Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8812 |
| ensemblid | ENSG00000090061.17 |
| hgncid | 1596 |
| symbol | CCNK |
| name | cyclin K |
| refseq_nuc | NM_001099402.2 |
| refseq_prot | NP_001092872.1 |
| ensembl_nuc | ENST00000389879.9 |
| ensembl_prot | ENSP00000374529.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 99481409 |
| end | 99512440 |
| strand | + |
| ver | v1.2 |
| region | chr14:99481409-99512440 |
| region5000 | chr14:99476409-99517440 |
| regionname0 | CCNK_chr14_99481409_99512440 |
| regionname5000 | CCNK_chr14_99476409_99517440 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 580 | 324 | 84 | 55 | 131 | 16 | 36 | 102 | CCNK_chr14_99476409_99517440 | CCNK | MKENK others(575): Show |
chr14 | 99476409 | 99517440 |
| a0002 | 0/0 | 580 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | MKENK others(575): Show |
chr14 | 99476409 | 99517440 |
| a0003 | 0/0 | 580 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | MKENK others(575): Show |
chr14 | 99476409 | 99517440 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1740 | 316 | 84 | 55 | 123 | 16 | 36 | CCNK_chr14_99476409_99517440 | CCNK | ATGAA others(1735): Show |
chr14 | 99476409 | 99517440 | ||
| a0001c0002 | 0/0 | 1740 | 6 | 0 | 0 | 6 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | ATGAA others(1735): Show |
chr14 | 99476409 | 99517440 | ||
| a0001c0004 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | ATGAA others(1735): Show |
chr14 | 99476409 | 99517440 | ||
| a0001c0005 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | ATGAA others(1735): Show |
chr14 | 99476409 | 99517440 | ||
| a0002c0006 | 0/0 | 1740 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | ATGAA others(1735): Show |
chr14 | 99476409 | 99517440 | ||
| a0003c0003 | 0/0 | 1740 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | ATGAA others(1735): Show |
chr14 | 99476409 | 99517440 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3524 | 279 | 60 | 51 | 117 | 16 | 33 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0002 | 0/0 | 3523 | 9 | 9 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3518): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0003 | 0/0 | 3525 | 9 | 8 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3520): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0004 | 0/0 | 3524 | 6 | 5 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0005 | 0/0 | 3524 | 5 | 0 | 0 | 5 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0006 | 0/0 | 3524 | 2 | 0 | 0 | 0 | 0 | 2 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0007 | 0/0 | 3524 | 2 | 0 | 2 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0008 | 0/0 | 3524 | 2 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0009 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0001t0010 | 0/0 | 3524 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0002t0001 | 0/0 | 3524 | 6 | 0 | 0 | 6 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0004t0001 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0001c0005t0001 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0002c0006t0001 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| a0003c0003t0001 | 0/0 | 3524 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | GACAT others(3519): Show |
chr14 | 99476409 | 99517440 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 8 | 6 | 7 | 1 | 3 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0002 | 0/0 | 23 | 1 | 6 | 15 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0003 | 0/0 | 23 | 1 | 4 | 8 | 4 | 6 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0004 | 0/0 | 22 | 3 | 9 | 5 | 2 | 3 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0005 | 0/0 | 21 | 7 | 0 | 14 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0017 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0003g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0004g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0005g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0001c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0002c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| a0003c0003t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00597 | hp1 | a0002 | c0006 | t0001 | g0084 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0033 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0097 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0098 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0122 | SAS | BEB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0003 | SAS | BEB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0004 | SAS | STU | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | YRI | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19063 | hp1 | a0001 | c0005 | t0001 | g0071 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | USA | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | USA | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | USA | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0078 | REF | REF | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0017 | REF | REF | CCNK_chr14_99476409_99517440 | CCNK | chr14 | 99476409 | 99517440 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99502925 | C | G | 1 | a0002 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.952C>G | p.Gln318Glu | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 8/11 | 1075/3524 | 952/1743 | 318/580 | chr14 | 99502925 | |||
| chr14:99510735 | G | A | 1 | a0003 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.1696G>A | p.Gly566Ser | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 1819/3524 | 1696/1743 | 566/580 | chr14 | 99510735 | |||
| chr14:99512428 | GA | G | 1 | a0001 | 9 | HG01884.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
splice_region_variant | LOW | c.*1658delA | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 99512428 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99500849 | A | T | 1 | a0001c0002 | 6 | NA18951.hp1 NA18964.hp1 NA18972.hp1 others(3): Show |
synonymous_variant | LOW | c.495A>T | p.Leu165Leu | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 5/11 | 618/3524 | 495/1743 | 165/580 | chr14 | 99500849 | |||
| chr14:99510569 | A | C | 1 | a0001c0005 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.1530A>C | p.Pro510Pro | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 1653/3524 | 1530/1743 | 510/580 | chr14 | 99510569 | |||
| chr14:99510701 | A | G | 1 | a0001c0004 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1662A>G | p.Gly554Gly | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 1785/3524 | 1662/1743 | 554/580 | chr14 | 99510701 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99481440 | C | T | 1 | a0001c0001t0005 | 5 | NA18966.hp2 NA18967.hp2 NA18969.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-92C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/11 | 11238 | chr14 | 99481440 | ||||||
