0001 | g0031 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19088 | hp2 | a0004 | c0006 | t0001 | g0107 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19089 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19091 | hp1 | a0002 | c0004 | t0001 | g0103 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19091 | hp2 | a0004 | c0007 | t0001 | g0269 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19240 | hp1 | a0001 | c0068 | t0002 | g0056 | AFR | YRI | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0041 | AFR | YRI | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20129 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | ASW | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20129 | hp2 | a0012 | c0029 | t0001 | g0020 | AFR | ASW | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20752 | hp1 | a0002 | c0004 | t0001 | g0304 | EUR | TSI | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20752 | hp2 | a0036 | c0064 | t0001 | g0074 | EUR | TSI | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20805 | hp1 | a0002 | c0056 | t0001 | g0302 | EUR | TSI | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0219 | EUR | TSI | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20905 | hp1 | a0004 | c0006 | t0001 | g0034 | SAS | GIH | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20905 | hp2 | a0005 | c0005 | t0001 | g0298 | SAS | GIH | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0237 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG01123 | hp2 | a0004 | c0006 | t0001 | g0341 | AMR | CLM | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02109 | hp1 | a0011 | c0059 | t0001 | g0353 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0150 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0048 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02486 | hp2 | a0005 | c0005 | t0001 | g0265 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02559 | hp1 | a0013 | c0016 | t0001 | g0038 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0101 | AFR | ACB | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03471 | hp1 | a0010 | c0039 | t0002 | g0226 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG03471 | hp2 | a0010 | c0058 | t0002 | g0344 | AFR | MSL | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG06807 | hp1 | a0001 | c0034 | t0002 | g0035 | AFR | USA | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| HG06807 | hp2 | a0010 | c0031 | t0002 | g0241 | AFR | USA | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18955 | hp1 | a0003 | c0001 | t0001 | g0001 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA18955 | hp2 | a0009 | c0050 | t0001 | g0029 | EAS | JPT | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20300 | hp1 | a0007 | c0008 | t0001 | g0290 | AFR | USA | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA20300 | hp2 | a0002 | c0004 | t0010 | g0079 | AFR | USA | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA21309 | hp1 | a0012 | c0020 | t0003 | g0318 | AFR | LWK | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| NA21309 | hp2 | a0001 | c0023 | t0002 | g0258 | AFR | LWK | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| homoSapiens | chm13v2 | a0008 | c0017 | t0002 | g0165 | REF | REF | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0011 | g0050 | REF | REF | PLEKHH1_chr14_67528290_67594612 | PLEKHH1 | chr14 | 67528290 | 67594612 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67557303 | A | G | 3 | a0013 a0026 a0029 |
9 | HG02257.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
missense_variant | MODERATE | c.224A>G | p.Asn75Ser | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/29 | 367/6615 | 224/4095 | 75/1364 | chr14 | 67557303 | |||
| chr14:67557342 | A | G | 1 | a0018 | 2 | HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.263A>G | p.Lys88Arg | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/29 | 406/6615 | 263/4095 | 88/1364 | chr14 | 67557342 | |||
| chr14:67557417 | A | T | 5 | a0004 a0005 a0006 others(2): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
missense_variant&splice_region_variant | MODERATE | c.338A>T | p.Gln113Leu | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/29 | 481/6615 | 338/4095 | 113/1364 | chr14 | 67557417 | |||
| chr14:67562334 | C | T | 1 | a0017 | 2 | HG02886.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.703C>T | p.Pro235Ser | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/29 | 846/6615 | 703/4095 | 235/1364 | chr14 | 67562334 | |||
| chr14:67562401 | C | A | 4 | a0008 a0009 a0022 others(1): Show |
28 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(25): Show |
missense_variant | MODERATE | c.770C>A | p.Pro257His | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/29 | 913/6615 | 770/4095 | 257/1364 | chr14 | 67562401 | |||
| chr14:67562596 | G | A | 6 | a0004 a0005 a0006 others(3): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
missense_variant | MODERATE | c.965G>A | p.Arg322Gln | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/29 | 1108/6615 | 965/4095 | 322/1364 | chr14 | 67562596 | |||
| chr14:67569162 | A | G | 7 | a0003 a0010 a0011 others(4): Show |
81 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(78): Show |
missense_variant | MODERATE | c.1288A>G | p.Thr430Ala | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/29 | 1431/6615 | 1288/4095 | 430/1364 | chr14 | 67569162 | |||
| chr14:67569166 | C | T | 1 | a0023 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.1292C>T | p.Ser431Leu | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/29 | 1435/6615 | 1292/4095 | 431/1364 | chr14 | 67569166 | |||
| chr14:67569186 | A | G | 3 | a0012 a0029 a0030 |
10 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
missense_variant | MODERATE | c.1312A>G | p.Met438Val | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/29 | 1455/6615 | 1312/4095 | 438/1364 | chr14 | 67569186 | |||
| chr14:67574344 | G | A | 8 | a0005 a0007 a0010 others(5): Show |
54 | HG00423.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
missense_variant | MODERATE | c.2029G>A | p.Gly677Arg | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/29 | 2172/6615 | 2029/4095 | 677/1364 | chr14 | 67574344 | |||
| chr14:67575824 | G | A | 1 | a0032 | 1 | HG04228.hp2 | missense_variant&splice_region_variant | MODERATE | c.2171G>A | p.Arg724Gln | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 16/29 | 2314/6615 | 2171/4095 | 724/1364 | chr14 | 67575824 | |||
| chr14:67575856 | C | A | 1 | a0002 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.2203C>A | p.His735Asn | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 16/29 | 2346/6615 | 2203/4095 | 735/1364 | chr14 | 67575856 | |||
| chr14:67575857 | A | G | 20 | a0002 a0004 a0005 others(17): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
missense_variant | MODERATE | c.2204A>G | p.His735Arg | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 16/29 | 2347/6615 | 2204/4095 | 735/1364 | chr14 | 67575857 | |||
| chr14:67575919 | C | T | 1 | a0033 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2266C>T | p.Arg756Trp | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 16/29 | 2409/6615 | 2266/4095 | 756/1364 | chr14 | 67575919 | |||
| chr14:67576404 | C | T | 1 | a0035 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.2362C>T | p.Leu788Phe | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 17/29 | 2505/6615 | 2362/4095 | 788/1364 | chr14 | 67576404 | |||
| chr14:67578042 | A | G | 1 | a0019 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.2594A>G | p.Asn865Ser | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 19/29 | 2737/6615 | 2594/4095 | 865/1364 | chr14 | 67578042 | |||
| chr14:67578095 | G | A | 1 | a0034 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.2647G>A | p.Ala883Thr | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 19/29 | 2790/6615 | 2647/4095 | 883/1364 | chr14 | 67578095 | |||
| chr14:67579247 | G | A | 1 | a0028 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2963G>A | p.Arg988His | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 21/29 | 3106/6615 | 2963/4095 | 988/1364 | chr14 | 67579247 | |||
| chr14:67579289 | A | G | 1 | a0025 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.3005A>G | p.His1002Arg | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 21/29 | 3148/6615 | 3005/4095 | 1002/1364 | chr14 | 67579289 | |||
| chr14:67582089 | T | C | 1 | a0024 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.3305T>C | p.Val1102Ala | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/29 | 3448/6615 | 3305/4095 | 1102/1364 | chr14 | 67582089 | |||
| chr14:67583774 | C | T | 1 | a0016 | 5 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(2): Show |
missense_variant | MODERATE | c.3460C>T | p.Pro1154Ser | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 25/29 | 3603/6615 | 3460/4095 | 1154/1364 | chr14 | 67583774 | |||
| chr14:67583798 | G | A | 1 | a0020 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.3484G>A | p.Ala1162Thr | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 25/29 | 3627/6615 | 3484/4095 | 1162/1364 | chr14 | 67583798 | |||
| chr14:67584039 | G | A | 1 | a0027 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.3614G>A | p.Gly1205Glu | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/29 | 3757/6615 | 3614/4095 | 1205/1364 | chr14 | 67584039 | |||
| chr14:67587182 | C | T | 1 | a0036 | 1 | NA20752.hp2 | stop_gained | HIGH | c.4042C>T | p.Arg1348* | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 4185/6615 | 4042/4095 | 1348/1364 | chr14 | 67587182 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67555875 | C | T | 1 | a0002c0047 | 2 | HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.177C>T | p.Asn59Asn | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/29 | 320/6615 | 177/4095 | 59/1364 | chr14 | 67555875 | |||
| chr14:67557296 | C | T | 1 | a0001c0086 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.217C>T | p.Leu73Leu | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/29 | 360/6615 | 217/4095 | 73/1364 | chr14 | 67557296 | |||
| chr14:67562669 | G | A | 13 | a0001c0022 a0001c0023 a0001c0034 others(10): Show |
28 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(25): Show |
synonymous_variant | LOW | c.1038G>A | p.Val346Val | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/29 | 1181/6615 | 1038/4095 | 346/1364 | chr14 | 67562669 | |||
| chr14:67571871 | C | T | 7 | a0001c0034 a0001c0068 a0001c0069 others(4): Show |
11 | HG01074.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
synonymous_variant | LOW | c.1554C>T | p.Ser518Ser | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 10/29 | 1697/6615 | 1554/4095 | 518/1364 | chr14 | 67571871 | |||
| chr14:67572172 | C | T | 2 | a0002c0038 a0010c0031 |
5 | HG01074.hp2 HG01099.hp1 HG02717.hp2 others(2): Show |
synonymous_variant | LOW | c.1623C>T | p.Tyr541Tyr | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/29 | 1766/6615 | 1623/4095 | 541/1364 | chr14 | 67572172 | |||
| chr14:67572187 | C | T | 1 | a0006c0081 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.1638C>T | p.Asp546Asp | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/29 | 1781/6615 | 1638/4095 | 546/1364 | chr14 | 67572187 | |||
| chr14:67575424 | C | T | 1 | a0002c0067 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.2121C>T | p.Cys707Cys | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 15/29 | 2264/6615 | 2121/4095 | 707/1364 | chr14 | 67575424 | |||
| chr14:67575876 | A | G | 1 | a0015c0053 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.2223A>G | p.Arg741Arg | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 16/29 | 2366/6615 | 2223/4095 | 741/1364 | chr14 | 67575876 | |||
| chr14:67576463 | G | A | 1 | a0010c0072 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.2421G>A | p.Glu807Glu | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 17/29 | 2564/6615 | 2421/4095 | 807/1364 | chr14 | 67576463 | |||
| chr14:67577309 | G | A | 1 | a0002c0036 | 2 | HG02258.hp1 HG02965.hp2 |
synonymous_variant | LOW | c.2469G>A | p.Pro823Pro | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 18/29 | 2612/6615 | 2469/4095 | 823/1364 | chr14 | 67577309 | |||
| chr14:67578542 | G | A | 1 | a0003c0075 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.2760G>A | p.Gln920Gln | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 20/29 | 2903/6615 | 2760/4095 | 920/1364 | chr14 | 67578542 | |||
| chr14:67579218 | G | A | 53 | a0001c0010 a0001c0019 a0002c0004 others(50): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
synonymous_variant | LOW | c.2934G>A | p.Ser978Ser | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 21/29 | 3077/6615 | 2934/4095 | 978/1364 | chr14 | 67579218 | |||
| chr14:67579236 | C | T | 1 | a0004c0079 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.2952C>T | p.Ser984Ser | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 21/29 | 3095/6615 | 2952/4095 | 984/1364 | chr14 | 67579236 | |||
| chr14:67579735 | C | T | 2 | a0001c0069 a0003c0042 |
3 | HG01074.hp1 HG02630.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.3042C>T | p.Asp1014Asp | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/29 | 3185/6615 | 3042/4095 | 1014/1364 | chr14 | 67579735 | |||
| chr14:67579825 | G | A | 1 | a0002c0037 | 2 | HG02622.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.3132G>A | p.Thr1044Thr | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/29 | 3275/6615 | 3132/4095 | 1044/1364 | chr14 | 67579825 | |||
| chr14:67585651 | T | C | 1 | a0002c0047 | 2 | HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.3783T>C | p.Thr1261Thr | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 27/29 | 3926/6615 | 3783/4095 | 1261/1364 | chr14 | 67585651 | |||
| chr14:67587085 | T | C | 36 | a0001c0002 a0001c0010 a0001c0022 others(33): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
synonymous_variant | LOW | c.3945T>C | p.Ala1315Ala | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 4088/6615 | 3945/4095 | 1315/1364 | chr14 | 67587085 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67587260 | A | C | 117 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0009 others(114): Show |
407 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(404): Show |
3_prime_UTR_variant | MODIFIER | c.*25A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 25 | chr14 | 67587260 | ||||||
| chr14:67587596 | T | TG | 16 | a0001c0002t0009 a0001c0003t0009 a0001c0010t0004 others(13): Show |
24 | HG00408.hp1 HG00558.hp2 HG00639.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*369dupG | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 370 | INFO_REALIGN_3_PRIME | chr14 | 67587596 | |||||
| chr14:67587598 | G | C | 4 | a0002c0011t0005 a0002c0025t0005 a0002c0067t0005 others(1): Show |
10 | HG01516.hp1 HG01517.hp2 HG02602.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*363G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 363 | chr14 | 67587598 | ||||||
| chr14:67587605 | C | T | 3 | a0001c0003t0007 a0002c0028t0007 a0017c0043t0007 |
4 | HG02572.hp2 HG02886.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*370C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 370 | chr14 | 67587605 | ||||||
| chr14:67587677 | G | A | 117 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0009 others(114): Show |
407 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(404): Show |
3_prime_UTR_variant | MODIFIER | c.*442G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 442 | chr14 | 67587677 | ||||||
| chr14:67587709 | G | A | 4 | a0002c0011t0005 a0002c0025t0005 a0002c0067t0005 others(1): Show |
10 | HG01516.hp1 HG01517.hp2 HG02602.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*474G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 474 | chr14 | 67587709 | ||||||
| chr14:67587890 | G | C | 4 | a0002c0011t0005 a0002c0025t0005 a0002c0067t0005 others(1): Show |
10 | HG01516.hp1 HG01517.hp2 HG02602.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*655G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 655 | chr14 | 67587890 | ||||||
| chr14:67587903 | C | T | 3 | a0001c0069t0008 a0002c0070t0008 a0003c0042t0008 |
4 | HG01074.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*668C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 668 | chr14 | 67587903 | ||||||
| chr14:67588493 | A | G | 1 | a0012c0029t0014 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1258A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 1258 | chr14 | 67588493 | ||||||
| chr14:67588896 | C | G | 82 | a0001c0002t0001 a0001c0010t0001 a0001c0010t0004 others(79): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1661C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 1661 | chr14 | 67588896 | ||||||
| chr14:67589163 | G | T | 4 | a0002c0011t0005 a0002c0025t0005 a0002c0067t0005 others(1): Show |
10 | HG01516.hp1 HG01517.hp2 HG02602.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1928G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 1928 | chr14 | 67589163 | ||||||
| chr14:67589167 | A | G | 14 | a0002c0004t0003 a0002c0004t0010 a0002c0004t0015 others(11): Show |
28 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1932A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 1932 | chr14 | 67589167 | ||||||
| chr14:67589202 | A | C | 2 | a0001c0010t0006 a0014c0033t0006 |
5 | HG01884.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1967A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 1967 | chr14 | 67589202 | ||||||
| chr14:67589375 | T | C | 2 | a0002c0004t0010 a0013c0016t0010 |
3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2140T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 2140 | chr14 | 67589375 | ||||||
| chr14:67589451 | C | T | 1 | a0002c0004t0013 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2216C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 29/29 | 2216 | chr14 | 67589451 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:67533489 | C | T | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+91C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67533489 | |||||||
| chr14:67533492 | A | G | 218 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(215): Show |
