Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 150468 |
| ensemblid | ENSG00000169607.13 |
| hgncid | 26877 |
| symbol | CKAP2L |
| name | cytoskeleton associated protein 2 like |
| refseq_nuc | NM_152515.5 |
| refseq_prot | NP_689728.3 |
| ensembl_nuc | ENST00000302450.11 |
| ensembl_prot | ENSP00000305204.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 112736349 |
| end | 112764609 |
| strand | - |
| ver | v1.2 |
| region | chr2:112736349-112764609 |
| region5000 | chr2:112731349-112769609 |
| regionname0 | CKAP2L_chr2_112736349_112764609 |
| regionname5000 | CKAP2L_chr2_112731349_112769609 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 745 | 159 | 56 | 33 | 51 | 7 | 12 | 41 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0002 | 0/0 | 745 | 89 | 6 | 20 | 52 | 2 | 9 | 40 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0003 | 0/0 | 745 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0004 | 0/0 | 745 | 7 | 2 | 5 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0005 | 0/0 | 745 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0006 | 0/1 | 745 | 4 | 1 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0007 | 0/0 | 745 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0008 | 0/0 | 745 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0009 | 0/0 | 745 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0010 | 0/0 | 745 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0011 | 0/0 | 745 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0012 | 1/0 | 745 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0013 | 0/0 | 745 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0014 | 0/0 | 745 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0015 | 0/0 | 745 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0016 | 0/0 | 745 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| a0017 | 0/0 | 745 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | MVGPG others(740): Show |
chr2 | 112731349 | 112769609 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2235 | 144 | 43 | 33 | 50 | 7 | 11 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0001c0004 | 0/0 | 2235 | 8 | 8 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0001c0010 | 0/0 | 2235 | 3 | 3 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0001c0013 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0001c0017 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0001c0019 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0002c0002 | 0/0 | 2235 | 89 | 6 | 20 | 52 | 2 | 9 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0003c0003 | 0/0 | 2235 | 14 | 14 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0003c0011 | 0/0 | 2235 | 3 | 3 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0004c0005 | 0/0 | 2235 | 6 | 2 | 4 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0004c0024 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0005c0006 | 0/0 | 2235 | 5 | 5 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0006c0008 | 0/1 | 2235 | 4 | 1 | 2 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0007c0007 | 0/0 | 2235 | 4 | 4 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0008c0009 | 0/0 | 2235 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0009c0014 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0010c0012 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0011c0015 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0012c0018 | 1/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0013c0016 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0014c0023 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0015c0021 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0016c0022 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 | ||
| a0017c0020 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ATGGT others(2230): Show |
chr2 | 112731349 | 112769609 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4723 | 123 | 28 | 28 | 49 | 7 | 11 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0003 | 0/0 | 4723 | 5 | 5 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0008 | 0/0 | 4723 | 4 | 3 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0013 | 0/0 | 4723 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0014 | 0/0 | 4723 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0017 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0018 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0019 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0022 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0023 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0024 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0025 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0001t0026 | 0/0 | 4723 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0004t0006 | 0/0 | 4720 | 7 | 7 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4715): Show |
chr2 | 112731349 | 112769609 |
| a0001c0004t0016 | 0/0 | 4720 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4715): Show |
chr2 | 112731349 | 112769609 |
| a0001c0010t0011 | 0/0 | 4723 | 3 | 3 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0013t0012 | 0/0 | 4720 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4715): Show |
chr2 | 112731349 | 112769609 |
| a0001c0017t0001 | 0/0 | 4723 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0001c0019t0001 | 0/0 | 4723 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0002c0002t0002 | 0/0 | 4723 | 82 | 6 | 20 | 45 | 2 | 9 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0002c0002t0007 | 0/0 | 4719 | 6 | 0 | 0 | 6 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4714): Show |
chr2 | 112731349 | 112769609 |
| a0002c0002t0021 | 0/0 | 4723 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0003c0003t0003 | 0/0 | 4723 | 9 | 9 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0003c0003t0009 | 0/0 | 4723 | 4 | 4 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0003c0003t0020 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0003c0011t0010 | 0/0 | 4716 | 3 | 3 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4711): Show |
chr2 | 112731349 | 112769609 |
| a0004c0005t0004 | 0/0 | 4723 | 6 | 2 | 4 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0004c0024t0004 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0005c0006t0005 | 0/0 | 4723 | 5 | 5 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0006c0008t0002 | 0/1 | 4723 | 4 | 1 | 2 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0007c0007t0001 | 0/0 | 4723 | 4 | 4 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0008c0009t0002 | 0/0 | 4723 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0009c0014t0004 | 0/0 | 4723 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0010c0012t0005 | 0/0 | 4723 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0011c0015t0015 | 0/0 | 4723 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0012c0018t0004 | 1/0 | 4723 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0013c0016t0002 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0014c0023t0002 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0015c0021t0002 | 0/0 | 4723 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0016c0022t0001 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| a0017c0020t0002 | 0/0 | 4723 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | ACTGA others(4718): Show |
chr2 | 112731349 | 112769609 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 21 | 0 | 2 | 17 | 2 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 8 | 4 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0008g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0013g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0014g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0017g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0018g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0019g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0022g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0023g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0024g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0025g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0001t0026g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0004t0006g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0004t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0004t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0004t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0004t0016g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0010t0011g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0010t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0013t0012g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0017t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0001c0019t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0001 | 0/0 | 29 | 0 | 8 | 16 | 2 | 3 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0007g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0002c0002t0021g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0003g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0003t0020g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0003c0011t0010g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0004c0005t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0004c0005t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0004c0005t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0004c0005t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0004c0005t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0004c0024t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0005c0006t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0005c0006t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0005c0006t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0006c0008t0002g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0006c0008t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0006c0008t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0006c0008t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0007c0007t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0007c0007t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0008c0009t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0008c0009t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0009c0014t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0009c0014t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0010c0012t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0010c0012t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0011c0015t0015g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0011c0015t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0012c0018t0004g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0013c0016t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0014c0023t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0015c0021t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0016c0022t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| a0017c0020t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | GBR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00558 | hp2 | a0001 | c0017 | t0001 | g0058 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00639 | hp1 | a0001 | c0001 | t0024 | g0045 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00639 | hp2 | a0001 | c0001 | t0014 | g0030 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00733 | hp2 | a0001 | c0001 | t0022 | g0070 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01069 | hp1 | a0004 | c0005 | t0004 | g0018 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01071 | hp2 | a0004 | c0005 | t0004 | g0018 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0152 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01106 | hp1 | a0013 | c0016 | t0002 | g0174 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0165 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01243 | hp1 | a0004 | c0024 | t0004 | g0092 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01257 | hp2 | a0001 | c0001 | t0023 | g0073 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01258 | hp2 | a0006 | c0008 | t0002 | g0180 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01261 | hp2 | a0006 | c0008 | t0002 | g0178 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01346 | hp2 | a0014 | c0023 | t0002 | g0146 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01358 | hp2 | a0004 | c0005 | t0004 | g0048 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01517 | hp1 | a0015 | c0021 | t0002 | g0143 | EUR | IBS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01884 | hp1 | a0003 | c0011 | t0010 | g0009 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01884 | hp2 | a0003 | c0003 | t0009 | g0104 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01891 | hp1 | a0001 | c0004 | t0016 | g0129 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0150 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0163 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02055 | hp2 | a0006 | c0008 | t0002 | g0179 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | KHV | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | KHV | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | KHV | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02145 | hp1 | a0003 | c0003 | t0003 | g0096 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02145 | hp2 | a0004 | c0005 | t0004 | g0091 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02257 | hp2 | a0001 | c0013 | t0012 | g0027 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02280 | hp1 | a0003 | c0003 | t0009 | g0105 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02280 | hp2 | a0007 | c0007 | t0001 | g0013 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02293 | hp2 | a0004 | c0005 | t0004 | g0047 | AMR | PEL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02451 | hp1 | a0009 | c0014 | t0004 | g0089 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02451 | hp2 | a0001 | c0010 | t0011 | g0029 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0181 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02572 | hp2 | a0005 | c0006 | t0005 | g0031 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02615 | hp2 | a0003 | c0003 | t0003 | g0008 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02630 | hp1 | a0001 | c0001 | t0019 | g0133 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02630 | hp2 | a0003 | c0003 | t0020 | g0183 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02647 | hp1 | a0009 | c0014 | t0004 | g0090 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02647 | hp2 | a0010 | c0012 | t0005 | g0109 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02717 | hp1 | a0001 | c0004 | t0006 | g0007 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02717 | hp2 | a0011 | c0015 | t0015 | g0176 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02723 | hp1 | a0007 | c0007 | t0001 | g0112 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0182 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02809 | hp2 | a0007 | c0007 | t0001 | g0013 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0063 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0184 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02896 | hp1 | a0003 | c0003 | t0009 | g0103 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02896 | hp2 | a0003 | c0003 | t0003 | g0008 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02897 | hp2 | a0003 | c0003 | t0003 | g0008 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02965 | hp2 | a0005 | c0006 | t0005 | g0032 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02970 | hp1 | a0005 | c0006 | t0005 | g0031 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02976 | hp2 | a0001 | c0004 | t0006 | g0127 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0023 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0030 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03139 | hp1 | a0001 | c0010 | t0011 | g0029 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03139 | hp2 | a0001 | c0004 | t0006 | g0126 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03209 | hp2 | a0016 | c0022 | t0001 | g0054 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03225 | hp1 | a0007 | c0007 | t0001 | g0013 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03225 | hp2 | a0003 | c0003 | t0003 | g0008 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03453 | hp1 | a0001 | c0004 | t0006 | g0007 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03516 | hp2 | a0003 | c0003 | t0009 | g0106 | AFR | ESN | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | GWD | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03579 | hp1 | a0004 | c0005 | t0004 | g0088 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0162 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03654 | hp2 | a0001 | c0019 | t0001 | g0059 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0173 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03669 | hp2 | a0017 | c0020 | t0002 | g0156 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | STU | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0144 | SAS | BEB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | STU | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0026 | AFR | YRI | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18522 | hp2 | a0001 | c0001 | t0025 | g0114 | AFR | YRI | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | YRI | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18941 | hp1 | a0008 | c0009 | t0002 | g0036 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18946 | hp2 | a0002 | c0002 | t0007 | g0004 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18948 | hp2 | a0002 | c0002 | t0007 | g0004 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18960 | hp1 | a0002 | c0002 | t0007 | g0004 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18963 | hp2 | a0008 | c0009 | t0002 | g0036 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18993 | hp2 | a0008 | c0009 | t0002 | g0158 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19000 | hp2 | a0001 | c0001 | t0026 | g0069 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19004 | hp1 | a0002 | c0002 | t0007 | g0004 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19030 | hp1 | a0010 | c0012 | t0005 | g0108 | AFR | LWK | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19030 | hp2 | a0001 | c0004 | t0006 | g0128 | AFR | LWK | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19043 | hp2 | a0001 | c0004 | t0006 | g0007 | AFR | LWK | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19074 | hp1 | a0002 | c0002 | t0007 | g0004 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19084 | hp1 | a0002 | c0002 | t0007 | g0004 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19240 | hp1 | a0005 | c0006 | t0005 | g0032 | AFR | YRI | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA19240 | hp2 | a0003 | c0011 | t0010 | g0009 | AFR | YRI | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA20129 | hp2 | a0003 | c0011 | t0010 | g0009 | AFR | ASW | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | GIH | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | GIH | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02109 | hp1 | a0001 | c0004 | t0006 | g0007 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02109 | hp2 | a0001 | c0010 | t0011 | g0101 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0171 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0102 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02559 | hp1 | a0003 | c0003 | t0003 | g0026 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0100 | AFR | ACB | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03471 | hp1 | a0011 | c0015 | t0015 | g0175 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| HG06807 | hp2 | a0001 | c0013 | t0012 | g0027 | AFR | USA | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA18955 | hp2 | a0002 | c0002 | t0021 | g0159 | EAS | JPT | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA20300 | hp1 | a0005 | c0006 | t0005 | g0107 | AFR | USA | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA20300 | hp2 | a0001 | c0001 | t0017 | g0086 | AFR | USA | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA21309 | hp1 | a0003 | c0003 | t0003 | g0097 | AFR | LWK | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0023 | AFR | LWK | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| homoSapiens | chm13v2 | a0006 | c0008 | t0002 | g0177 | REF | REF | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| homoSapiens | grch38p0 | a0012 | c0018 | t0004 | g0147 | REF | REF | CKAP2L_chr2_112731349_112769609 | CKAP2L | chr2 | 112731349 | 112769609 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112738875 | C | T | 1 | a0009 | 2 | HG02451.hp1 HG02647.hp1 |