| chr14:99510881 | A | T | 1 | a0001c0001t0008 | 2 | HG02615.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*99A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 99 | chr14 | 99510881 | ||||||
| chr14:99511802 | G | A | 2 | a0001c0001t0004 a0001c0001t0008 |
8 | HG01123.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1020G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 1020 | chr14 | 99511802 | ||||||
| chr14:99511816 | G | A | 1 | a0001c0001t0006 | 2 | HG03831.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 1034 | chr14 | 99511816 | ||||||
| chr14:99511884 | G | A | 1 | a0001c0001t0009 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1102G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 1102 | chr14 | 99511884 | ||||||
| chr14:99511935 | C | T | 1 | a0001c0001t0010 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 1153 | chr14 | 99511935 | ||||||
| chr14:99511963 | G | A | 1 | a0001c0001t0007 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1181G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 11/11 | 1181 | chr14 | 99511963 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99481519 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
5 | HG02451.hp2 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53+40C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99481519 | |||||||
| chr14:99481521 | G | T | 1 | a0001c0001t0003g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-53+42G>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99481521 | |||||||
| chr14:99481609 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-53+130C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99481609 | |||||||
| chr14:99481801 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
4 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+322C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99481801 | |||||||
| chr14:99482020 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-53+541C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99482020 | |||||||
| chr14:99482113 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-53+634C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99482113 | |||||||
| chr14:99482171 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-53+692C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99482171 | |||||||
| chr14:99482248 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(64): Show |
145 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-53+769A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99482248 | |||||||
| chr14:99482467 | A | T | 1 | a0001c0001t0001g0093 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-53+988A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99482467 | |||||||
| chr14:99482695 | T | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0039 others(3): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53+1216T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99482695 | |||||||
| chr14:99482793 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0001t0001g0096 |
7 | HG02109.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53+1314T>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99482793 | |||||||
| chr14:99482858 | ACT | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(64): Show |
145 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-53+1382_-53+1383d others(4): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 99482858 | ||||||
| chr14:99483021 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-53+1542G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99483021 | |||||||
| chr14:99483185 | A | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.-53+1706A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99483185 | |||||||
| chr14:99483186 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-53+1707G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99483186 | |||||||
| chr14:99483546 | T | A | 10 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(7): Show |
12 | HG00639.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-53+2067T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99483546 | |||||||
| chr14:99483818 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-53+2339A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99483818 | |||||||
| chr14:99483937 | A | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-53+2458A>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99483937 | |||||||
| chr14:99483999 | C | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-53+2520C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99483999 | |||||||
| chr14:99484194 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-53+2715A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99484194 | |||||||
| chr14:99484243 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-53+2764G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99484243 | |||||||
| chr14:99484320 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-53+2841G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99484320 | |||||||
| chr14:99484564 | C | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0039 others(3): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53+3085C>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99484564 | |||||||
| chr14:99484675 | G | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
15 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-53+3196G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99484675 | |||||||
| chr14:99484869 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-53+3390A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99484869 | |||||||
| chr14:99485236 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53+3757A>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99485236 | |||||||
| chr14:99485244 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-53+3765T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99485244 | |||||||
| chr14:99485358 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-53+3879A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99485358 | |||||||
| chr14:99486251 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-53+4772T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99486251 | |||||||
| chr14:99486446 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-53+4967C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99486446 | |||||||
| chr14:99486558 | G | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
5 | HG02451.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53+5079G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99486558 | |||||||
| chr14:99486748 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-53+5269A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99486748 | |||||||
| chr14:99486791 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-53+5312C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99486791 | |||||||