239 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-35+94A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67533492 | |||||||
| chr14:67533511 | G | C | 1 | a0026c0084t0002g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-35+113G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67533511 | |||||||
| chr14:67533535 | T | C | 39 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0002c0004t0003g0173 others(36): Show |
40 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-35+137T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67533535 | |||||||
| chr14:67533642 | T | C | 44 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(41): Show |
46 | HG00323.hp2 HG01123.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.-35+244T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67533642 | |||||||
| chr14:67533971 | T | C | 1 | a0001c0003t0002g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-35+573T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67533971 | |||||||
| chr14:67534239 | T | C | 35 | a0002c0004t0003g0173 a0002c0004t0003g0189 a0002c0004t0015g0190 others(32): Show |
36 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-35+841T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67534239 | |||||||
| chr14:67534651 | G | T | 5 | a0001c0003t0002g0161 a0001c0010t0006g0159 a0010c0031t0002g0162 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+1253G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67534651 | |||||||
| chr14:67534691 | T | C | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+1293T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67534691 | |||||||
| chr14:67534761 | G | A | 210 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(207): Show |
231 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-35+1363G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67534761 | |||||||
| chr14:67534928 | C | T | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+1530C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67534928 | |||||||
| chr14:67535017 | C | T | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+1619C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67535017 | |||||||
| chr14:67535064 | C | T | 220 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(217): Show |
241 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-35+1666C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67535064 | |||||||
| chr14:67535150 | C | T | 1 | a0002c0013t0001g0156 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-35+1752C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67535150 | |||||||
| chr14:67535370 | C | CT | 86 | a0001c0002t0001g0117 a0001c0002t0002g0004 a0001c0002t0002g0005 others(83): Show |
104 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-35+2000dupT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67535370 | ||||||
| chr14:67535370 | C | CTT | 38 | a0001c0002t0002g0024 a0001c0002t0002g0127 a0001c0002t0002g0131 others(35): Show |
43 | HG00621.hp2 HG00735.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-35+1999_-35+2000d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67535370 | ||||||
| chr14:67535370 | C | CTTT | 11 | a0001c0002t0002g0153 a0001c0003t0002g0155 a0001c0003t0002g0161 others(8): Show |
12 | HG00738.hp2 HG01433.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+1998_-35+2000d others(5): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67535370 | ||||||
| chr14:67535370 | CT | C | 80 | a0001c0002t0002g0300 a0001c0002t0002g0313 a0001c0003t0002g0308 others(77): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-35+2000delT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67535370 | ||||||
| chr14:67535370 | CTT | C | 6 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(3): Show |
8 | HG01074.hp1 HG01256.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+1999_-35+2000d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67535370 | ||||||
| chr14:67535370 | CTTTTTTT others(4): Show |
C | 1 | a0002c0004t0003g0247 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-35+1990_-35+2000d others(13): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67535370 | ||||||
| chr14:67535400 | A | T | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+2002A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67535400 | |||||||
| chr14:67535669 | C | T | 171 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(168): Show |
189 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-35+2271C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67535669 | |||||||
| chr14:67535682 | G | A | 1 | a0004c0018t0003g0251 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-35+2284G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67535682 | |||||||
| chr14:67536019 | C | T | 2 | a0002c0004t0003g0189 a0002c0004t0015g0190 |
2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-35+2621C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536019 | |||||||
| chr14:67536095 | TCTCAAGG others(1464): Show |
T | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+2698_-35+4168d others(2): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536095 | |||||||
| chr14:67536154 | G | A | 1 | a0001c0003t0002g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-35+2756G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536154 | |||||||
| chr14:67536472 | T | C | 319 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0024 others(316): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.-35+3074T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536472 | |||||||
| chr14:67536659 | A | C | 1 | a0001c0003t0002g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-35+3261A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536659 | |||||||
| chr14:67536803 | G | C | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-35+3405G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536803 | |||||||
| chr14:67536805 | G | A | 1 | a0005c0005t0001g0336 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-35+3407G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536805 | |||||||
| chr14:67536925 | C | T | 1 | a0007c0008t0001g0224 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-35+3527C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536925 | |||||||
| chr14:67536926 | G | A | 94 | a0001c0002t0001g0117 a0001c0002t0002g0024 a0001c0002t0002g0102 others(91): Show |
114 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-35+3528G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67536926 | |||||||
| chr14:67537027 | G | A | 33 | a0002c0004t0003g0173 a0002c0004t0003g0189 a0002c0004t0015g0190 others(30): Show |
34 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.-35+3629G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537027 | |||||||
| chr14:67537078 | T | G | 1 | a0001c0023t0002g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-35+3680T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537078 | |||||||
| chr14:67537227 | C | G | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-35+3829C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537227 | |||||||
| chr14:67537275 | C | T | 7 | a0003c0001t0001g0075 a0011c0027t0001g0126 a0011c0027t0003g0070 others(4): Show |
7 | HG00280.hp1 HG00642.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+3877C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537275 | |||||||
| chr14:67537276 | G | A | 33 | a0002c0004t0003g0173 a0002c0004t0003g0189 a0002c0004t0015g0190 others(30): Show |
34 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.-35+3878G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537276 | |||||||
| chr14:67537346 | A | AAAT | 20 | a0001c0002t0002g0004 a0001c0002t0002g0313 a0002c0004t0001g0304 others(17): Show |
20 | HG02109.hp1 HG02129.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35+3981_-35+3983d others(5): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537346 | ||||||
| chr14:67537346 | A | AAATAAT | 21 | a0001c0003t0002g0013 a0001c0003t0002g0308 a0001c0003t0002g0309 others(18): Show |
22 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.-35+3978_-35+3983d others(8): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537346 | ||||||
| chr14:67537346 | A | AAATAATA others(2): Show |
72 | a0001c0002t0001g0117 a0001c0002t0002g0105 a0001c0002t0009g0120 others(69): Show |
85 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-35+3975_-35+3983d others(11): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537346 | ||||||
| chr14:67537346 | A | AAATAATA others(5): Show |
15 | a0001c0003t0002g0116 a0001c0069t0008g0200 a0002c0004t0003g0173 others(12): Show |
16 | HG00423.hp1 HG01255.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-35+3972_-35+3983d others(14): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537346 | ||||||
| chr14:67537346 | A | AAATAATA others(8): Show |
6 | a0001c0010t0001g0142 a0003c0042t0008g0201 a0008c0012t0002g0191 others(3): Show |
7 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35+3969_-35+3983d others(17): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537346 | ||||||
| chr14:67537346 | AAAT | A | 10 | a0001c0002t0002g0138 a0001c0003t0002g0161 a0001c0010t0006g0159 others(7): Show |
10 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35+3981_-35+3983d others(5): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537346 | ||||||
| chr14:67537349 | T | A | 1 | a0001c0023t0002g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-35+3951T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537349 | |||||||
| chr14:67537367 | TAATAATA others(8): Show |
T | 2 | a0002c0004t0001g0320 a0002c0004t0004g0352 |
2 | HG00558.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-35+3972_-35+3986d others(17): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537367 | ||||||
| chr14:67537376 | TAATAAA | T | 3 | a0001c0002t0002g0030 a0001c0002t0002g0242 a0013c0016t0010g0324 |
3 | HG02015.hp1 HG02135.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-35+3981_-35+3986d others(8): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537376 | ||||||
| chr14:67537379 | TAAA | T | 60 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0354 others(57): Show |
63 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-35+3984_-35+3986d others(5): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67537379 | ||||||
| chr14:67537382 | A | T | 115 | a0001c0002t0002g0212 a0001c0002t0002g0300 a0001c0002t0002g0313 others(112): Show |
128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-35+3984A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537382 | |||||||
| chr14:67537519 | G | C | 2 | a0001c0068t0002g0056 a0002c0070t0008g0055 |
2 | HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-35+4121G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537519 | |||||||
| chr14:67537567 | A | G | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+4169A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537567 | |||||||
| chr14:67537745 | G | A | 1 | a0007c0008t0004g0202 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-34-4089G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537745 | |||||||
| chr14:67537869 | T | C | 1 | a0011c0030t0001g0076 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-34-3965T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67537869 | |||||||
| chr14:67538168 | T | G | 178 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(175): Show |
196 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.-34-3666T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67538168 | |||||||
| chr14:67538393 | C | T | 319 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0024 others(316): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.-34-3441C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67538393 | |||||||
| chr14:67538430 | T | C | 102 | a0001c0002t0001g0117 a0001c0002t0002g0024 a0001c0002t0002g0102 others(99): Show |
122 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-34-3404T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67538430 | |||||||
| chr14:67538432 | C | T | 1 | a0006c0032t0002g0348 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-34-3402C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67538432 | |||||||
| chr14:67538453 | T | G | 1 | a0007c0008t0001g0078 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-34-3381T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67538453 | |||||||
| chr14:67538617 | A | G | 186 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(183): Show |
206 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.-34-3217A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67538617 | |||||||
| chr14:67538638 | G | A | 1 | a0002c0013t0003g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-34-3196G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67538638 | |||||||
| chr14:67538906 | A | G | 3 | a0001c0002t0002g0313 a0002c0004t0003g0247 a0002c0013t0001g0347 |
3 | HG02129.hp2 NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-34-2928A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67538906 | |||||||
| chr14:67539001 | A | G | 1 | a0021c0052t0004g0346 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-34-2833A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67539001 | |||||||
| chr14:67539091 | C | G | 2 | a0001c0019t0001g0137 a0012c0020t0001g0095 |
2 | HG01109.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-34-2743C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67539091 | |||||||
| chr14:67539139 | T | G | 1 | a0001c0002t0002g0127 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-34-2695T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67539139 | |||||||
| chr14:67539458 | G | A | 3 | a0003c0001t0001g0014 a0003c0001t0004g0014 a0011c0030t0001g0096 |
3 | HG00639.hp1 HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-34-2376G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67539458 | |||||||
| chr14:67539470 | G | T | 1 | a0014c0083t0001g0357 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-34-2364G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67539470 | |||||||
| chr14:67539756 | C | T | 7 | a0003c0001t0001g0075 a0011c0027t0001g0126 a0011c0027t0003g0070 others(4): Show |
7 | HG00280.hp1 HG00642.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34-2078C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67539756 | |||||||
| chr14:67539794 | G | A | 5 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0002c0028t0007g0098 others(2): Show |
6 | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-2040G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67539794 | |||||||
| chr14:67539962 | G | C | 1 | a0007c0008t0001g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-34-1872G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67539962 | |||||||
| chr14:67540011 | T | G | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-1823T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540011 | |||||||
| chr14:67540115 | T | C | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-1719T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540115 | |||||||
| chr14:67540223 | C | T | 223 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(220): Show |
244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.-34-1611C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540223 | |||||||
| chr14:67540291 | T | C | 221 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0138 others(218): Show |
242 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.-34-1543T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540291 | |||||||
| chr14:67540312 | A | G | 4 | a0014c0033t0006g0012 a0014c0083t0001g0357 a0017c0043t0007g0249 others(1): Show |
6 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-1522A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540312 | |||||||
| chr14:67540397 | C | A | 223 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(220): Show |
244 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.-34-1437C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540397 | |||||||
| chr14:67540436 | G | T | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-1398G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540436 | |||||||
| chr14:67540587 | T | C | 1 | a0001c0003t0002g0314 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-34-1247T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540587 | |||||||
| chr14:67540625 | C | CA | 18 | a0001c0003t0002g0139 a0001c0022t0002g0252 a0001c0068t0002g0056 others(15): Show |
18 | HG00621.hp2 HG01099.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.-34-1193dupA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67540625 | ||||||
| chr14:67540625 | C | CAA | 28 | a0002c0004t0003g0173 a0002c0004t0003g0189 a0002c0011t0001g0245 others(25): Show |
29 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.-34-1194_-34-1193d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67540625 | ||||||
| chr14:67540625 | CA | C | 37 | a0001c0002t0002g0354 a0001c0003t0002g0026 a0001c0003t0002g0041 others(34): Show |
38 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-34-1193delA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67540625 | ||||||
| chr14:67540651 | TA | T | 3 | a0005c0005t0001g0307 a0005c0005t0001g0312 a0031c0082t0001g0306 |
3 | HG02735.hp2 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-34-1177delA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr14 | 67540651 | ||||||
| chr14:67540730 | T | C | 3 | a0008c0012t0002g0168 a0008c0012t0002g0169 a0008c0012t0002g0191 |
3 | HG00423.hp2 HG02083.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-34-1104T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540730 | |||||||
| chr14:67540856 | C | T | 38 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0053 others(35): Show |
43 | HG00544.hp1 HG00735.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.-34-978C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540856 | |||||||
| chr14:67540921 | G | C | 2 | a0001c0003t0002g0161 a0016c0065t0003g0160 |
2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-34-913G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67540921 | |||||||
