Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57082 |
|---|---|
| ensemblid | ENSG00000137812.21 |
| hgncid | 24054 |
| symbol | KNL1 |
| name | kinetochore scaffold 1 |
| refseq_nuc | NM_144508.5 |
| refseq_prot | NP_653091.3 |
| ensembl_nuc | ENST00000399668.7 |
| ensembl_prot | ENSP00000382576.3 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 40594249 |
| end | 40664342 |
| strand | + |
| ver | v1.2 |
| region | chr15:40594249-40664342 |
| region5000 | chr15:40589249-40669342 |
| regionname0 | KNL1_chr15_40594249_40664342 |
| regionname5000 | KNL1_chr15_40589249_40669342 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 2316 | 119 | 4 | 20 | 75 | 6 | 13 | 57 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002 | 0/1 | 2316 | 99 | 8 | 18 | 52 | 2 | 18 | 40 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0003 | 0/0 | 2316 | 48 | 2 | 15 | 18 | 3 | 10 | 9 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0004 | 0/0 | 2316 | 27 | 26 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0005 | 0/0 | 2316 | 19 | 18 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0006 | 0/0 | 2316 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0007 | 0/0 | 2316 | 7 | 0 | 6 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0008 | 0/0 | 2316 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0009 | 0/0 | 2316 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0010 | 0/0 | 2316 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0011 | 0/0 | 2316 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0012 | 0/0 | 2316 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0013 | 0/0 | 2316 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0014 | 0/0 | 2316 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0015 | 0/0 | 2316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0016 | 0/0 | 2316 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0017 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0018 | 0/0 | 2316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0019 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0020 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0021 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0022 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0023 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0024 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0025 | 0/0 | 2316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0026 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0027 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0028 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0029 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0030 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0031 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0032 | 0/0 | 2316 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0033 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 6951 | 102 | 4 | 19 | 59 | 6 | 13 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0002 | 0/1 | 6951 | 95 | 6 | 18 | 51 | 2 | 17 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0003 | 0/0 | 6951 | 48 | 2 | 15 | 18 | 3 | 10 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0004 | 0/0 | 6951 | 23 | 22 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0005 | 0/0 | 6951 | 16 | 15 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0006 | 0/0 | 6951 | 15 | 0 | 1 | 14 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0007 | 0/0 | 6951 | 9 | 9 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0008 | 0/0 | 6951 | 7 | 0 | 6 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0009 | 0/0 | 6951 | 4 | 3 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0010 | 0/0 | 6951 | 4 | 0 | 0 | 4 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0011 | 0/0 | 6951 | 4 | 4 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0012 | 0/0 | 6951 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0013 | 0/0 | 6951 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0014 | 0/0 | 6951 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0015 | 0/0 | 6951 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0016 | 0/0 | 6951 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0017 | 0/0 | 6951 | 2 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0018 | 0/0 | 6951 | 2 | 2 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0019 | 0/0 | 6951 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0020 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0021 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0022 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0023 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0024 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0025 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0026 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0027 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0028 | 0/0 | 6951 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0029 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0030 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0031 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0032 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0033 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0034 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0035 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0036 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0037 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0038 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0039 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0040 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0041 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| c0042 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2316 | 199 | 50 | 12 | 111 | 6 | 18 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0002 | 0/0 | 2316 | 70 | 24 | 17 | 17 | 3 | 9 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0003 | 0/0 | 2316 | 66 | 1 | 16 | 34 | 2 | 13 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0004 | 0/0 | 2316 | 13 | 0 | 13 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0005 | 0/0 | 2316 | 7 | 0 | 6 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0006 | 0/0 | 2316 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0007 | 0/0 | 2316 | 2 | 1 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0008 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0009 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0010 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0011 | 0/0 | 2316 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0012 | 0/0 | 2370 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0013 | 0/0 | 2316 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0014 | 0/0 | 2316 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0015 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0016 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| t0017 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0350 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 6951 | 102 | 4 | 19 | 59 | 6 | 13 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0001c0006 | 0/0 | 6951 | 15 | 0 | 1 | 14 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0001c0038 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0001c0039 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0002 | 0/1 | 6951 | 95 | 6 | 18 | 51 | 2 | 17 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0022 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0024 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0025 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0028 | 0/0 | 6951 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0003c0003 | 0/0 | 6951 | 48 | 2 | 15 | 18 | 3 | 10 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0004c0004 | 0/0 | 6951 | 23 | 22 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0004c0011 | 0/0 | 6951 | 4 | 4 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0005c0005 | 0/0 | 6951 | 16 | 15 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0005c0015 | 0/0 | 6951 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0006c0007 | 0/0 | 6951 | 9 | 9 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0007c0008 | 0/0 | 6951 | 7 | 0 | 6 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0008c0010 | 0/0 | 6951 | 4 | 0 | 0 | 4 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0009c0009 | 0/0 | 6951 | 4 | 3 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0010c0013 | 0/0 | 6951 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0011c0014 | 0/0 | 6951 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0012c0012 | 0/0 | 6951 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0013c0017 | 0/0 | 6951 | 2 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0014c0016 | 0/0 | 6951 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0015c0018 | 0/0 | 6951 | 2 | 2 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0016c0019 | 0/0 | 6951 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0017c0042 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0018c0037 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0019c0040 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0020c0041 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0021c0036 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0022c0035 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0023c0020 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0024c0033 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0025c0030 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0026c0029 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0027c0031 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0028c0027 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0029c0026 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0030c0023 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0031c0032 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0032c0034 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0033c0021 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 9266 | 88 | 4 | 6 | 59 | 6 | 12 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0001c0001t0004 | 0/0 | 9266 | 13 | 0 | 13 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0001c0001t0012 | 0/0 | 9320 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0001c0006t0001 | 0/0 | 9266 | 15 | 0 | 1 | 14 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0001c0038t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0001c0039t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0002t0001 | 0/1 | 9266 | 35 | 5 | 3 | 20 | 0 | 6 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0002t0003 | 0/0 | 9266 | 58 | 1 | 15 | 29 | 2 | 11 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0002t0008 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0002t0016 | 0/0 | 9206 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0022t0015 | 0/0 | 9311 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0024t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0025t0001 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0002c0028t0003 | 0/0 | 9266 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0003c0003t0002 | 0/0 | 9266 | 45 | 2 | 15 | 16 | 3 | 9 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0003c0003t0010 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0003c0003t0011 | 0/0 | 9266 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0003c0003t0014 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0004c0004t0001 | 0/0 | 9266 | 23 | 22 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0004c0011t0001 | 0/0 | 9266 | 4 | 4 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0005c0005t0002 | 0/0 | 9266 | 16 | 15 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0005c0015t0002 | 0/0 | 9266 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0006c0007t0001 | 0/0 | 9266 | 9 | 9 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0007c0008t0005 | 0/0 | 9266 | 7 | 0 | 6 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0008c0010t0001 | 0/0 | 9266 | 4 | 0 | 0 | 4 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0009c0009t0006 | 0/0 | 9266 | 2 | 2 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0009c0009t0007 | 0/0 | 9266 | 2 | 1 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0010c0013t0001 | 0/0 | 9266 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0011c0014t0001 | 0/0 | 9266 | 3 | 0 | 0 | 3 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0012c0012t0001 | 0/0 | 9266 | 3 | 3 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0013c0017t0003 | 0/0 | 9266 | 2 | 0 | 1 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0014c0016t0003 | 0/0 | 9266 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0015c0018t0002 | 0/0 | 9266 | 2 | 2 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0016c0019t0003 | 0/0 | 9266 | 2 | 0 | 0 | 2 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0017c0042t0001 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0018c0037t0001 | 0/0 | 9266 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0019c0040t0001 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0020c0041t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0021c0036t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0022c0035t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0023c0020t0002 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0024c0033t0017 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0025c0030t0002 | 0/0 | 9266 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0026c0029t0009 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0027c0031t0002 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0028c0027t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0029c0026t0003 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0030c0023t0006 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0031c0032t0001 | 0/0 | 9266 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0032c0034t0013 | 0/0 | 9266 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| a0033c0021t0002 | 0/0 | 9266 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | copy fasta | chr15 | 40589249 | 40669342 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0350 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0001t0012g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0006t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0038t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0001c0039t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0002t0016g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0022t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0024t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0025t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0002c0028t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0010g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0011g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0003c0003t0014g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0004t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0011t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0011t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0011t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0004c0011t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0005t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0015t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0015t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0005c0015t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0006c0007t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0007c0008t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0007c0008t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0007c0008t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0007c0008t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0007c0008t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0007c0008t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0007c0008t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0008c0010t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0008c0010t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0008c0010t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0008c0010t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0009c0009t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0009c0009t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0009c0009t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0009c0009t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0010c0013t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0010c0013t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0010c0013t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0011c0014t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0011c0014t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0011c0014t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0012c0012t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0012c0012t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0012c0012t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0013c0017t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0013c0017t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0014c0016t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0014c0016t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0015c0018t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0015c0018t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0016c0019t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0016c0019t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0017c0042t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0018c0037t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0019c0040t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0020c0041t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0021c0036t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0022c0035t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0023c0020t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0024c0033t0017g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0025c0030t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0026c0029t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0027c0031t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0028c0027t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0029c0026t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0030c0023t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0031c0032t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0032c0034t0013g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| a0033c0021t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0002 | g0171 | EUR | GBR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0040 | EUR | GBR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0355 | EUR | FIN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00280 | hp2 | a0003 | c0003 | t0002 | g0183 | EUR | FIN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0197 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00544 | hp1 | a0001 | c0039 | t0001 | g0349 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00544 | hp2 | a0014 | c0016 | t0003 | g0034 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00558 | hp1 | a0003 | c0003 | t0002 | g0176 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00558 | hp2 | a0001 | c0006 | t0001 | g0230 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00597 | hp2 | a0010 | c0013 | t0001 | g0103 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00609 | hp1 | a0003 | c0003 | t0002 | g0160 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00609 | hp2 | a0002 | c0002 | t0003 | g0059 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0132 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00639 | hp2 | a0003 | c0003 | t0002 | g0188 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00642 | hp1 | a0007 | c0008 | t0005 | g0036 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0262 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00673 | hp2 | a0001 | c0006 | t0001 | g0228 | EAS | CHS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0071 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00733 | hp2 | a0003 | c0003 | t0002 | g0158 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00738 | hp1 | a0007 | c0008 | t0005 | g0053 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00738 | hp2 | a0003 | c0003 | t0002 | g0363 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00741 | hp1 | a0032 | c0034 | t0013 | g0013 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0073 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01069 | hp2 | a0007 | c0008 | t0005 | g0052 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0364 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01071 | hp1 | a0003 | c0003 | t0002 | g0365 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01071 | hp2 | a0007 | c0008 | t0005 | g0054 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0012 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01074 | hp2 | a0003 | c0003 | t0002 | g0361 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01081 | hp2 | a0007 | c0008 | t0005 | g0083 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0048 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0318 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01109 | hp2 | a0009 | c0009 | t0007 | g0005 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01167 | hp1 | a0003 | c0003 | t0002 | g0187 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01167 | hp2 | a0002 | c0002 | t0003 | g0033 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0157 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0315 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0086 | AMR | PUR | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01255 | hp1 | a0005 | c0005 | t0002 | g0168 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01255 | hp2 | a0007 | c0008 | t0005 | g0078 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0159 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01256 | hp2 | a0018 | c0037 | t0001 | g0270 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01346 | hp1 | a0003 | c0003 | t0002 | g0184 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0324 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01358 | hp2 | a0003 | c0003 | t0002 | g0362 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01361 | hp1 | a0003 | c0003 | t0002 | g0204 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01361 | hp2 | a0002 | c0002 | t0003 | g0069 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0295 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0108 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01515 | hp2 | a0007 | c0008 | t0005 | g0051 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0174 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | IBS | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01891 | hp1 | a0003 | c0003 | t0002 | g0201 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01891 | hp2 | a0004 | c0004 | t0001 | g0246 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01928 | hp1 | a0002 | c0002 | t0003 | g0056 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01928 | hp2 | a0001 | c0006 | t0001 | g0237 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01952 | hp1 | a0002 | c0002 | t0003 | g0079 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0065 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0055 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0317 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01978 | hp2 | a0003 | c0003 | t0002 | g0196 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0149 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0325 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01993 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02015 | hp2 | a0003 | c0003 | t0002 | g0189 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02027 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02040 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02055 | hp1 | a0004 | c0004 | t0001 | g0255 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02055 | hp2 | a0015 | c0018 | t0002 | g0205 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02056 | hp2 | a0003 | c0003 | t0014 | g0190 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02080 | hp1 | a0001 | c0006 | t0001 | g0226 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02083 | hp2 | a0020 | c0041 | t0001 | g0220 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02132 | hp1 | a0003 | c0003 | t0002 | g0154 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02135 | hp2 | a0003 | c0003 | t0002 | g0151 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02145 | hp1 | a0033 | c0021 | t0002 | g0209 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02145 | hp2 | a0004 | c0011 | t0001 | g0241 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0298 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02148 | hp2 | a0002 | c0002 | t0003 | g0035 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0047 | EAS | CDX | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | CDX | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CDX | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0175 | EAS | CDX | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02257 | hp1 | a0026 | c0029 | t0009 | g0193 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02257 | hp2 | a0004 | c0011 | t0001 | g0240 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02273 | hp2 | a0002 | c0002 | t0003 | g0057 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02280 | hp1 | a0023 | c0020 | t0002 | g0211 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02280 | hp2 | a0004 | c0004 | t0001 | g0358 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02293 | hp1 | a0013 | c0017 | t0003 | g0067 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02300 | hp2 | a0003 | c0003 | t0002 | g0191 | AMR | PEL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02451 | hp1 | a0009 | c0009 | t0006 | g0010 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02451 | hp2 | a0006 | c0007 | t0001 | g0017 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02523 | hp2 | a0002 | c0002 | t0003 | g0030 | EAS | KHV | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02572 | hp1 | a0004 | c0004 | t0001 | g0359 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02572 | hp2 | a0005 | c0005 | t0002 | g0146 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0087 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02622 | hp1 | a0004 | c0011 | t0001 | g0263 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02622 | hp2 | a0005 | c0005 | t0002 | g0207 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02630 | hp1 | a0004 | c0004 | t0001 | g0244 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02647 | hp2 | a0004 | c0004 | t0001 | g0256 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0150 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02698 | hp2 | a0002 | c0028 | t0003 | g0075 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02717 | hp1 | a0004 | c0011 | t0001 | g0348 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02717 | hp2 | a0005 | c0005 | t0002 | g0145 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02735 | hp1 | a0003 | c0003 | t0002 | g0170 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0032 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0022 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0222 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02818 | hp1 | a0004 | c0004 | t0001 | g0247 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02818 | hp2 | a0003 | c0003 | t0002 | g0165 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02886 | hp2 | a0004 | c0004 | t0001 | g0259 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02895 | hp1 | a0005 | c0015 | t0002 | g0178 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02895 | hp2 | a0012 | c0012 | t0001 | g0129 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02896 | hp1 | a0009 | c0009 | t0006 | g0008 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02896 | hp2 | a0005 | c0005 | t0002 | g0163 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02897 | hp1 | a0012 | c0012 | t0001 | g0130 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02897 | hp2 | a0005 | c0005 | t0002 | g0180 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02922 | hp1 | a0006 | c0007 | t0001 | g0028 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02922 | hp2 | a0005 | c0005 | t0002 | g0208 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02965 | hp1 | a0005 | c0005 | t0002 | g0203 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02965 | hp2 | a0005 | c0005 | t0002 | g0210 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02976 | hp1 | a0004 | c0004 | t0001 | g0357 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03017 | hp2 | a0003 | c0003 | t0002 | g0001 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03041 | hp1 | a0006 | c0007 | t0001 | g0018 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03041 | hp2 | a0004 | c0004 | t0001 | g0250 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03098 | hp2 | a0005 | c0015 | t0002 | g0147 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03130 | hp1 | a0015 | c0018 | t0002 | g0206 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03130 | hp2 | a0004 | c0004 | t0001 | g0252 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03139 | hp1 | a0006 | c0007 | t0001 | g0141 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03139 | hp2 | a0004 | c0004 | t0001 | g0253 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03209 | hp1 | a0004 | c0004 | t0001 | g0258 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03225 | hp1 | a0005 | c0005 | t0002 | g0179 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03225 | hp2 | a0012 | c0012 | t0001 | g0029 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0046 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03453 | hp1 | a0024 | c0033 | t0017 | g0148 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0243 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03486 | hp1 | a0004 | c0004 | t0001 | g0261 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03486 | hp2 | a0005 | c0005 | t0002 | g0202 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03490 | hp1 | a0003 | c0003 | t0011 | g0156 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0031 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03491 | hp1 | a0013 | c0017 | t0003 | g0042 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0072 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03516 | hp1 | a0004 | c0004 | t0001 | g0242 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03516 | hp2 | a0005 | c0005 | t0002 | g0185 | AFR | ESN | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03540 | hp1 | a0004 | c0004 | t0001 | g0248 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03540 | hp2 | a0006 | c0007 | t0001 | g0027 | AFR | GWD | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03654 | hp1 | a0003 | c0003 | t0002 | g0164 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0043 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0125 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03710 | hp1 | a0003 | c0003 | t0002 | g0186 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03834 | hp1 | a0003 | c0003 | t0002 | g0166 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0098 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03927 | hp1 | a0002 | c0002 | t0003 | g0064 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0106 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0161 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03942 | hp2 | a0002 | c0002 | t0003 | g0084 | SAS | BEB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0080 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG04228 | hp2 | a0003 | c0003 | t0002 | g0195 | SAS | STU | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18522 | hp1 | a0005 | c0005 | t0002 | g0181 | AFR | YRI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18522 | hp2 | a0019 | c0040 | t0001 | g0213 | AFR | YRI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18747 | hp1 | a0001 | c0006 | t0001 | g0227 | EAS | CHB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18942 | hp1 | a0003 | c0003 | t0002 | g0198 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18944 | hp2 | a0029 | c0026 | t0003 | g0002 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18945 | hp1 | a0002 | c0002 | t0003 | g0014 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18945 | hp2 | a0021 | c0036 | t0001 | g0294 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18946 | hp2 | a0011 | c0014 | t0001 | g0135 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18950 | hp1 | a0014 | c0016 | t0003 | g0127 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18950 | hp2 | a0008 | c0010 | t0001 | g0215 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18951 | hp1 | a0003 | c0003 | t0002 | g0167 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18957 | hp2 | a0003 | c0003 | t0002 | g0182 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18960 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18960 | hp2 | a0002 | c0024 | t0001 | g0102 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18961 | hp2 | a0003 | c0003 | t0002 | g0199 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18962 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18964 | hp2 | a0001 | c0006 | t0001 | g0229 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18965 | hp1 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18965 | hp2 | a0002 | c0002 | t0016 | g0093 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18967 | hp1 | a0003 | c0003 | t0002 | g0153 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18967 | hp2 | a0031 | c0032 | t0001 | g0109 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18969 | hp1 | a0002 | c0002 | t0003 | g0123 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18970 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18972 | hp1 | a0001 | c0038 | t0001 | g0234 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18973 | hp1 | a0001 | c0006 | t0001 | g0360 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0124 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18974 | hp1 | a0022 | c0035 | t0001 | g0268 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18978 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18979 | hp1 | a0011 | c0014 | t0001 | g0088 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18979 | hp2 | a0001 | c0006 | t0001 | g0238 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18983 | hp1 | a0008 | c0010 | t0001 | g0217 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18983 | hp2 | a0010 | c0013 | t0001 | g0021 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18988 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18989 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18990 | hp1 | a0002 | c0002 | t0008 | g0011 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18991 | hp1 | a0001 | c0006 | t0001 | g0232 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18991 | hp2 | a0002 | c0002 | t0003 | g0085 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18993 | hp1 | a0001 | c0006 | t0001 | g0239 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18993 | hp2 | a0011 | c0014 | t0001 | g0099 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18994 | hp2 | a0016 | c0019 | t0003 | g0081 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18999 | hp2 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19001 | hp1 | a0003 | c0003 | t0010 | g0152 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19001 | hp2 | a0028 | c0027 | t0001 | g0111 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19002 | hp1 | a0008 | c0010 | t0001 | g0354 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19003 | hp1 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19004 | hp2 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19005 | hp2 | a0002 | c0002 | t0003 | g0041 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19007 | hp1 | a0010 | c0013 | t0001 | g0107 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19009 | hp2 | a0001 | c0006 | t0001 | g0225 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19010 | hp2 | a0001 | c0006 | t0001 | g0235 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0192 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19011 | hp2 | a0002 | c0002 | t0003 | g0082 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19012 | hp1 | a0016 | c0019 | t0003 | g0063 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19030 | hp1 | a0004 | c0004 | t0001 | g0254 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19043 | hp1 | a0004 | c0004 | t0001 | g0251 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19043 | hp2 | a0005 | c0005 | t0002 | g0173 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0058 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19058 | hp2 | a0002 | c0002 | t0003 | g0131 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0037 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19060 | hp2 | a0027 | c0031 | t0002 | g0001 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0074 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19064 | hp2 | a0003 | c0003 | t0002 | g0200 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19065 | hp2 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19070 | hp1 | a0001 | c0006 | t0001 | g0233 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0155 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19075 | hp1 | a0002 | c0002 | t0003 | g0134 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19075 | hp2 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19085 | hp2 | a0001 | c0006 | t0001 | g0231 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19090 | hp1 | a0008 | c0010 | t0001 | g0216 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19240 | hp1 | a0030 | c0023 | t0006 | g0009 | AFR | YRI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA19240 | hp2 | a0017 | c0042 | t0001 | g0260 | AFR | YRI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA20129 | hp1 | a0009 | c0009 | t0007 | g0007 | AFR | ASW | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA20129 | hp2 | a0002 | c0025 | t0001 | g0138 | AFR | ASW | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0020 | EUR | TSI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | TSI | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | GIH | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA20905 | hp2 | a0003 | c0003 | t0002 | g0169 | SAS | GIH | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01123 | hp1 | a0025 | c0030 | t0002 | g0194 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | CLM | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02109 | hp2 | a0005 | c0005 | t0002 | g0172 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02486 | hp1 | a0002 | c0022 | t0015 | g0006 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0061 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02559 | hp1 | a0006 | c0007 | t0001 | g0019 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG02559 | hp2 | a0004 | c0004 | t0001 | g0245 | AFR | ACB | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03471 | hp1 | a0006 | c0007 | t0001 | g0140 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG03471 | hp2 | a0006 | c0007 | t0001 | g0015 | AFR | MSL | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG06807 | hp1 | a0004 | c0004 | t0001 | g0249 | AFR | USA | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| HG06807 | hp2 | a0005 | c0015 | t0002 | g0177 | AFR | USA | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA20300 | hp1 | a0005 | c0005 | t0002 | g0162 | AFR | USA | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA20300 | hp2 | a0004 | c0004 | t0001 | g0257 | AFR | USA | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| NA21309 | hp2 | a0006 | c0007 | t0001 | g0016 | AFR | LWK | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0100 | REF | REF | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0350 | REF | REF | KNL1_chr15_40589249_40669342 | KNL1 | chr15 | 40589249 | 40669342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:40606445
|
G | C | 24 | a0002a0003a0005others(21): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
missense_variant | MODERATE | c.128G>C | p.Arg43Thr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/26 | 289/9266 | 128/6951 | 43/2316 | chr15 | 40606445 | ||
| chr15:40610276
|
G | A | 1 | a0023 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.229G>A | p.Val77Met | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/26 | 390/9266 | 229/6951 | 77/2316 | chr15 | 40610276 | ||
| chr15:40610292
|
T | C | 2 | a0006a0012 | 12 | HG02451.hp2 HG02559.hp1 HG02895.hp2 others(9): Show |
missense_variant | MODERATE | c.245T>C | p.Met82Thr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/26 | 406/9266 | 245/6951 | 82/2316 | chr15 | 40610292 | ||
| chr15:40611486
|
A | G | 26 | a0002a0003a0004others(23): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(239): Show |
missense_variant | MODERATE | c.259A>G | p.Thr87Ala | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/26 | 420/9266 | 259/6951 | 87/2316 | chr15 | 40611486 | ||
| chr15:40620715
|
A | G | 1 | a0017 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.451A>G | p.Met151Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 612/9266 | 451/6951 | 151/2316 | chr15 | 40620715 | ||
| chr15:40620761
|
T | C | 1 | a0033 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.497T>C | p.Leu166Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 658/9266 | 497/6951 | 166/2316 | chr15 | 40620761 | ||
| chr15:40620835
|
G | A | 1 | a0022 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.571G>A | p.Glu191Lys | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 732/9266 | 571/6951 | 191/2316 | chr15 | 40620835 | ||
| chr15:40620991
|
A | G | 1 | a0032 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.727A>G | p.Ile243Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 888/9266 | 727/6951 | 243/2316 | chr15 | 40620991 | ||
| chr15:40621033
|
A | G | 1 | a0016 | 2 | NA18994.hp2 NA19012.hp1 |
missense_variant | MODERATE | c.769A>G | p.Met257Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 930/9266 | 769/6951 | 257/2316 | chr15 | 40621033 | ||
| chr15:40621076
|
C | G | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.812C>G | p.Thr271Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 973/9266 | 812/6951 | 271/2316 | chr15 | 40621076 | ||
| chr15:40621258
|
G | C | 1 | a0021 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.994G>C | p.Ala332Pro | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1155/9266 | 994/6951 | 332/2316 | chr15 | 40621258 | ||
| chr15:40621393
|
A | G | 1 | a0015 | 2 | HG02055.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.1129A>G | p.Ile377Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1290/9266 | 1129/6951 | 377/2316 | chr15 | 40621393 | ||
| chr15:40621642
|
G | T | 24 | a0002a0003a0005others(21): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
missense_variant | MODERATE | c.1378G>T | p.Ala460Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1539/9266 | 1378/6951 | 460/2316 | chr15 | 40621642 | ||
| chr15:40621742
|
C | T | 1 | a0031 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.1478C>T | p.Ala493Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1639/9266 | 1478/6951 | 493/2316 | chr15 | 40621742 | ||
| chr15:40621757
|
T | A | 3 | a0009a0012a0030 | 8 | HG01109.hp2 HG02451.hp1 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.1493T>A | p.Ile498Asn | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1654/9266 | 1493/6951 | 498/2316 | chr15 | 40621757 | ||
| chr15:40621979
|
T | C | 14 | a0002a0006a0007others(11): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
missense_variant | MODERATE | c.1715T>C | p.Met572Thr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1876/9266 | 1715/6951 | 572/2316 | chr15 | 40621979 | ||
| chr15:40622018
|
A | G | 1 | a0027 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.1754A>G | p.Gln585Arg | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1915/9266 | 1754/6951 | 585/2316 | chr15 | 40622018 | ||
| chr15:40622278
|
A | C | 1 | a0017 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2014A>C | p.Ile672Leu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2175/9266 | 2014/6951 | 672/2316 | chr15 | 40622278 | ||
| chr15:40622633
|
C | G | 1 | a0013 | 2 | HG02293.hp1 HG03491.hp1 |
missense_variant | MODERATE | c.2369C>G | p.Thr790Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2530/9266 | 2369/6951 | 790/2316 | chr15 | 40622633 | ||
| chr15:40622992
|
A | G | 26 | a0002a0003a0004others(23): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(239): Show |
missense_variant | MODERATE | c.2728A>G | p.Arg910Gly | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2889/9266 | 2728/6951 | 910/2316 | chr15 | 40622992 | ||
| chr15:40623079
|
A | T | 1 | a0025 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.2815A>T | p.Met939Leu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2976/9266 | 2815/6951 | 939/2316 | chr15 | 40623079 | ||
| chr15:40623171
|
A | C | 1 | a0011 | 3 | NA18946.hp2 NA18979.hp1 NA18993.hp2 |
missense_variant | MODERATE | c.2907A>C | p.Arg969Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3068/9266 | 2907/6951 | 969/2316 | chr15 | 40623171 | ||
| chr15:40623754
|
C | G | 2 | a0009a0030 | 5 | HG01109.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.3490C>G | p.Leu1164Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3651/9266 | 3490/6951 | 1164/2316 | chr15 | 40623754 | ||
| chr15:40623923
|
G | T | 1 | a0020 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.3659G>T | p.Gly1220Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3820/9266 | 3659/6951 | 1220/2316 | chr15 | 40623923 | ||
| chr15:40624013
|
C | T | 1 | a0019 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.3749C>T | p.Ala1250Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3910/9266 | 3749/6951 | 1250/2316 | chr15 | 40624013 | ||
| chr15:40624039
|
A | G | 3 | a0003a0025a0027 | 50 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(47): Show |
missense_variant | MODERATE | c.3775A>G | p.Lys1259Glu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3936/9266 | 3775/6951 | 1259/2316 | chr15 | 40624039 | ||
| chr15:40624264
|
C | T | 1 | a0014 | 2 | HG00544.hp2 NA18950.hp1 |
missense_variant | MODERATE | c.4000C>T | p.Pro1334Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4161/9266 | 4000/6951 | 1334/2316 | chr15 | 40624264 | ||
| chr15:40624434
|
T | A | 3 | a0010a0011a0031 | 7 | HG00597.hp2 NA18946.hp2 NA18967.hp2 others(4): Show |
missense_variant | MODERATE | c.4170T>A | p.Asp1390Glu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4331/9266 | 4170/6951 | 1390/2316 | chr15 | 40624434 | ||
| chr15:40624603
|
A | G | 1 | a0007 | 7 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(4): Show |
missense_variant | MODERATE | c.4339A>G | p.Thr1447Ala | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4500/9266 | 4339/6951 | 1447/2316 | chr15 | 40624603 | ||
| chr15:40624766
|
C | T | 1 | a0016 | 2 | NA18994.hp2 NA19012.hp1 |
missense_variant | MODERATE | c.4502C>T | p.Ala1501Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4663/9266 | 4502/6951 | 1501/2316 | chr15 | 40624766 | ||
| chr15:40624837
|
A | G | 1 | a0028 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.4573A>G | p.Asn1525Asp | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4734/9266 | 4573/6951 | 1525/2316 | chr15 | 40624837 | ||
| chr15:40625036
|
A | G | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.4772A>G | p.Asn1591Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4933/9266 | 4772/6951 | 1591/2316 | chr15 | 40625036 | ||
| chr15:40625195
|
A | G | 1 | a0032 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.4931A>G | p.Lys1644Arg | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 5092/9266 | 4931/6951 | 1644/2316 | chr15 | 40625195 | ||
| chr15:40645051
|
C | A | 1 | a0029 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.5853C>A | p.Asn1951Lys | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/26 | 6014/9266 | 5853/6951 | 1951/2316 | chr15 | 40645051 | ||
| chr15:40647014
|
A | G | 1 | a0026 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.6034A>G | p.Ile2012Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/26 | 6195/9266 | 6034/6951 | 2012/2316 | chr15 | 40647014 | ||
| chr15:40647023
|
A | C | 1 | a0008 | 4 | NA18950.hp2 NA18983.hp1 NA19002.hp1 others(1): Show |
missense_variant | MODERATE | c.6043A>C | p.Met2015Leu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/26 | 6204/9266 | 6043/6951 | 2015/2316 | chr15 | 40647023 | ||
| chr15:40662172
|
G | A | 1 | a0030 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6935G>A | p.Cys2312Tyr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 7096/9266 | 6935/6951 | 2312/2316 | chr15 | 40662172 | ||
| chr15:40662174
|
C | T | 1 | a0018 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.6937C>T | p.His2313Tyr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 7098/9266 | 6937/6951 | 2313/2316 | chr15 | 40662174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:40621563
|
T | C | 1 | a0002c0022 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1299T>C | p.Cys433Cys | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 1460/9266 | 1299/6951 | 433/2316 | chr15 | 40621563 | ||
| chr15:40622532
|
A | G | 1 | a0002c0028 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.2268A>G | p.Ser756Ser | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2429/9266 | 2268/6951 | 756/2316 | chr15 | 40622532 | ||
| chr15:40622574
|
C | T | 18 | a0002c0002a0002c0022a0002c0024others(15): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
synonymous_variant | LOW | c.2310C>T | p.Val770Val | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2471/9266 | 2310/6951 | 770/2316 | chr15 | 40622574 | ||
| chr15:40622847
|
T | G | 18 | a0002c0002a0002c0022a0002c0024others(15): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
synonymous_variant | LOW | c.2583T>G | p.Thr861Thr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 2744/9266 | 2583/6951 | 861/2316 | chr15 | 40622847 | ||
| chr15:40623429
|
T | C | 1 | a0002c0024 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.3165T>C | p.Asn1055Asn | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3326/9266 | 3165/6951 | 1055/2316 | chr15 | 40623429 | ||
| chr15:40623669
|
C | T | 3 | a0010c0013a0011c0014a0031c0032 | 7 | HG00597.hp2 NA18946.hp2 NA18967.hp2 others(4): Show |
synonymous_variant | LOW | c.3405C>T | p.Ala1135Ala | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3566/9266 | 3405/6951 | 1135/2316 | chr15 | 40623669 | ||
| chr15:40623696
|
T | C | 18 | a0002c0002a0002c0022a0002c0024others(15): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
synonymous_variant | LOW | c.3432T>C | p.Asn1144Asn | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3593/9266 | 3432/6951 | 1144/2316 | chr15 | 40623696 | ||
| chr15:40624026
|
A | G | 1 | a0001c0039 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.3762A>G | p.Glu1254Glu | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3923/9266 | 3762/6951 | 1254/2316 | chr15 | 40624026 | ||
| chr15:40624074
|
G | A | 1 | a0005c0015 | 3 | HG02895.hp1 HG03098.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.3810G>A | p.Ala1270Ala | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 3971/9266 | 3810/6951 | 1270/2316 | chr15 | 40624074 | ||
| chr15:40624482
|
T | C | 1 | a0002c0025 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.4218T>C | p.Tyr1406Tyr | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 4379/9266 | 4218/6951 | 1406/2316 | chr15 | 40624482 | ||
| chr15:40625415
|
T | C | 3 | a0001c0006a0008c0010a0020c0041 | 20 | HG00558.hp2 HG00673.hp2 HG01928.hp2 others(17): Show |
synonymous_variant | LOW | c.5151T>C | p.Pro1717Pro | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 5312/9266 | 5151/6951 | 1717/2316 | chr15 | 40625415 | ||
| chr15:40625535
|
C | T | 1 | a0004c0011 | 4 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(1): Show |
synonymous_variant | LOW | c.5271C>T | p.Cys1757Cys | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/26 | 5432/9266 | 5271/6951 | 1757/2316 | chr15 | 40625535 | ||
| chr15:40628126
|
A | T | 1 | a0001c0038 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.5433A>T | p.Ile1811Ile | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 11/26 | 5594/9266 | 5433/6951 | 1811/2316 | chr15 | 40628126 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:40594279
|
G | A | 1 | a0002c0002t0008 | 1 | NA18990.hp1 | 5_prime_UTR_variant | MODIFIER | c.-131G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/26 | 8653 | chr15 | 40594279 | |||||
| chr15:40594355
|
G | A | 1 | a0007c0008t0005 | 7 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-55G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/26 | 8577 | chr15 | 40594355 | |||||
| chr15:40594381
|
T | G | 1 | a0009c0009t0007 | 2 | HG01109.hp2 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-29T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/26 | 8551 | chr15 | 40594381 | |||||
| chr15:40662216
|
A | G | 1 | a0024c0033t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 28 | chr15 | 40662216 | |||||
| chr15:40662324
|
TATGTTTT others(53): Show |
T | 1 | a0002c0002t0016 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137_*196delATGTTT others(54): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 137 | chr15 | 40662324 | |||||
| chr15:40662393
|
A | G | 4 | a0002c0022t0015a0009c0009t0006a0009c0009t0007others(1): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*205A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 205 | chr15 | 40662393 | |||||
| chr15:40662538
|