| chr14:99486893 | TAA | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-53+5415_-53+5416d others(4): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99486893 | |||||||
| chr14:99487114 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-52-5512A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99487114 | |||||||
| chr14:99487180 | G | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG00639.hp1 HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-52-5446G>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99487180 | |||||||
| chr14:99487302 | C | G | 1 | a0001c0001t0002g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52-5324C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99487302 | |||||||
| chr14:99487335 | A | G | 3 | a0001c0001t0004g0012 a0001c0001t0008g0097 a0001c0001t0008g0098 |
6 | HG01123.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-5291A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99487335 | |||||||
| chr14:99487464 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-52-5162A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99487464 | |||||||
| chr14:99487566 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.-52-5060T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99487566 | |||||||
| chr14:99487747 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(64): Show |
145 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-52-4879A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99487747 | |||||||
| chr14:99488085 | G | C | 1 | a0001c0001t0001g0024 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-52-4541G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99488085 | |||||||
| chr14:99488094 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-52-4532A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99488094 | |||||||
| chr14:99488277 | TA | T | 19 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0050 others(16): Show |
25 | HG00099.hp1 HG00280.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.-52-4334delA | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 99488277 | ||||||
| chr14:99488278 | A | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0024 others(12): Show |
19 | HG00639.hp1 HG00738.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-52-4348A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99488278 | |||||||
| chr14:99488279 | A | T | 2 | a0001c0001t0001g0094 a0001c0001t0002g0041 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-52-4347A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99488279 | |||||||
| chr14:99488455 | T | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
40 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-52-4171T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99488455 | |||||||
| chr14:99488747 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-52-3879C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99488747 | |||||||
| chr14:99488913 | C | CT | 11 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0124 others(8): Show |
37 | HG00558.hp1 HG00673.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-52-3699dupT | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 99488913 | ||||||
| chr14:99488981 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-52-3645G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99488981 | |||||||
| chr14:99489137 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-52-3489A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99489137 | |||||||
| chr14:99489139 | T | A | 18 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
21 | HG00639.hp1 HG01257.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.-52-3487T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99489139 | |||||||
| chr14:99489256 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-52-3370G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99489256 | |||||||
| chr14:99489257 | G | T | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0039 others(3): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-3369G>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99489257 | |||||||
| chr14:99489483 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52-3143T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99489483 | |||||||
| chr14:99489639 | G | A | 1 | a0001c0001t0001g0011 | 4 | HG03490.hp2 HG03492.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2987G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99489639 | |||||||
| chr14:99489707 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-52-2919G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99489707 | |||||||
| chr14:99489908 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-52-2718A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99489908 | |||||||
| chr14:99490445 | A | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0039 others(3): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2181A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99490445 | |||||||
| chr14:99490579 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0085 |
2 | HG00738.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-52-2047A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99490579 | |||||||
| chr14:99490655 | C | T | 1 | a0002c0006t0001g0084 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-52-1971C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99490655 | |||||||
| chr14:99490743 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-52-1883C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99490743 | |||||||
| chr14:99490761 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG01978.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-52-1865A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99490761 | |||||||
| chr14:99490788 | C | T | 1 | a0001c0001t0006g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-52-1838C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99490788 | |||||||
| chr14:99490859 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.-52-1767T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99490859 | |||||||
| chr14:99491197 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG01516.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-52-1429T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491197 | |||||||
| chr14:99491239 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-52-1387T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491239 | |||||||
| chr14:99491362 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-52-1264A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491362 | |||||||
| chr14:99491366 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.-52-1260T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491366 | |||||||
| chr14:99491588 | AC | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-52-1037delC | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491588 | |||||||
| chr14:99491590 | T | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-52-1036T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491590 | |||||||