| chr14:67541042 | A | G | 1 | a0033c0055t0011g0311 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-34-792A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67541042 | |||||||
| chr14:67541445 | A | G | 1 | a0003c0001t0001g0121 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-34-389A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67541445 | |||||||
| chr14:67541506 | A | G | 2 | a0002c0047t0012g0045 a0002c0047t0012g0046 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-34-328A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67541506 | |||||||
| chr14:67541681 | C | A | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-153C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67541681 | |||||||
| chr14:67541699 | A | T | 1 | a0004c0006t0001g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-34-135A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67541699 | |||||||
| chr14:67541741 | T | C | 4 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-93T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 1/28 | chr14 | 67541741 | |||||||
| chr14:67542075 | C | G | 37 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(34): Show |
38 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.126+82C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542075 | |||||||
| chr14:67542085 | A | G | 6 | a0001c0022t0002g0252 a0001c0022t0002g0301 a0001c0022t0002g0303 others(3): Show |
7 | HG01099.hp2 HG03490.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+92A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542085 | |||||||
| chr14:67542150 | G | A | 61 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(58): Show |
64 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.126+157G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542150 | |||||||
| chr14:67542176 | C | G | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+183C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542176 | |||||||
| chr14:67542182 | T | TA | 37 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(34): Show |
38 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.126+189_126+190ins others(1): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542182 | |||||||
| chr14:67542183 | C | A | 37 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(34): Show |
38 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.126+190C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542183 | |||||||
| chr14:67542562 | G | T | 6 | a0001c0002t0002g0300 a0003c0075t0002g0342 a0004c0006t0001g0034 others(3): Show |
7 | HG00140.hp1 HG00280.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+569G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542562 | |||||||
| chr14:67542676 | C | CTATTT | 8 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(5): Show |
9 | HG00621.hp2 HG01109.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+709_126+713dup others(5): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67542676 | ||||||
| chr14:67542676 | CTATTT | C | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+709_126+713del others(5): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67542676 | ||||||
| chr14:67542747 | C | A | 1 | a0014c0033t0006g0012 | 3 | HG01891.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.126+754C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542747 | |||||||
| chr14:67542761 | C | T | 6 | a0002c0004t0001g0304 a0002c0011t0001g0245 a0002c0011t0001g0246 others(3): Show |
6 | HG00621.hp2 HG02129.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+768C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542761 | |||||||
| chr14:67542775 | G | A | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+782G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542775 | |||||||
| chr14:67542906 | G | A | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+913G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542906 | |||||||
| chr14:67542919 | C | G | 169 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(166): Show |
187 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.126+926C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67542919 | |||||||
| chr14:67543039 | C | G | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1046C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543039 | |||||||
| chr14:67543287 | C | T | 1 | a0002c0011t0001g0185 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.126+1294C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543287 | |||||||
| chr14:67543300 | G | C | 1 | a0001c0023t0002g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126+1307G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543300 | |||||||
| chr14:67543439 | C | T | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1446C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543439 | |||||||
| chr14:67543507 | G | C | 169 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(166): Show |
187 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.126+1514G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543507 | |||||||
| chr14:67543600 | A | G | 4 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1607A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543600 | |||||||
| chr14:67543703 | A | G | 2 | a0001c0002t0002g0138 a0012c0020t0001g0154 |
2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.126+1710A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543703 | |||||||
| chr14:67543736 | G | A | 84 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(81): Show |
89 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.126+1743G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543736 | |||||||
| chr14:67543781 | CA | C | 219 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(216): Show |
240 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.126+1798delA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67543781 | ||||||
| chr14:67543791 | A | C | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1798A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543791 | |||||||
| chr14:67543947 | C | G | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1954C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543947 | |||||||
| chr14:67543992 | G | T | 2 | a0002c0004t0001g0320 a0002c0004t0004g0352 |
2 | HG00558.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.126+1999G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67543992 | |||||||
| chr14:67544043 | G | T | 1 | a0014c0045t0002g0157 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.126+2050G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544043 | |||||||
| chr14:67544071 | A | G | 1 | a0006c0081t0002g0297 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.126+2078A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544071 | |||||||
| chr14:67544074 | C | T | 1 | a0003c0001t0001g0148 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.126+2081C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544074 | |||||||
| chr14:67544116 | T | A | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+2123T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544116 | |||||||
| chr14:67544169 | G | A | 1 | a0011c0027t0003g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.126+2176G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544169 | |||||||
| chr14:67544269 | C | T | 4 | a0004c0079t0003g0340 a0005c0005t0001g0294 a0005c0044t0005g0295 others(1): Show |
4 | HG00735.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+2276C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544269 | |||||||
| chr14:67544291 | G | A | 208 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(205): Show |
229 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.126+2298G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544291 | |||||||
| chr14:67544373 | G | A | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+2380G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544373 | |||||||
| chr14:67544779 | T | C | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+2786T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544779 | |||||||
| chr14:67544848 | A | G | 1 | a0001c0019t0001g0151 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+2855A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67544848 | |||||||
| chr14:67545051 | A | G | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+3058A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67545051 | |||||||
| chr14:67545077 | A | C | 2 | a0002c0047t0012g0045 a0002c0047t0012g0046 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.126+3084A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67545077 | |||||||
| chr14:67545518 | G | A | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+3525G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67545518 | |||||||
| chr14:67545631 | T | C | 4 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+3638T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67545631 | |||||||
| chr14:67545936 | C | T | 1 | a0002c0013t0001g0156 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.126+3943C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67545936 | |||||||
| chr14:67545945 | T | TA | 40 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(37): Show |
41 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+3966dupA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67545945 | ||||||
| chr14:67545945 | TA | T | 8 | a0001c0068t0002g0056 a0002c0011t0001g0245 a0002c0011t0001g0246 others(5): Show |
8 | HG00323.hp1 HG00621.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+3966delA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67545945 | ||||||
| chr14:67546110 | T | C | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.126+4117T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546110 | |||||||
| chr14:67546167 | T | C | 1 | a0002c0004t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+4174T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546167 | |||||||
| chr14:67546174 | A | G | 22 | a0001c0002t0001g0117 a0001c0002t0009g0120 a0001c0003t0002g0116 others(19): Show |
31 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+4181A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546174 | |||||||
| chr14:67546192 | C | T | 2 | a0002c0004t0001g0203 a0002c0004t0001g0237 |
2 | HG01123.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.126+4199C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546192 | |||||||
| chr14:67546390 | GTTTTGT | G | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+4421_126+4426d others(8): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67546390 | ||||||
| chr14:67546499 | T | C | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+4506T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546499 | |||||||
| chr14:67546516 | G | A | 2 | a0005c0005t0001g0259 a0005c0005t0001g0327 |
2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.126+4523G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546516 | |||||||
| chr14:67546535 | C | T | 40 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(37): Show |
41 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+4542C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546535 | |||||||
| chr14:67546537 | C | T | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+4544C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546537 | |||||||
| chr14:67546637 | G | A | 1 | a0002c0004t0004g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.126+4644G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546637 | |||||||
| chr14:67546674 | G | A | 1 | a0011c0030t0001g0076 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.126+4681G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546674 | |||||||
| chr14:67546679 | C | T | 2 | a0002c0047t0012g0045 a0002c0047t0012g0046 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.126+4686C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546679 | |||||||
| chr14:67546696 | C | T | 4 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0013t0001g0244 others(1): Show |
4 | HG00621.hp2 HG02129.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+4703C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546696 | |||||||
| chr14:67546738 | G | A | 2 | a0003c0042t0008g0198 a0003c0042t0008g0201 |
2 | HG01074.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.126+4745G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546738 | |||||||
| chr14:67546805 | G | A | 1 | a0002c0028t0001g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.126+4812G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546805 | |||||||
| chr14:67546831 | C | T | 44 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(41): Show |
47 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.126+4838C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546831 | |||||||
| chr14:67546936 | G | A | 1 | a0001c0003t0002g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.126+4943G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546936 | |||||||
| chr14:67546999 | A | T | 36 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(33): Show |
37 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.126+5006A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67546999 | |||||||
| chr14:67547209 | G | A | 2 | a0013c0016t0004g0323 a0013c0016t0010g0322 |
2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.126+5216G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67547209 | |||||||
| chr14:67547465 | G | A | 1 | a0001c0003t0002g0308 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.126+5472G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67547465 | |||||||
| chr14:67547566 | C | T | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.126+5573C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67547566 | |||||||
| chr14:67547593 | G | A | 2 | a0011c0027t0003g0071 a0011c0027t0003g0072 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.126+5600G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67547593 | |||||||
| chr14:67547704 | T | C | 1 | a0002c0004t0003g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+5711T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67547704 | |||||||
| chr14:67547705 | G | A | 2 | a0003c0040t0001g0051 a0003c0040t0001g0052 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.126+5712G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67547705 | |||||||
| chr14:67547732 | C | T | 1 | a0004c0006t0001g0292 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.126+5739C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67547732 | |||||||
| chr14:67547797 | CAG | C | 38 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0053 others(35): Show |
43 | HG00544.hp1 HG00735.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.126+5805_126+5806d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67547797 | |||||||
| chr14:67548401 | A | G | 2 | a0006c0014t0001g0033 a0006c0014t0001g0321 |
3 | NA18948.hp2 NA19010.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.126+6408A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67548401 | |||||||
| chr14:67548527 | G | A | 1 | a0001c0003t0002g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126+6534G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67548527 | |||||||
| chr14:67548700 | A | T | 1 | a0008c0017t0009g0028 | 2 | HG00408.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.126+6707A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67548700 | |||||||
| chr14:67548755 | A | C | 169 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0094 others(166): Show |
187 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.126+6762A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67548755 | |||||||
| chr14:67548772 | C | T | 1 | a0010c0072t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.126+6779C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67548772 | |||||||
| chr14:67548934 | T | C | 217 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0094 others(214): Show |
238 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.127-6891T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67548934 | |||||||
| chr14:67548976 | C | T | 26 | a0001c0010t0001g0063 a0002c0011t0005g0065 a0002c0013t0001g0110 others(23): Show |
27 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.127-6849C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67548976 | |||||||
| chr14:67549054 | T | G | 13 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0011t0001g0262 others(10): Show |
15 | HG00621.hp2 HG00733.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.127-6771T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549054 | |||||||
| chr14:67549127 | G | A | 1 | a0029c0085t0001g0254 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-6698G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549127 | |||||||
| chr14:67549155 | A | T | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.127-6670A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549155 | |||||||
| chr14:67549214 | C | T | 2 | a0003c0040t0001g0051 a0003c0040t0001g0052 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.127-6611C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549214 | |||||||
| chr14:67549219 | G | C | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.127-6606G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549219 | |||||||
| chr14:67549220 | C | G | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.127-6605C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549220 | |||||||
| chr14:67549266 | ATTT | A | 4 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-6556_127-6554d others(5): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67549266 | ||||||
| chr14:67549342 | C | T | 1 | a0001c0003t0002g0236 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.127-6483C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549342 | |||||||
| chr14:67549356 | C | T | 1 | a0007c0008t0001g0093 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.127-6469C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549356 | |||||||
| chr14:67549518 | G | C | 34 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(31): Show |
35 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-6307G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549518 | |||||||