A | G | 4 | a0002c0022t0015a0009c0009t0006a0009c0009t0007others(1): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*350A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 350 | chr15 | 40662538 | |||||
| chr15:40662597
|
A | G | 1 | a0003c0003t0014 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 409 | chr15 | 40662597 | |||||
| chr15:40662638
|
C | T | 1 | a0032c0034t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 450 | chr15 | 40662638 | |||||
| chr15:40662863
|
G | C | 1 | a0032c0034t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*675G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 675 | chr15 | 40662863 | |||||
| chr15:40662871
|
G | A | 12 | a0003c0003t0002a0003c0003t0010a0003c0003t0011others(9): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*683G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 683 | chr15 | 40662871 | |||||
| chr15:40662966
|
A | G | 1 | a0032c0034t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*778A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 778 | chr15 | 40662966 | |||||
| chr15:40663105
|
G | GCTGGAGT others(38): Show |
1 | a0002c0022t0015 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922_*966dupAGTGCA others(39): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 967 | INFO_REALIGN_3_PRIME | chr15 | 40663105 | ||||
| chr15:40663282
|
A | G | 1 | a0003c0003t0011 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1094A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1094 | chr15 | 40663282 | |||||
| chr15:40663441
|
T | A | 1 | a0024c0033t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1253T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1253 | chr15 | 40663441 | |||||
| chr15:40663795
|
C | T | 1 | a0003c0003t0010 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1607C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1607 | chr15 | 40663795 | |||||
| chr15:40663862
|
G | A | 1 | a0001c0001t0004 | 13 | HG01109.hp1 HG01123.hp2 HG01168.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1674G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1674 | chr15 | 40663862 | |||||
| chr15:40663909
|
G | GGTATGTT others(47): Show |
1 | a0001c0001t0012 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1721_*1722insGTAT others(50): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1722 | chr15 | 40663909 | |||||
| chr15:40663910
|
A | T | 1 | a0001c0001t0012 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1722A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1722 | chr15 | 40663910 | |||||
| chr15:40663911
|
G | T | 1 | a0001c0001t0012 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1723G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1723 | chr15 | 40663911 | |||||
| chr15:40664053
|
A | C | 1 | a0026c0029t0009 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1865A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1865 | chr15 | 40664053 | |||||
| chr15:40664118
|
G | A | 1 | a0024c0033t0017 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1930G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1930 | chr15 | 40664118 | |||||
| chr15:40664154
|
G | A | 1 | a0032c0034t0013 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1966G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 1966 | chr15 | 40664154 | |||||
| chr15:40664273
|
A | C | 7 | a0002c0002t0003a0002c0028t0003a0007c0008t0005others(4): Show | 73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2085A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 26/26 | 2085 | chr15 | 40664273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:40594423
|
T | C | 139 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(136): Show | 139 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18+31T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594423 | ||||||
| chr15:40594469
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | NA18957.hp1 NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-18+77G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594469 | ||||||
| chr15:40594613
|
T | C | 1 | a0005c0005t0002g0145 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18+221T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594613 | ||||||
| chr15:40594625
|
C | T | 2 | a0006c0007t0001g0140a0006c0007t0001g0141 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-18+233C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594625 | ||||||
| chr15:40594643
|
C | T | 5 | a0003c0003t0002g0361a0003c0003t0002g0362a0003c0003t0002g0363others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+251C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594643 | ||||||
| chr15:40594677
|
C | A | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+285C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594677 | ||||||
| chr15:40594694
|
C | G | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+302C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594694 | ||||||
| chr15:40594790
|
T | C | 1 | a0005c0005t0002g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-18+398T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594790 | ||||||
| chr15:40594791
|
T | A | 1 | a0002c0002t0008g0011 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-18+399T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594791 | ||||||
| chr15:40594900
|
T | C | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+508T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594900 | ||||||
| chr15:40594958
|
T | C | 1 | a0002c0002t0003g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-18+566T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40594958 | ||||||
| chr15:40595456
|
T | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18+1064T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595456 | ||||||
| chr15:40595565
|
G | T | 1 | a0001c0006t0001g0360 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-18+1173G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595565 | ||||||
| chr15:40595603
|
T | G | 1 | a0002c0002t0003g0014 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-18+1211T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595603 | ||||||
| chr15:40595787
|
C | A | 210 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.-18+1395C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595787 | ||||||
| chr15:40595805
|
T | C | 5 | a0006c0007t0001g0015a0006c0007t0001g0016a0006c0007t0001g0017others(2): Show | 5 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+1413T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595805 | ||||||
| chr15:40595813
|
A | G | 7 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(4): Show | 7 | HG00741.hp1 HG01109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+1421A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595813 | ||||||
| chr15:40595836
|
G | A | 2 | a0001c0001t0001g0212a0019c0040t0001g0213 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18+1444G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40595836 | ||||||
| chr15:40596029
|
TA | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+1644delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40596029 | |||||
| chr15:40596046
|
C | T | 3 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359 | 3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18+1654C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596046 | ||||||
| chr15:40596124
|
G | A | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+1732G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596124 | ||||||
| chr15:40596401
|
G | A | 1 | a0002c0002t0003g0020 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-18+2009G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596401 | ||||||
| chr15:40596555
|
T | C | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-18+2163T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596555 | ||||||
| chr15:40596577
|
A | G | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+2185A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596577 | ||||||
| chr15:40596601
|
C | G | 1 | a0003c0003t0002g0204 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-18+2209C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596601 | ||||||
| chr15:40596686
|
C | A | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+2294C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596686 | ||||||
| chr15:40596838
|
T | C | 1 | a0010c0013t0001g0021 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-18+2446T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596838 | ||||||
| chr15:40596993
|
T | A | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-18+2601T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40596993 | ||||||
| chr15:40597000
|
CA | C | 86 | a0001c0001t0001g0355a0001c0001t0001g0356a0002c0002t0001g0023others(83): Show | 87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-18+2629delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40597000 | |||||
| chr15:40597000
|
CAA | C | 119 | a0002c0002t0001g0089a0002c0002t0001g0090a0002c0002t0001g0091others(116): Show | 119 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-18+2628_-18+2629d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40597000 | |||||
| chr15:40597000
|
CAAA | C | 8 | a0002c0002t0001g0136a0002c0002t0003g0131a0002c0002t0003g0132others(5): Show | 8 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+2627_-18+2629d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40597000 | |||||
| chr15:40597021
|
A | G | 1 | a0003c0003t0002g0149 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-18+2629A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597021 | ||||||
| chr15:40597054
|
A | G | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+2662A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597054 | ||||||
| chr15:40597215
|
G | C | 28 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(25): Show | 28 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+2823G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597215 | ||||||
| chr15:40597240
|
C | T | 1 | a0002c0002t0001g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+2848C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597240 | ||||||
| chr15:40597372
|
A | G | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-18+2980A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597372 | ||||||
| chr15:40597411
|
T | C | 5 | a0009c0009t0006g0008a0009c0009t0006g0010a0009c0009t0007g0005others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+3019T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597411 | ||||||
| chr15:40597564
|
C | T | 1 | a0001c0001t0001g0353 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-18+3172C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597564 | ||||||
| chr15:40597626
|
T | C | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-18+3234T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597626 | ||||||
| chr15:40597632
|
A | T | 1 | a0014c0016t0003g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18+3240A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597632 | ||||||
| chr15:40597633
|
T | A | 1 | a0014c0016t0003g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18+3241T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597633 | ||||||
| chr15:40597634
|
A | T | 1 | a0014c0016t0003g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18+3242A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597634 | ||||||
| chr15:40597796
|
T | G | 4 | a0006c0007t0001g0027a0006c0007t0001g0028a0006c0007t0001g0140others(1): Show | 4 | HG02922.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+3404T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597796 | ||||||
| chr15:40597929
|
T | C | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-18+3537T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40597929 | ||||||
| chr15:40598078
|
G | A | 1 | a0003c0003t0002g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-18+3686G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598078 | ||||||
| chr15:40598099
|
A | G | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-18+3707A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598099 | ||||||
| chr15:40598143
|
T | C | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-18+3751T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598143 | ||||||
| chr15:40598210
|
A | G | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-18+3818A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598210 | ||||||
| chr15:40598212
|
T | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18+3820T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598212 | ||||||
| chr15:40598297
|
C | T | 1 | a0002c0002t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-18+3905C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598297 | ||||||
| chr15:40598312
|
G | T | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-18+3920G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598312 | ||||||
| chr15:40598352
|
T | G | 1 | a0004c0011t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+3960T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598352 | ||||||
| chr15:40598439
|
G | A | 2 | a0002c0002t0001g0137a0002c0025t0001g0138 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-18+4047G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598439 | ||||||
| chr15:40598589
|
A | C | 1 | a0002c0002t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-18+4197A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598589 | ||||||
| chr15:40598599
|
A | G | 2 | a0002c0002t0003g0123a0002c0002t0003g0124 | 2 | NA18969.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-18+4207A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598599 | ||||||
| chr15:40598609
|
T | G | 3 | a0006c0007t0001g0027a0006c0007t0001g0140a0006c0007t0001g0141 | 3 | HG03139.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+4217T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598609 | ||||||
| chr15:40598629
|
T | G | 1 | a0014c0016t0003g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18+4237T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598629 | ||||||
| chr15:40598632
|
A | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-18+4240A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598632 | ||||||
| chr15:40598809
|
T | A | 3 | a0008c0010t0001g0215a0008c0010t0001g0216a0008c0010t0001g0217 | 3 | NA18950.hp2 NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-17-4106T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598809 | ||||||
| chr15:40598873
|
G | A | 75 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(72): Show | 75 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-17-4042G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40598873 | ||||||
| chr15:40599120
|
A | T | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-17-3795A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599120 | ||||||
| chr15:40599121
|
T | A | 230 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-17-3794T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599121 | ||||||
| chr15:40599122
|
T | A | 4 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130others(1): Show | 4 | HG00741.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-3793T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599122 | ||||||
| chr15:40599260
|
C | T | 1 | a0002c0002t0003g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17-3655C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599260 | ||||||
| chr15:40599312
|
C | CA | 18 | a0001c0001t0001g0218a0001c0001t0001g0264a0001c0001t0001g0265others(15): Show | 18 | HG01070.hp2 HG02135.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.-17-3585dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40599312 | |||||
| chr15:40599404
|
G | A | 1 | a0002c0002t0008g0011 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-17-3511G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599404 | ||||||
| chr15:40599419
|
T | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3496T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599419 | ||||||
| chr15:40599426
|
C | T | 3 | a0003c0003t0002g0363a0003c0003t0002g0364a0003c0003t0002g0365 | 3 | HG00738.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-17-3489C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599426 | ||||||
| chr15:40599454
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-17-3461G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599454 | ||||||
| chr15:40599487
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3428G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599487 | ||||||
| chr15:40599515
|
C | T | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-17-3400C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599515 | ||||||
| chr15:40599516
|
T | C | 1 | a0003c0003t0002g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-17-3399T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599516 | ||||||
| chr15:40599571
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3344G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599571 | ||||||
| chr15:40599584
|
G | C | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3331G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599584 | ||||||
| chr15:40599619
|
G | C | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-3296G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599619 | ||||||
| chr15:40599661
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-3254G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40599661 | ||||||
| chr15:40599793
|
CT | C | 148 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0212others(145): Show | 150 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.-17-3101delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40599793 | |||||
| chr15:40599793
|
CTT | C | 206 | a0001c0001t0001g0142a0001c0001t0001g0219a0001c0001t0001g0269others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-17-3102_-17-3101d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40599793 | |||||
| chr15:40599793
|
CTTT | C | 8 | a0002c0002t0001g0089a0002c0002t0003g0030a0002c0002t0003g0031others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-3103_-17-3101d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40599793 | |||||
| chr15:40600003
|
C | A | 1 | a0002c0002t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-2912C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600003 | ||||||
| chr15:40600005
|
A | C | 1 | a0002c0002t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-2910A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600005 | ||||||
| chr15:40600075
|
C | CT | 7 | a0001c0001t0001g0347a0001c0001t0001g0353a0001c0039t0001g0349others(4): Show | 7 | HG00544.hp1 HG00642.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-2822dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40600075 | |||||
| chr15:40600075
|
CT | C | 205 | a0001c0001t0001g0274a0002c0002t0001g0023a0002c0002t0001g0024others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.-17-2822delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40600075 | |||||
| chr15:40600207
|
C | G | 1 | a0006c0007t0001g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-17-2708C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600207 | ||||||
| chr15:40600236
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-17-2679G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600236 | ||||||
| chr15:40600364
|
C | A | 1 | a0002c0002t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-2551C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600364 | ||||||
| chr15:40600366
|
C | T | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-2549C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600366 | ||||||
| chr15:40600403
|
G | A | 132 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(129): Show | 132 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.-17-2512G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600403 | ||||||
| chr15:40600478
|
T | C | 1 | a0012c0012t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-17-2437T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600478 | ||||||
| chr15:40600499
|
A | T | 1 | a0002c0002t0003g0087 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17-2416A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600499 | ||||||
| chr15:40600523
|
A | G | 1 | a0001c0001t0001g0346 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17-2392A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600523 | ||||||
| chr15:40600841
|
C | A | 1 | a0002c0002t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-2074C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40600841 | ||||||
| chr15:40601023
|
C | G | 8 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(5): Show | 8 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-1892C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601023 | ||||||
| chr15:40601024
|
T | A | 1 | a0002c0002t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-1891T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601024 | ||||||
| chr15:40601043
|
C | T | 1 | a0007c0008t0005g0083 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-17-1872C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601043 | ||||||
| chr15:40601268
|
C | A | 1 | a0002c0002t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-1647C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601268 | ||||||
| chr15:40601301
|
T | A | 1 | a0002c0002t0001g0126 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-17-1614T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601301 | ||||||
| chr15:40601320
|
C | A | 212 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-17-1595C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601320 | ||||||
| chr15:40601375
|
C | A | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.-17-1540C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601375 | ||||||
| chr15:40601611
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-17-1304C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601611 | ||||||
| chr15:40601688
|
G | T | 3 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359 | 3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-17-1227G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601688 | ||||||
| chr15:40601741
|
T | G | 1 | a0014c0016t0003g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-17-1174T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601741 | ||||||
| chr15:40601778
|
A | C | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-1137A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601778 | ||||||
| chr15:40601827
|
C | CA | 76 | a0001c0001t0001g0275a0001c0001t0012g0222a0002c0002t0001g0090others(73): Show | 76 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.-17-1073dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601827 | |||||
| chr15:40601827
|
C | CAA | 8 | a0002c0002t0003g0022a0002c0002t0003g0035a0002c0002t0003g0037others(5): Show | 8 | HG00544.hp2 HG00642.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-1074_-17-1073d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601827 | |||||
| chr15:40601859
|
C | CT | 154 | a0001c0001t0001g0142a0001c0001t0001g0212a0001c0001t0001g0218others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-17-1030dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601859 | |||||
| chr15:40601859
|
C | CTT | 85 | a0001c0001t0001g0344a0002c0002t0001g0023a0002c0002t0001g0024others(82): Show | 85 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.-17-1031_-17-1030d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601859 | |||||
| chr15:40601859
|
C | CTTT | 24 | a0002c0002t0001g0026a0002c0002t0001g0089a0002c0002t0001g0112others(21): Show | 24 | HG00423.hp1 HG01071.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17-1032_-17-1030d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601859 | |||||
| chr15:40601859
|
CTTTTTTT others(4): Show |
C | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-1040_-17-1030d others(13): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40601859 | |||||
| chr15:40601955
|
C | T | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-960C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40601955 | ||||||
| chr15:40602053
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-862G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602053 | ||||||
| chr15:40602175
|
C | T | 1 | a0002c0002t0003g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-17-740C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602175 | ||||||
| chr15:40602215
|
A | G | 1 | a0006c0007t0001g0141 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17-700A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602215 | ||||||
| chr15:40602279
|
C | T | 1 | a0026c0029t0009g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-636C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602279 | ||||||
| chr15:40602303
|
A | AT | 63 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(60): Show | 63 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.-17-599dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602303 | |||||
| chr15:40602303
|
A | ATT | 111 | a0001c0001t0012g0222a0002c0002t0001g0023a0002c0002t0001g0024others(108): Show | 111 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-17-600_-17-599dup others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602303 | |||||
| chr15:40602303
|
A | ATTT | 8 | a0002c0002t0001g0026a0002c0002t0001g0110a0002c0002t0001g0117others(5): Show | 8 | HG00673.hp1 HG02647.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-601_-17-599dup others(3): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602303 | |||||
| chr15:40602338
|
G | C | 1 | a0002c0022t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-17-577G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602338 | ||||||
| chr15:40602363
|
C | T | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-17-552C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602363 | ||||||
| chr15:40602387
|
C | T | 1 | a0002c0002t0003g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-17-528C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602387 | ||||||
| chr15:40602388
|
G | A | 7 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0001t0001g0276others(4): Show | 7 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-527G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602388 | ||||||
| chr15:40602423
|
A | G | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-492A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602423 | ||||||
| chr15:40602479
|
C | CGTT | 3 | a0002c0022t0015g0006a0009c0009t0007g0005a0009c0009t0007g0007 | 3 | HG01109.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-17-436_-17-435ins others(3): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602479 | ||||||
| chr15:40602479
|
C | CGTTT | 3 | a0009c0009t0006g0008a0009c0009t0006g0010a0030c0023t0006g0009 | 3 | HG02451.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-17-436_-17-435ins others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602479 | ||||||
| chr15:40602480