| chr14:99491641 | G | T | 1 | a0001c0001t0001g0031 | 2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-52-985G>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491641 | |||||||
| chr14:99491651 | G | C | 1 | a0001c0002t0001g0059 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-52-975G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491651 | |||||||
| chr14:99491851 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-52-775T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99491851 | |||||||
| chr14:99491923 | T | TTTTC | 4 | a0001c0001t0002g0021 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
5 | HG02451.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-689_-52-686dup others(4): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 99491923 | ||||||
| chr14:99492043 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-52-583A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99492043 | |||||||
| chr14:99492203 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
4 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-423G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99492203 | |||||||
| chr14:99492258 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-52-368A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99492258 | |||||||
| chr14:99492283 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-52-343G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99492283 | |||||||
| chr14:99492528 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-52-98A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99492528 | |||||||
| chr14:99492579 | A | T | 1 | a0001c0001t0001g0081 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-52-47A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99492579 | |||||||
| chr14:99492601 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-52-25A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99492601 | |||||||
| chr14:99492622 | A | G | 1 | a0001c0001t0004g0123 | 1 | HG03209.hp1 | splice_region_variant&intron_variant | LOW | c.-52-4A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 1/10 | chr14 | 99492622 | |||||||
| chr14:99493151 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.197+277C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 2/10 | chr14 | 99493151 | |||||||
| chr14:99493420 | TTTG | T | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.198-82_198-80delGT others(1): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 99493420 | ||||||
| chr14:99493644 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.279+49C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99493644 | |||||||
| chr14:99493924 | A | C | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.279+329A>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99493924 | |||||||
| chr14:99493945 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.279+350G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99493945 | |||||||
| chr14:99494290 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0003g0034 |
2 | HG01978.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.279+695A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99494290 | |||||||
| chr14:99494328 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.279+733T>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99494328 | |||||||
| chr14:99494333 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0057 |
3 | HG02723.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.279+738C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99494333 | |||||||
| chr14:99494655 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.280-843C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99494655 | |||||||
| chr14:99494749 | A | G | 1 | a0001c0001t0001g0014 | 4 | HG01081.hp1 HG01106.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-749A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99494749 | |||||||
| chr14:99494870 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.280-628C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99494870 | |||||||
| chr14:99494905 | C | T | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.280-593C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99494905 | |||||||
| chr14:99495134 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0002g0022 a0001c0001t0002g0041 |
6 | HG01891.hp2 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-364G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99495134 | |||||||
| chr14:99495342 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.280-156T>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99495342 | |||||||
| chr14:99495362 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.280-136T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99495362 | |||||||
| chr14:99495474 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.280-24C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99495474 | |||||||
| chr14:99495493 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
splice_region_variant&intron_variant | LOW | c.280-5T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 3/10 | chr14 | 99495493 | |||||||
| chr14:99496068 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.411+439C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496068 | |||||||
| chr14:99496258 | C | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.411+629C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496258 | |||||||
| chr14:99496459 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.411+830C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496459 | |||||||
| chr14:99496566 | C | T | 1 | a0001c0001t0003g0075 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.411+937C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496566 | |||||||
| chr14:99496567 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0003g0088 |
2 | HG03041.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.411+938G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496567 | |||||||
| chr14:99496653 | T | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG00639.hp1 HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.411+1024T>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496653 | |||||||
| chr14:99496799 | T | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0041 |
3 | HG02258.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.411+1170T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496799 | |||||||
| chr14:99496915 | GA | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(64): Show |
142 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.411+1298delA | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr14 | 99496915 | ||||||
| chr14:99496929 | G | GT | 2 | a0001c0001t0001g0020 a0001c0001t0001g0119 |
4 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1300_411+1301i others(3): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496929 | |||||||
