Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 91807 |
|---|---|
| ensemblid | ENSG00000140795.13 |
| hgncid | 29826 |
| symbol | MYLK3 |
| name | myosin light chain kinase 3 |
| refseq_nuc | NM_182493.3 |
| refseq_prot | NP_872299.2 |
| ensembl_nuc | ENST00000394809.9 |
| ensembl_prot | ENSP00000378288.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 46702282 |
| end | 46748344 |
| strand | - |
| ver | v1.2 |
| region | chr16:46702282-46748344 |
| region5000 | chr16:46697282-46753344 |
| regionname0 | MYLK3_chr16_46702282_46748344 |
| regionname5000 | MYLK3_chr16_46697282_46753344 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 819 | 127 | 66 | 27 | 22 | 4 | 7 | 17 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002 | 0/1 | 819 | 85 | 9 | 20 | 22 | 6 | 27 | 19 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0003 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0004 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0005 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0006 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0007 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0008 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2460 | 125 | 64 | 27 | 22 | 4 | 7 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0002 | 0/1 | 2460 | 82 | 9 | 18 | 22 | 5 | 27 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0003 | 0/0 | 2460 | 3 | 0 | 2 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0004 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0005 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0006 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0007 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0008 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0009 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0010 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| c0011 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 5573 | 144 | 42 | 34 | 40 | 7 | 20 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0002 | 0/0 | 5574 | 40 | 21 | 12 | 1 | 3 | 3 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0003 | 1/0 | 5574 | 8 | 6 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0004 | 0/0 | 5573 | 5 | 0 | 0 | 0 | 0 | 5 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0005 | 0/0 | 5573 | 3 | 0 | 0 | 3 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0006 | 0/0 | 5574 | 3 | 3 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0007 | 0/0 | 5574 | 2 | 1 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0008 | 0/0 | 5574 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0009 | 0/0 | 5573 | 2 | 0 | 0 | 0 | 0 | 2 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0010 | 0/0 | 5574 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0011 | 0/0 | 5573 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0012 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0013 | 0/0 | 5573 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0014 | 0/0 | 5573 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0015 | 0/0 | 5573 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0016 | 0/0 | 5573 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0017 | 0/0 | 5573 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| t0018 | 0/0 | 5574 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2460 | 125 | 64 | 27 | 22 | 4 | 7 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0007 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0011 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002 | 0/1 | 2460 | 82 | 9 | 18 | 22 | 5 | 27 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0003 | 0/0 | 2460 | 3 | 0 | 2 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0003c0010 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0004c0009 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0005c0008 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0006c0006 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0007c0005 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0008c0004 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8032 | 66 | 29 | 13 | 20 | 1 | 3 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0002 | 0/0 | 8033 | 40 | 21 | 12 | 1 | 3 | 3 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0003 | 1/0 | 8033 | 8 | 6 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0005 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0006 | 0/0 | 8033 | 3 | 3 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0007 | 0/0 | 8033 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0008 | 0/0 | 8033 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0010 | 0/0 | 8033 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0011 | 0/0 | 8032 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0015 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0001t0017 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0007t0001 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0001c0011t0001 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0001 | 0/1 | 8032 | 68 | 9 | 18 | 18 | 5 | 17 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0004 | 0/0 | 8032 | 5 | 0 | 0 | 0 | 0 | 5 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0005 | 0/0 | 8032 | 2 | 0 | 0 | 2 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0007 | 0/0 | 8033 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0009 | 0/0 | 8032 | 2 | 0 | 0 | 0 | 0 | 2 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0012 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0013 | 0/0 | 8032 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0014 | 0/0 | 8032 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0002t0016 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0002c0003t0001 | 0/0 | 8032 | 3 | 0 | 2 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0003c0010t0001 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0004c0009t0018 | 0/0 | 8033 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0005c0008t0001 | 0/0 | 8032 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0006c0006t0001 | 0/0 | 8032 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0007c0005t0001 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| a0008c0004t0001 | 0/0 | 8032 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | copy fasta | chr16 | 46697282 | 46753344 