|
C | CT | 135 | a0001c0001t0001g0221a0001c0001t0001g0272a0001c0001t0001g0273others(132): Show | 135 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.-17-413dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602480 | |||||
| chr15:40602480
|
C | CTT | 21 | a0001c0006t0001g0233a0001c0006t0001g0239a0002c0002t0001g0092others(18): Show | 21 | HG00741.hp1 HG02602.hp2 HG02647.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-414_-17-413dup others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602480 | |||||
| chr15:40602480
|
C | T | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-435C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602480 | ||||||
| chr15:40602480
|
CT | C | 65 | a0001c0001t0001g0311a0003c0003t0002g0001a0003c0003t0002g0149others(62): Show | 66 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-17-413delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr15 | 40602480 | |||||
| chr15:40602517
|
G | A | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-17-398G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602517 | ||||||
| chr15:40602559
|
T | C | 1 | a0002c0002t0001g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-17-356T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602559 | ||||||
| chr15:40602637
|
C | A | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-17-278C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602637 | ||||||
| chr15:40602862
|
G | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-17-53G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 1/25 | chr15 | 40602862 | ||||||
| chr15:40603100
|
T | A | 2 | a0003c0003t0002g0186a0003c0003t0002g0191 | 2 | HG02300.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.35+134T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603100 | ||||||
| chr15:40603101
|
A | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.35+135A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603101 | ||||||
| chr15:40603242
|
T | C | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.35+276T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603242 | ||||||
| chr15:40603402
|
A | G | 293 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.35+436A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603402 | ||||||
| chr15:40603417
|
T | A | 1 | a0002c0002t0003g0080 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.35+451T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603417 | ||||||
| chr15:40603432
|
T | G | 3 | a0002c0002t0003g0038a0002c0002t0003g0039a0002c0002t0003g0066 | 3 | NA18960.hp1 NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.35+466T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603432 | ||||||
| chr15:40603573
|
A | G | 5 | a0006c0007t0001g0015a0006c0007t0001g0016a0006c0007t0001g0017others(2): Show | 5 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.35+607A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603573 | ||||||
| chr15:40603610
|
A | C | 1 | a0002c0002t0003g0139 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.35+644A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603610 | ||||||
| chr15:40603866
|
T | C | 12 | a0006c0007t0001g0015a0006c0007t0001g0016a0006c0007t0001g0017others(9): Show | 12 | HG02451.hp2 HG02559.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.35+900T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40603866 | ||||||
| chr15:40604090
|
C | T | 1 | a0001c0001t0001g0328 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.36-1020C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604090 | ||||||
| chr15:40604098
|
T | C | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.36-1012T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604098 | ||||||
| chr15:40604116
|
T | TATC | 89 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0312others(86): Show | 90 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.36-960_36-958dupAT others(1): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr15 | 40604116 | |||||
| chr15:40604116
|
TATC | T | 16 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359others(13): Show | 16 | HG00741.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.36-960_36-958delAT others(1): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr15 | 40604116 | |||||
| chr15:40604193
|
TCCTATCT others(45): Show |
T | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.36-873_36-822delAA others(50): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr15 | 40604193 | |||||
| chr15:40604303
|
C | T | 1 | a0005c0005t0002g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.36-807C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604303 | ||||||
| chr15:40604328
|
G | A | 1 | a0002c0002t0003g0020 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.36-782G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604328 | ||||||
| chr15:40604590
|
C | T | 1 | a0003c0003t0002g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.36-520C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604590 | ||||||
| chr15:40604613
|
G | A | 10 | a0001c0006t0001g0225a0001c0006t0001g0226a0001c0006t0001g0227others(7): Show | 10 | HG00558.hp2 HG00673.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.36-497G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604613 | ||||||
| chr15:40604907
|
A | G | 1 | a0002c0002t0003g0061 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.36-203A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604907 | ||||||
| chr15:40604974
|
A | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.36-136A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 2/25 | chr15 | 40604974 | ||||||
| chr15:40605169
|
A | G | 1 | a0002c0002t0003g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.75+20A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605169 | ||||||
| chr15:40605207
|
A | G | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.75+58A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605207 | ||||||
| chr15:40605388
|
G | A | 73 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(70): Show | 73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.75+239G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605388 | ||||||
| chr15:40605490
|
C | T | 9 | a0002c0002t0003g0060a0002c0002t0003g0062a0005c0005t0002g0207others(6): Show | 9 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+341C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605490 | ||||||
| chr15:40605690
|
T | C | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.75+541T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605690 | ||||||
| chr15:40605737
|
A | G | 1 | a0001c0001t0001g0300 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75+588A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605737 | ||||||
| chr15:40605819
|
C | T | 42 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.76-574C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605819 | ||||||
| chr15:40605938
|
C | G | 1 | a0001c0001t0001g0328 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.76-455C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605938 | ||||||
| chr15:40605943
|
A | G | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.76-450A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605943 | ||||||
| chr15:40605990
|
A | T | 1 | a0003c0003t0002g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.76-403A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40605990 | ||||||
| chr15:40606225
|
T | C | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.76-168T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 3/25 | chr15 | 40606225 | ||||||
| chr15:40606590
|
G | A | 37 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(34): Show | 37 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.135+138G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40606590 | ||||||
| chr15:40606823
|
G | A | 5 | a0005c0005t0002g0208a0005c0005t0002g0210a0015c0018t0002g0205others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+371G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40606823 | ||||||
| chr15:40606850
|
C | G | 1 | a0002c0002t0003g0059 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.135+398C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40606850 | ||||||
| chr15:40606863
|
G | A | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.135+411G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40606863 | ||||||
| chr15:40607055
|
C | G | 11 | a0002c0002t0003g0002a0002c0002t0003g0037a0002c0002t0003g0055others(8): Show | 11 | HG01192.hp2 HG01928.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+603C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607055 | ||||||
| chr15:40607246
|
G | A | 4 | a0006c0007t0001g0027a0006c0007t0001g0028a0006c0007t0001g0140others(1): Show | 4 | HG02922.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+794G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607246 | ||||||
| chr15:40607293
|
C | T | 7 | a0007c0008t0005g0036a0007c0008t0005g0051a0007c0008t0005g0052others(4): Show | 7 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+841C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607293 | ||||||
| chr15:40607297
|
T | C | 24 | a0004c0004t0001g0242a0004c0004t0001g0243a0004c0004t0001g0244others(21): Show | 24 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.135+845T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607297 | ||||||
| chr15:40607361
|
A | T | 5 | a0006c0007t0001g0015a0006c0007t0001g0016a0006c0007t0001g0017others(2): Show | 5 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+909A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607361 | ||||||
| chr15:40607495
|
A | G | 12 | a0006c0007t0001g0015a0006c0007t0001g0016a0006c0007t0001g0017others(9): Show | 12 | HG02451.hp2 HG02559.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+1043A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607495 | ||||||
| chr15:40607665
|
G | T | 1 | a0004c0004t0001g0357 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.136-1182G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607665 | ||||||
| chr15:40607793
|
A | G | 1 | a0001c0038t0001g0234 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.136-1054A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607793 | ||||||
| chr15:40607801
|
T | A | 1 | a0002c0002t0001g0119 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.136-1046T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607801 | ||||||
| chr15:40607894
|
C | G | 1 | a0003c0003t0002g0182 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.136-953C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40607894 | ||||||
| chr15:40608036
|
G | A | 1 | a0002c0002t0003g0040 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.136-811G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608036 | ||||||
| chr15:40608081
|
TGTG | T | 3 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359 | 3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.136-763_136-761del others(3): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr15 | 40608081 | |||||
| chr15:40608139
|
C | G | 9 | a0006c0007t0001g0015a0006c0007t0001g0016a0006c0007t0001g0017others(6): Show | 9 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-708C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608139 | ||||||
| chr15:40608426
|
C | T | 1 | a0002c0002t0003g0050 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.136-421C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608426 | ||||||
| chr15:40608433
|
G | GA | 10 | a0001c0006t0001g0225a0001c0038t0001g0234a0002c0002t0001g0117others(7): Show | 10 | HG00597.hp2 HG02027.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-392dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr15 | 40608433 | |||||
| chr15:40608433
|
GA | G | 24 | a0001c0001t0001g0144a0002c0002t0001g0128a0004c0004t0001g0242others(21): Show | 24 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.136-392delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr15 | 40608433 | |||||
| chr15:40608511
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.136-336C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608511 | ||||||
| chr15:40608521
|
C | G | 293 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.136-326C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608521 | ||||||
| chr15:40608544
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136-303G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608544 | ||||||
| chr15:40608606
|
G | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136-241G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608606 | ||||||
| chr15:40608675
|
G | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-172G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608675 | ||||||
| chr15:40608704
|
C | T | 7 | a0001c0006t0001g0225a0001c0006t0001g0228a0001c0006t0001g0229others(4): Show | 7 | HG00558.hp2 HG00673.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-143C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | chr15 | 40608704 | ||||||
| chr15:40608745
|
CA | C | 133 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(130): Show | 133 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.136-86delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr15 | 40608745 | |||||
| chr15:40609002
|
T | C | 1 | a0002c0002t0001g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.197+94T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609002 | ||||||
| chr15:40609127
|
G | T | 4 | a0002c0002t0003g0037a0002c0002t0003g0058a0002c0002t0003g0060others(1): Show | 4 | NA18970.hp2 NA18999.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+219G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609127 | ||||||
| chr15:40609202
|
G | A | 1 | a0009c0009t0007g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.197+294G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609202 | ||||||
| chr15:40609210
|
C | T | 1 | a0001c0001t0001g0334 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.197+302C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609210 | ||||||
| chr15:40609244
|
C | CA | 36 | a0001c0001t0001g0214a0001c0001t0001g0273a0001c0001t0001g0279others(33): Show | 36 | HG00408.hp1 HG00621.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.197+357dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr15 | 40609244 | |||||
| chr15:40609244
|
CA | C | 13 | a0002c0002t0001g0101a0002c0002t0001g0110a0002c0002t0001g0112others(10): Show | 13 | HG01167.hp2 HG02897.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.197+357delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr15 | 40609244 | |||||
| chr15:40609805
|
A | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.198-440A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609805 | ||||||
| chr15:40609934
|
G | C | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.198-311G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 5/25 | chr15 | 40609934 | ||||||
| chr15:40610438
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.250+141C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40610438 | ||||||
| chr15:40610853
|
G | A | 8 | a0003c0003t0002g0183a0005c0005t0002g0207a0005c0005t0002g0208others(5): Show | 8 | HG00280.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+556G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40610853 | ||||||
| chr15:40611108
|
AT | A | 238 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.251-356delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr15 | 40611108 | |||||
| chr15:40611240
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.251-238C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611240 | ||||||
| chr15:40611258
|
G | A | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.251-220G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611258 | ||||||
| chr15:40611308
|
C | T | 2 | a0012c0012t0001g0129a0012c0012t0001g0130 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.251-170C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611308 | ||||||
| chr15:40611328
|
C | T | 1 | a0003c0003t0014g0190 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.251-150C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611328 | ||||||
| chr15:40611329
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.251-149G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611329 | ||||||
| chr15:40611358
|
C | T | 1 | a0002c0002t0003g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.251-120C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611358 | ||||||
| chr15:40611392
|
C | G | 2 | a0001c0001t0001g0331a0001c0001t0001g0353 | 2 | NA19062.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.251-86C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611392 | ||||||
| chr15:40611419
|
T | G | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.251-59T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 6/25 | chr15 | 40611419 | ||||||
| chr15:40611544
|
A | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+33A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611544 | ||||||
| chr15:40611554
|
A | G | 1 | a0003c0003t0002g0182 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.284+43A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611554 | ||||||
| chr15:40611616
|
C | A | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.284+105C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611616 | ||||||
| chr15:40611684
|
A | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.284+173A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611684 | ||||||
| chr15:40611873
|
G | A | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.284+362G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611873 | ||||||
| chr15:40611946
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.284+435G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611946 | ||||||
| chr15:40611977
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.284+466C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611977 | ||||||
| chr15:40611996
|
A | G | 9 | a0006c0007t0001g0015a0006c0007t0001g0016a0006c0007t0001g0017others(6): Show | 9 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+485A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40611996 | ||||||
| chr15:40612024
|
A | G | 1 | a0002c0002t0003g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.284+513A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612024 | ||||||
| chr15:40612039
|
C | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.284+528C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612039 | ||||||
| chr15:40612048
|
T | G | 1 | a0001c0006t0001g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.284+537T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612048 | ||||||
| chr15:40612323
|
C | CA | 7 | a0001c0001t0001g0280a0001c0001t0001g0313a0001c0001t0004g0281others(4): Show | 7 | HG00597.hp2 HG01123.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+820dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40612323 | |||||
| chr15:40612331
|
A | C | 70 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(67): Show | 70 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.284+820A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612331 | ||||||
| chr15:40612332
|
C | A | 43 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0089others(40): Show | 43 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.284+821C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612332 | ||||||
| chr15:40612345
|
G | A | 6 | a0001c0001t0001g0273a0001c0001t0001g0307a0001c0001t0001g0329others(3): Show | 6 | NA18951.hp2 NA18962.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+834G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612345 | ||||||
| chr15:40612407
|
G | T | 1 | a0001c0001t0001g0310 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.284+896G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612407 | ||||||
| chr15:40612610
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.284+1099G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612610 | ||||||
| chr15:40612804
|
A | C | 1 | a0001c0001t0012g0222 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284+1293A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612804 | ||||||
| chr15:40612903
|
A | T | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+1392A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612903 | ||||||
| chr15:40612984
|
C | T | 1 | a0009c0009t0006g0008 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.284+1473C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40612984 | ||||||
| chr15:40613104
|
A | G | 1 | a0001c0006t0001g0232 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.284+1593A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613104 | ||||||
| chr15:40613155
|
G | A | 3 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359 | 3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.284+1644G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613155 | ||||||
| chr15:40613250
|
A | AGT | 5 | a0002c0002t0003g0057a0009c0009t0006g0008a0009c0009t0007g0005others(2): Show | 5 | HG01109.hp2 HG02273.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+1740_284+1741i others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40613250 | |||||
| chr15:40613252
|
C | T | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.284+1741C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613252 | ||||||
| chr15:40613359
|
T | C | 7 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0001t0001g0276others(4): Show | 7 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.284+1848T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613359 | ||||||
| chr15:40613442
|
A | G | 43 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(40): Show | 43 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.285-1899A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613442 | ||||||
| chr15:40613461
|
TGAAAC | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-1876_285-1872d others(7): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40613461 | |||||
| chr15:40613828
|
C | T | 1 | a0002c0002t0003g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.285-1513C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613828 | ||||||
| chr15:40613883
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.285-1458C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613883 | ||||||
| chr15:40613943
|
G | A | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.285-1398G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613943 | ||||||
| chr15:40613999
|
T | C | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.285-1342T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40613999 | ||||||
| chr15:40614089
|
C | T | 1 | a0002c0002t0001g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.285-1252C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614089 | ||||||
| chr15:40614101
|
C | CT | 120 | a0001c0001t0001g0337a0002c0002t0001g0023a0002c0002t0001g0024others(117): Show | 120 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.285-1226dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40614101 | |||||
| chr15:40614101
|
C | CTT | 15 | a0001c0001t0001g0221a0002c0002t0003g0022a0002c0002t0003g0055others(12): Show | 15 | HG01975.hp2 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.285-1227_285-1226d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr15 | 40614101 | |||||
| chr15:40614240
|
G | A | 1 | a0001c0001t0001g0328 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.285-1101G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614240 | ||||||
| chr15:40614295
|
A | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.285-1046A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614295 | ||||||
| chr15:40614435
|
G | T | 1 | a0017c0042t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.285-906G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614435 | ||||||
| chr15:40614541
|
C | G | 1 | a0026c0029t0009g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.285-800C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614541 | ||||||
| chr15:40614895
|
A | G | 1 | a0022c0035t0001g0268 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.285-446A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614895 | ||||||
| chr15:40614932
|
C | G | 1 | a0017c0042t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.285-409C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 7/25 | chr15 | 40614932 | ||||||
| chr15:40615469
|
C | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.322+91C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615469 | ||||||
| chr15:40615493
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.322+115G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615493 | ||||||
| chr15:40615500
|
T | TG | 366 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(363): Show | 369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.322+123dupG | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40615500 | |||||
| chr15:40615608
|
A | G | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.322+230A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615608 | ||||||
| chr15:40615637
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.322+259C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615637 | ||||||
| chr15:40615697
|
G | A | 1 | a0002c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322+319G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615697 | ||||||
| chr15:40615721
|
C | T | 2 | a0001c0001t0001g0327a0017c0042t0001g0260 | 2 | HG02056.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.322+343C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615721 | ||||||
| chr15:40615762
|
C | CT | 7 | a0001c0001t0012g0222a0001c0006t0001g0233a0002c0002t0003g0022others(4): Show | 7 | HG02738.hp1 HG02738.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.322+399dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40615762 | |||||
| chr15:40615779
|
T | G | 28 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(25): Show | 28 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.322+401T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615779 | ||||||
| chr15:40615853
|
C | A | 2 | a0001c0001t0001g0218a0001c0001t0012g0222 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.322+475C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615853 | ||||||
| chr15:40615994
|
T | TG | 366 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(363): Show | 369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.322+616_322+617ins others(1): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40615994 | ||||||
| chr15:40616009
|
A | C | 293 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.322+631A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616009 | ||||||
| chr15:40616057
|
G | A | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.322+679G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616057 | ||||||
| chr15:40616102
|
A | G | 7 | a0001c0001t0001g0271a0001c0001t0001g0303a0001c0001t0001g0304others(4): Show | 7 | HG01081.hp1 HG01106.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.322+724A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616102 | ||||||