| chr14:99496930 | C | CT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.411+1314dupT | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr14 | 99496930 | ||||||
| chr14:99496930 | C | CTT | 11 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0049 others(8): Show |
14 | HG00639.hp2 HG00642.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.411+1313_411+1314d others(4): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr14 | 99496930 | ||||||
| chr14:99496930 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0118 a0001c0001t0001g0119 |
5 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+1301C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99496930 | |||||||
| chr14:99497021 | CAG | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0025 others(21): Show |
54 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.411+1393_411+1394d others(4): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497021 | |||||||
| chr14:99497178 | T | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(64): Show |
145 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.411+1549T>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497178 | |||||||
| chr14:99497235 | T | G | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.411+1606T>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497235 | |||||||
| chr14:99497296 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.411+1667C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497296 | |||||||
| chr14:99497345 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.411+1716T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497345 | |||||||
| chr14:99497548 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.411+1919T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497548 | |||||||
| chr14:99497616 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.411+1987C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497616 | |||||||
| chr14:99497691 | T | C | 1 | a0001c0002t0001g0063 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.411+2062T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497691 | |||||||
| chr14:99497698 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.411+2069A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99497698 | |||||||
| chr14:99497824 | CTT | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0041 |
3 | HG02258.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.411+2198_411+2199d others(4): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr14 | 99497824 | ||||||
| chr14:99498095 | A | G | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.411+2466A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99498095 | |||||||
| chr14:99498166 | G | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.411+2537G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99498166 | |||||||
| chr14:99498184 | CCTTTA | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0067 |
8 | HG00597.hp2 HG02080.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+2560_411+2564d others(7): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr14 | 99498184 | ||||||
| chr14:99498309 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG00639.hp1 HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.412-2457A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99498309 | |||||||
| chr14:99498470 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0041 |
3 | HG02258.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.412-2296A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99498470 | |||||||
| chr14:99498476 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0107 |
7 | NA18940.hp1 NA18977.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.412-2290T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99498476 | |||||||
| chr14:99498766 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0114 |
5 | HG00673.hp1 NA18941.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-2000C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99498766 | |||||||
| chr14:99499041 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.412-1725T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99499041 | |||||||
| chr14:99499150 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(14): Show |
51 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.412-1616C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99499150 | |||||||
| chr14:99499182 | C | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0041 |
3 | HG02258.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.412-1584C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99499182 | |||||||
| chr14:99499290 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.412-1476G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99499290 | |||||||
| chr14:99499301 | G | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
5 | HG02451.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-1465G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99499301 | |||||||
| chr14:99499821 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.412-945T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99499821 | |||||||
| chr14:99500051 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-715T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99500051 | |||||||
| chr14:99500189 | GTGT | G | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.412-571_412-569del others(3): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr14 | 99500189 | ||||||
| chr14:99500191 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0085 |
3 | HG00738.hp2 HG01109.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.412-575G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99500191 | |||||||
| chr14:99500211 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.412-555C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 4/10 | chr14 | 99500211 | |||||||
| chr14:99501188 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.518-168A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 5/10 | chr14 | 99501188 | |||||||
| chr14:99501630 | T | C | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.575+217T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 6/10 | chr14 | 99501630 | |||||||
| chr14:99501659 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.575+246G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 6/10 | chr14 | 99501659 | |||||||
| chr14:99501820 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.576-387G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 6/10 | chr14 | 99501820 | |||||||
| chr14:99501964 | A | C | 1 | a0001c0001t0002g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.576-243A>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 6/10 | chr14 | 99501964 | |||||||
| chr14:99502040 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(80): Show |
166 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.576-167C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 6/10 | chr14 | 99502040 | |||||||