missense_variant | MODERATE | c.2186G>A | p.Arg729His | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2197/4723 | 2186/2238 | 729/745 | chr2 | 112738875 | |||
| chr2:112738943 | T | A | 1 | a0008 | 3 | NA18941.hp1 NA18963.hp2 NA18993.hp2 |
missense_variant | MODERATE | c.2118A>T | p.Glu706Asp | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2129/4723 | 2118/2238 | 706/745 | chr2 | 112738943 | |||
| chr2:112738977 | C | T | 1 | a0015 | 1 | HG01517.hp1 | missense_variant | MODERATE | c.2084G>A | p.Arg695Gln | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2095/4723 | 2084/2238 | 695/745 | chr2 | 112738977 | |||
| chr2:112739023 | C | T | 1 | a0017 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2038G>A | p.Asp680Asn | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2049/4723 | 2038/2238 | 680/745 | chr2 | 112739023 | |||
| chr2:112740989 | A | G | 8 | a0002 a0006 a0008 others(5): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
missense_variant | MODERATE | c.1841T>C | p.Leu614Ser | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/9 | 1852/4723 | 1841/2238 | 614/745 | chr2 | 112740989 | |||
| chr2:112752314 | T | C | 2 | a0005 a0010 |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
missense_variant | MODERATE | c.1555A>G | p.Ser519Gly | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/9 | 1566/4723 | 1555/2238 | 519/745 | chr2 | 112752314 | |||
| chr2:112756226 | G | C | 1 | a0010 | 2 | HG02647.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.1145C>G | p.Thr382Arg | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 1156/4723 | 1145/2238 | 382/745 | chr2 | 112756226 | |||
| chr2:112756248 | T | C | 14 | a0001 a0002 a0003 others(11): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
missense_variant | MODERATE | c.1123A>G | p.Ile375Val | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 1134/4723 | 1123/2238 | 375/745 | chr2 | 112756248 | |||
| chr2:112756521 | G | A | 1 | a0016 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.850C>T | p.Arg284Trp | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 861/4723 | 850/2238 | 284/745 | chr2 | 112756521 | |||
| chr2:112756582 | T | A | 3 | a0003 a0004 a0009 |
26 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(23): Show |
missense_variant | MODERATE | c.789A>T | p.Arg263Ser | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 800/4723 | 789/2238 | 263/745 | chr2 | 112756582 | |||
| chr2:112756970 | A | C | 1 | a0007 | 4 | HG02280.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
missense_variant | MODERATE | c.401T>G | p.Leu134Arg | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 412/4723 | 401/2238 | 134/745 | chr2 | 112756970 | |||
| chr2:112756986 | A | G | 1 | a0013 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.385T>C | p.Ser129Pro | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 396/4723 | 385/2238 | 129/745 | chr2 | 112756986 | |||
| chr2:112757185 | G | C | 1 | a0014 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.186C>G | p.Asn62Lys | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 197/4723 | 186/2238 | 62/745 | chr2 | 112757185 | |||
| chr2:112757186 | T | C | 2 | a0004 a0009 |
9 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(6): Show |
missense_variant | MODERATE | c.185A>G | p.Asn62Ser | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 196/4723 | 185/2238 | 62/745 | chr2 | 112757186 | |||
| chr2:112762530 | T | C | 1 | a0011 | 2 | HG02717.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.77A>G | p.Lys26Arg | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/9 | 88/4723 | 77/2238 | 26/745 | chr2 | 112762530 | |||
| chr2:112762552 | G | A | 1 | a0006 | 3 | HG01258.hp2 HG01261.hp2 HG02055.hp2 |
missense_variant | MODERATE | c.55C>T | p.Leu19Phe | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/9 | 66/4723 | 55/2238 | 19/745 | chr2 | 112762552 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112739003 | A | G | 1 | a0001c0010 | 3 | HG02109.hp2 HG02451.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.2058T>C | p.Pro686Pro | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2069/4723 | 2058/2238 | 686/745 | chr2 | 112739003 | |||
| chr2:112752423 | A | G | 3 | a0001c0004 a0001c0013 a0003c0011 |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
synonymous_variant | LOW | c.1446T>C | p.Pro482Pro | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/9 | 1457/4723 | 1446/2238 | 482/745 | chr2 | 112752423 | |||
| chr2:112756237 | C | T | 1 | a0001c0019 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.1134G>A | p.Arg378Arg | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 1145/4723 | 1134/2238 | 378/745 | chr2 | 112756237 | |||
| chr2:112756603 | T | C | 5 | a0003c0003 a0003c0011 a0004c0005 others(2): Show |
26 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(23): Show |
synonymous_variant | LOW | c.768A>G | p.Val256Val | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 779/4723 | 768/2238 | 256/745 | chr2 | 112756603 | |||
| chr2:112756615 | C | T | 1 | a0001c0017 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.756G>A | p.Arg252Arg | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 767/4723 | 756/2238 | 252/745 | chr2 | 112756615 | |||
| chr2:112757149 | G | A | 1 | a0001c0013 | 2 | HG02257.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.222C>T | p.Ile74Ile | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 233/4723 | 222/2238 | 74/745 | chr2 | 112757149 | |||
| chr2:112757188 | G | A | 1 | a0004c0024 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.183C>T | p.Thr61Thr | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/9 | 194/4723 | 183/2238 | 61/745 | chr2 | 112757188 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112736412 | A | G | 1 | a0001c0001t0019 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2411T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2411 | chr2 | 112736412 | ||||||
| chr2:112736446 | GATTAAC | G | 4 | a0001c0004t0006 a0001c0004t0016 a0001c0013t0012 others(1): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2371_*2376delGTTA others(2): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2371 | chr2 | 112736446 | ||||||
| chr2:112736482 | G | T | 1 | a0003c0003t0020 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2341C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2341 | chr2 | 112736482 | ||||||
| chr2:112736493 | C | G | 1 | a0002c0002t0021 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2330G>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2330 | chr2 | 112736493 | ||||||
| chr2:112736554 | G | C | 1 | a0001c0001t0018 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2269 | chr2 | 112736554 | ||||||
| chr2:112736563 | A | T | 1 | a0001c0001t0017 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2260T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2260 | chr2 | 112736563 | ||||||
| chr2:112736673 | T | C | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(34): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*2150A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2150 | chr2 | 112736673 | ||||||
| chr2:112736800 | C | T | 2 | a0001c0001t0008 a0001c0001t0019 |
5 | HG01167.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2023G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2023 | chr2 | 112736800 | ||||||
| chr2:112736818 | TTTTC | T | 1 | a0002c0002t0007 | 6 | NA18946.hp2 NA18948.hp2 NA18960.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2001_*2004delGAAA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 2001 | chr2 | 112736818 | ||||||
| chr2:112736897 | T | G | 4 | a0001c0004t0006 a0001c0004t0016 a0001c0013t0012 others(1): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1926A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1926 | chr2 | 112736897 | ||||||
| chr2:112736932 | C | CTTCT | 3 | a0001c0004t0006 a0001c0004t0016 a0001c0013t0012 |
10 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1890_*1891insAGAA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1890 | chr2 | 112736932 | ||||||
| chr2:112736943 | T | C | 9 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0021 others(6): Show |
99 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1880A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1880 | chr2 | 112736943 | ||||||
| chr2:112736952 | A | C | 14 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(11): Show |
141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1871T>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1871 | chr2 | 112736952 | ||||||
| chr2:112737039 | G | A | 2 | a0005c0006t0005 a0010c0012t0005 |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1784C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1784 | chr2 | 112737039 | ||||||
| chr2:112737295 | A | G | 1 | a0003c0011t0010 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1528T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1528 | chr2 | 112737295 | ||||||
| chr2:112737314 | A | G | 6 | a0001c0004t0006 a0001c0004t0016 a0001c0013t0012 others(3): Show |
20 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1509T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1509 | chr2 | 112737314 | ||||||
| chr2:112737336 | C | T | 4 | a0001c0004t0006 a0001c0004t0016 a0001c0013t0012 others(1): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1487G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1487 | chr2 | 112737336 | ||||||
| chr2:112737337 | G | A | 1 | a0001c0001t0022 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1486C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1486 | chr2 | 112737337 | ||||||
| chr2:112737407 | T | C | 1 | a0001c0001t0023 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1416A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1416 | chr2 | 112737407 | ||||||
| chr2:112737543 | C | T | 3 | a0001c0004t0006 a0001c0004t0016 a0001c0013t0012 |
10 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1280G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1280 | chr2 | 112737543 | ||||||