| chr14:67549626 | A | G | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-6199A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549626 | |||||||
| chr14:67549679 | T | C | 3 | a0003c0001t0001g0025 a0003c0001t0001g0027 a0003c0001t0001g0143 |
5 | NA18945.hp1 NA18962.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-6146T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549679 | |||||||
| chr14:67549758 | A | G | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-6067A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549758 | |||||||
| chr14:67549969 | G | A | 1 | a0005c0005t0001g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127-5856G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549969 | |||||||
| chr14:67549981 | C | G | 205 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(202): Show |
226 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.127-5844C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549981 | |||||||
| chr14:67549985 | T | A | 1 | a0008c0012t0002g0192 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.127-5840T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67549985 | |||||||
| chr14:67550158 | T | TAAAA | 7 | a0001c0002t0002g0138 a0001c0022t0002g0303 a0007c0008t0001g0224 others(4): Show |
9 | HG01891.hp2 HG01993.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-5656_127-5653d others(6): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67550158 | ||||||
| chr14:67550158 | T | TAAAAA | 98 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(95): Show |
103 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.127-5657_127-5653d others(7): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67550158 | ||||||
| chr14:67550158 | T | TAAAAAA | 68 | a0002c0011t0001g0245 a0004c0006t0001g0003 a0004c0006t0001g0032 others(65): Show |
78 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.127-5658_127-5653d others(8): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67550158 | ||||||
| chr14:67550158 | T | TAAAAAAA | 11 | a0004c0007t0001g0010 a0004c0007t0001g0031 a0004c0007t0001g0039 others(8): Show |
14 | HG00609.hp2 HG00741.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-5659_127-5653d others(9): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67550158 | ||||||
| chr14:67550241 | T | G | 1 | a0013c0016t0010g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-5584T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550241 | |||||||
| chr14:67550377 | C | T | 1 | a0010c0039t0002g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.127-5448C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550377 | |||||||
| chr14:67550452 | G | A | 7 | a0001c0022t0002g0252 a0001c0022t0002g0301 a0001c0022t0002g0303 others(4): Show |
8 | HG01099.hp2 HG02109.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-5373G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550452 | |||||||
| chr14:67550675 | G | T | 8 | a0001c0002t0002g0138 a0001c0003t0007g0199 a0001c0069t0008g0200 others(5): Show |
8 | HG01074.hp1 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-5150G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550675 | |||||||
| chr14:67550697 | T | A | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.127-5128T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550697 | |||||||
| chr14:67550699 | A | C | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.127-5126A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550699 | |||||||
| chr14:67550771 | A | T | 166 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0094 others(163): Show |
184 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.127-5054A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550771 | |||||||
| chr14:67550820 | G | A | 2 | a0006c0014t0001g0328 a0006c0014t0001g0329 |
2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.127-5005G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550820 | |||||||
| chr14:67550917 | A | G | 9 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0011t0001g0262 others(6): Show |
9 | HG00621.hp2 HG00733.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-4908A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550917 | |||||||
| chr14:67550972 | A | G | 1 | a0010c0026t0001g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.127-4853A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67550972 | |||||||
| chr14:67551117 | T | C | 1 | a0025c0060t0001g0205 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.127-4708T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551117 | |||||||
| chr14:67551238 | G | C | 7 | a0001c0022t0002g0252 a0001c0022t0002g0301 a0001c0022t0002g0303 others(4): Show |
8 | HG01099.hp2 HG02109.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-4587G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551238 | |||||||
| chr14:67551266 | C | T | 4 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-4559C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551266 | |||||||
| chr14:67551367 | T | C | 4 | a0001c0002t0002g0102 a0001c0003t0002g0100 a0001c0003t0002g0101 others(1): Show |
4 | HG00639.hp2 HG02559.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-4458T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551367 | |||||||
| chr14:67551468 | A | T | 2 | a0009c0049t0003g0183 a0022c0048t0001g0184 |
2 | HG01106.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.127-4357A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551468 | |||||||
| chr14:67551470 | A | T | 40 | a0001c0002t0002g0138 a0001c0003t0002g0308 a0001c0003t0002g0309 others(37): Show |
41 | HG00408.hp1 HG00423.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-4355A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551470 | |||||||
| chr14:67551500 | G | A | 1 | a0002c0036t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.127-4325G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551500 | |||||||
| chr14:67551530 | C | G | 85 | a0001c0002t0002g0094 a0001c0003t0002g0314 a0002c0011t0001g0245 others(82): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.127-4295C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551530 | |||||||
| chr14:67551658 | G | A | 1 | a0006c0014t0004g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.127-4167G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551658 | |||||||
| chr14:67551834 | A | T | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-3991A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551834 | |||||||
| chr14:67551869 | C | T | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-3956C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551869 | |||||||
| chr14:67551959 | C | T | 3 | a0004c0007t0001g0270 a0015c0021t0001g0332 a0015c0021t0004g0333 |
3 | HG00741.hp2 HG03710.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.127-3866C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551959 | |||||||
| chr14:67551996 | C | T | 84 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(81): Show |
89 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.127-3829C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67551996 | |||||||
| chr14:67552139 | T | A | 135 | a0001c0002t0002g0094 a0001c0002t0002g0138 a0001c0003t0002g0308 others(132): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.127-3686T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552139 | |||||||
| chr14:67552331 | A | G | 5 | a0001c0002t0002g0024 a0001c0002t0002g0102 a0001c0003t0002g0100 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-3494A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552331 | |||||||
| chr14:67552390 | G | A | 1 | a0002c0036t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.127-3435G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552390 | |||||||
| chr14:67552479 | A | G | 1 | a0014c0033t0006g0012 | 3 | HG01891.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.127-3346A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552479 | |||||||
| chr14:67552533 | C | T | 1 | a0010c0031t0002g0241 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-3292C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552533 | |||||||
| chr14:67552538 | T | C | 221 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0094 others(218): Show |
242 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.127-3287T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552538 | |||||||
| chr14:67552591 | C | T | 2 | a0001c0002t0002g0138 a0012c0020t0001g0154 |
2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.127-3234C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552591 | |||||||
| chr14:67552595 | G | A | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-3230G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552595 | |||||||
| chr14:67552649 | C | T | 2 | a0002c0047t0012g0045 a0002c0047t0012g0046 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.127-3176C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552649 | |||||||
| chr14:67552654 | C | CTA | 81 | a0001c0002t0002g0094 a0004c0006t0001g0003 a0004c0006t0001g0032 others(78): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.127-3170_127-3169d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67552654 | ||||||
| chr14:67552663 | A | C | 1 | a0001c0002t0002g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.127-3162A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552663 | |||||||
| chr14:67552668 | A | G | 1 | a0007c0008t0001g0235 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.127-3157A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552668 | |||||||
| chr14:67552699 | G | A | 5 | a0001c0002t0002g0024 a0001c0002t0002g0102 a0001c0003t0002g0100 others(2): Show |
6 | HG00639.hp2 HG01243.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-3126G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552699 | |||||||
| chr14:67552724 | A | G | 321 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0024 others(318): Show |
362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.127-3101A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552724 | |||||||
| chr14:67552745 | C | T | 1 | a0006c0015t0002g0291 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.127-3080C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552745 | |||||||
| chr14:67552762 | G | A | 34 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(31): Show |
35 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-3063G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552762 | |||||||
| chr14:67552766 | C | CA | 165 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0030 others(162): Show |
189 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.127-3047dupA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67552766 | ||||||
| chr14:67552766 | C | CAA | 51 | a0001c0002t0002g0138 a0001c0003t0002g0308 a0001c0003t0002g0309 others(48): Show |
52 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.127-3048_127-3047d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67552766 | ||||||
| chr14:67552779 | C | A | 1 | a0002c0004t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.127-3046C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552779 | |||||||
| chr14:67552846 | C | T | 1 | a0003c0001t0001g0068 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.127-2979C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552846 | |||||||
| chr14:67552891 | A | G | 135 | a0001c0002t0002g0094 a0001c0002t0002g0138 a0001c0003t0002g0308 others(132): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.127-2934A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552891 | |||||||
| chr14:67552958 | G | T | 3 | a0009c0009t0001g0180 a0009c0009t0001g0181 a0009c0009t0001g0182 |
3 | NA18959.hp1 NA18992.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.127-2867G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67552958 | |||||||
| chr14:67553094 | T | C | 84 | a0001c0002t0002g0094 a0001c0003t0002g0314 a0004c0006t0001g0003 others(81): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.127-2731T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67553094 | |||||||
| chr14:67553140 | CAG | C | 6 | a0015c0021t0001g0332 a0015c0021t0003g0331 a0015c0021t0003g0356 others(3): Show |
6 | HG00741.hp2 HG01346.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-2683_127-2682d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67553140 | ||||||
| chr14:67553376 | T | TA | 11 | a0001c0003t0002g0208 a0007c0008t0001g0009 a0007c0008t0001g0209 others(8): Show |
12 | HG01167.hp1 HG01168.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-2439dupA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67553376 | ||||||
| chr14:67553386 | A | C | 79 | a0001c0002t0002g0094 a0001c0002t0002g0136 a0001c0003t0002g0314 others(76): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.127-2439A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67553386 | |||||||
| chr14:67553387 | C | A | 2 | a0002c0028t0001g0021 a0027c0057t0001g0021 |
2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.127-2438C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67553387 | |||||||
| chr14:67553422 | G | A | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.127-2403G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67553422 | |||||||
| chr14:67553617 | A | T | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.127-2208A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67553617 | |||||||
| chr14:67553743 | G | A | 38 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(35): Show |
39 | HG00408.hp1 HG00423.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.127-2082G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67553743 | |||||||
| chr14:67553801 | T | C | 1 | a0001c0010t0001g0082 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.127-2024T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67553801 | |||||||
| chr14:67554045 | G | A | 34 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(31): Show |
35 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-1780G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67554045 | |||||||
| chr14:67554122 | G | GA | 3 | a0001c0002t0002g0354 a0001c0010t0001g0036 a0001c0010t0001g0349 |
4 | HG00438.hp1 HG00609.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1696dupA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr14 | 67554122 | ||||||
| chr14:67554150 | T | C | 3 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 |
3 | HG02809.hp2 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.127-1675T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67554150 | |||||||
| chr14:67554179 | T | C | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-1646T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67554179 | |||||||
| chr14:67554316 | C | T | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-1509C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67554316 | |||||||
| chr14:67554400 | G | C | 83 | a0001c0002t0002g0094 a0001c0003t0002g0314 a0004c0006t0001g0003 others(80): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.127-1425G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67554400 | |||||||
| chr14:67554453 | T | C | 75 | a0001c0002t0001g0117 a0001c0002t0002g0105 a0001c0002t0009g0120 others(72): Show |
93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.127-1372T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67554453 | |||||||
| chr14:67554568 | T | C | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-1257T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67554568 | |||||||
| chr14:67555021 | G | A | 2 | a0004c0006t0001g0248 a0004c0006t0001g0341 |
2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.127-804G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555021 | |||||||
| chr14:67555042 | A | T | 1 | a0001c0068t0002g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.127-783A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555042 | |||||||
| chr14:67555069 | C | T | 86 | a0001c0002t0002g0094 a0001c0003t0002g0314 a0002c0011t0001g0245 others(83): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.127-756C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555069 | |||||||
| chr14:67555070 | G | A | 5 | a0003c0001t0001g0015 a0003c0001t0001g0060 a0003c0001t0001g0108 others(2): Show |
6 | HG00140.hp2 HG00733.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-755G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555070 | |||||||
| chr14:67555072 | T | C | 128 | a0001c0002t0002g0094 a0001c0002t0002g0138 a0001c0003t0002g0308 others(125): Show |
144 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.127-753T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555072 | |||||||
| chr14:67555169 | T | G | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127-656T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555169 | |||||||
| chr14:67555332 | C | T | 1 | a0001c0002t0009g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.127-493C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555332 | |||||||
| chr14:67555372 | A | C | 1 | a0001c0003t0002g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-453A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555372 | |||||||
| chr14:67555449 | C | T | 1 | a0001c0019t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-376C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555449 | |||||||
| chr14:67555526 | A | T | 1 | a0010c0058t0002g0344 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.127-299A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555526 | |||||||
| chr14:67555629 | C | T | 1 | a0002c0011t0001g0245 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.127-196C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555629 | |||||||
| chr14:67555693 | C | T | 313 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0024 others(310): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.127-132C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555693 | |||||||
| chr14:67555697 | C | T | 76 | a0001c0003t0002g0314 a0004c0006t0001g0003 a0004c0006t0001g0032 others(73): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.127-128C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 2/28 | chr14 | 67555697 | |||||||