| chr14:99502064 | CTT | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(64): Show |
145 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.576-142_576-141del others(2): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 6/10 | chr14 | 99502064 | |||||||
| chr14:99502142 | A | G | 4 | a0001c0001t0002g0021 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
5 | HG02451.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.576-65A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 6/10 | chr14 | 99502142 | |||||||
| chr14:99502475 | A | G | 1 | a0001c0001t0001g0028 | 2 | NA18967.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.745+99A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 7/10 | chr14 | 99502475 | |||||||
| chr14:99502591 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.746-128A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 7/10 | chr14 | 99502591 | |||||||
| chr14:99502636 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0120 |
4 | HG00408.hp1 HG01928.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.746-83G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 7/10 | chr14 | 99502636 | |||||||
| chr14:99502683 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.746-36A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 7/10 | chr14 | 99502683 | |||||||
| chr14:99502684 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.746-35A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 7/10 | chr14 | 99502684 | |||||||
| chr14:99503021 | T | A | 1 | a0001c0001t0008g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1011+37T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 8/10 | chr14 | 99503021 | |||||||
| chr14:99503024 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1011+40C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 8/10 | chr14 | 99503024 | |||||||
| chr14:99503154 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0002g0051 |
3 | HG01884.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1011+170C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 8/10 | chr14 | 99503154 | |||||||
| chr14:99503264 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1011+280G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 8/10 | chr14 | 99503264 | |||||||
| chr14:99503556 | T | C | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1012-55T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 8/10 | chr14 | 99503556 | |||||||
| chr14:99503956 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1045+312C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99503956 | |||||||
| chr14:99504007 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0004g0012 |
5 | HG01123.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045+363G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99504007 | |||||||
| chr14:99504007 | G | T | 1 | a0001c0001t0001g0072 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1045+363G>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99504007 | |||||||
| chr14:99504008 | G | GGGGGGCA others(3): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG00639.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1045+370_1045+379d others(12): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr14 | 99504008 | ||||||
| chr14:99504008 | G | GGGGGGGC others(4): Show |
1 | a0001c0001t0001g0045 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1045+369_1045+370i others(13): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr14 | 99504008 | ||||||
| chr14:99504418 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1045+774T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99504418 | |||||||
| chr14:99504451 | A | AT | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1045+823dupT | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr14 | 99504451 | ||||||
| chr14:99504458 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1045+814T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99504458 | |||||||
| chr14:99504581 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1045+937G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99504581 | |||||||
| chr14:99504622 | G | C | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1045+978G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99504622 | |||||||
| chr14:99504943 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1045+1299A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99504943 | |||||||
| chr14:99504957 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1045+1313C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99504957 | |||||||
| chr14:99505024 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0066 |
3 | HG00099.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1045+1380G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99505024 | |||||||
| chr14:99505402 | C | T | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1046-1674C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99505402 | |||||||
| chr14:99505441 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1046-1635C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99505441 | |||||||
| chr14:99505490 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1046-1586C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99505490 | |||||||
| chr14:99505510 | A | AT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1046-1562dupT | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr14 | 99505510 | ||||||
| chr14:99505694 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1046-1382C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99505694 | |||||||
| chr14:99505806 | A | G | 11 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
12 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1046-1270A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99505806 | |||||||
| chr14:99506019 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0080 |
3 | HG00438.hp1 HG02129.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1046-1057A>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506019 | |||||||
| chr14:99506031 | AAGGT | A | 11 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
12 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1046-1042_1046-103 others(8): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr14 | 99506031 | ||||||
| chr14:99506038 | A | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1046-1038A>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506038 | |||||||
| chr14:99506042 | T | C | 1 | a0001c0001t0001g0013 | 4 | NA18945.hp2 NA18953.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046-1034T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506042 | |||||||
| chr14:99506073 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1046-1003C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506073 | |||||||