| chr2:112737592 | G | C | 1 | a0001c0001t0024 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1231C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1231 | chr2 | 112737592 | ||||||
| chr2:112737650 | G | A | 1 | a0003c0011t0010 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1173C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1173 | chr2 | 112737650 | ||||||
| chr2:112737723 | T | C | 1 | a0001c0004t0016 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1100A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1100 | chr2 | 112737723 | ||||||
| chr2:112737739 | G | A | 1 | a0003c0011t0010 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1084C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1084 | chr2 | 112737739 | ||||||
| chr2:112737757 | T | A | 1 | a0001c0001t0025 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1066A>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 1066 | chr2 | 112737757 | ||||||
| chr2:112737868 | A | G | 1 | a0001c0001t0014 | 2 | HG00639.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*955T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 955 | chr2 | 112737868 | ||||||
| chr2:112737959 | CA | C | 4 | a0001c0004t0006 a0001c0004t0016 a0001c0013t0012 others(1): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*863delT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 863 | chr2 | 112737959 | ||||||
| chr2:112738002 | T | C | 1 | a0003c0003t0009 | 4 | HG01884.hp2 HG02280.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*821A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 821 | chr2 | 112738002 | ||||||
| chr2:112738029 | C | T | 1 | a0001c0001t0013 | 2 | HG03041.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*794G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 794 | chr2 | 112738029 | ||||||
| chr2:112738126 | T | A | 1 | a0001c0010t0011 | 3 | HG02109.hp2 HG02451.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*697A>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 697 | chr2 | 112738126 | ||||||
| chr2:112738136 | C | A | 1 | a0001c0013t0012 | 2 | HG02257.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*687G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 687 | chr2 | 112738136 | ||||||
| chr2:112738137 | C | A | 1 | a0001c0013t0012 | 2 | HG02257.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*686G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 686 | chr2 | 112738137 | ||||||
| chr2:112738208 | T | C | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(34): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*615A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 615 | chr2 | 112738208 | ||||||
| chr2:112738554 | A | T | 4 | a0001c0004t0006 a0001c0004t0016 a0001c0013t0012 others(1): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*269T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 269 | chr2 | 112738554 | ||||||
| chr2:112738609 | A | G | 2 | a0005c0006t0005 a0010c0012t0005 |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*214T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 214 | chr2 | 112738609 | ||||||
| chr2:112738745 | T | C | 1 | a0011c0015t0015 | 2 | HG02717.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*78A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 78 | chr2 | 112738745 | ||||||
| chr2:112738767 | T | A | 1 | a0001c0001t0026 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56A>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 9/9 | 56 | chr2 | 112738767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112739377 | T | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0136 |
2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2013-329A>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739377 | |||||||
| chr2:112739474 | T | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(87): Show |
146 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.2013-426A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739474 | |||||||
| chr2:112739532 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0052 others(3): Show |
8 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.2013-484A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739532 | |||||||
| chr2:112739584 | AC | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0110 |
4 | NA18946.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2013-537delG | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739584 | |||||||
| chr2:112739718 | A | G | 63 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(60): Show |
114 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.2013-670T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739718 | |||||||
| chr2:112739764 | T | C | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2013-716A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739764 | |||||||
| chr2:112739841 | T | A | 1 | a0001c0001t0019g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2013-793A>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739841 | |||||||
| chr2:112739905 | C | T | 1 | a0016c0022t0001g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2013-857G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739905 | |||||||
| chr2:112739913 | C | G | 1 | a0016c0022t0001g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2013-865G>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112739913 | |||||||
| chr2:112740229 | G | A | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2012+589C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112740229 | |||||||
| chr2:112740254 | G | C | 1 | a0001c0001t0026g0069 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2012+564C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112740254 | |||||||
| chr2:112740373 | A | G | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2012+445T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112740373 | |||||||
| chr2:112740404 | A | C | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2012+414T>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112740404 | |||||||
| chr2:112740587 | C | A | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2012+231G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112740587 | |||||||
| chr2:112740760 | C | T | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2012+58G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 8/8 | chr2 | 112740760 | |||||||
| chr2:112741053 | T | C | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1823-46A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741053 | |||||||
| chr2:112741176 | C | T | 6 | a0003c0003t0003g0008 a0003c0003t0003g0026 a0003c0003t0003g0096 others(3): Show |
10 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1823-169G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741176 | |||||||
| chr2:112741177 | G | A | 56 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0015 others(53): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1823-170C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741177 | |||||||
| chr2:112741341 | C | T | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1823-334G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741341 | |||||||
| chr2:112741363 | A | C | 2 | a0011c0015t0015g0175 a0011c0015t0015g0176 |
2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1823-356T>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741363 | |||||||
| chr2:112741388 | C | T | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1823-381G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741388 | |||||||
| chr2:112741672 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(99): Show |
161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1823-665G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741672 | |||||||
| chr2:112741888 | G | A | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1822+818C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741888 | |||||||
| chr2:112741902 | A | G | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1822+804T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741902 | |||||||
| chr2:112741907 | C | T | 1 | a0002c0002t0002g0154 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1822+799G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741907 | |||||||
| chr2:112741940 | G | GT | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0055 others(10): Show |
15 | HG00544.hp1 HG01981.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1822+765dupA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741940 | |||||||
| chr2:112741940 | GT | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(93): Show |
170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1822+765delA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741940 | |||||||
| chr2:112741940 | GTT | G | 5 | a0001c0013t0012g0027 a0002c0002t0002g0157 a0003c0011t0010g0009 others(2): Show |
8 | HG01496.hp2 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1822+764_1822+765d others(4): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741940 | |||||||
| chr2:112741940 | GTTTT | G | 4 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(1): Show |
7 | HG02109.hp1 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822+762_1822+765d others(6): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741940 | |||||||
| chr2:112741991 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(106): Show |
174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1822+715G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741991 | |||||||
| chr2:112741992 | G | T | 1 | a0002c0002t0021g0159 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1822+714C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112741992 | |||||||
| chr2:112742057 | C | T | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822+649G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112742057 | |||||||
| chr2:112742058 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0077 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1822+648C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112742058 | |||||||
| chr2:112742352 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1822+354A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112742352 | |||||||
| chr2:112742453 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0110 |