| chr14:67555957 | G | A | 4 | a0001c0023t0002g0253 a0001c0023t0002g0255 a0001c0023t0002g0256 others(1): Show |
4 | HG03041.hp1 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+70G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67555957 | |||||||
| chr14:67555974 | T | C | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.189+87T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67555974 | |||||||
| chr14:67556215 | A | C | 6 | a0001c0002t0002g0138 a0001c0003t0007g0199 a0001c0069t0008g0200 others(3): Show |
6 | HG01074.hp1 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+328A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556215 | |||||||
| chr14:67556265 | C | T | 1 | a0001c0069t0008g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.189+378C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556265 | |||||||
| chr14:67556397 | A | T | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.189+510A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556397 | |||||||
| chr14:67556412 | A | G | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.189+525A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556412 | |||||||
| chr14:67556421 | C | G | 1 | a0004c0007t0001g0269 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.189+534C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556421 | |||||||
| chr14:67556609 | G | A | 1 | a0007c0008t0001g0224 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.190-660G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556609 | |||||||
| chr14:67556618 | C | T | 1 | a0013c0016t0010g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.190-651C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556618 | |||||||
| chr14:67556631 | T | G | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.190-638T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556631 | |||||||
| chr14:67556632 | G | T | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.190-637G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556632 | |||||||
| chr14:67556726 | A | T | 1 | a0014c0033t0006g0012 | 3 | HG01891.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.190-543A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556726 | |||||||
| chr14:67556788 | T | C | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.190-481T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556788 | |||||||
| chr14:67556803 | T | C | 3 | a0006c0015t0002g0266 a0014c0045t0002g0157 a0014c0045t0002g0158 |
3 | HG00438.hp2 HG02074.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.190-466T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556803 | |||||||
| chr14:67556821 | T | C | 1 | a0028c0076t0001g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.190-448T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67556821 | |||||||
| chr14:67557152 | G | A | 10 | a0001c0022t0002g0252 a0001c0022t0002g0257 a0001c0022t0002g0301 others(7): Show |
11 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-117G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67557152 | |||||||
| chr14:67557172 | G | A | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.190-97G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 3/28 | chr14 | 67557172 | |||||||
| chr14:67557431 | G | C | 6 | a0003c0001t0001g0006 a0003c0001t0001g0099 a0003c0001t0001g0122 others(3): Show |
7 | NA18949.hp1 NA18950.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+13G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67557431 | |||||||
| chr14:67557525 | G | A | 2 | a0002c0047t0012g0045 a0002c0047t0012g0046 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.339+107G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67557525 | |||||||
| chr14:67557656 | G | A | 3 | a0003c0001t0001g0025 a0003c0001t0001g0027 a0003c0001t0001g0143 |
5 | NA18945.hp1 NA18962.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+238G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67557656 | |||||||
| chr14:67557810 | G | A | 5 | a0002c0011t0001g0262 a0002c0011t0001g0263 a0003c0001t0001g0261 others(2): Show |
5 | HG00733.hp2 HG01071.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+392G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67557810 | |||||||
| chr14:67557934 | C | T | 1 | a0002c0004t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.339+516C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67557934 | |||||||
| chr14:67558060 | A | G | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.339+642A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558060 | |||||||
| chr14:67558111 | T | C | 1 | a0010c0026t0002g0113 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.339+693T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558111 | |||||||
| chr14:67558136 | C | A | 3 | a0004c0018t0003g0251 a0004c0018t0003g0272 a0004c0018t0003g0273 |
3 | HG02300.hp2 NA18747.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.339+718C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558136 | |||||||
| chr14:67558341 | A | C | 219 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(216): Show |
240 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.339+923A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558341 | |||||||
| chr14:67558399 | C | G | 74 | a0004c0006t0001g0003 a0004c0006t0001g0032 a0004c0006t0001g0034 others(71): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.339+981C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558399 | |||||||
| chr14:67558543 | T | C | 220 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(217): Show |
241 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.340-1065T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558543 | |||||||
| chr14:67558549 | G | C | 2 | a0001c0002t0002g0138 a0012c0020t0001g0154 |
2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.340-1059G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558549 | |||||||
| chr14:67558644 | G | A | 5 | a0001c0022t0002g0252 a0001c0022t0002g0301 a0001c0022t0002g0303 others(2): Show |
6 | HG01099.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-964G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558644 | |||||||
| chr14:67558731 | G | A | 6 | a0015c0021t0001g0332 a0015c0021t0003g0331 a0015c0021t0003g0356 others(3): Show |
6 | HG00741.hp2 HG01346.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-877G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67558731 | |||||||
| chr14:67559016 | T | A | 1 | a0007c0035t0001g0206 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.340-592T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67559016 | |||||||
| chr14:67559028 | T | A | 2 | a0001c0003t0002g0013 a0001c0003t0002g0047 |
3 | HG01192.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.340-580T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67559028 | |||||||
| chr14:67559041 | G | A | 1 | a0005c0005t0001g0334 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.340-567G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67559041 | |||||||
| chr14:67559119 | C | T | 219 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(216): Show |
240 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.340-489C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67559119 | |||||||
| chr14:67559312 | T | C | 362 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0004 others(359): Show |
408 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(405): Show |
intron_variant | MODIFIER | c.340-296T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67559312 | |||||||
| chr14:67559402 | C | T | 39 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0053 others(36): Show |
44 | HG00544.hp1 HG00735.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.340-206C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 4/28 | chr14 | 67559402 | |||||||
| chr14:67559713 | G | A | 2 | a0003c0040t0001g0051 a0003c0040t0001g0052 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.423+22G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67559713 | |||||||
| chr14:67560316 | C | T | 2 | a0005c0044t0005g0295 a0005c0044t0005g0296 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.423+625C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560316 | |||||||
| chr14:67560384 | T | C | 1 | a0014c0033t0006g0012 | 3 | HG01891.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.423+693T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560384 | |||||||
| chr14:67560407 | G | A | 1 | a0007c0008t0001g0235 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.423+716G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560407 | |||||||
| chr14:67560425 | G | C | 1 | a0002c0004t0001g0316 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.423+734G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560425 | |||||||
| chr14:67560544 | G | A | 3 | a0006c0014t0001g0033 a0006c0014t0001g0274 a0006c0014t0001g0321 |
4 | NA18948.hp2 NA18972.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+853G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560544 | |||||||
| chr14:67560544 | G | C | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+853G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560544 | |||||||
| chr14:67560674 | C | G | 4 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+983C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560674 | |||||||
| chr14:67560727 | C | CT | 94 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(91): Show |
100 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.423+1056dupT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr14 | 67560727 | ||||||
| chr14:67560727 | C | CTT | 6 | a0002c0004t0001g0320 a0002c0025t0005g0223 a0002c0028t0007g0098 others(3): Show |
6 | HG00558.hp1 HG01978.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+1055_423+1056d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr14 | 67560727 | ||||||
| chr14:67560727 | CT | C | 8 | a0001c0002t0002g0138 a0001c0003t0007g0199 a0001c0019t0001g0151 others(5): Show |
8 | HG01074.hp1 HG01256.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.423+1056delT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr14 | 67560727 | ||||||
| chr14:67560727 | CTTT | C | 75 | a0004c0006t0001g0003 a0004c0006t0001g0032 a0004c0006t0001g0034 others(72): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.423+1054_423+1056d others(5): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr14 | 67560727 | ||||||
| chr14:67560728 | T | C | 6 | a0001c0002t0002g0024 a0001c0002t0002g0102 a0001c0003t0002g0100 others(3): Show |
7 | HG00639.hp2 HG01243.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+1037T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560728 | |||||||
| chr14:67560747 | T | G | 4 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+1056T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560747 | |||||||
| chr14:67560762 | C | T | 82 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(79): Show |
86 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.423+1071C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560762 | |||||||
| chr14:67560799 | C | T | 2 | a0003c0040t0001g0051 a0003c0040t0001g0052 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.423+1108C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560799 | |||||||
| chr14:67560805 | T | A | 218 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(215): Show |
239 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.423+1114T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560805 | |||||||
| chr14:67560824 | G | C | 1 | a0031c0082t0001g0306 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.424-1130G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560824 | |||||||
| chr14:67560974 | G | T | 2 | a0002c0047t0012g0045 a0002c0047t0012g0046 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.424-980G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560974 | |||||||
| chr14:67560978 | G | A | 90 | a0001c0002t0001g0117 a0001c0002t0002g0024 a0001c0002t0002g0102 others(87): Show |
110 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.424-976G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67560978 | |||||||
| chr14:67561007 | G | A | 309 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0024 others(306): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.424-947G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561007 | |||||||
| chr14:67561020 | C | G | 2 | a0002c0054t0001g0343 a0010c0058t0002g0344 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.424-934C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561020 | |||||||
| chr14:67561026 | C | T | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.424-928C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561026 | |||||||
| chr14:67561049 | C | T | 1 | a0002c0013t0003g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.424-905C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561049 | |||||||
| chr14:67561087 | G | T | 1 | a0002c0004t0001g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.424-867G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561087 | |||||||
| chr14:67561092 | A | G | 123 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(120): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.424-862A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561092 | |||||||
| chr14:67561156 | T | A | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.424-798T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561156 | |||||||
| chr14:67561177 | C | A | 9 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0011t0001g0262 others(6): Show |
9 | HG00621.hp2 HG00733.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.424-777C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561177 | |||||||
| chr14:67561190 | C | T | 1 | a0002c0013t0003g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.424-764C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561190 | |||||||
| chr14:67561290 | G | A | 4 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0003c0042t0008g0198 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-664G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561290 | |||||||
| chr14:67561408 | G | A | 74 | a0004c0006t0001g0003 a0004c0006t0001g0032 a0004c0006t0001g0034 others(71): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.424-546G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561408 | |||||||
| chr14:67561777 | G | A | 78 | a0004c0006t0001g0003 a0004c0006t0001g0032 a0004c0006t0001g0034 others(75): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.424-177G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561777 | |||||||
| chr14:67561781 | G | T | 2 | a0004c0006t0001g0034 a0004c0006t0001g0299 |
3 | HG00140.hp1 HG00280.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.424-173G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | chr14 | 67561781 | |||||||
| chr14:67561869 | C | CA | 6 | a0002c0004t0001g0317 a0002c0036t0001g0170 a0003c0001t0001g0145 others(3): Show |
8 | HG00140.hp1 HG01358.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-68dupA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr14 | 67561869 | ||||||
| chr14:67561869 | C | CAA | 11 | a0001c0003t0002g0314 a0002c0011t0001g0245 a0002c0011t0001g0246 others(8): Show |
11 | HG00621.hp2 HG00733.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.424-69_424-68dupAA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr14 | 67561869 | ||||||
| chr14:67561869 | CA | C | 6 | a0003c0001t0001g0092 a0003c0001t0001g0143 a0004c0006t0001g0248 others(3): Show |
6 | HG01256.hp1 HG02886.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-68delA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr14 | 67561869 | ||||||
| chr14:67562098 | CG | C | 64 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(61): Show |
67 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.506-36delG | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr14 | 67562098 | ||||||
| chr14:67562910 | C | T | 2 | a0001c0002t0002g0138 a0012c0020t0001g0154 |
2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1263+16C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67562910 | |||||||
| chr14:67562995 | C | T | 2 | a0002c0054t0001g0343 a0010c0058t0002g0344 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1263+101C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67562995 | |||||||
| chr14:67563010 | C | A | 1 | a0012c0020t0003g0318 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1263+116C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563010 | |||||||
| chr14:67563065 | C | T | 1 | a0001c0003t0002g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1263+171C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563065 | |||||||
| chr14:67563066 | G | A | 1 | a0003c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1263+172G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563066 | |||||||
| chr14:67563092 | C | T | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263+198C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563092 | |||||||
| chr14:67563240 | T | C | 1 | a0001c0003t0009g0211 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1263+346T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563240 | |||||||
| chr14:67563434 | T | G | 1 | a0002c0004t0001g0317 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1263+540T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563434 | |||||||
| chr14:67563435 | G | T | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1263+541G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563435 | |||||||
| chr14:67563440 | GT | G | 7 | a0001c0003t0002g0026 a0001c0003t0002g0041 a0001c0003t0002g0124 others(4): Show |
8 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1263+547delT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563440 | |||||||
| chr14:67563441 | T | C | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1263+547T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563441 | |||||||
| chr14:67563614 | G | C | 1 | a0004c0018t0003g0272 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1263+720G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563614 | |||||||