| chr14:99506100 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1046-976T>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506100 | |||||||
| chr14:99506119 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1046-957T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506119 | |||||||
| chr14:99506122 | T | A | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1046-954T>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506122 | |||||||
| chr14:99506320 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0073 |
2 | HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1046-756G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506320 | |||||||
| chr14:99506355 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1046-721G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506355 | |||||||
| chr14:99506451 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG00639.hp1 HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1046-625C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506451 | |||||||
| chr14:99506935 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1046-141C>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506935 | |||||||
| chr14:99506991 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0002c0006t0001g0084 |
4 | HG00597.hp1 HG02683.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046-85A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 9/10 | chr14 | 99506991 | |||||||
| chr14:99507205 | G | A | 1 | a0001c0001t0008g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1117+58G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99507205 | |||||||
| chr14:99507432 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1117+285G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99507432 | |||||||
| chr14:99507455 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1117+308C>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99507455 | |||||||
| chr14:99507515 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0041 |
3 | HG02258.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1117+368A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99507515 | |||||||
| chr14:99507637 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0077 |
2 | NA18979.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1117+490T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99507637 | |||||||
| chr14:99507702 | C | T | 2 | a0001c0001t0008g0097 a0001c0001t0008g0098 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1117+555C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99507702 | |||||||
| chr14:99508041 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1117+894G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508041 | |||||||
| chr14:99508140 | T | C | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1117+993T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508140 | |||||||
| chr14:99508449 | T | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0039 a0001c0001t0002g0040 others(1): Show |
5 | HG02451.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117+1302T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508449 | |||||||
| chr14:99508555 | G | C | 1 | a0001c0001t0006g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1117+1408G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508555 | |||||||
| chr14:99508577 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1117+1430G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508577 | |||||||
| chr14:99508626 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1117+1479C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508626 | |||||||
| chr14:99508841 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG00642.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1118-1316G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508841 | |||||||
| chr14:99508879 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0002g0051 |
2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1118-1278T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508879 | |||||||
| chr14:99508996 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1118-1161C>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99508996 | |||||||
| chr14:99509053 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1118-1104G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509053 | |||||||
| chr14:99509074 | T | G | 1 | a0001c0001t0001g0023 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1118-1083T>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509074 | |||||||
| chr14:99509118 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1118-1039G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509118 | |||||||
| chr14:99509229 | C | T | 1 | a0001c0005t0001g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1118-928C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509229 | |||||||
| chr14:99509230 | T | C | 1 | a0001c0005t0001g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1118-927T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509230 | |||||||
| chr14:99509340 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1118-817G>A | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509340 | |||||||
| chr14:99509384 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0002g0051 |
2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1118-773G>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509384 | |||||||
| chr14:99509445 | C | T | 1 | a0001c0001t0001g0016 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1118-712C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509445 | |||||||
| chr14:99509510 | A | ACACGCAG others(21): Show |
10 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(7): Show |
12 | HG00639.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1118-631_1118-604d others(30): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 99509510 | ||||||
| chr14:99509541 | C | CGCAGCAC others(10): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0002g0051 |
3 | HG01884.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1118-604_1118-603i others(19): Show |
CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 99509541 | ||||||
| chr14:99509553 | A | G | 1 | a0001c0002t0001g0059 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1118-604A>G | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509553 | |||||||
| chr14:99509610 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1118-547G>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509610 | |||||||
| chr14:99509765 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
5 | HG00597.hp1 HG02683.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1118-392C>T | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509765 | |||||||
| chr14:99509944 | T | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0039 others(3): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1118-213T>C | CCNK | ENSG00000090061.17 | transcript | ENST00000389879.9 | protein_coding | 10/10 | chr14 | 99509944 |