4 | NA18946.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1822+253A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 7/8 | chr2 | 112742453 | |||||||
| chr2:112742810 | T | G | 1 | a0003c0003t0003g0026 | 2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1759-41A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112742810 | |||||||
| chr2:112742993 | G | T | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1759-224C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112742993 | |||||||
| chr2:112743028 | A | G | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1759-259T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743028 | |||||||
| chr2:112743049 | T | C | 1 | a0001c0001t0019g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1759-280A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743049 | |||||||
| chr2:112743098 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0072 |
3 | HG02698.hp1 HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1759-329G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743098 | |||||||
| chr2:112743180 | T | C | 1 | a0003c0011t0010g0009 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1759-411A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743180 | |||||||
| chr2:112743288 | G | A | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1759-519C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743288 | |||||||
| chr2:112743364 | G | A | 56 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0015 others(53): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1759-595C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743364 | |||||||
| chr2:112743389 | G | T | 1 | a0002c0002t0002g0153 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1759-620C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743389 | |||||||
| chr2:112743393 | C | T | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1759-624G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743393 | |||||||
| chr2:112743402 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0077 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1759-633T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743402 | |||||||
| chr2:112743419 | C | T | 1 | a0006c0008t0002g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1759-650G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743419 | |||||||
| chr2:112743564 | A | G | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1759-795T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743564 | |||||||
| chr2:112743626 | C | T | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1759-857G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743626 | |||||||
| chr2:112743634 | C | T | 1 | a0002c0002t0002g0016 | 3 | HG00735.hp1 HG01934.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1759-865G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743634 | |||||||
| chr2:112743637 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1759-868A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743637 | |||||||
| chr2:112743654 | T | G | 1 | a0001c0001t0022g0070 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1759-885A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743654 | |||||||
| chr2:112743974 | T | A | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1759-1205A>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112743974 | |||||||
| chr2:112744019 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1759-1250G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112744019 | |||||||
| chr2:112744176 | T | TA | 5 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(2): Show |
8 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1759-1408dupT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112744176 | |||||||
| chr2:112744742 | C | T | 2 | a0003c0003t0003g0096 a0003c0003t0003g0097 |
2 | HG02145.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1758+1678G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112744742 | |||||||
| chr2:112744755 | T | C | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1758+1665A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112744755 | |||||||
| chr2:112744952 | G | C | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1758+1468C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112744952 | |||||||
| chr2:112744961 | A | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1758+1459T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112744961 | |||||||
| chr2:112745238 | C | G | 1 | a0007c0007t0001g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1758+1182G>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112745238 | |||||||
| chr2:112745239 | G | A | 4 | a0002c0002t0002g0138 a0002c0002t0002g0160 a0002c0002t0002g0167 others(1): Show |
4 | HG02083.hp1 NA18955.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1758+1181C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112745239 | |||||||
| chr2:112745259 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1758+1161T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112745259 | |||||||
| chr2:112745439 | G | A | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1758+981C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112745439 | |||||||
| chr2:112745661 | G | A | 1 | a0001c0017t0001g0058 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1758+759C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112745661 | |||||||
| chr2:112746005 | C | T | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1758+415G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112746005 | |||||||
| chr2:112746010 | C | T | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0120 others(3): Show |
6 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1758+410G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112746010 | |||||||
| chr2:112746100 | C | T | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1758+320G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112746100 | |||||||
| chr2:112746101 | A | G | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1758+319T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112746101 | |||||||
| chr2:112746253 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1758+167G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 6/8 | chr2 | 112746253 | |||||||
| chr2:112746795 | A | T | 1 | a0001c0004t0006g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1603-220T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112746795 | |||||||
| chr2:112746819 | GCT | G | 1 | a0003c0011t0010g0009 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1603-246_1603-245d others(4): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112746819 | |||||||
| chr2:112746916 | T | C | 5 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(2): Show |
8 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603-341A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112746916 | |||||||
| chr2:112746918 | G | C | 4 | a0001c0001t0008g0028 a0001c0001t0008g0100 a0001c0001t0008g0102 others(1): Show |
5 | HG01167.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603-343C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112746918 | |||||||
| chr2:112746991 | G | A | 1 | a0002c0002t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1603-416C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112746991 | |||||||
| chr2:112747031 | C | T | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-456G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747031 | |||||||
| chr2:112747097 | CT | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(106): Show |
174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1603-523delA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747097 | |||||||
| chr2:112747175 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1603-600G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747175 | |||||||
| chr2:112747249 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1603-674G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747249 | |||||||
| chr2:112747317 | A | C | 1 | a0002c0002t0002g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1603-742T>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747317 | |||||||
| chr2:112747365 | CTAGAG | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
158 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1603-795_1603-791d others(7): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747365 | |||||||
| chr2:112747366 | TAGAGTA | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0087 a0001c0001t0023g0073 |
3 | HG00735.hp2 HG01257.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1603-797_1603-792d others(8): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747366 | |||||||
| chr2:112747479 | C | T | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603-904G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747479 | |||||||
| chr2:112747491 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1603-916C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747491 | |||||||
| chr2:112747559 | G | A | 2 | a0002c0002t0002g0161 a0002c0002t0002g0172 |
2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1603-984C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747559 | |||||||
| chr2:112747563 | A | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1603-988T>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747563 | |||||||
| chr2:112747632 | A | AG | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603-1058_1603-105 others(5): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112747632 | |||||||
| chr2:112748267 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0120 others(2): Show |
5 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-1692C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748267 | |||||||
| chr2:112748344 | A | G | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1603-1769T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748344 | |||||||
| chr2:112748424 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(99): Show |
161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1603-1849A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748424 | |||||||
| chr2:112748459 | C | CA | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1603-1885dupT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748459 | |||||||