| chr14:67563621 | C | T | 1 | a0011c0059t0001g0353 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1263+727C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563621 | |||||||
| chr14:67563624 | G | C | 1 | a0001c0003t0002g0013 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1263+730G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563624 | |||||||
| chr14:67563731 | CT | C | 263 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0024 others(260): Show |
303 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.1263+856delT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67563731 | ||||||
| chr14:67563731 | CTT | C | 32 | a0001c0002t0002g0212 a0001c0003t0002g0308 a0001c0003t0002g0309 others(29): Show |
33 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1263+855_1263+856d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67563731 | ||||||
| chr14:67563878 | T | C | 1 | a0001c0002t0002g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1263+984T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67563878 | |||||||
| chr14:67563903 | GT | G | 300 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0024 others(297): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1263+1023delT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67563903 | ||||||
| chr14:67564062 | C | T | 3 | a0002c0025t0005g0220 a0002c0025t0005g0221 a0002c0025t0005g0223 |
3 | HG03654.hp2 HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1263+1168C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564062 | |||||||
| chr14:67564137 | G | A | 1 | a0002c0004t0001g0129 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1263+1243G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564137 | |||||||
| chr14:67564288 | C | T | 3 | a0007c0008t0001g0209 a0007c0008t0001g0233 a0007c0035t0001g0206 |
3 | HG01168.hp2 HG01358.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1263+1394C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564288 | |||||||
| chr14:67564289 | G | A | 10 | a0007c0008t0001g0009 a0007c0008t0001g0209 a0007c0008t0001g0224 others(7): Show |
11 | HG01167.hp1 HG01168.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1263+1395G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564289 | |||||||
| chr14:67564329 | C | A | 1 | a0007c0008t0001g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1263+1435C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564329 | |||||||
| chr14:67564335 | A | G | 306 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0024 others(303): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1263+1441A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564335 | |||||||
| chr14:67564397 | G | A | 37 | a0001c0003t0002g0308 a0001c0003t0002g0309 a0001c0003t0002g0310 others(34): Show |
38 | HG00408.hp1 HG00423.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1263+1503G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564397 | |||||||
| chr14:67564554 | C | T | 14 | a0001c0022t0002g0252 a0001c0022t0002g0257 a0001c0022t0002g0301 others(11): Show |
15 | HG01099.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1263+1660C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564554 | |||||||
| chr14:67564574 | C | A | 6 | a0001c0022t0002g0252 a0001c0022t0002g0301 a0001c0022t0002g0303 others(3): Show |
7 | HG01099.hp2 HG02109.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263+1680C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564574 | |||||||
| chr14:67564589 | C | G | 1 | a0005c0005t0002g0339 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1263+1695C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564589 | |||||||
| chr14:67564654 | C | T | 1 | a0001c0019t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1263+1760C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67564654 | |||||||
| chr14:67564675 | AT | A | 9 | a0001c0003t0002g0026 a0001c0003t0002g0041 a0001c0003t0002g0124 others(6): Show |
10 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1263+1791delT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67564675 | ||||||
| chr14:67564709 | CAG | C | 2 | a0014c0033t0006g0012 a0014c0083t0001g0357 |
4 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263+1818_1263+181 others(6): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67564709 | ||||||
| chr14:67565513 | T | G | 1 | a0004c0018t0001g0275 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1263+2619T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67565513 | |||||||
| chr14:67565518 | C | T | 74 | a0004c0006t0001g0003 a0004c0006t0001g0032 a0004c0006t0001g0034 others(71): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1263+2624C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67565518 | |||||||
| chr14:67565599 | G | A | 1 | a0002c0011t0005g0065 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1263+2705G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67565599 | |||||||
| chr14:67565647 | C | G | 92 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(89): Show |
97 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1263+2753C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67565647 | |||||||
| chr14:67565719 | G | C | 1 | a0008c0012t0002g0171 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1263+2825G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67565719 | |||||||
| chr14:67565781 | G | A | 1 | a0010c0058t0002g0344 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1263+2887G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67565781 | |||||||
| chr14:67565842 | G | A | 2 | a0002c0037t0002g0022 a0002c0070t0008g0055 |
3 | HG02622.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1263+2948G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67565842 | |||||||
| chr14:67565990 | C | T | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1263+3096C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67565990 | |||||||
| chr14:67566075 | C | T | 3 | a0003c0001t0001g0014 a0003c0001t0004g0014 a0011c0030t0001g0096 |
3 | HG00639.hp1 HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1264-3063C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566075 | |||||||
| chr14:67566157 | C | T | 92 | a0001c0002t0001g0219 a0001c0002t0002g0030 a0001c0002t0002g0212 others(89): Show |
97 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1264-2981C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566157 | |||||||
| chr14:67566236 | A | G | 1 | a0017c0043t0007g0250 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1264-2902A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566236 | |||||||
| chr14:67566309 | G | A | 10 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0011t0001g0262 others(7): Show |
10 | HG00621.hp2 HG00733.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-2829G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566309 | |||||||
| chr14:67566374 | G | A | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1264-2764G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566374 | |||||||
| chr14:67566466 | C | T | 1 | a0002c0004t0001g0304 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1264-2672C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566466 | |||||||
| chr14:67566564 | GC | G | 74 | a0004c0006t0001g0003 a0004c0006t0001g0032 a0004c0006t0001g0034 others(71): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1264-2573delC | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566564 | |||||||
| chr14:67566590 | A | G | 1 | a0001c0002t0002g0024 | 2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1264-2548A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566590 | |||||||
| chr14:67566613 | T | C | 1 | a0002c0011t0005g0350 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1264-2525T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566613 | |||||||
| chr14:67566618 | C | A | 2 | a0005c0005t0001g0276 a0005c0005t0004g0285 |
2 | HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1264-2520C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566618 | |||||||
| chr14:67566749 | G | GA | 22 | a0001c0002t0002g0138 a0002c0028t0001g0021 a0002c0028t0001g0097 others(19): Show |
23 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1264-2373dupA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67566749 | ||||||
| chr14:67566749 | GA | G | 135 | a0001c0002t0001g0117 a0001c0002t0002g0024 a0001c0002t0002g0102 others(132): Show |
158 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1264-2373delA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67566749 | ||||||
| chr14:67566749 | GAA | G | 80 | a0001c0003t0002g0161 a0001c0010t0006g0159 a0002c0038t0001g0064 others(77): Show |
93 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1264-2374_1264-237 others(6): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67566749 | ||||||
| chr14:67566834 | G | A | 10 | a0002c0011t0001g0245 a0002c0011t0001g0246 a0002c0011t0001g0262 others(7): Show |
10 | HG00621.hp2 HG00733.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-2304G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566834 | |||||||
| chr14:67566846 | C | T | 1 | a0001c0003t0002g0147 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1264-2292C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67566846 | |||||||
| chr14:67567048 | T | C | 1 | a0007c0008t0001g0078 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1264-2090T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567048 | |||||||
| chr14:67567101 | A | G | 1 | a0001c0003t0002g0310 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1264-2037A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567101 | |||||||
| chr14:67567138 | TCGTGTTC | T | 87 | a0001c0003t0002g0026 a0001c0003t0002g0041 a0001c0003t0002g0124 others(84): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1264-1990_1264-198 others(11): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67567138 | ||||||
| chr14:67567146 | C | T | 1 | a0002c0011t0001g0263 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1264-1992C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567146 | |||||||
| chr14:67567278 | A | G | 2 | a0029c0085t0001g0254 a0033c0055t0011g0311 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1264-1860A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567278 | |||||||
| chr14:67567285 | G | A | 1 | a0007c0008t0001g0233 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1264-1853G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567285 | |||||||
| chr14:67567484 | T | C | 2 | a0012c0029t0001g0020 a0012c0029t0014g0149 |
3 | HG01433.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1264-1654T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567484 | |||||||
| chr14:67567525 | T | C | 154 | a0001c0002t0002g0024 a0001c0002t0002g0053 a0001c0002t0002g0084 others(151): Show |
180 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1264-1613T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567525 | |||||||
| chr14:67567549 | A | G | 4 | a0001c0019t0001g0151 a0001c0019t0001g0227 a0001c0019t0001g0238 others(1): Show |
4 | HG02280.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-1589A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567549 | |||||||
| chr14:67567587 | A | C | 89 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(86): Show |
97 | HG00438.hp2 HG00544.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1264-1551A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567587 | |||||||
| chr14:67567639 | T | C | 10 | a0001c0019t0001g0151 a0001c0019t0001g0225 a0001c0019t0001g0227 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-1499T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567639 | |||||||
| chr14:67567715 | A | G | 11 | a0001c0002t0002g0138 a0001c0003t0002g0208 a0001c0019t0001g0151 others(8): Show |
11 | HG01496.hp2 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1264-1423A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567715 | |||||||
| chr14:67567784 | C | T | 4 | a0005c0005t0001g0011 a0005c0005t0001g0265 a0005c0005t0001g0307 others(1): Show |
6 | HG01081.hp1 HG01106.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264-1354C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67567784 | |||||||
| chr14:67567843 | CGTCAGCC others(5): Show |
C | 5 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0002c0047t0012g0045 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-1293_1264-128 others(16): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67567843 | ||||||
| chr14:67568139 | T | C | 15 | a0001c0010t0004g0319 a0002c0004t0001g0037 a0002c0004t0001g0316 others(12): Show |
15 | HG00558.hp1 HG02129.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264-999T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568139 | |||||||
| chr14:67568255 | C | T | 1 | a0002c0070t0008g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1264-883C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568255 | |||||||
| chr14:67568345 | CA | C | 58 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0001c0003t0002g0100 others(55): Show |
70 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1264-791delA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr14 | 67568345 | ||||||
| chr14:67568541 | A | G | 2 | a0018c0046t0001g0213 a0018c0046t0001g0222 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1264-597A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568541 | |||||||
| chr14:67568619 | A | T | 1 | a0002c0004t0001g0317 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1264-519A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568619 | |||||||
| chr14:67568645 | T | A | 1 | a0002c0070t0008g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1264-493T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568645 | |||||||
| chr14:67568650 | A | C | 1 | a0013c0016t0001g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1264-488A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568650 | |||||||
| chr14:67568704 | G | C | 133 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0004 others(130): Show |
154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1264-434G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568704 | |||||||
| chr14:67568722 | C | T | 125 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0004 others(122): Show |
146 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1264-416C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568722 | |||||||
| chr14:67568762 | A | G | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1264-376A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568762 | |||||||
| chr14:67568765 | G | T | 19 | a0002c0004t0001g0017 a0002c0011t0001g0185 a0002c0011t0001g0246 others(16): Show |
20 | HG00621.hp2 HG00733.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.1264-373G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568765 | |||||||
| chr14:67568775 | C | T | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1264-363C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568775 | |||||||
| chr14:67568871 | G | A | 7 | a0001c0003t0007g0199 a0001c0069t0008g0200 a0002c0028t0001g0021 others(4): Show |
7 | HG02451.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1264-267G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568871 | |||||||
| chr14:67568871 | G | C | 1 | a0002c0004t0004g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1264-267G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568871 | |||||||
| chr14:67568891 | G | A | 12 | a0001c0010t0004g0319 a0002c0004t0001g0037 a0002c0004t0001g0316 others(9): Show |
12 | HG00558.hp1 HG02129.hp2 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.1264-247G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568891 | |||||||
| chr14:67568928 | A | G | 2 | a0017c0043t0007g0249 a0017c0043t0007g0250 |
2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1264-210A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67568928 | |||||||
| chr14:67569093 | G | A | 10 | a0001c0019t0001g0137 a0012c0020t0001g0095 a0012c0020t0001g0154 others(7): Show |
11 | HG01109.hp2 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1264-45G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 7/28 | chr14 | 67569093 | |||||||
| chr14:67569257 | G | A | 5 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0017c0043t0007g0249 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1342+41G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569257 | |||||||
| chr14:67569373 | G | GTCCCACC others(97): Show |
11 | a0002c0011t0001g0262 a0002c0011t0001g0263 a0002c0011t0005g0133 others(8): Show |
11 | HG00733.hp2 HG01167.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1342+166_1342+269d others(106): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr14 | 67569373 | ||||||
| chr14:67569399 | C | T | 2 | a0001c0068t0002g0056 a0002c0054t0001g0343 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1342+183C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569399 | |||||||
| chr14:67569476 | C | A | 9 | a0002c0004t0001g0017 a0002c0011t0001g0141 a0002c0011t0001g0185 others(6): Show |
10 | HG02015.hp2 HG02040.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1342+260C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569476 | |||||||
| chr14:67569497 | G | C | 185 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(182): Show |
211 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1342+281G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569497 | |||||||
| chr14:67569536 | A | G | 1 | a0019c0073t0001g0059 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1342+320A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569536 | |||||||
| chr14:67569678 | T | G | 3 | a0003c0001t0001g0014 a0003c0001t0004g0014 a0011c0030t0001g0096 |
3 | HG00639.hp1 HG00738.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1343-243T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569678 | |||||||
| chr14:67569728 | T | C | 99 | a0001c0010t0004g0319 a0001c0022t0002g0257 a0002c0004t0001g0007 others(96): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1343-193T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569728 | |||||||