| chr15:40616125
|
C | CT | 72 | a0001c0001t0001g0330a0003c0003t0002g0001a0003c0003t0002g0149others(69): Show | 73 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.322+762dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40616125 | |||||
| chr15:40616498
|
C | T | 296 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0218others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.322+1120C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616498 | ||||||
| chr15:40616563
|
G | A | 1 | a0002c0025t0001g0138 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.322+1185G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616563 | ||||||
| chr15:40616601
|
C | T | 1 | a0002c0002t0003g0030 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.322+1223C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616601 | ||||||
| chr15:40616706
|
A | G | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.322+1328A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616706 | ||||||
| chr15:40616794
|
A | G | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.322+1416A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616794 | ||||||
| chr15:40616920
|
T | C | 3 | a0003c0003t0002g0363a0003c0003t0002g0364a0003c0003t0002g0365 | 3 | HG00738.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.322+1542T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40616920 | ||||||
| chr15:40617012
|
G | T | 38 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(35): Show | 38 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.322+1634G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617012 | ||||||
| chr15:40617073
|
C | T | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.322+1695C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617073 | ||||||
| chr15:40617255
|
C | T | 1 | a0002c0002t0001g0112 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.323-1704C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617255 | ||||||
| chr15:40617269
|
A | G | 72 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(69): Show | 72 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.323-1690A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617269 | ||||||
| chr15:40617358
|
CAA | C | 9 | a0006c0007t0001g0015a0006c0007t0001g0016a0006c0007t0001g0017others(6): Show | 9 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.323-1599_323-1598d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617358 | |||||
| chr15:40617419
|
A | G | 2 | a0005c0005t0002g0179a0005c0005t0002g0185 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.323-1540A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617419 | ||||||
| chr15:40617498
|
T | C | 73 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(70): Show | 73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.323-1461T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617498 | ||||||
| chr15:40617522
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.323-1437G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617522 | ||||||
| chr15:40617750
|
C | T | 2 | a0003c0003t0002g0151a0003c0003t0002g0189 | 2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.323-1209C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617750 | ||||||
| chr15:40617808
|
A | G | 2 | a0016c0019t0003g0063a0016c0019t0003g0081 | 2 | NA18994.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.323-1151A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617808 | ||||||
| chr15:40617918
|
G | A | 1 | a0002c0002t0001g0023 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.323-1041G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617918 | ||||||
| chr15:40617939
|
A | G | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.323-1020A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40617939 | ||||||
| chr15:40617975
|
T | TA | 14 | a0001c0001t0001g0212a0001c0001t0001g0219a0001c0001t0001g0223others(11): Show | 14 | HG00597.hp1 HG00673.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.323-945dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
T | TAAAA | 7 | a0001c0001t0001g0264a0001c0001t0001g0275a0001c0001t0001g0276others(4): Show | 7 | HG01069.hp1 HG01070.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-948_323-945dup others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TA | T | 55 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0214others(52): Show | 56 | HG00408.hp1 HG00741.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.323-945delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAA | T | 15 | a0001c0001t0001g0224a0001c0001t0001g0302a0001c0001t0001g0338others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.323-946_323-945del others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAA | T | 9 | a0003c0003t0002g0158a0003c0003t0002g0159a0003c0003t0002g0160others(6): Show | 9 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.323-947_323-945del others(3): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAA | T | 13 | a0003c0003t0002g0149a0003c0003t0002g0150a0003c0003t0002g0153others(10): Show | 13 | HG00639.hp2 HG00738.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.323-948_323-945del others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAA | T | 27 | a0003c0003t0002g0001a0003c0003t0002g0151a0003c0003t0002g0154others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.323-949_323-945del others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAA | T | 10 | a0003c0003t0002g0174a0003c0003t0002g0175a0003c0003t0002g0176others(7): Show | 10 | HG00558.hp1 HG01516.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.323-950_323-945del others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(1): Show |
T | 17 | a0002c0002t0001g0091a0002c0002t0001g0110a0002c0002t0001g0115others(14): Show | 17 | HG00597.hp2 HG02135.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.323-952_323-945del others(8): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(2): Show |
T | 49 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(46): Show | 49 | HG00423.hp1 HG01109.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.323-953_323-945del others(9): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0001g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.323-954_323-945del others(10): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(6): Show |
T | 3 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359 | 3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.323-957_323-945del others(13): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(7): Show |
T | 7 | a0001c0001t0001g0266a0001c0001t0001g0342a0001c0001t0001g0343others(4): Show | 7 | HG02895.hp1 HG03098.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-958_323-945del others(14): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(8): Show |
T | 7 | a0001c0001t0001g0299a0002c0002t0003g0022a0002c0002t0003g0037others(4): Show | 7 | HG02738.hp1 HG03688.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-959_323-945del others(15): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(9): Show |
T | 64 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(61): Show | 64 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.323-960_323-945del others(16): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(10): Show |
T | 2 | a0002c0002t0003g0077a0002c0002t0003g0123 | 2 | NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.323-961_323-945del others(17): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(11): Show |
T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.323-962_323-945del others(18): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(15): Show |
T | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.323-966_323-945del others(22): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(16): Show |
T | 1 | a0001c0001t0001g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.323-967_323-945del others(23): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(17): Show |
T | 1 | a0001c0001t0001g0326 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.323-968_323-945del others(24): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40617975
|
TAAAAAAA others(19): Show |
T | 1 | a0003c0003t0002g0191 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.323-970_323-945del others(26): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr15 | 40617975 | |||||
| chr15:40618237
|
A | G | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.323-722A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618237 | ||||||
| chr15:40618470
|
C | T | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.323-489C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618470 | ||||||
| chr15:40618472
|
C | G | 1 | a0001c0006t0001g0232 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.323-487C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618472 | ||||||
| chr15:40618509
|
T | C | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.323-450T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618509 | ||||||
| chr15:40618705
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.323-254G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618705 | ||||||
| chr15:40618724
|
A | G | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.323-235A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618724 | ||||||
| chr15:40618829
|
C | T | 1 | a0003c0003t0002g0195 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.323-130C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 8/25 | chr15 | 40618829 | ||||||
| chr15:40619102
|
A | T | 2 | a0008c0010t0001g0216a0008c0010t0001g0217 | 2 | NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.375+91A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619102 | ||||||
| chr15:40619254
|
A | G | 1 | a0002c0002t0003g0012 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.375+243A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619254 | ||||||
| chr15:40619328
|
T | C | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.375+317T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619328 | ||||||
| chr15:40619355
|
A | AAT | 130 | a0001c0001t0001g0221a0001c0001t0001g0284a0001c0001t0001g0311others(127): Show | 130 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.375+365_375+366dup others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619355 | |||||
| chr15:40619355
|
A | AATAT | 13 | a0002c0002t0001g0092a0002c0002t0001g0114a0002c0002t0003g0066others(10): Show | 13 | HG00639.hp1 HG01109.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.375+363_375+366dup others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619355 | |||||
| chr15:40619355
|
A | AATATAT | 4 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(1): Show | 4 | HG02015.hp1 HG02886.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+361_375+366dup others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619355 | |||||
| chr15:40619355
|
AAT | A | 62 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(59): Show | 63 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.375+365_375+366del others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619355 | |||||
| chr15:40619376
|
A | T | 1 | a0003c0003t0002g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.375+365A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619376 | ||||||
| chr15:40619377
|
T | TTAGGCTA others(3): Show |
1 | a0003c0003t0002g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.375+367_375+368ins others(10): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40619377 | |||||
| chr15:40619379
|
T | A | 1 | a0003c0003t0002g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.375+368T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619379 | ||||||
| chr15:40619725
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.375+714C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619725 | ||||||
| chr15:40619872
|
C | T | 1 | a0004c0011t0001g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.376-768C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619872 | ||||||
| chr15:40619902
|
A | G | 4 | a0002c0002t0003g0048a0002c0002t0003g0065a0002c0002t0003g0069others(1): Show | 4 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-738A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40619902 | ||||||
| chr15:40620188
|
C | T | 1 | a0003c0003t0002g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.376-452C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620188 | ||||||
| chr15:40620216
|
A | AT | 128 | a0001c0001t0001g0305a0002c0002t0001g0024a0002c0002t0001g0025others(125): Show | 128 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.376-409dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40620216 | |||||
| chr15:40620216
|
ATT | A | 67 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(64): Show | 68 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.376-410_376-409del others(2): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr15 | 40620216 | |||||
| chr15:40620387
|
T | C | 2 | a0003c0003t0002g0161a0003c0003t0002g0166 | 2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.376-253T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620387 | ||||||
| chr15:40620413
|
A | G | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.376-227A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620413 | ||||||
| chr15:40620505
|
T | C | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.376-135T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620505 | ||||||
| chr15:40620577
|
T | A | 2 | a0001c0001t0001g0342a0001c0001t0001g0343 | 2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.376-63T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620577 | ||||||
| chr15:40620618
|
T | C | 1 | a0003c0003t0002g0151 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.376-22T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 9/25 | chr15 | 40620618 | ||||||
| chr15:40625692
|
G | A | 1 | a0003c0003t0002g0195 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5376+52G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40625692 | ||||||
| chr15:40625931
|
A | G | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5376+291A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40625931 | ||||||
| chr15:40626327
|
C | CT | 34 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(31): Show | 34 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.5376+702dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr15 | 40626327 | |||||
| chr15:40626350
|
T | C | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5376+710T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626350 | ||||||
| chr15:40626355
|
G | A | 2 | a0002c0002t0001g0094a0002c0002t0001g0095 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5376+715G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626355 | ||||||
| chr15:40626386
|
G | A | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5376+746G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626386 | ||||||
| chr15:40626386
|
G | C | 1 | a0002c0002t0001g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.5376+746G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626386 | ||||||
| chr15:40626394
|
C | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5376+754C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626394 | ||||||
| chr15:40626405
|
A | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5376+765A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626405 | ||||||
| chr15:40626563
|
G | A | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5376+923G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626563 | ||||||
| chr15:40626563
|
G | C | 3 | a0004c0004t0001g0248a0004c0004t0001g0256a0004c0004t0001g0258 | 3 | HG02647.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5376+923G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626563 | ||||||
| chr15:40626628
|
G | T | 72 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(69): Show | 72 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.5376+988G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626628 | ||||||
| chr15:40626648
|
C | T | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5376+1008C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626648 | ||||||
| chr15:40626649
|
G | T | 1 | a0002c0002t0003g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5376+1009G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626649 | ||||||
| chr15:40626720
|
C | T | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5376+1080C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626720 | ||||||
| chr15:40626747
|
T | G | 24 | a0004c0004t0001g0242a0004c0004t0001g0243a0004c0004t0001g0244others(21): Show | 24 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.5376+1107T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626747 | ||||||
| chr15:40626781
|
C | T | 1 | a0002c0028t0003g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5376+1141C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626781 | ||||||
| chr15:40626832
|
G | A | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5376+1192G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626832 | ||||||
| chr15:40626888
|
T | C | 1 | a0017c0042t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5377-1182T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40626888 | ||||||
| chr15:40627087
|
G | A | 2 | a0001c0001t0001g0212a0019c0040t0001g0213 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5377-983G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40627087 | ||||||
| chr15:40627095
|
A | G | 1 | a0009c0009t0007g0005 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5377-975A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40627095 | ||||||
| chr15:40627513
|
CA | C | 8 | a0002c0002t0003g0074a0002c0022t0015g0006a0009c0009t0006g0008others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.5377-540delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr15 | 40627513 | |||||
| chr15:40627536
|
CA | C | 44 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(41): Show | 44 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.5377-530delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr15 | 40627536 | |||||
| chr15:40627858
|
C | T | 1 | a0004c0004t0001g0245 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5377-212C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40627858 | ||||||
| chr15:40627946
|
C | T | 293 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.5377-124C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 10/25 | chr15 | 40627946 | ||||||
| chr15:40628771
|
A | T | 2 | a0001c0001t0001g0312a0001c0001t0004g0298 | 2 | HG02148.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.5583+93A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 12/25 | chr15 | 40628771 | ||||||
| chr15:40628772
|
T | A | 1 | a0005c0005t0002g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5583+94T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 12/25 | chr15 | 40628772 | ||||||
| chr15:40628839
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5583+161A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 12/25 | chr15 | 40628839 | ||||||
| chr15:40628891
|
G | A | 1 | a0002c0002t0003g0131 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.5583+213G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 12/25 | chr15 | 40628891 | ||||||
| chr15:40629380
|
AGTTTCTT others(8): Show |
A | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5682+14_5682+28del others(15): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629380 | |||||
| chr15:40629471
|
C | CT | 192 | a0001c0001t0001g0296a0002c0002t0001g0023a0002c0002t0001g0024others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.5682+116dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629471 | |||||
| chr15:40629495
|
C | CT | 38 | a0001c0001t0001g0144a0001c0001t0001g0212a0001c0001t0001g0266others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.5682+150dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629495 | |||||
| chr15:40629495
|
C | CTT | 6 | a0001c0001t0001g0273a0001c0001t0001g0301a0001c0001t0001g0307others(3): Show | 6 | HG02717.hp1 HG03492.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.5682+149_5682+150d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629495 | |||||
| chr15:40629495
|
CT | C | 14 | a0001c0001t0001g0275a0001c0006t0001g0236a0002c0022t0015g0006others(11): Show | 14 | HG01516.hp2 HG01978.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.5682+150delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629495 | |||||
| chr15:40629495
|
CTTTTTTT others(6): Show |
C | 132 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(129): Show | 132 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.5682+138_5682+150d others(15): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629495 | |||||
| chr15:40629500
|
T | C | 2 | a0003c0003t0002g0196a0022c0035t0001g0268 | 2 | HG01978.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.5682+129T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629500 | ||||||
| chr15:40629506
|
T | C | 1 | a0001c0001t0001g0337 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5682+135T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629506 | ||||||
| chr15:40629736
|
C | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5682+365C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629736 | ||||||
| chr15:40629779
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5682+408G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629779 | ||||||
| chr15:40629793
|
G | A | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5682+422G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629793 | ||||||
| chr15:40629800
|
C | T | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5682+429C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629800 | ||||||
| chr15:40629862
|
A | G | 3 | a0001c0001t0001g0351a0001c0001t0001g0352a0003c0003t0002g0184 | 3 | HG01346.hp1 NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.5682+491A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40629862 | ||||||
| chr15:40629970
|
C | CT | 137 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(134): Show | 137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.5682+604dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40629970 | |||||
| chr15:40630204
|
T | A | 1 | a0003c0003t0002g0191 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5682+833T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630204 | ||||||
| chr15:40630205
|
T | C | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.5682+834T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630205 | ||||||
| chr15:40630326
|
ATT | A | 42 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5682+960_5682+961d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40630326 | |||||
| chr15:40630330
|
T | A | 42 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5682+959T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630330 | ||||||
| chr15:40630331
|
T | A | 42 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5682+960T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630331 | ||||||
| chr15:40630332
|
T | A | 42 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5682+961T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630332 | ||||||
| chr15:40630468
|
C | T | 1 | a0006c0007t0001g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5682+1097C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630468 | ||||||
| chr15:40630567
|
A | G | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.5682+1196A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630567 | ||||||
| chr15:40630717
|
G | C | 217 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.5682+1346G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630717 | ||||||
| chr15:40630787
|
A | G | 1 | a0002c0002t0003g0035 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5682+1416A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630787 | ||||||
| chr15:40630899
|
C | T | 1 | a0004c0004t0001g0245 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5682+1528C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630899 | ||||||
| chr15:40630917
|
C | T | 1 | a0003c0003t0002g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5682+1546C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630917 | ||||||
| chr15:40630975
|
G | T | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.5682+1604G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40630975 | ||||||
| chr15:40631141
|
AAAAAT | A | 8 | a0002c0002t0003g0030a0002c0002t0003g0038a0002c0002t0003g0039others(5): Show | 8 | HG02523.hp2 NA18960.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.5682+1780_5682+178 others(9): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40631141 | |||||
| chr15:40631157
|
CAAGG | C | 45 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(42): Show | 45 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.5682+1790_5682+179 others(8): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40631157 | |||||
| chr15:40631485
|
A | G | 7 | a0010c0013t0001g0021a0010c0013t0001g0103a0010c0013t0001g0107others(4): Show | 7 | HG00597.hp2 NA18946.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.5682+2114A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631485 | ||||||
| chr15:40631561
|
C | A | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.5682+2190C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631561 | ||||||
| chr15:40631714
|
G | A | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.5682+2343G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631714 | ||||||
| chr15:40631740
|
G | A | 6 | a0003c0003t0002g0158a0003c0003t0002g0159a0003c0003t0002g0164others(3): Show | 6 | HG00639.hp2 HG00733.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.5682+2369G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631740 | ||||||
| chr15:40631898
|
A | G | 1 | a0005c0005t0002g0145 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5682+2527A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631898 | ||||||
| chr15:40631914
|
T | G | 72 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(69): Show | 72 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.5682+2543T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40631914 | ||||||
| chr15:40632008
|
C | CA | 11 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0314others(8): Show | 11 | HG00280.hp2 HG02080.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.5682+2653dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40632008 | |||||
| chr15:40632109
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0356 | 2 | NA19003.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.5682+2738C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40632109 | ||||||
| chr15:40632210
|
A | AC | 78 | a0001c0001t0001g0223a0001c0001t0001g0267a0001c0001t0001g0335others(75): Show | 78 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.5682+2848dupC | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40632210 | |||||