| chr2:112748797 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(106): Show |
174 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1603-2222A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748797 | |||||||
| chr2:112748798 | A | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(99): Show |
161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1603-2223T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748798 | |||||||
| chr2:112748845 | A | G | 1 | a0002c0002t0002g0035 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1603-2270T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748845 | |||||||
| chr2:112748866 | TA | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0116 others(4): Show |
10 | HG00280.hp2 HG01884.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1603-2292delT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748866 | |||||||
| chr2:112748866 | TAA | T | 5 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(2): Show |
8 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603-2293_1603-229 others(6): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112748866 | |||||||
| chr2:112749096 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(99): Show |
161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1603-2521G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112749096 | |||||||
| chr2:112749131 | A | T | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1603-2556T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112749131 | |||||||
| chr2:112749222 | AAGAGCTA others(2): Show |
A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(99): Show |
161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1603-2656_1603-264 others(13): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112749222 | |||||||
| chr2:112749612 | GA | G | 56 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0015 others(53): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1602+2654delT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112749612 | |||||||
| chr2:112749699 | C | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1602+2568G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112749699 | |||||||
| chr2:112749719 | A | G | 5 | a0001c0001t0001g0099 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+2548T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112749719 | |||||||
| chr2:112750064 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1602+2203C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750064 | |||||||
| chr2:112750182 | A | G | 6 | a0003c0003t0003g0008 a0003c0003t0003g0026 a0003c0003t0003g0096 others(3): Show |
10 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1602+2085T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750182 | |||||||
| chr2:112750213 | T | C | 10 | a0003c0003t0003g0008 a0003c0003t0003g0026 a0003c0003t0003g0096 others(7): Show |
14 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1602+2054A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750213 | |||||||
| chr2:112750214 | T | C | 10 | a0003c0003t0003g0008 a0003c0003t0003g0026 a0003c0003t0003g0096 others(7): Show |
14 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1602+2053A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750214 | |||||||
| chr2:112750352 | CAG | C | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602+1913_1602+191 others(6): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750352 | |||||||
| chr2:112750365 | G | A | 1 | a0001c0001t0003g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1602+1902C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750365 | |||||||
| chr2:112750384 | C | T | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1602+1883G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750384 | |||||||
| chr2:112750433 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1602+1834G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750433 | |||||||
| chr2:112750441 | C | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(7): Show |
14 | HG01175.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1602+1826G>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750441 | |||||||
| chr2:112750518 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01175.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+1749G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750518 | |||||||
| chr2:112750632 | G | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(87): Show |
146 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1602+1635C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750632 | |||||||
| chr2:112750704 | T | G | 1 | a0002c0002t0002g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1602+1563A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750704 | |||||||
| chr2:112750783 | C | T | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+1484G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750783 | |||||||
| chr2:112750791 | T | TA | 5 | a0001c0001t0001g0084 a0001c0001t0008g0028 a0001c0001t0008g0100 others(2): Show |
6 | HG01167.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602+1475dupT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750791 | |||||||
| chr2:112750791 | TA | T | 5 | a0001c0001t0001g0115 a0001c0001t0023g0073 a0001c0010t0011g0029 others(2): Show |
6 | HG01257.hp2 HG01943.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602+1475delT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750791 | |||||||
| chr2:112750802 | AAAAG | A | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+1461_1602+146 others(8): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750802 | |||||||
| chr2:112750899 | A | C | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1602+1368T>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750899 | |||||||
| chr2:112750972 | A | G | 10 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(7): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+1295T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112750972 | |||||||
| chr2:112751083 | T | C | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602+1184A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112751083 | |||||||
| chr2:112751364 | T | C | 1 | a0003c0011t0010g0009 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1602+903A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112751364 | |||||||
| chr2:112751435 | T | C | 10 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(7): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+832A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112751435 | |||||||
| chr2:112751561 | C | T | 6 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(3): Show |
10 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1602+706G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112751561 | |||||||
| chr2:112751655 | A | G | 2 | a0001c0001t0008g0100 a0001c0001t0008g0102 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1602+612T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112751655 | |||||||
| chr2:112751881 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(162): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1602+386G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112751881 | |||||||
| chr2:112752062 | T | C | 1 | a0001c0001t0014g0030 | 2 | HG00639.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1602+205A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 5/8 | chr2 | 112752062 | |||||||
| chr2:112752656 | C | T | 7 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1395-182G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112752656 | |||||||
| chr2:112752670 | C | T | 1 | a0001c0001t0025g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1395-196G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112752670 | |||||||
| chr2:112752924 | C | T | 1 | a0002c0002t0002g0151 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1395-450G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112752924 | |||||||
| chr2:112753081 | G | C | 1 | a0002c0002t0002g0163 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1395-607C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753081 | |||||||
| chr2:112753146 | A | G | 5 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(2): Show |
8 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395-672T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753146 | |||||||
| chr2:112753229 | G | A | 6 | a0003c0003t0003g0008 a0003c0003t0003g0026 a0003c0003t0003g0096 others(3): Show |
10 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1395-755C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753229 | |||||||
| chr2:112753467 | C | T | 5 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(2): Show |
8 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395-993G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753467 | |||||||
| chr2:112753521 | CTTTTCT | C | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395-1053_1395-104 others(10): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753521 | |||||||
| chr2:112753526 | C | CT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(12): Show |
16 | HG00558.hp2 HG01169.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1395-1053dupA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753526 | |||||||
| chr2:112753526 | C | CTT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(69): Show |
119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1395-1054_1395-105 others(6): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753526 | |||||||
| chr2:112753526 | CT | C | 61 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(58): Show |
106 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1395-1053delA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753526 | |||||||
| chr2:112753526 | CTTTTTTT others(6): Show |
C | 10 | a0003c0003t0003g0008 a0003c0003t0003g0026 a0003c0003t0003g0096 others(7): Show |
14 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395-1065_1395-105 others(17): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753526 | |||||||
| chr2:112753531 | T | C | 6 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(3): Show |
10 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1395-1057A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753531 | |||||||