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0011g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0007t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0001c0011t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0009g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0009g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0013g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0014g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0002t0016g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0003c0010t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0004c0009t0018g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0005c0008t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0006c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0007c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| a0008c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0159 | EUR | GBR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0144 | EUR | FIN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | CHS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0014 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01074 | hp1 | a0005 | c0008 | t0001 | g0092 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0161 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0147 | AMR | PUR | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0150 | EUR | IBS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01517 | hp1 | a0002 | c0003 | t0001 | g0146 | EUR | IBS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | KHV | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | KHV | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0076 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02572 | hp1 | a0001 | c0011 | t0001 | g0179 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02622 | hp2 | a0008 | c0004 | t0001 | g0009 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02683 | hp1 | a0002 | c0002 | t0014 | g0167 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0173 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02698 | hp2 | a0002 | c0002 | t0009 | g0210 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02717 | hp1 | a0004 | c0009 | t0018 | g0109 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02738 | hp1 | a0002 | c0002 | t0009 | g0209 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02970 | hp2 | a0001 | c0007 | t0001 | g0058 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0165 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0208 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0192 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03239 | hp1 | a0001 | c0001 | t0010 | g0034 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03453 | hp1 | a0001 | c0001 | t0015 | g0203 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | GWD | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03654 | hp2 | a0002 | c0002 | t0004 | g0162 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03669 | hp1 | a0002 | c0002 | t0013 | g0122 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0136 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | PJL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | BEB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04115 | hp1 | a0002 | c0002 | t0007 | g0061 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04115 | hp2 | a0002 | c0002 | t0004 | g0074 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0108 | SAS | BEB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04184 | hp2 | a0002 | c0002 | t0004 | g0163 | SAS | BEB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04199 | hp2 | a0002 | c0002 | t0004 | g0164 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04204 | hp2 | a0002 | c0002 | t0004 | g0075 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | STU | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | YRI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18942 | hp1 | a0002 | c0002 | t0005 | g0119 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18998 | hp1 | a0002 | c0002 | t0016 | g0148 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19001 | hp2 | a0006 | c0006 | t0001 | g0080 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19043 | hp1 | a0007 | c0005 | t0001 | g0015 | AFR | LWK | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | LWK | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19076 | hp2 | a0003 | c0010 | t0001 | g0085 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19080 | hp1 | a0002 | c0002 | t0012 | g0073 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19088 | hp1 | a0002 | c0002 | t0005 | g0118 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | ASW | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0115 | EUR | TSI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0116 | EUR | TSI | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | USA | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | USA | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | USA | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | USA | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | LWK | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0140 | REF | REF | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0052 | REF | REF | MYLK3_chr16_46697282_46753344 | MYLK3 | chr16 | 46697282 | 46753344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46721148
|
T | C | 1 | a0005 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.1960A>G | p.Ile654Val | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/13 | 2111/8033 | 1960/2460 | 654/819 | chr16 | 46721148 | ||
| chr16:46721192
|
G | A | 1 | a0004 | 1 | HG02717.hp1 | missense_variant&splice_region_variant | MODERATE | c.1916C>T | p.Pro639Leu | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/13 | 2067/8033 | 1916/2460 | 639/819 | chr16 | 46721192 | ||
| chr16:46729124
|
T | C | 1 | a0003 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1672A>G | p.Lys558Glu | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/13 | 1823/8033 | 1672/2460 | 558/819 | chr16 | 46729124 | ||
| chr16:46730662
|
C | G | 1 | a0003 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1499G>C | p.Arg500Pro | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/13 | 1650/8033 | 1499/2460 | 500/819 | chr16 | 46730662 | ||
| chr16:46730663
|
G | C | 1 | a0003 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1498C>G | p.Arg500Gly | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/13 | 1649/8033 | 1498/2460 | 500/819 | chr16 | 46730663 | ||
| chr16:46732367
|