| chr14:67569734 | A | G | 10 | a0001c0019t0001g0137 a0012c0020t0001g0095 a0012c0020t0001g0154 others(7): Show |
11 | HG01109.hp2 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1343-187A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569734 | |||||||
| chr14:67569747 | C | G | 106 | a0001c0002t0002g0024 a0001c0002t0002g0102 a0001c0002t0002g0138 others(103): Show |
123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1343-174C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569747 | |||||||
| chr14:67569872 | T | C | 3 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0027c0057t0001g0021 |
3 | HG02451.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1343-49T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 8/28 | chr14 | 67569872 | |||||||
| chr14:67570036 | G | A | 10 | a0001c0019t0001g0137 a0012c0020t0001g0095 a0012c0020t0001g0154 others(7): Show |
11 | HG01109.hp2 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1434+24G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570036 | |||||||
| chr14:67570136 | G | C | 116 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(113): Show |
129 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1434+124G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570136 | |||||||
| chr14:67570146 | C | T | 2 | a0001c0002t0002g0086 a0036c0064t0001g0074 |
2 | NA18954.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1434+134C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570146 | |||||||
| chr14:67570309 | G | A | 2 | a0005c0005t0001g0011 a0022c0048t0001g0184 |
4 | HG01081.hp1 HG01106.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1434+297G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570309 | |||||||
| chr14:67570475 | T | C | 3 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0027c0057t0001g0021 |
3 | HG02451.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1434+463T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570475 | |||||||
| chr14:67570496 | G | C | 3 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0027c0057t0001g0021 |
3 | HG02451.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1434+484G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570496 | |||||||
| chr14:67570648 | A | C | 4 | a0005c0005t0001g0011 a0005c0005t0001g0307 a0005c0005t0001g0312 others(1): Show |
6 | HG01081.hp1 HG01106.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1434+636A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570648 | |||||||
| chr14:67570773 | G | T | 1 | a0014c0083t0001g0357 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1434+761G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570773 | |||||||
| chr14:67570778 | C | G | 3 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0027c0057t0001g0021 |
3 | HG02451.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1434+766C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570778 | |||||||
| chr14:67570826 | C | T | 1 | a0014c0083t0001g0357 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1434+814C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67570826 | |||||||
| chr14:67571046 | C | T | 5 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0017c0043t0007g0249 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435-706C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571046 | |||||||
| chr14:67571069 | C | G | 7 | a0007c0035t0002g0239 a0010c0072t0001g0066 a0016c0024t0003g0044 others(4): Show |
7 | HG00639.hp2 HG01243.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1435-683C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571069 | |||||||
| chr14:67571178 | G | T | 110 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(107): Show |
124 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1435-574G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571178 | |||||||
| chr14:67571244 | A | G | 1 | a0004c0018t0003g0251 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1435-508A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571244 | |||||||
| chr14:67571387 | A | G | 1 | a0001c0010t0001g0142 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1435-365A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571387 | |||||||
| chr14:67571414 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1435-338C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571414 | |||||||
| chr14:67571482 | G | A | 1 | a0015c0021t0003g0356 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1435-270G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571482 | |||||||
| chr14:67571513 | A | T | 4 | a0001c0003t0002g0048 a0001c0003t0002g0049 a0002c0047t0012g0045 others(1): Show |
4 | HG01081.hp2 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1435-239A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571513 | |||||||
| chr14:67571603 | A | G | 3 | a0001c0003t0007g0199 a0017c0043t0007g0249 a0017c0043t0007g0250 |
3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1435-149A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571603 | |||||||
| chr14:67571709 | T | C | 1 | a0002c0013t0001g0244 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1435-43T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571709 | |||||||
| chr14:67571736 | G | C | 2 | a0001c0010t0006g0159 a0014c0033t0006g0012 |
4 | HG01884.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1435-16G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 9/28 | chr14 | 67571736 | |||||||
| chr14:67571980 | C | G | 228 | a0001c0002t0002g0138 a0001c0003t0002g0026 a0001c0003t0002g0041 others(225): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1585+78C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 10/28 | chr14 | 67571980 | |||||||
| chr14:67572012 | A | G | 259 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(256): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1585+110A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 10/28 | chr14 | 67572012 | |||||||
| chr14:67572062 | T | G | 220 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(217): Show |
248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1586-73T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 10/28 | chr14 | 67572062 | |||||||
| chr14:67572291 | C | T | 10 | a0001c0002t0002g0005 a0001c0002t0002g0054 a0001c0002t0002g0090 others(7): Show |
12 | HG00735.hp2 HG01255.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.1728+14C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572291 | |||||||
| chr14:67572310 | A | G | 173 | a0001c0003t0002g0026 a0001c0003t0002g0041 a0001c0003t0002g0124 others(170): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1728+33A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572310 | |||||||
| chr14:67572318 | G | GT | 22 | a0002c0011t0005g0065 a0002c0011t0005g0133 a0002c0011t0005g0355 others(19): Show |
25 | HG00609.hp2 HG02080.hp2 HG02602.hp1 others(22): Show |
intron_variant | MODIFIER | c.1728+41_1728+42ins others(1): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572318 | |||||||
| chr14:67572380 | T | G | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1728+103T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572380 | |||||||
| chr14:67572381 | C | T | 1 | a0001c0003t0002g0139 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1728+104C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572381 | |||||||
| chr14:67572524 | A | G | 13 | a0002c0028t0007g0098 a0002c0070t0008g0055 a0007c0035t0002g0239 others(10): Show |
13 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1728+247A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572524 | |||||||
| chr14:67572609 | T | C | 1 | a0002c0054t0001g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1728+332T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572609 | |||||||
| chr14:67572617 | T | TAGAG | 82 | a0002c0004t0001g0007 a0002c0004t0001g0017 a0002c0004t0001g0018 others(79): Show |
93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1728+340_1728+341i others(6): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572617 | |||||||
| chr14:67572653 | C | G | 41 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(38): Show |
44 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.1728+376C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572653 | |||||||
| chr14:67572684 | T | C | 3 | a0001c0003t0007g0199 a0017c0043t0007g0249 a0017c0043t0007g0250 |
3 | HG02886.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1728+407T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572684 | |||||||
| chr14:67572805 | T | C | 21 | a0002c0004t0003g0128 a0002c0004t0003g0173 a0002c0004t0003g0189 others(18): Show |
21 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1729-471T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572805 | |||||||
| chr14:67572998 | C | G | 1 | a0001c0022t0002g0257 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1729-278C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67572998 | |||||||
| chr14:67573043 | T | G | 30 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(27): Show |
33 | HG00609.hp2 HG02015.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.1729-233T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67573043 | |||||||
| chr14:67573181 | C | G | 11 | a0002c0011t0001g0262 a0002c0011t0001g0263 a0002c0011t0005g0065 others(8): Show |
11 | HG00733.hp2 HG01167.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729-95C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67573181 | |||||||
| chr14:67573253 | A | G | 1 | a0001c0019t0001g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1729-23A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 11/28 | chr14 | 67573253 | |||||||
| chr14:67573430 | A | C | 1 | a0001c0019t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1839+44A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 12/28 | chr14 | 67573430 | |||||||
| chr14:67573464 | A | G | 1 | a0012c0020t0001g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1839+78A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 12/28 | chr14 | 67573464 | |||||||
| chr14:67573476 | G | T | 79 | a0002c0004t0003g0128 a0002c0004t0003g0173 a0002c0004t0003g0189 others(76): Show |
82 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1839+90G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 12/28 | chr14 | 67573476 | |||||||
| chr14:67573478 | C | T | 1 | a0002c0004t0001g0304 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1839+92C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 12/28 | chr14 | 67573478 | |||||||
| chr14:67573672 | T | C | 24 | a0001c0010t0001g0063 a0001c0010t0001g0082 a0001c0010t0004g0319 others(21): Show |
26 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1840-129T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 12/28 | chr14 | 67573672 | |||||||
| chr14:67573717 | C | T | 3 | a0001c0069t0008g0200 a0003c0042t0008g0198 a0003c0042t0008g0201 |
3 | HG01074.hp1 HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1840-84C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 12/28 | chr14 | 67573717 | |||||||
| chr14:67573741 | T | C | 30 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(27): Show |
33 | HG00609.hp2 HG02015.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.1840-60T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 12/28 | chr14 | 67573741 | |||||||
| chr14:67573933 | G | A | 7 | a0001c0019t0001g0151 a0001c0019t0001g0225 a0001c0019t0001g0227 others(4): Show |
7 | HG02258.hp2 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1926+46G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67573933 | |||||||
| chr14:67573964 | A | G | 42 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(39): Show |
45 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1926+77A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67573964 | |||||||
| chr14:67573978 | G | A | 1 | a0002c0036t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1926+91G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67573978 | |||||||
| chr14:67573997 | G | A | 1 | a0010c0026t0002g0113 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1926+110G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67573997 | |||||||
| chr14:67574104 | G | A | 2 | a0001c0019t0001g0137 a0012c0020t0001g0095 |
2 | HG01109.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1927-138G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67574104 | |||||||
| chr14:67574121 | G | A | 21 | a0002c0004t0003g0128 a0002c0004t0003g0173 a0002c0004t0003g0189 others(18): Show |
21 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1927-121G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67574121 | |||||||
| chr14:67574174 | C | T | 1 | a0002c0054t0001g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1927-68C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67574174 | |||||||
| chr14:67574208 | G | A | 78 | a0002c0004t0003g0128 a0002c0004t0003g0173 a0002c0004t0003g0189 others(75): Show |
81 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1927-34G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67574208 | |||||||
| chr14:67574220 | C | T | 1 | a0002c0036t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1927-22C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 13/28 | chr14 | 67574220 | |||||||
| chr14:67574407 | G | C | 204 | a0001c0003t0007g0199 a0001c0010t0006g0123 a0001c0010t0006g0159 others(201): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
splice_region_variant&intron_variant | LOW | c.2088+4G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67574407 | |||||||
| chr14:67574592 | G | A | 1 | a0011c0059t0001g0353 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2088+189G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67574592 | |||||||
| chr14:67574737 | G | C | 1 | a0004c0007t0001g0335 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2088+334G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67574737 | |||||||
| chr14:67574775 | C | A | 2 | a0003c0040t0001g0051 a0003c0040t0001g0052 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2088+372C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67574775 | |||||||
| chr14:67574852 | A | C | 30 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(27): Show |
33 | HG00609.hp2 HG02015.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.2088+449A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67574852 | |||||||
| chr14:67574933 | G | C | 21 | a0002c0004t0003g0128 a0002c0004t0003g0173 a0002c0004t0003g0189 others(18): Show |
21 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.2089-459G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67574933 | |||||||
| chr14:67575007 | C | A | 1 | a0011c0059t0001g0353 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2089-385C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67575007 | |||||||
| chr14:67575198 | T | C | 62 | a0001c0010t0001g0036 a0001c0010t0001g0063 a0001c0010t0001g0082 others(59): Show |
76 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2089-194T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67575198 | |||||||
| chr14:67575214 | A | G | 265 | a0001c0010t0001g0036 a0001c0010t0001g0063 a0001c0010t0001g0082 others(262): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.2089-178A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67575214 | |||||||
| chr14:67575348 | G | A | 2 | a0001c0034t0002g0035 a0001c0068t0002g0056 |
3 | HG06807.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2089-44G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 14/28 | chr14 | 67575348 | |||||||
| chr14:67575538 | A | G | 136 | a0001c0010t0001g0036 a0001c0010t0001g0063 a0001c0010t0001g0082 others(133): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.2169+66A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 15/28 | chr14 | 67575538 | |||||||
| chr14:67575778 | C | T | 1 | a0007c0008t0001g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2170-45C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 15/28 | chr14 | 67575778 | |||||||
| chr14:67575779 | A | G | 267 | a0001c0003t0007g0199 a0001c0010t0001g0036 a0001c0010t0001g0063 others(264): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.2170-44A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 15/28 | chr14 | 67575779 | |||||||
| chr14:67576755 | A | G | 4 | a0002c0036t0001g0170 a0002c0036t0002g0210 a0002c0047t0012g0045 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461+252A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 17/28 | chr14 | 67576755 | |||||||
| chr14:67576768 | G | C | 1 | a0011c0059t0001g0353 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2461+265G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 17/28 | chr14 | 67576768 | |||||||
| chr14:67576839 | A | T | 4 | a0002c0036t0001g0170 a0002c0036t0002g0210 a0002c0047t0012g0045 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461+336A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 17/28 | chr14 | 67576839 | |||||||
| chr14:67577193 | C | T | 1 | a0002c0036t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2462-109C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 17/28 | chr14 | 67577193 | |||||||
| chr14:67577288 | C | T | 329 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(326): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.2462-14C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 17/28 | chr14 | 67577288 | |||||||
| chr14:67577472 | A | G | 1 | a0001c0003t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2574+58A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 18/28 | chr14 | 67577472 | |||||||
| chr14:67577485 | T | C | 5 | a0001c0019t0001g0151 a0001c0019t0001g0225 a0001c0019t0001g0227 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2574+71T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 18/28 | chr14 | 67577485 | |||||||
| chr14:67577603 | G | A | 2 | a0002c0036t0001g0170 a0002c0036t0002g0210 |
2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2574+189G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 18/28 | chr14 | 67577603 | |||||||
| chr14:67577769 | T | C | 1 | a0013c0016t0001g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2575-254T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 18/28 | chr14 | 67577769 | |||||||