| chr2:112753532 | T | C | 1 | a0002c0002t0002g0164 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1395-1058A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753532 | |||||||
| chr2:112753554 | G | A | 56 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0015 others(53): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1395-1080C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753554 | |||||||
| chr2:112753689 | G | A | 1 | a0003c0011t0010g0009 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1395-1215C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753689 | |||||||
| chr2:112753734 | G | A | 6 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(3): Show |
10 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1395-1260C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753734 | |||||||
| chr2:112753741 | C | T | 1 | a0003c0003t0009g0104 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1395-1267G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753741 | |||||||
| chr2:112753820 | A | T | 1 | a0003c0011t0010g0009 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1395-1346T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753820 | |||||||
| chr2:112753870 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1395-1396G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112753870 | |||||||
| chr2:112754058 | C | T | 2 | a0011c0015t0015g0175 a0011c0015t0015g0176 |
2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1395-1584G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112754058 | |||||||
| chr2:112754186 | A | T | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1395-1712T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112754186 | |||||||
| chr2:112754253 | G | T | 1 | a0003c0011t0010g0009 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1394+1724C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112754253 | |||||||
| chr2:112754526 | C | T | 1 | a0001c0001t0001g0019 | 2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1394+1451G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112754526 | |||||||
| chr2:112754639 | A | C | 1 | a0002c0002t0002g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1394+1338T>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112754639 | |||||||
| chr2:112755171 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1394+806A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755171 | |||||||
| chr2:112755264 | T | C | 56 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0015 others(53): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1394+713A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755264 | |||||||
| chr2:112755289 | G | C | 5 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(2): Show |
8 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+688C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755289 | |||||||
| chr2:112755469 | T | C | 1 | a0002c0002t0002g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1394+508A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755469 | |||||||
| chr2:112755738 | GAAAA | G | 6 | a0003c0003t0003g0008 a0003c0003t0003g0026 a0003c0003t0003g0096 others(3): Show |
10 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1394+235_1394+238d others(6): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755738 | |||||||
| chr2:112755756 | G | T | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1394+221C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755756 | |||||||
| chr2:112755766 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1394+211C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755766 | |||||||
| chr2:112755774 | A | G | 5 | a0002c0002t0002g0015 a0002c0002t0002g0142 a0002c0002t0002g0148 others(2): Show |
7 | NA18977.hp1 NA18984.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.1394+203T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755774 | |||||||
| chr2:112755794 | T | C | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1394+183A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755794 | |||||||
| chr2:112755927 | A | G | 56 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0015 others(53): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1394+50T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 4/8 | chr2 | 112755927 | |||||||
| chr2:112757306 | AT | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.157-93delA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757306 | |||||||
| chr2:112757385 | G | GT | 18 | a0002c0002t0002g0035 a0002c0002t0002g0037 a0002c0002t0002g0131 others(15): Show |
23 | HG01069.hp1 HG01071.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.157-172dupA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757385 | |||||||
| chr2:112757385 | GT | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(101): Show |
165 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.157-172delA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757385 | |||||||
| chr2:112757385 | GTT | G | 5 | a0001c0001t0001g0056 a0001c0001t0023g0073 a0005c0006t0005g0031 others(2): Show |
7 | HG01257.hp2 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-173_157-172del others(2): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757385 | |||||||
| chr2:112757556 | T | C | 2 | a0009c0014t0004g0089 a0009c0014t0004g0090 |
2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.157-342A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757556 | |||||||
| chr2:112757678 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0055 a0001c0001t0001g0056 |
5 | HG00099.hp1 HG00741.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-464G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757678 | |||||||
| chr2:112757686 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.157-472C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757686 | |||||||
| chr2:112757693 | C | T | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.157-479G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757693 | |||||||
| chr2:112757695 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.157-481C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757695 | |||||||
| chr2:112757813 | A | G | 1 | a0016c0022t0001g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157-599T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757813 | |||||||
| chr2:112757852 | C | T | 1 | a0002c0002t0002g0141 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.157-638G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757852 | |||||||
| chr2:112757863 | C | G | 1 | a0003c0003t0003g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.157-649G>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757863 | |||||||
| chr2:112757879 | C | A | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-665G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757879 | |||||||
| chr2:112757903 | C | T | 3 | a0001c0001t0008g0028 a0001c0001t0008g0100 a0001c0001t0008g0102 |
4 | HG01167.hp2 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-689G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757903 | |||||||
| chr2:112757953 | T | G | 1 | a0002c0002t0002g0166 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.157-739A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757953 | |||||||
| chr2:112757958 | C | T | 5 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(2): Show |
8 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.157-744G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112757958 | |||||||
| chr2:112758378 | G | C | 1 | a0004c0005t0004g0018 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.157-1164C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758378 | |||||||
| chr2:112758526 | C | T | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.157-1312G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758526 | |||||||
| chr2:112758538 | C | T | 1 | a0002c0002t0002g0168 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.157-1324G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758538 | |||||||
| chr2:112758599 | A | T | 1 | a0002c0002t0002g0035 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.157-1385T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758599 | |||||||
| chr2:112758624 | T | C | 1 | a0002c0002t0002g0167 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.157-1410A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758624 | |||||||
| chr2:112758669 | G | A | 1 | a0002c0002t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.157-1455C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758669 | |||||||
| chr2:112758672 | C | T | 1 | a0001c0004t0006g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157-1458G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758672 | |||||||
| chr2:112758703 | T | G | 6 | a0001c0004t0006g0007 a0001c0004t0006g0126 a0001c0004t0006g0127 others(3): Show |
10 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.157-1489A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758703 | |||||||
| chr2:112758739 | T | C | 8 | a0004c0005t0004g0018 a0004c0005t0004g0047 a0004c0005t0004g0048 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-1525A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758739 | |||||||
| chr2:112758961 | G | A | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.157-1747C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112758961 | |||||||
| chr2:112759184 | G | A | 1 | a0001c0001t0023g0073 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.156+1529C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112759184 | |||||||
| chr2:112759244 | C | CA | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(123): Show |
196 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.156+1468dupT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112759244 | |||||||
| chr2:112759685 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.156+1028G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112759685 | |||||||
| chr2:112759762 | G | A | 1 | a0001c0001t0017g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156+951C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112759762 | |||||||
| chr2:112759773 | C | CATATGCA others(135): Show |