| chr15:40632210
|
A | ACC | 39 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0089others(36): Show | 39 | HG00597.hp2 HG00673.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.5682+2847_5682+284 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40632210 | |||||
| chr15:40632210
|
A | ACCC | 18 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0090others(15): Show | 18 | HG00423.hp1 HG01109.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.5682+2846_5682+284 others(7): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40632210 | |||||
| chr15:40632220
|
A | C | 1 | a0012c0012t0001g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5682+2849A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40632220 | ||||||
| chr15:40632380
|
A | G | 269 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.5682+3009A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40632380 | ||||||
| chr15:40632589
|
C | T | 2 | a0002c0002t0001g0094a0002c0002t0001g0095 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5682+3218C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40632589 | ||||||
| chr15:40633005
|
C | T | 2 | a0002c0002t0001g0094a0002c0002t0001g0095 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5682+3634C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633005 | ||||||
| chr15:40633016
|
T | A | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.5682+3645T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633016 | ||||||
| chr15:40633029
|
C | T | 1 | a0002c0002t0016g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5682+3658C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633029 | ||||||
| chr15:40633200
|
G | A | 43 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(40): Show | 43 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5682+3829G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633200 | ||||||
| chr15:40633201
|
T | C | 1 | a0002c0002t0003g0124 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5682+3830T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633201 | ||||||
| chr15:40633258
|
C | T | 1 | a0002c0002t0016g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5682+3887C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633258 | ||||||
| chr15:40633262
|
G | A | 4 | a0004c0011t0001g0240a0004c0011t0001g0241a0004c0011t0001g0263others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.5682+3891G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633262 | ||||||
| chr15:40633310
|
C | CA | 78 | a0001c0001t0001g0267a0001c0001t0001g0331a0001c0001t0004g0315others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.5682+3959dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40633310 | |||||
| chr15:40633310
|
C | CAA | 122 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(119): Show | 122 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.5682+3958_5682+395 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40633310 | |||||
| chr15:40633310
|
C | CAAA | 9 | a0002c0002t0001g0023a0002c0002t0001g0115a0002c0002t0001g0120others(6): Show | 9 | HG03471.hp2 HG03831.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.5682+3957_5682+395 others(7): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40633310 | |||||
| chr15:40633443
|
G | A | 3 | a0003c0003t0002g0157a0003c0003t0002g0187a0003c0003t0002g0196 | 3 | HG01167.hp1 HG01169.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.5682+4072G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633443 | ||||||
| chr15:40633461
|
T | C | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5682+4090T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633461 | ||||||
| chr15:40633666
|
A | C | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5682+4295A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633666 | ||||||
| chr15:40633703
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5682+4332G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633703 | ||||||
| chr15:40633738
|
G | A | 74 | a0002c0002t0001g0026a0003c0003t0002g0001a0003c0003t0002g0149others(71): Show | 75 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.5682+4367G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633738 | ||||||
| chr15:40633750
|
A | G | 2 | a0002c0002t0001g0094a0002c0002t0001g0095 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5682+4379A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40633750 | ||||||
| chr15:40634085
|
T | TTTG | 3 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359 | 3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5682+4732_5682+473 others(7): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40634085 | |||||
| chr15:40634189
|
C | G | 1 | a0002c0002t0001g0096 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5682+4818C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634189 | ||||||
| chr15:40634398
|
C | T | 3 | a0006c0007t0001g0015a0006c0007t0001g0027a0006c0007t0001g0141 | 3 | HG03139.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5682+5027C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634398 | ||||||
| chr15:40634423
|
T | C | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5682+5052T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634423 | ||||||
| chr15:40634426
|
G | A | 1 | a0010c0013t0001g0021 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5682+5055G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634426 | ||||||
| chr15:40634456
|
C | G | 132 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(129): Show | 132 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.5682+5085C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634456 | ||||||
| chr15:40634509
|
G | A | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5682+5138G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634509 | ||||||
| chr15:40634552
|
AATTGGGA others(18): Show |
A | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.5682+5182_5682+520 others(29): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634552 | ||||||
| chr15:40634740
|
A | G | 1 | a0003c0003t0002g0170 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5682+5369A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634740 | ||||||
| chr15:40634781
|
A | G | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.5682+5410A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634781 | ||||||
| chr15:40634957
|
A | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5682+5586A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40634957 | ||||||
| chr15:40635025
|
C | T | 1 | a0017c0042t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5682+5654C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635025 | ||||||
| chr15:40635050
|
A | AT | 6 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0038t0001g0234others(3): Show | 6 | HG02145.hp2 HG02717.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.5682+5695dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40635050 | |||||
| chr15:40635050
|
AT | A | 132 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(129): Show | 132 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.5682+5695delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40635050 | |||||
| chr15:40635288
|
G | C | 7 | a0001c0001t0001g0271a0001c0001t0001g0303a0001c0001t0001g0304others(4): Show | 7 | HG01081.hp1 HG01106.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.5683-5624G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635288 | ||||||
| chr15:40635524
|
T | C | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5683-5388T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635524 | ||||||
| chr15:40635553
|
C | T | 42 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5683-5359C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635553 | ||||||
| chr15:40635628
|
A | G | 1 | a0001c0001t0001g0334 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.5683-5284A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635628 | ||||||
| chr15:40635743
|
A | G | 1 | a0025c0030t0002g0194 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.5683-5169A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635743 | ||||||
| chr15:40635955
|
G | C | 1 | a0002c0002t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5683-4957G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635955 | ||||||
| chr15:40635977
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-4935G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635977 | ||||||
| chr15:40635995
|
G | A | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-4917G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40635995 | ||||||
| chr15:40636012
|
A | G | 2 | a0005c0005t0002g0179a0005c0005t0002g0185 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5683-4900A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636012 | ||||||
| chr15:40636127
|
C | T | 1 | a0001c0001t0001g0319 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.5683-4785C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636127 | ||||||
| chr15:40636205
|
G | A | 1 | a0002c0002t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5683-4707G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636205 | ||||||
| chr15:40636415
|
T | C | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5683-4497T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636415 | ||||||
| chr15:40636458
|
T | C | 1 | a0002c0022t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5683-4454T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636458 | ||||||
| chr15:40636486
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0092 | 3 | NA18955.hp2 NA18972.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.5683-4426G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636486 | ||||||
| chr15:40636754
|
C | A | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5683-4158C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40636754 | ||||||
| chr15:40637004
|
T | A | 43 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(40): Show | 43 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5683-3908T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637004 | ||||||
| chr15:40637037
|
C | A | 1 | a0004c0004t0001g0243 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5683-3875C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637037 | ||||||
| chr15:40637047
|
C | CT | 42 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5683-3855dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637047 | |||||
| chr15:40637070
|
T | A | 366 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(363): Show | 369 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.5683-3842T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637070 | ||||||
| chr15:40637135
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5683-3777C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637135 | ||||||
| chr15:40637175
|
C | CT | 76 | a0001c0001t0001g0297a0001c0006t0001g0232a0002c0002t0001g0094others(73): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.5683-3724dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637175 | |||||
| chr15:40637256
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5683-3656G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637256 | ||||||
| chr15:40637323
|
C | CT | 135 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(132): Show | 135 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.5683-3578dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637323 | |||||
| chr15:40637368
|
G | GT | 69 | a0001c0001t0001g0274a0001c0001t0001g0313a0001c0001t0001g0332others(66): Show | 69 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.5683-3532dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637368 | |||||
| chr15:40637368
|
G | GTT | 61 | a0002c0002t0001g0023a0002c0002t0001g0026a0002c0002t0001g0089others(58): Show | 61 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.5683-3533_5683-353 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637368 | |||||
| chr15:40637596
|
G | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-3316G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637596 | ||||||
| chr15:40637616
|
T | C | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.5683-3296T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637616 | ||||||
| chr15:40637625
|
A | G | 1 | a0002c0022t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5683-3287A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637625 | ||||||
| chr15:40637873
|
G | GA | 12 | a0001c0001t0004g0281a0003c0003t0002g0153a0006c0007t0001g0015others(9): Show | 12 | HG01123.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.5683-3029dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40637873 | |||||
| chr15:40637885
|
C | G | 1 | a0001c0001t0001g0305 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5683-3027C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40637885 | ||||||
| chr15:40638167
|
G | C | 20 | a0002c0002t0003g0002a0002c0002t0003g0037a0002c0002t0003g0047others(17): Show | 20 | HG00609.hp2 HG01192.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.5683-2745G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638167 | ||||||
| chr15:40638250
|
A | AG | 25 | a0001c0001t0001g0142a0001c0001t0001g0219a0001c0001t0001g0269others(22): Show | 25 | HG00408.hp1 HG00741.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.5683-2656dupG | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40638250 | |||||
| chr15:40638251
|
GGGGGGA | G | 122 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(119): Show | 122 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.5683-2648_5683-264 others(10): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40638251 | |||||
| chr15:40638252
|
GGGGGA | G | 9 | a0002c0002t0001g0092a0002c0002t0001g0101a0002c0002t0001g0108others(6): Show | 9 | HG01496.hp2 HG02738.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.5683-2655_5683-265 others(9): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40638252 | |||||
| chr15:40638257
|
A | G | 2 | a0001c0001t0001g0356a0003c0003t0002g0150 | 2 | HG02698.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.5683-2655A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638257 | ||||||
| chr15:40638512
|
G | T | 1 | a0004c0004t0001g0359 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5683-2400G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638512 | ||||||
| chr15:40638669
|
T | A | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-2243T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638669 | ||||||
| chr15:40638670
|
T | C | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.5683-2242T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638670 | ||||||
| chr15:40638709
|
T | C | 1 | a0003c0003t0002g0200 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5683-2203T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638709 | ||||||
| chr15:40638782
|
C | T | 1 | a0001c0006t0001g0230 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5683-2130C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638782 | ||||||
| chr15:40638784
|
C | T | 3 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0092 | 3 | NA18955.hp2 NA18972.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.5683-2128C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638784 | ||||||
| chr15:40638816
|
C | CT | 12 | a0005c0005t0002g0145a0005c0005t0002g0162a0005c0005t0002g0163others(9): Show | 12 | HG01255.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5683-2084dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40638816 | |||||
| chr15:40638950
|
T | C | 1 | a0003c0003t0002g0204 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5683-1962T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40638950 | ||||||
| chr15:40639089
|
A | G | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.5683-1823A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639089 | ||||||
| chr15:40639159
|
C | CT | 68 | a0002c0002t0001g0126a0002c0002t0003g0035a0003c0003t0002g0001others(65): Show | 69 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.5683-1740dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40639159 | |||||
| chr15:40639234
|
C | T | 1 | a0005c0005t0002g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5683-1678C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639234 | ||||||
| chr15:40639414
|
C | T | 3 | a0007c0008t0005g0052a0007c0008t0005g0053a0007c0008t0005g0054 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5683-1498C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639414 | ||||||
| chr15:40639425
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5683-1487A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639425 | ||||||
| chr15:40639483
|
G | A | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5683-1429G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639483 | ||||||
| chr15:40639510
|
A | G | 215 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.5683-1402A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639510 | ||||||
| chr15:40639585
|
CA | C | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.5683-1314delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40639585 | |||||
| chr15:40639610
|
A | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-1302A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639610 | ||||||
| chr15:40639704
|
G | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-1208G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639704 | ||||||
| chr15:40639710
|
G | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5683-1202G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639710 | ||||||
| chr15:40639872
|
C | T | 3 | a0009c0009t0006g0008a0009c0009t0006g0010a0030c0023t0006g0009 | 3 | HG02451.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5683-1040C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639872 | ||||||
| chr15:40639936
|
G | A | 1 | a0001c0001t0001g0306 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.5683-976G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40639936 | ||||||
| chr15:40640082
|
T | C | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5683-830T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640082 | ||||||
| chr15:40640085
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5683-819_5683-798d others(24): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40640085 | |||||
| chr15:40640098
|
C | CT | 14 | a0001c0001t0001g0266a0001c0001t0001g0296a0001c0001t0001g0334others(11): Show | 14 | HG00621.hp2 HG01978.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.5683-798dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40640098 | |||||
| chr15:40640098
|
C | CTT | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-799_5683-798d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40640098 | |||||
| chr15:40640098
|
CT | C | 8 | a0001c0001t0001g0314a0002c0002t0001g0092a0002c0002t0003g0039others(5): Show | 8 | HG00733.hp2 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.5683-798delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr15 | 40640098 | |||||
| chr15:40640103
|
T | C | 1 | a0002c0002t0003g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5683-809T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640103 | ||||||
| chr15:40640157
|
C | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-755C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640157 | ||||||
| chr15:40640182
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5683-730C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640182 | ||||||
| chr15:40640245
|
C | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5683-667C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640245 | ||||||
| chr15:40640330
|
A | T | 2 | a0001c0001t0001g0342a0001c0001t0001g0343 | 2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.5683-582A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640330 | ||||||
| chr15:40640331
|
A | G | 2 | a0003c0003t0002g0186a0003c0003t0002g0191 | 2 | HG02300.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.5683-581A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640331 | ||||||
| chr15:40640445
|
T | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5683-467T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640445 | ||||||
| chr15:40640515
|
G | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | NA18970.hp1 NA18974.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.5683-397G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640515 | ||||||
| chr15:40640731
|
C | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5683-181C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 13/25 | chr15 | 40640731 | ||||||
| chr15:40641347
|
G | A | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.5798+320G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641347 | ||||||
| chr15:40641397
|
A | T | 6 | a0003c0003t0002g0158a0003c0003t0002g0159a0003c0003t0002g0164others(3): Show | 6 | HG00639.hp2 HG00733.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.5798+370A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641397 | ||||||
| chr15:40641454
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5798+427G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641454 | ||||||
| chr15:40641483
|
G | A | 24 | a0004c0004t0001g0242a0004c0004t0001g0243a0004c0004t0001g0244others(21): Show | 24 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.5798+456G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641483 | ||||||
| chr15:40641779
|
A | T | 1 | a0009c0009t0007g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5798+752A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641779 | ||||||
| chr15:40641838
|
A | G | 17 | a0002c0002t0003g0002a0002c0002t0003g0037a0002c0002t0003g0047others(14): Show | 17 | HG00609.hp2 HG01192.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.5798+811A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641838 | ||||||
| chr15:40641842
|
A | G | 1 | a0003c0003t0002g0183 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5798+815A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641842 | ||||||
| chr15:40641927
|
A | ACCCCTCC others(3): Show |
1 | a0003c0003t0010g0152 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5798+900_5798+901i others(12): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641927 | ||||||
| chr15:40641928
|
T | C | 1 | a0003c0003t0010g0152 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5798+901T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641928 | ||||||
| chr15:40641976
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0001g0337 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.5798+949A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40641976 | ||||||
| chr15:40642002
|
A | C | 1 | a0002c0002t0003g0061 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5798+975A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642002 | ||||||
| chr15:40642030
|
G | T | 1 | a0004c0004t0001g0257 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5798+1003G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642030 | ||||||
| chr15:40642142
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.5798+1115G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642142 | ||||||
| chr15:40642259
|
C | T | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5798+1232C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642259 | ||||||
| chr15:40642291
|
C | T | 28 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(25): Show | 28 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.5798+1264C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642291 | ||||||
| chr15:40642316
|
G | A | 1 | a0002c0022t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5798+1289G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642316 | ||||||
| chr15:40642422
|
C | T | 1 | a0017c0042t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5798+1395C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642422 | ||||||
| chr15:40642423
|
G | A | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.5798+1396G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642423 | ||||||
| chr15:40642794
|
A | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5798+1767A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642794 | ||||||
| chr15:40642876
|
C | T | 1 | a0005c0005t0002g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5798+1849C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642876 | ||||||
| chr15:40642880
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5798+1853G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642880 | ||||||
| chr15:40642993
|
C | T | 3 | a0006c0007t0001g0015a0006c0007t0001g0027a0006c0007t0001g0141 | 3 | HG03139.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5798+1966C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40642993 | ||||||
| chr15:40643165
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5799-1832T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643165 | ||||||
| chr15:40643353
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5799-1644C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643353 | ||||||
| chr15:40643366
|
T | C | 2 | a0003c0003t0002g0151a0003c0003t0002g0189 | 2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.5799-1631T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643366 | ||||||
| chr15:40643456
|
G | A | 3 | a0002c0002t0001g0108a0002c0002t0001g0114a0002c0002t0001g0117 | 3 | HG01496.hp2 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.5799-1541G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643456 | ||||||
| chr15:40643489
|
A | T | 2 | a0016c0019t0003g0063a0016c0019t0003g0081 | 2 | NA18994.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.5799-1508A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643489 | ||||||
| chr15:40643515
|
C | T | 137 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(134): Show | 137 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.5799-1482C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643515 | ||||||
| chr15:40643517
|
C | T | 3 | a0002c0002t0001g0108a0002c0002t0001g0114a0002c0002t0001g0117 | 3 | HG01496.hp2 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.5799-1480C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643517 | ||||||
| chr15:40643519
|
C | G | 1 | a0002c0002t0008g0011 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.5799-1478C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643519 | ||||||
| chr15:40643646
|
C | T | 2 | a0024c0033t0017g0148a0032c0034t0013g0013 | 2 | HG00741.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.5799-1351C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643646 | ||||||
| chr15:40643824
|
A | G | 43 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(40): Show | 43 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.5799-1173A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40643824 | ||||||
| chr15:40644390
|
C | T | 2 | a0001c0001t0001g0331a0001c0001t0001g0353 | 2 | NA19062.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.5799-607C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644390 | ||||||