| chr14:67577771 | G | GT | 11 | a0002c0011t0001g0262 a0002c0011t0001g0263 a0002c0011t0005g0065 others(8): Show |
11 | HG00733.hp2 HG01167.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.2575-244dupT | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr14 | 67577771 | ||||||
| chr14:67578291 | G | A | 6 | a0001c0019t0001g0137 a0012c0020t0001g0095 a0012c0020t0003g0318 others(3): Show |
7 | HG01109.hp2 HG01433.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2751+92G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 19/28 | chr14 | 67578291 | |||||||
| chr14:67578407 | A | G | 10 | a0001c0019t0001g0137 a0012c0020t0001g0095 a0012c0020t0001g0154 others(7): Show |
11 | HG01109.hp2 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2752-127A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 19/28 | chr14 | 67578407 | |||||||
| chr14:67578506 | C | T | 1 | a0002c0004t0003g0189 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2752-28C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 19/28 | chr14 | 67578506 | |||||||
| chr14:67578507 | A | C | 1 | a0002c0004t0003g0189 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2752-27A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 19/28 | chr14 | 67578507 | |||||||
| chr14:67578508 | C | A | 1 | a0002c0004t0003g0189 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2752-26C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 19/28 | chr14 | 67578508 | |||||||
| chr14:67579036 | T | C | 73 | a0001c0010t0001g0036 a0001c0010t0001g0063 a0001c0010t0001g0082 others(70): Show |
89 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2850-98T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 20/28 | chr14 | 67579036 | |||||||
| chr14:67579060 | TAGATAGG others(16): Show |
T | 1 | a0002c0004t0003g0189 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2850-73_2850-51del others(23): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 20/28 | chr14 | 67579060 | |||||||
| chr14:67579123 | C | CTTCT | 264 | a0001c0010t0001g0036 a0001c0010t0001g0063 a0001c0010t0001g0082 others(261): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.2850-11_2850-10ins others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 20/28 | chr14 | 67579123 | |||||||
| chr14:67579336 | C | T | 29 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(26): Show |
32 | HG00609.hp2 HG02015.hp2 HG02080.hp2 others(29): Show |
intron_variant | MODIFIER | c.3027+25C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 21/28 | chr14 | 67579336 | |||||||
| chr14:67579337 | C | T | 1 | a0009c0009t0001g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3027+26C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 21/28 | chr14 | 67579337 | |||||||
| chr14:67579502 | G | A | 1 | a0002c0028t0007g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3027+191G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 21/28 | chr14 | 67579502 | |||||||
| chr14:67579558 | C | T | 62 | a0001c0010t0001g0036 a0001c0010t0001g0063 a0001c0010t0001g0082 others(59): Show |
76 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.3028-163C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 21/28 | chr14 | 67579558 | |||||||
| chr14:67579885 | C | T | 61 | a0002c0004t0001g0007 a0002c0004t0001g0017 a0002c0004t0001g0018 others(58): Show |
72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.3183+9C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67579885 | |||||||
| chr14:67580022 | C | T | 10 | a0001c0019t0001g0137 a0012c0020t0001g0095 a0012c0020t0001g0154 others(7): Show |
11 | HG01109.hp2 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3183+146C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580022 | |||||||
| chr14:67580125 | G | A | 2 | a0004c0006t0001g0040 a0004c0006t0004g0282 |
3 | NA19067.hp2 NA19068.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.3183+249G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580125 | |||||||
| chr14:67580193 | C | T | 1 | a0005c0005t0001g0336 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3183+317C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580193 | |||||||
| chr14:67580196 | G | A | 4 | a0003c0001t0001g0015 a0003c0001t0001g0060 a0003c0001t0004g0042 others(1): Show |
5 | HG00140.hp2 HG01071.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.3183+320G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580196 | |||||||
| chr14:67580198 | C | G | 3 | a0009c0009t0001g0180 a0009c0009t0001g0181 a0009c0009t0001g0182 |
3 | NA18959.hp1 NA18992.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.3183+322C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580198 | |||||||
| chr14:67580399 | T | C | 1 | a0013c0016t0001g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3183+523T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580399 | |||||||
| chr14:67580426 | A | G | 45 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(42): Show |
48 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.3184-512A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580426 | |||||||
| chr14:67580642 | C | G | 1 | a0007c0008t0001g0093 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3184-296C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580642 | |||||||
| chr14:67580822 | G | A | 9 | a0001c0019t0001g0137 a0012c0020t0001g0154 a0012c0020t0001g0228 others(6): Show |
10 | HG01109.hp2 HG01433.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.3184-116G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580822 | |||||||
| chr14:67580916 | T | C | 1 | a0004c0007t0001g0335 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3184-22T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 22/28 | chr14 | 67580916 | |||||||
| chr14:67581065 | C | T | 1 | a0003c0001t0004g0104 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3284+27C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581065 | |||||||
| chr14:67581151 | T | A | 3 | a0001c0069t0008g0200 a0003c0042t0008g0198 a0003c0042t0008g0201 |
3 | HG01074.hp1 HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3284+113T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581151 | |||||||
| chr14:67581197 | G | A | 1 | a0010c0026t0001g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3284+159G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581197 | |||||||
| chr14:67581249 | A | G | 2 | a0001c0003t0002g0308 a0001c0003t0002g0310 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3284+211A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581249 | |||||||
| chr14:67581256 | G | A | 37 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(34): Show |
45 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.3284+218G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581256 | |||||||
| chr14:67581274 | G | GCA | 116 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(113): Show |
137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.3284+261_3284+262d others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr14 | 67581274 | ||||||
| chr14:67581274 | G | GCACA | 4 | a0001c0002t0002g0091 a0001c0003t0002g0314 a0004c0018t0001g0283 others(1): Show |
4 | HG02165.hp2 HG02647.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.3284+259_3284+262d others(6): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr14 | 67581274 | ||||||
| chr14:67581274 | GCACA | G | 47 | a0001c0003t0007g0199 a0002c0011t0001g0141 a0002c0011t0001g0185 others(44): Show |
50 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.3284+259_3284+262d others(6): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr14 | 67581274 | ||||||
| chr14:67581274 | GCACACAC others(3): Show |
G | 1 | a0002c0004t0001g0316 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3284+253_3284+262d others(12): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr14 | 67581274 | ||||||
| chr14:67581430 | G | T | 8 | a0001c0019t0001g0151 a0001c0019t0001g0225 a0001c0019t0001g0227 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3284+392G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581430 | |||||||
| chr14:67581461 | G | A | 2 | a0005c0005t0001g0259 a0005c0005t0001g0327 |
2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.3284+423G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581461 | |||||||
| chr14:67581692 | A | G | 1 | a0011c0059t0001g0353 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3285-377A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581692 | |||||||
| chr14:67581839 | G | T | 1 | a0002c0056t0001g0302 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3285-230G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581839 | |||||||
| chr14:67581961 | G | A | 2 | a0004c0006t0001g0034 a0004c0006t0001g0299 |
3 | HG00140.hp1 HG00280.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.3285-108G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67581961 | |||||||
| chr14:67582042 | C | T | 11 | a0002c0011t0001g0262 a0002c0011t0001g0263 a0002c0011t0005g0065 others(8): Show |
11 | HG00733.hp2 HG01167.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.3285-27C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67582042 | |||||||
| chr14:67582047 | T | C | 41 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(38): Show |
44 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.3285-22T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 23/28 | chr14 | 67582047 | |||||||
| chr14:67582386 | G | A | 1 | a0001c0003t0002g0236 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3426+176G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67582386 | |||||||
| chr14:67582400 | C | T | 51 | a0002c0013t0001g0110 a0002c0036t0002g0210 a0005c0005t0001g0011 others(48): Show |
54 | HG00423.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.3426+190C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67582400 | |||||||
| chr14:67582401 | G | A | 41 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(38): Show |
44 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.3426+191G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67582401 | |||||||
| chr14:67582477 | A | AGG | 41 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(38): Show |
44 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.3426+268_3426+269i others(4): Show |
PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr14 | 67582477 | ||||||
| chr14:67582516 | A | G | 3 | a0001c0002t0002g0138 a0001c0034t0002g0035 a0001c0068t0002g0056 |
4 | HG02970.hp2 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3426+306A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67582516 | |||||||
| chr14:67582579 | G | C | 93 | a0001c0002t0001g0117 a0002c0004t0001g0007 a0002c0004t0001g0017 others(90): Show |
104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.3426+369G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67582579 | |||||||
| chr14:67582652 | GA | G | 330 | a0001c0002t0001g0117 a0001c0002t0001g0219 a0001c0002t0002g0004 others(327): Show |
375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.3426+450delA | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr14 | 67582652 | ||||||
| chr14:67582815 | C | T | 1 | a0009c0049t0003g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3426+605C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67582815 | |||||||
| chr14:67583201 | A | C | 3 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0027c0057t0001g0021 |
3 | HG02451.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3427-540A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67583201 | |||||||
| chr14:67583436 | G | C | 1 | a0010c0026t0002g0113 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3427-305G>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67583436 | |||||||
| chr14:67583622 | A | T | 41 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(38): Show |
44 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.3427-119A>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 24/28 | chr14 | 67583622 | |||||||
| chr14:67583970 | A | G | 41 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(38): Show |
44 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.3570-25A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 25/28 | chr14 | 67583970 | |||||||
| chr14:67584370 | G | A | 60 | a0001c0002t0001g0117 a0002c0004t0001g0007 a0002c0004t0001g0017 others(57): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.3699+246G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67584370 | |||||||
| chr14:67584378 | C | G | 1 | a0004c0018t0001g0275 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3699+254C>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67584378 | |||||||
| chr14:67584861 | T | C | 1 | a0002c0036t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3700-707T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67584861 | |||||||
| chr14:67584882 | T | G | 1 | a0002c0011t0005g0355 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3700-686T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67584882 | |||||||
| chr14:67584887 | T | C | 9 | a0001c0002t0002g0138 a0001c0003t0002g0026 a0001c0003t0002g0041 others(6): Show |
11 | HG02109.hp2 HG02572.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3700-681T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67584887 | |||||||
| chr14:67584904 | G | A | 1 | a0001c0023t0002g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3700-664G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67584904 | |||||||
| chr14:67584918 | G | T | 1 | a0004c0007t0001g0268 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3700-650G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67584918 | |||||||
| chr14:67585160 | C | T | 2 | a0002c0004t0001g0129 a0002c0013t0001g0156 |
2 | HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.3700-408C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67585160 | |||||||
| chr14:67585166 | G | T | 55 | a0001c0010t0001g0036 a0001c0010t0001g0063 a0001c0010t0001g0082 others(52): Show |
69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.3700-402G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67585166 | |||||||
| chr14:67585167 | G | T | 55 | a0001c0010t0001g0036 a0001c0010t0001g0063 a0001c0010t0001g0082 others(52): Show |
69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.3700-401G>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67585167 | |||||||
| chr14:67585260 | T | G | 41 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(38): Show |
44 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.3700-308T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 26/28 | chr14 | 67585260 | |||||||
| chr14:67585684 | C | T | 1 | a0002c0054t0001g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3786+30C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 27/28 | chr14 | 67585684 | |||||||
| chr14:67585701 | A | G | 9 | a0001c0019t0001g0151 a0001c0019t0001g0225 a0001c0019t0001g0227 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3786+47A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 27/28 | chr14 | 67585701 | |||||||
| chr14:67585766 | C | A | 1 | a0001c0002t0002g0090 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3786+112C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 27/28 | chr14 | 67585766 | |||||||
| chr14:67586266 | G | A | 41 | a0002c0011t0001g0141 a0002c0011t0001g0185 a0002c0011t0001g0245 others(38): Show |
44 | HG00609.hp2 HG00733.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.3933+169G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586266 | |||||||
| chr14:67586307 | G | A | 3 | a0002c0028t0001g0021 a0002c0028t0001g0097 a0027c0057t0001g0021 |
3 | HG02451.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3933+210G>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586307 | |||||||
| chr14:67586402 | C | T | 1 | a0015c0021t0004g0333 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3933+305C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586402 | |||||||
| chr14:67586407 | T | A | 25 | a0002c0004t0003g0128 a0002c0004t0003g0173 a0002c0004t0003g0189 others(22): Show |
25 | HG00280.hp1 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.3933+310T>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586407 | |||||||
| chr14:67586430 | T | G | 1 | a0003c0041t0002g0083 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3933+333T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586430 | |||||||
| chr14:67586432 | A | G | 147 | a0001c0002t0001g0117 a0001c0010t0001g0142 a0001c0010t0006g0123 others(144): Show |
163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.3933+335A>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586432 | |||||||
| chr14:67586542 | T | G | 60 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(57): Show |
71 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.3933+445T>G | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586542 | |||||||
| chr14:67586624 | T | C | 4 | a0001c0019t0001g0151 a0001c0019t0001g0225 a0001c0019t0001g0227 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3934-450T>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586624 | |||||||
| chr14:67586629 | A | C | 9 | a0001c0019t0001g0151 a0001c0019t0001g0225 a0001c0019t0001g0227 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3934-445A>C | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586629 | |||||||
| chr14:67586722 | C | T | 61 | a0001c0002t0001g0219 a0001c0002t0002g0004 a0001c0002t0002g0005 others(58): Show |
72 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.3934-352C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586722 | |||||||
| chr14:67586855 | C | T | 1 | a0001c0003t0007g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3934-219C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586855 | |||||||
| chr14:67586896 | C | T | 11 | a0002c0036t0001g0170 a0002c0036t0002g0210 a0002c0037t0002g0022 others(8): Show |
12 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.3934-178C>T | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67586896 | |||||||
| chr14:67587066 | C | A | 1 | a0010c0026t0002g0231 | 1 | HG02896.hp1 | splice_region_variant&intron_variant | LOW | c.3934-8C>A | PLEKHH1 | ENSG00000054690.14 | transcript | ENST00000329153.10 | protein_coding | 28/28 | chr14 | 67587066 |