1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.156+798_156+939dup others(142): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112759773 | |||||||
| chr2:112760237 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.156+476C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112760237 | |||||||
| chr2:112760283 | C | T | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.156+430G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112760283 | |||||||
| chr2:112760332 | A | G | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.156+381T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112760332 | |||||||
| chr2:112760343 | A | T | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.156+370T>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112760343 | |||||||
| chr2:112760367 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(124): Show |
197 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.156+346A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112760367 | |||||||
| chr2:112760429 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.156+284C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 3/8 | chr2 | 112760429 | |||||||
| chr2:112760836 | TA | T | 4 | a0001c0001t0008g0028 a0001c0001t0008g0100 a0001c0001t0008g0102 others(1): Show |
5 | HG01167.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-73delT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112760836 | |||||||
| chr2:112760971 | C | T | 6 | a0003c0003t0003g0008 a0003c0003t0003g0026 a0003c0003t0003g0096 others(3): Show |
10 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.105-207G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112760971 | |||||||
| chr2:112761290 | C | T | 1 | a0002c0002t0002g0140 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.105-526G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112761290 | |||||||
| chr2:112761291 | G | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(124): Show |
197 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.105-527C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112761291 | |||||||
| chr2:112761354 | G | A | 1 | a0013c0016t0002g0174 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.105-590C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112761354 | |||||||
| chr2:112761417 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0135 |
5 | NA18979.hp2 NA18980.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.105-653G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112761417 | |||||||
| chr2:112761460 | C | CA | 39 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0034 others(36): Show |
47 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.105-697dupT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112761460 | |||||||
| chr2:112761460 | CA | C | 9 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0004t0006g0007 others(6): Show |
13 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.105-697delT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112761460 | |||||||
| chr2:112761634 | T | C | 1 | a0001c0004t0016g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.104+869A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112761634 | |||||||
| chr2:112761800 | T | C | 9 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(6): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.104+703A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112761800 | |||||||
| chr2:112762197 | T | C | 2 | a0001c0013t0012g0027 a0003c0011t0010g0009 |
5 | HG01884.hp1 HG02257.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.104+306A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112762197 | |||||||
| chr2:112762266 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.104+237G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112762266 | |||||||
| chr2:112762377 | G | A | 5 | a0005c0006t0005g0031 a0005c0006t0005g0032 a0005c0006t0005g0107 others(2): Show |
7 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+126C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112762377 | |||||||
| chr2:112762448 | T | C | 1 | a0003c0011t0010g0009 | 3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.104+55A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 2/8 | chr2 | 112762448 | |||||||
| chr2:112762586 | C | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.38-17G>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112762586 | |||||||
| chr2:112762785 | C | CT | 6 | a0001c0001t0001g0072 a0005c0006t0005g0031 a0005c0006t0005g0032 others(3): Show |
8 | HG02572.hp2 HG02647.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.38-217dupA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112762785 | |||||||
| chr2:112762785 | C | CTT | 12 | a0001c0013t0012g0027 a0003c0003t0003g0008 a0003c0003t0003g0026 others(9): Show |
19 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.38-218_38-217dupAA | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112762785 | |||||||
| chr2:112762785 | C | CTTTT | 8 | a0004c0005t0004g0018 a0004c0005t0004g0047 a0004c0005t0004g0048 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.38-220_38-217dupAA others(2): Show |
CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112762785 | |||||||
| chr2:112762846 | C | A | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.38-277G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112762846 | |||||||
| chr2:112762934 | C | T | 3 | a0003c0003t0003g0008 a0003c0003t0003g0184 a0003c0003t0020g0183 |
6 | HG02615.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.38-365G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112762934 | |||||||
| chr2:112762952 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.38-383A>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112762952 | |||||||
| chr2:112762953 | T | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(102): Show |
165 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.38-384A>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112762953 | |||||||
| chr2:112763022 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.38-453C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763022 | |||||||
| chr2:112763066 | G | A | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.38-497C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763066 | |||||||
| chr2:112763101 | G | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(124): Show |
197 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.38-532C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763101 | |||||||
| chr2:112763168 | C | G | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.38-599G>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763168 | |||||||
| chr2:112763356 | T | C | 8 | a0004c0005t0004g0018 a0004c0005t0004g0047 a0004c0005t0004g0048 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.38-787A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763356 | |||||||
| chr2:112763392 | C | T | 6 | a0001c0001t0008g0028 a0001c0001t0008g0100 a0001c0001t0008g0102 others(3): Show |
9 | HG00639.hp2 HG01167.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.38-823G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763392 | |||||||
| chr2:112763407 | G | T | 1 | a0002c0002t0002g0134 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.38-838C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763407 | |||||||
| chr2:112763530 | C | A | 1 | a0001c0013t0012g0027 | 2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.38-961G>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763530 | |||||||
| chr2:112763555 | G | A | 3 | a0002c0002t0002g0038 a0002c0002t0002g0181 a0002c0002t0002g0182 |
4 | HG02572.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-986C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763555 | |||||||
| chr2:112763559 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.38-990T>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763559 | |||||||
| chr2:112763572 | A | G | 2 | a0001c0001t0019g0133 a0001c0013t0012g0027 |
3 | HG02257.hp2 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.37+990T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763572 | |||||||
| chr2:112763580 | C | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(113): Show |
182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.37+982G>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763580 | |||||||
| chr2:112763604 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.37+958C>T | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763604 | |||||||
| chr2:112763845 | C | T | 7 | a0001c0001t0003g0098 a0003c0003t0003g0008 a0003c0003t0003g0026 others(4): Show |
11 | HG02145.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.37+717G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763845 | |||||||
| chr2:112763852 | T | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0095 |
4 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+710A>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763852 | |||||||
| chr2:112763893 | T | TA | 3 | a0003c0003t0003g0008 a0003c0003t0003g0184 a0003c0003t0020g0183 |
6 | HG02615.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+668dupT | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763893 | |||||||
| chr2:112763945 | T | C | 1 | a0001c0001t0003g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.37+617A>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763945 | |||||||
| chr2:112763970 | A | G | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.37+592T>C | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112763970 | |||||||
| chr2:112764015 | G | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0043 others(6): Show |
11 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.37+547C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112764015 | |||||||
| chr2:112764150 | G | C | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.37+412C>G | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112764150 | |||||||
| chr2:112764177 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(66): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.37+385G>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112764177 | |||||||
| chr2:112764366 | G | T | 3 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.37+196C>A | CKAP2L | ENSG00000169607.13 | transcript | ENST00000302450.11 | protein_coding | 1/8 | chr2 | 112764366 |