| chr15:40644408
|
A | G | 293 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.5799-589A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644408 | ||||||
| chr15:40644470
|
C | G | 1 | a0001c0001t0001g0285 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5799-527C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644470 | ||||||
| chr15:40644614
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5799-383C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644614 | ||||||
| chr15:40644646
|
C | T | 3 | a0009c0009t0006g0008a0009c0009t0006g0010a0030c0023t0006g0009 | 3 | HG02451.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5799-351C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644646 | ||||||
| chr15:40644655
|
T | C | 15 | a0002c0002t0003g0014a0002c0002t0003g0030a0002c0002t0003g0038others(12): Show | 15 | HG02027.hp1 HG02523.hp2 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.5799-342T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644655 | ||||||
| chr15:40644810
|
T | G | 2 | a0003c0003t0002g0186a0003c0003t0002g0191 | 2 | HG02300.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.5799-187T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644810 | ||||||
| chr15:40644914
|
C | T | 2 | a0012c0012t0001g0129a0012c0012t0001g0130 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5799-83C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644914 | ||||||
| chr15:40644917
|
CT | C | 42 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.5799-77delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr15 | 40644917 | |||||
| chr15:40644984
|
T | C | 1 | a0001c0006t0001g0231 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.5799-13T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 14/25 | chr15 | 40644984 | ||||||
| chr15:40645139
|
T | C | 3 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359 | 3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5889+52T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645139 | ||||||
| chr15:40645214
|
G | C | 1 | a0001c0001t0001g0305 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5889+127G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645214 | ||||||
| chr15:40645377
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5890-279G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645377 | ||||||
| chr15:40645384
|
T | C | 2 | a0012c0012t0001g0129a0012c0012t0001g0130 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5890-272T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645384 | ||||||
| chr15:40645444
|
C | G | 1 | a0001c0001t0004g0318 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5890-212C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645444 | ||||||
| chr15:40645449
|
A | G | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.5890-207A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645449 | ||||||
| chr15:40645529
|
C | T | 354 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(351): Show | 357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.5890-127C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645529 | ||||||
| chr15:40645603
|
C | T | 1 | a0003c0003t0002g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5890-53C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645603 | ||||||
| chr15:40645615
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5890-41G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 15/25 | chr15 | 40645615 | ||||||
| chr15:40645796
|
TAGAA | T | 11 | a0005c0005t0002g0145a0005c0005t0002g0162a0005c0005t0002g0163others(8): Show | 11 | HG01255.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.6006+28_6006+31del others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr15 | 40645796 | |||||
| chr15:40645841
|
A | T | 2 | a0002c0002t0001g0094a0002c0002t0001g0095 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6006+69A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40645841 | ||||||
| chr15:40645938
|
C | T | 3 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359 | 3 | HG02280.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.6006+166C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40645938 | ||||||
| chr15:40645979
|
A | G | 1 | a0001c0001t0004g0295 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6006+207A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40645979 | ||||||
| chr15:40646141
|
G | A | 1 | a0004c0004t0001g0248 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6006+369G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646141 | ||||||
| chr15:40646347
|
A | G | 1 | a0001c0038t0001g0234 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.6006+575A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646347 | ||||||
| chr15:40646646
|
G | A | 8 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(5): Show | 8 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.6007-341G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646646 | ||||||
| chr15:40646685
|
A | G | 1 | a0001c0006t0001g0230 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6007-302A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646685 | ||||||
| chr15:40646714
|
A | T | 2 | a0002c0002t0001g0137a0002c0025t0001g0138 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6007-273A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646714 | ||||||
| chr15:40646718
|
A | G | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.6007-269A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646718 | ||||||
| chr15:40646725
|
C | T | 1 | a0006c0007t0001g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6007-262C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646725 | ||||||
| chr15:40646856
|
C | CA | 24 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0012g0222others(21): Show | 24 | HG00609.hp2 HG01891.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.6007-109dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr15 | 40646856 | |||||
| chr15:40646856
|
CA | C | 15 | a0001c0001t0001g0271a0001c0001t0001g0307a0001c0001t0001g0343others(12): Show | 15 | HG00099.hp1 HG00280.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.6007-109delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr15 | 40646856 | |||||
| chr15:40646896
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.6007-91T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646896 | ||||||
| chr15:40646920
|
A | G | 1 | a0002c0022t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6007-67A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 16/25 | chr15 | 40646920 | ||||||
| chr15:40647155
|
C | T | 1 | a0002c0002t0003g0139 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.6094+81C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647155 | ||||||
| chr15:40647213
|
G | A | 1 | a0002c0002t0003g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6094+139G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647213 | ||||||
| chr15:40647250
|
G | A | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.6094+176G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647250 | ||||||
| chr15:40647454
|
G | A | 241 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.6094+380G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647454 | ||||||
| chr15:40647489
|
A | T | 1 | a0002c0002t0003g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6094+415A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647489 | ||||||
| chr15:40647515
|
C | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6094+441C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647515 | ||||||
| chr15:40647528
|
C | T | 1 | a0002c0025t0001g0138 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6094+454C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647528 | ||||||
| chr15:40647628
|
C | T | 1 | a0004c0004t0001g0258 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6094+554C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647628 | ||||||
| chr15:40647769
|
G | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6094+695G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647769 | ||||||
| chr15:40647915
|
T | G | 2 | a0002c0002t0003g0046a0002c0002t0003g0064 | 2 | HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.6094+841T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647915 | ||||||
| chr15:40647950
|
A | G | 73 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(70): Show | 73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.6094+876A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40647950 | ||||||
| chr15:40648041
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.6094+967G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648041 | ||||||
| chr15:40648077
|
TAA | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6094+1007_6094+100 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648077 | |||||
| chr15:40648244
|
G | A | 4 | a0001c0001t0001g0266a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | NA18970.hp1 NA18974.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.6094+1170G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648244 | ||||||
| chr15:40648442
|
AT | A | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6094+1369delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648442 | ||||||
| chr15:40648495
|
T | G | 1 | a0006c0007t0001g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6094+1421T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648495 | ||||||
| chr15:40648508
|
G | T | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6094+1434G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648508 | ||||||
| chr15:40648611
|
G | A | 1 | a0004c0004t0001g0255 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6094+1537G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648611 | ||||||
| chr15:40648829
|
CT | C | 205 | a0001c0001t0001g0212a0001c0001t0001g0273a0001c0001t0001g0286others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.6095-1454delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648829 | |||||
| chr15:40648843
|
T | G | 1 | a0002c0002t0003g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6095-1458T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648843 | ||||||
| chr15:40648864
|
G | C | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.6095-1437G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648864 | ||||||
| chr15:40648869
|
TACCCAGG others(9): Show |
T | 1 | a0001c0001t0001g0333 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6095-1430_6095-141 others(20): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648869 | |||||
| chr15:40648888
|
G | T | 1 | a0001c0001t0001g0333 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6095-1413G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648888 | ||||||
| chr15:40648889
|
G | T | 1 | a0001c0001t0001g0333 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6095-1412G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648889 | ||||||
| chr15:40648916
|
G | A | 1 | a0001c0001t0001g0287 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.6095-1385G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648916 | ||||||
| chr15:40648964
|
G | A | 1 | a0001c0006t0001g0232 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.6095-1337G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648964 | ||||||
| chr15:40648970
|
C | T | 1 | a0005c0005t0002g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6095-1331C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648970 | ||||||
| chr15:40648988
|
C | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6095-1313C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40648988 | ||||||
| chr15:40648996
|
A | AT | 131 | a0001c0001t0001g0271a0001c0001t0001g0303a0001c0001t0001g0304others(128): Show | 131 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.6095-1292dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648996 | |||||
| chr15:40648996
|
A | ATT | 11 | a0002c0002t0001g0126a0002c0002t0003g0044a0006c0007t0001g0015others(8): Show | 11 | HG01256.hp2 HG02895.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.6095-1293_6095-129 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40648996 | |||||
| chr15:40649044
|
G | A | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6095-1257G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649044 | ||||||
| chr15:40649115
|
G | T | 1 | a0002c0022t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6095-1186G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649115 | ||||||
| chr15:40649130
|
G | A | 3 | a0004c0004t0001g0248a0004c0004t0001g0256a0004c0004t0001g0258 | 3 | HG02647.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.6095-1171G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649130 | ||||||
| chr15:40649180
|
A | G | 5 | a0002c0002t0001g0090a0002c0002t0001g0096a0002c0002t0001g0100others(2): Show | 5 | HG01168.hp2 HG02293.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.6095-1121A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649180 | ||||||
| chr15:40649197
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6095-1104T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649197 | ||||||
| chr15:40649549
|
C | T | 1 | a0001c0006t0001g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.6095-752C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649549 | ||||||
| chr15:40649616
|
A | G | 2 | a0002c0002t0003g0044a0002c0002t0003g0133 | 2 | NA18962.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.6095-685A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649616 | ||||||
| chr15:40649700
|
G | T | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6095-601G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649700 | ||||||
| chr15:40649762
|
C | T | 12 | a0002c0002t0003g0002a0002c0002t0003g0037a0002c0002t0003g0049others(9): Show | 12 | HG01192.hp2 HG01928.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.6095-539C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649762 | ||||||
| chr15:40649811
|
C | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6095-490C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | chr15 | 40649811 | ||||||
| chr15:40650125
|
GA | G | 45 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(42): Show | 45 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.6095-161delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr15 | 40650125 | |||||
| chr15:40650517
|
G | GT | 13 | a0001c0001t0001g0282a0001c0001t0004g0281a0001c0001t0012g0222others(10): Show | 13 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.6173-13dupT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr15 | 40650517 | |||||
| chr15:40650517
|
GT | G | 104 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(101): Show | 104 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.6173-13delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr15 | 40650517 | |||||
| chr15:40650588
|
G | A | 2 | a0005c0005t0002g0181a0005c0005t0002g0203 | 2 | HG02965.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.6212+5G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40650588 | ||||||
| chr15:40650852
|
A | G | 1 | a0002c0002t0001g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.6212+269A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40650852 | ||||||
| chr15:40650922
|
A | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6212+339A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40650922 | ||||||
| chr15:40651075
|
C | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6213-396C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651075 | ||||||
| chr15:40651075
|
C | CA | 15 | a0001c0001t0001g0266a0001c0001t0004g0318a0001c0038t0001g0234others(12): Show | 15 | HG00099.hp2 HG01109.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.6213-383dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651075 | |||||
| chr15:40651124
|
A | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6213-347A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651124 | ||||||
| chr15:40651290
|
TTA | T | 67 | a0002c0002t0001g0089a0002c0002t0001g0112a0002c0002t0001g0126others(64): Show | 68 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.6213-176_6213-175d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651290 | |||||
| chr15:40651292
|
A | T | 1 | a0004c0004t0001g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6213-179A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651292 | ||||||
| chr15:40651293
|
TATA | T | 72 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(69): Show | 72 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.6213-176_6213-174d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651293 | |||||
| chr15:40651293
|
TATAA | T | 71 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(68): Show | 71 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.6213-176_6213-173d others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651293 | |||||
| chr15:40651295
|
T | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6213-176T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651295 | ||||||
| chr15:40651295
|
TA | T | 12 | a0001c0001t0001g0273a0001c0001t0001g0307a0001c0001t0001g0329others(9): Show | 12 | HG01928.hp2 NA18951.hp2 NA18962.hp2 others(9): Show |
intron_variant | MODIFIER | c.6213-159delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr15 | 40651295 | |||||
| chr15:40651413
|
A | C | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6213-58A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 19/25 | chr15 | 40651413 | ||||||
| chr15:40651905
|
C | T | 1 | a0002c0002t0003g0069 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6315-100C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 20/25 | chr15 | 40651905 | ||||||
| chr15:40651906
|
A | T | 1 | a0004c0004t0001g0258 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6315-99A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 20/25 | chr15 | 40651906 | ||||||
| chr15:40651945
|
A | T | 1 | a0002c0002t0003g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6315-60A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 20/25 | chr15 | 40651945 | ||||||
| chr15:40652133
|
T | A | 1 | a0002c0002t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6415+28T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652133 | ||||||
| chr15:40652186
|
A | G | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.6415+81A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652186 | ||||||
| chr15:40652196
|
C | T | 3 | a0012c0012t0001g0029a0012c0012t0001g0129a0012c0012t0001g0130 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.6415+91C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652196 | ||||||
| chr15:40652211
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6415+106G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652211 | ||||||
| chr15:40652250
|
A | G | 2 | a0001c0001t0001g0212a0019c0040t0001g0213 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6415+145A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652250 | ||||||
| chr15:40652455
|
CT | C | 205 | a0001c0001t0001g0288a0002c0002t0001g0023a0002c0002t0001g0024others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.6415+367delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652455 | |||||
| chr15:40652455
|
CTT | C | 8 | a0002c0002t0001g0096a0002c0002t0003g0022a0002c0002t0003g0057others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.6415+366_6415+367d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652455 | |||||
| chr15:40652508
|
G | A | 1 | a0013c0017t0003g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6415+403G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652508 | ||||||
| chr15:40652583
|
C | A | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6415+478C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652583 | ||||||
| chr15:40652583
|
C | T | 9 | a0001c0001t0001g0282a0001c0001t0001g0293a0001c0001t0001g0310others(6): Show | 9 | HG00621.hp1 HG02056.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.6415+478C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652583 | ||||||
| chr15:40652750
|
A | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6415+645A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652750 | ||||||
| chr15:40652753
|
A | ACT | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6415+649_6415+650d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652753 | |||||
| chr15:40652760
|
C | CAA | 130 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(127): Show | 131 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.6415+672_6415+673d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652760 | |||||
| chr15:40652760
|
C | CAAA | 80 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0115others(77): Show | 80 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.6415+671_6415+673d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40652760 | |||||
| chr15:40652771
|
A | G | 1 | a0004c0004t0001g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6415+666A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652771 | ||||||
| chr15:40652791
|
A | T | 1 | a0001c0001t0001g0288 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.6415+686A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652791 | ||||||
| chr15:40652861
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6415+756G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40652861 | ||||||
| chr15:40653071
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6415+966G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653071 | ||||||
| chr15:40653073
|
G | A | 2 | a0013c0017t0003g0042a0013c0017t0003g0067 | 2 | HG02293.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.6415+968G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653073 | ||||||
| chr15:40653205
|
T | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6415+1100T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653205 | ||||||
| chr15:40653350
|
G | T | 2 | a0012c0012t0001g0129a0012c0012t0001g0130 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6415+1245G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653350 | ||||||
| chr15:40653547
|
T | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6416-1362T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653547 | ||||||
| chr15:40653701
|
G | A | 1 | a0002c0002t0001g0119 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6416-1208G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653701 | ||||||
| chr15:40653702
|
T | C | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6416-1207T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653702 | ||||||
| chr15:40653760
|
G | A | 1 | a0017c0042t0001g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6416-1149G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653760 | ||||||
| chr15:40653862
|
C | A | 1 | a0001c0001t0004g0317 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.6416-1047C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653862 | ||||||
| chr15:40653864
|
C | T | 1 | a0009c0009t0007g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6416-1045C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653864 | ||||||
| chr15:40653868
|
C | T | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6416-1041C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40653868 | ||||||
| chr15:40653872
|
GT | G | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.6416-1033delT | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40653872 | |||||
| chr15:40654003
|
G | A | 2 | a0002c0002t0001g0094a0002c0002t0001g0095 | 2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6416-906G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654003 | ||||||
| chr15:40654036
|
T | G | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.6416-873T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654036 | ||||||
| chr15:40654095
|
T | A | 73 | a0002c0002t0003g0002a0002c0002t0003g0012a0002c0002t0003g0014others(70): Show | 73 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.6416-814T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654095 | ||||||
| chr15:40654249
|
T | G | 1 | a0002c0002t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6416-660T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654249 | ||||||
| chr15:40654423
|
GTAGTTGA others(6): Show |
G | 11 | a0005c0005t0002g0145a0005c0005t0002g0162a0005c0005t0002g0163others(8): Show | 11 | HG01255.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.6416-484_6416-472d others(15): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40654423 | |||||
| chr15:40654573
|
T | TA | 9 | a0001c0001t0001g0219a0001c0001t0001g0305a0002c0002t0001g0092others(6): Show | 9 | HG01256.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.6416-322dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40654573 | |||||
| chr15:40654573
|
T | TAA | 65 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(62): Show | 66 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.6416-323_6416-322d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40654573 | |||||
| chr15:40654573
|
T | TAAA | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6416-324_6416-322d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr15 | 40654573 | |||||
| chr15:40654597
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0277 | 2 | HG01070.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.6416-312C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654597 | ||||||
| chr15:40654706
|
A | G | 3 | a0002c0002t0003g0085a0014c0016t0003g0034a0014c0016t0003g0127 | 3 | HG00544.hp2 NA18950.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.6416-203A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654706 | ||||||
| chr15:40654730
|
G | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6416-179G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654730 | ||||||
| chr15:40654825
|
C | T | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6416-84C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654825 | ||||||
| chr15:40654833
|
C | T | 1 | a0002c0002t0001g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.6416-76C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654833 | ||||||
| chr15:40654856
|
G | A | 1 | a0002c0022t0015g0006 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6416-53G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 21/25 | chr15 | 40654856 | ||||||
| chr15:40655126
|
C | T | 3 | a0007c0008t0005g0052a0007c0008t0005g0053a0007c0008t0005g0054 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.6484+149C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655126 | ||||||
| chr15:40655188
|
C | T | 1 | a0020c0041t0001g0220 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6484+211C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655188 | ||||||
| chr15:40655210
|
A | G | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6484+233A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655210 | ||||||
| chr15:40655230
|
G | A | 1 | a0001c0006t0001g0233 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.6484+253G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655230 | ||||||
| chr15:40655288
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0283a0001c0001t0001g0336 | 3 | NA18946.hp1 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.6484+311C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655288 | ||||||
| chr15:40655505
|
C | T | 361 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(358): Show | 364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.6484+528C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655505 | ||||||
| chr15:40655540
|
G | A | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6484+563G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655540 | ||||||
| chr15:40655590
|
C | CA | 7 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0299others(4): Show | 7 | HG03098.hp1 HG03453.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.6484+634dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655590 | |||||
| chr15:40655590
|
CAA | C | 73 | a0002c0002t0003g0076a0003c0003t0002g0001a0003c0003t0002g0149others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6484+633_6484+634d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655590 | |||||
| chr15:40655590
|
CAAAA | C | 133 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(130): Show | 133 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.6484+631_6484+634d others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655590 | |||||
| chr15:40655636
|
C | T | 4 | a0002c0002t0003g0012a0002c0002t0003g0046a0002c0002t0003g0061others(1): Show | 4 | HG01074.hp1 HG02486.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.6484+659C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40655636 | ||||||
| chr15:40655915
|
C | CA | 11 | a0001c0006t0001g0229a0002c0002t0001g0092a0002c0002t0001g0115others(8): Show | 11 | HG02055.hp2 HG02293.hp1 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.6484+955dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655915 | |||||
| chr15:40655915
|
CA | C | 6 | a0001c0001t0001g0338a0002c0002t0003g0055a0002c0002t0003g0085others(3): Show | 6 | HG01975.hp2 HG02572.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.6484+955delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40655915 | |||||
| chr15:40656006
|
G | A | 2 | a0005c0005t0002g0181a0005c0005t0002g0203 | 2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6484+1029G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656006 | ||||||
| chr15:40656006
|
G | C | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6484+1029G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656006 | ||||||
| chr15:40656055
|
C | T | 3 | a0001c0001t0001g0290a0001c0001t0001g0314a0024c0033t0017g0148 | 3 | HG02040.hp1 HG03453.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.6485-987C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656055 | ||||||
| chr15:40656293
|
C | CATTGTGG others(30): Show |
1 | a0001c0001t0001g0299 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.6485-730_6485-729i others(39): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr15 | 40656293 | |||||
| chr15:40656346
|
T | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6485-696T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656346 | ||||||
| chr15:40656444
|
T | C | 1 | a0005c0005t0002g0202 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6485-598T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656444 | ||||||
| chr15:40656688
|
G | C | 213 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.6485-354G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656688 | ||||||
| chr15:40656733
|
A | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-309A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656733 | ||||||
| chr15:40656734
|
A | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-308A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656734 | ||||||
| chr15:40656735
|
A | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-307A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656735 | ||||||
| chr15:40656736
|
A | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-306A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656736 | ||||||
| chr15:40656743
|
G | A | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-299G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656743 | ||||||
| chr15:40656745
|
G | A | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-297G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656745 | ||||||
| chr15:40656749
|
G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-293G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656749 | ||||||
| chr15:40656750
|
G | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-292G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656750 | ||||||
| chr15:40656758
|
C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-284C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656758 | ||||||
| chr15:40656759
|
G | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-283G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656759 | ||||||
| chr15:40656771
|
A | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-271A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656771 | ||||||
| chr15:40656773
|
C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-269C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656773 | ||||||
| chr15:40656775
|
A | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-267A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656775 | ||||||
| chr15:40656776
|
C | A | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-266C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656776 | ||||||
| chr15:40656777
|
T | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-265T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656777 | ||||||
| chr15:40656785
|
C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-257C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656785 | ||||||
| chr15:40656786
|
T | A | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-256T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656786 | ||||||
| chr15:40656787
|
G | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-255G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656787 | ||||||
| chr15:40656789
|
G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-253G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656789 | ||||||
| chr15:40656790
|
G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-252G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656790 | ||||||
| chr15:40656794
|
G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-248G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656794 | ||||||
| chr15:40656801
|
G | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-241G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656801 | ||||||
| chr15:40656803
|
T | G | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-239T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656803 | ||||||
| chr15:40656804
|
T | G | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-238T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656804 | ||||||
| chr15:40656805
|
G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-237G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656805 | ||||||
| chr15:40656808
|
C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-234C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656808 | ||||||
| chr15:40656812
|
G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-230G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656812 | ||||||
| chr15:40656813
|
A | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-229A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656813 | ||||||
| chr15:40656817
|
C | G | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-225C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656817 | ||||||
| chr15:40656824
|
T | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-218T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656824 | ||||||
| chr15:40656825
|
G | C | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-217G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656825 | ||||||
| chr15:40656826
|
C | T | 1 | a0016c0019t0003g0063 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6485-216C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656826 | ||||||
| chr15:40656843
|
G | A | 1 | a0002c0002t0003g0085 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6485-199G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656843 | ||||||
| chr15:40656850
|
T | C | 2 | a0005c0005t0002g0162a0005c0005t0002g0168 | 2 | HG01255.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6485-192T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 22/25 | chr15 | 40656850 | ||||||
| chr15:40657303
|
G | A | 1 | a0009c0009t0006g0008 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.6595-52G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 23/25 | chr15 | 40657303 | ||||||
| chr15:40657328
|
C | T | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6595-27C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 23/25 | chr15 | 40657328 | ||||||
| chr15:40657596
|
G | T | 1 | a0001c0001t0001g0328 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.6713+123G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657596 | ||||||
| chr15:40657705
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6713+232G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657705 | ||||||
| chr15:40657903
|
G | T | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6713+430G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657903 | ||||||
| chr15:40657957
|
T | C | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6713+484T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657957 | ||||||
| chr15:40657965
|
T | A | 216 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.6713+492T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40657965 | ||||||
| chr15:40658177
|
A | G | 16 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0301others(13): Show | 16 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.6713+704A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658177 | ||||||
| chr15:40658247
|
A | G | 2 | a0013c0017t0003g0042a0013c0017t0003g0067 | 2 | HG02293.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.6713+774A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658247 | ||||||
| chr15:40658269
|
C | T | 1 | a0002c0002t0001g0092 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.6713+796C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658269 | ||||||
| chr15:40658290
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6713+817G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658290 | ||||||
| chr15:40658335
|
C | T | 2 | a0003c0003t0002g0175a0003c0003t0002g0176 | 2 | HG00558.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.6713+862C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658335 | ||||||
| chr15:40658375
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0001g0337 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.6713+902A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658375 | ||||||
| chr15:40658485
|
C | T | 1 | a0002c0002t0003g0022 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.6714-854C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658485 | ||||||
| chr15:40658523
|
ATCTCAAA others(27): Show |
A | 2 | a0001c0001t0001g0289a0001c0001t0001g0345 | 2 | HG00423.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.6714-793_6714-760d others(36): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658523 | |||||
| chr15:40658527
|
C | CA | 9 | a0001c0001t0001g0340a0001c0001t0001g0356a0003c0003t0002g0184others(6): Show | 9 | HG01346.hp1 HG02056.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.6714-793dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658527 | |||||
| chr15:40658527
|
CA | C | 7 | a0001c0001t0001g0269a0001c0001t0001g0272a0001c0001t0001g0278others(4): Show | 7 | HG01256.hp2 HG01516.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.6714-793delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658527 | |||||
| chr15:40658544
|
AAAG | A | 131 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(128): Show | 131 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.6714-793_6714-791d others(5): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658544 | |||||
| chr15:40658561
|
CA | C | 204 | a0001c0001t0001g0271a0001c0001t0001g0283a0001c0001t0001g0319others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.6714-760delA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658561 | |||||
| chr15:40658561
|
CAA | C | 15 | a0002c0002t0003g0132a0004c0004t0001g0251a0005c0005t0002g0145others(12): Show | 15 | HG00639.hp1 HG01255.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.6714-761_6714-760d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658561 | |||||
| chr15:40658576
|
A | G | 35 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0219others(32): Show | 35 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.6714-763A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658576 | ||||||
| chr15:40658590
|
A | C | 1 | a0024c0033t0017g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6714-749A>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658590 | ||||||
| chr15:40658711
|
C | T | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6714-628C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658711 | ||||||
| chr15:40658788
|
G | T | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6714-551G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658788 | ||||||
| chr15:40658929
|
C | CA | 7 | a0001c0001t0001g0273a0001c0001t0001g0307a0001c0001t0001g0329others(4): Show | 7 | HG00741.hp1 NA18951.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.6714-397dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658929 | |||||
| chr15:40658939
|
A | AAAAG | 134 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(131): Show | 134 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.6714-396_6714-393d others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr15 | 40658939 | |||||
| chr15:40658982
|
C | T | 1 | a0002c0002t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6714-357C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40658982 | ||||||
| chr15:40659017
|
G | A | 3 | a0009c0009t0006g0008a0009c0009t0006g0010a0030c0023t0006g0009 | 3 | HG02451.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6714-322G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40659017 | ||||||
| chr15:40659061
|
C | A | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6714-278C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40659061 | ||||||
| chr15:40659241
|
G | A | 1 | a0001c0001t0004g0281 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6714-98G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 24/25 | chr15 | 40659241 | ||||||
| chr15:40659482
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6836+21G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659482 | ||||||
| chr15:40659630
|
C | A | 1 | a0007c0008t0005g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6836+169C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659630 | ||||||
| chr15:40659892
|
T | TTGTGTGT others(3): Show |
25 | a0003c0003t0002g0151a0003c0003t0002g0158a0003c0003t0002g0159others(22): Show | 25 | HG00733.hp2 HG01123.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.6836+432_6836+433i others(12): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | |||||
| chr15:40659892
|
T | TTGTGTGT others(5): Show |
7 | a0003c0003t0002g0154a0003c0003t0002g0157a0003c0003t0002g0164others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.6836+432_6836+433i others(14): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | |||||
| chr15:40659892
|
T | TTGTGTGT others(7): Show |
27 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0153others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.6836+432_6836+433i others(16): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | |||||
| chr15:40659892
|
T | TTGTGTGT others(9): Show |
6 | a0003c0003t0002g0161a0003c0003t0002g0166a0003c0003t0002g0170others(3): Show | 6 | HG02735.hp1 HG02895.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.6836+432_6836+433i others(18): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | |||||
| chr15:40659892
|
T | TTGTGTGT others(15): Show |
3 | a0003c0003t0002g0182a0003c0003t0002g0197a0003c0003t0014g0190 | 3 | HG00408.hp2 HG02056.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.6836+432_6836+433i others(24): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659892 | |||||
| chr15:40659894
|
A | ATG | 30 | a0001c0001t0001g0271a0001c0001t0001g0276a0001c0001t0001g0278others(27): Show | 30 | HG00423.hp2 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.6836+465_6836+466d others(4): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | |||||
| chr15:40659894
|
A | ATGTG | 41 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(38): Show | 41 | HG00423.hp1 HG00673.hp1 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.6836+463_6836+466d others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | |||||
| chr15:40659894
|
A | ATGTGTG | 53 | a0002c0002t0001g0115a0002c0002t0001g0122a0002c0002t0003g0002others(50): Show | 53 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.6836+461_6836+466d others(8): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | |||||
| chr15:40659894
|
A | ATGTGTGT others(1): Show |
12 | a0002c0002t0001g0091a0002c0002t0003g0032a0002c0002t0003g0038others(9): Show | 12 | HG00639.hp1 HG00642.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.6836+459_6836+466d others(10): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | |||||
| chr15:40659894
|
A | ATGTGTGT others(3): Show |
16 | a0002c0002t0003g0040a0002c0002t0003g0048a0002c0002t0003g0062others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.6836+457_6836+466d others(12): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | |||||
| chr15:40659894
|
A | ATGTGTGT others(5): Show |
7 | a0002c0002t0001g0128a0002c0002t0003g0082a0006c0007t0001g0015others(4): Show | 7 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.6836+455_6836+466d others(14): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40659894 | |||||
| chr15:40659894
|
A | G | 73 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.6836+433A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659894 | ||||||
| chr15:40659927
|
T | TGTGTGTG others(4): Show |
1 | a0007c0008t0005g0052 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.6836+466_6836+467i others(13): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659927 | ||||||
| chr15:40659927
|
T | TGTGTGTG others(8): Show |
1 | a0003c0003t0002g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6836+466_6836+467i others(17): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659927 | ||||||
| chr15:40659927
|
T | TGTGTGTG others(10): Show |
2 | a0005c0005t0002g0146a0005c0015t0002g0147 | 2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.6836+466_6836+467i others(19): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659927 | ||||||
| chr15:40659948
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6836+487G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40659948 | ||||||
| chr15:40660063
|
C | T | 34 | a0002c0002t0003g0012a0002c0002t0003g0020a0002c0002t0003g0022others(31): Show | 34 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.6836+602C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660063 | ||||||
| chr15:40660100
|
T | G | 1 | a0002c0002t0003g0085 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.6836+639T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660100 | ||||||
| chr15:40660122
|
A | G | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6836+661A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660122 | ||||||
| chr15:40660392
|
C | T | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6836+931C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660392 | ||||||
| chr15:40660464
|
A | T | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6836+1003A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660464 | ||||||
| chr15:40660506
|
A | T | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6836+1045A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660506 | ||||||
| chr15:40660508
|
T | C | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6836+1047T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660508 | ||||||
| chr15:40660510
|
C | A | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6836+1049C>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660510 | ||||||
| chr15:40660664
|
C | CA | 263 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0218others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.6836+1224dupA | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40660664 | |||||
| chr15:40660664
|
C | CAA | 29 | a0001c0001t0001g0223a0001c0001t0012g0222a0002c0002t0001g0089others(26): Show | 29 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.6836+1223_6836+122 others(6): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40660664 | |||||
| chr15:40660793
|
T | C | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-1281T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660793 | ||||||
| chr15:40660871
|
G | A | 1 | a0002c0002t0003g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.6837-1203G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660871 | ||||||
| chr15:40660886
|
C | G | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-1188C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660886 | ||||||
| chr15:40660987
|
G | A | 66 | a0003c0003t0002g0001a0003c0003t0002g0149a0003c0003t0002g0150others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.6837-1087G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40660987 | ||||||
| chr15:40661038
|
T | C | 4 | a0004c0004t0001g0357a0004c0004t0001g0358a0004c0004t0001g0359others(1): Show | 4 | HG02280.hp2 HG02572.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.6837-1036T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661038 | ||||||
| chr15:40661086
|
C | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6837-988C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661086 | ||||||
| chr15:40661095
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0278 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.6837-979C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661095 | ||||||
| chr15:40661127
|
A | T | 4 | a0008c0010t0001g0215a0008c0010t0001g0216a0008c0010t0001g0217others(1): Show | 4 | NA18950.hp2 NA18983.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.6837-947A>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661127 | ||||||
| chr15:40661129
|
T | A | 1 | a0001c0001t0001g0319 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.6837-945T>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661129 | ||||||
| chr15:40661165
|
T | G | 138 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(135): Show | 138 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.6837-909T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661165 | ||||||
| chr15:40661218
|
C | T | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG02015.hp1 NA18943.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.6837-856C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661218 | ||||||
| chr15:40661259
|
G | A | 4 | a0002c0002t0001g0104a0002c0002t0001g0105a0002c0002t0001g0113others(1): Show | 4 | HG00423.hp1 HG02155.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.6837-815G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661259 | ||||||
| chr15:40661293
|
C | CCATCCTG others(78): Show |
1 | a0002c0002t0016g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.6837-773_6837-772i others(87): Show |
KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr15 | 40661293 | |||||
| chr15:40661327
|
C | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6837-747C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661327 | ||||||
| chr15:40661352
|
C | G | 1 | a0002c0002t0016g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.6837-722C>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661352 | ||||||
| chr15:40661352
|
C | T | 7 | a0005c0005t0002g0207a0005c0005t0002g0208a0005c0005t0002g0210others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.6837-722C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661352 | ||||||
| chr15:40661353
|
G | C | 1 | a0002c0002t0016g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.6837-721G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661353 | ||||||
| chr15:40661363
|
G | C | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6837-711G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661363 | ||||||
| chr15:40661380
|
T | C | 1 | a0002c0002t0003g0082 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.6837-694T>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661380 | ||||||
| chr15:40661387
|
G | A | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-687G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661387 | ||||||
| chr15:40661388
|
A | G | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-686A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661388 | ||||||
| chr15:40661452
|
A | G | 43 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(40): Show | 43 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.6837-622A>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661452 | ||||||
| chr15:40661770
|
C | T | 132 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0025others(129): Show | 132 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.6837-304C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661770 | ||||||
| chr15:40661809
|
G | C | 39 | a0002c0002t0001g0023a0002c0002t0001g0089a0002c0002t0001g0090others(36): Show | 39 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.6837-265G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661809 | ||||||
| chr15:40661844
|
C | T | 1 | a0025c0030t0002g0194 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.6837-230C>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661844 | ||||||
| chr15:40661852
|
G | C | 6 | a0002c0022t0015g0006a0009c0009t0006g0008a0009c0009t0006g0010others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.6837-222G>C | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661852 | ||||||
| chr15:40661903
|
T | G | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-171T>G | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661903 | ||||||
| chr15:40661904
|
G | T | 1 | a0002c0002t0003g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6837-170G>T | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661904 | ||||||
| chr15:40661944
|
G | A | 1 | a0032c0034t0013g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6837-130G>A | KNL1 | ENSG00000137812.21 | transcript | ENST00000399668.7 | protein_coding | 25/25 | chr15 | 40661944 |