C | G | 1 | a0006 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.1303G>C | p.Asp435His | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/13 | 1454/8033 | 1303/2460 | 435/819 | chr16 | 46732367 | ||
| chr16:46732502
|
C | T | 1 | a0007 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1168G>A | p.Gly390Arg | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/13 | 1319/8033 | 1168/2460 | 390/819 | chr16 | 46732502 | ||
| chr16:46740087
|
C | A | 1 | a0002 | 85 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(82): Show |
missense_variant | MODERATE | c.538G>T | p.Val180Leu | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/13 | 689/8033 | 538/2460 | 180/819 | chr16 | 46740087 | ||
| chr16:46747965
|
C | T | 1 | a0008 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.229G>A | p.Gly77Arg | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/13 | 380/8033 | 229/2460 | 77/819 | chr16 | 46747965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46710684
|
C | T | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2220G>A | p.Ser740Ser | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/13 | 2371/8033 | 2220/2460 | 740/819 | chr16 | 46710684 | ||
| chr16:46729125
|
C | T | 1 | a0003c0010 | 1 | NA19076.hp2 | synonymous_variant | LOW | c.1671G>A | p.Val557Val | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/13 | 1822/8033 | 1671/2460 | 557/819 | chr16 | 46729125 | ||
| chr16:46730673
|
A | G | 1 | a0002c0003 | 3 | HG01109.hp2 HG01243.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.1488T>C | p.Pro496Pro | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/13 | 1639/8033 | 1488/2460 | 496/819 | chr16 | 46730673 | ||
| chr16:46732650
|
T | C | 1 | a0001c0011 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1020A>G | p.Gln340Gln | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/13 | 1171/8033 | 1020/2460 | 340/819 | chr16 | 46732650 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46702292
|
G | A | 1 | a0002c0002t0014 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5412C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 5412 | chr16 | 46702292 | |||||
| chr16:46702351
|
C | T | 23 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(20): Show | 163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*5353G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 5353 | chr16 | 46702351 | |||||
| chr16:46702956
|
TA | T | 21 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(18): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*4747delT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 4747 | chr16 | 46702956 | |||||
| chr16:46703598
|
T | C | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(24): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*4106A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 4106 | chr16 | 46703598 | |||||
| chr16:46704397
|
T | C | 1 | a0001c0001t0015 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3307A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 3307 | chr16 | 46704397 | |||||
| chr16:46704506
|
T | C | 24 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(21): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*3198A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 3198 | chr16 | 46704506 | |||||
| chr16:46704536
|
C | G | 1 | a0002c0002t0004 | 5 | HG03654.hp2 HG04115.hp2 HG04184.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3168G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 3168 | chr16 | 46704536 | |||||
| chr16:46704657
|
G | A | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(25): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*3047C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 3047 | chr16 | 46704657 | |||||
| chr16:46705224
|
C | T | 1 | a0002c0002t0013 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2480G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 2480 | chr16 | 46705224 | |||||
| chr16:46705476
|
C | T | 2 | a0001c0001t0005a0002c0002t0005 | 3 | NA18942.hp1 NA18968.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2228G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 2228 | chr16 | 46705476 | |||||
| chr16:46705628
|
A | T | 1 | a0002c0002t0012 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2076T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 2076 | chr16 | 46705628 | |||||
| chr16:46705991
|
G | A | 1 | a0001c0001t0006 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1713C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1713 | chr16 | 46705991 | |||||
| chr16:46706067
|
T | C | 1 | a0001c0001t0006 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1637A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1637 | chr16 | 46706067 | |||||
| chr16:46706361
|
T | G | 1 | a0002c0002t0016 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1343A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1343 | chr16 | 46706361 | |||||
| chr16:46706442
|
C | A | 3 | a0001c0001t0002a0001c0001t0010a0001c0001t0017 | 42 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1262G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1262 | chr16 | 46706442 | |||||
| chr16:46706688
|
G | T | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(24): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1016C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 1016 | chr16 | 46706688 | |||||
| chr16:46706970
|
G | T | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(25): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*734C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 734 | chr16 | 46706970 | |||||
| chr16:46707131
|
C | G | 1 | a0001c0001t0011 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 573 | chr16 | 46707131 | |||||
| chr16:46707133
|
T | C | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(25): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*571A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 571 | chr16 | 46707133 | |||||
| chr16:46707358
|
G | A | 1 | a0004c0009t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*346C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 346 | chr16 | 46707358 | |||||
| chr16:46707488
|
C | T | 1 | a0001c0001t0010 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*216G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 13/13 | 216 | chr16 | 46707488 | |||||
| chr16:46748335
|
T | C | 1 | a0002c0002t0009 | 2 | HG02698.hp2 HG02738.hp1 |
5_prime_UTR_variant | MODIFIER | c.-142A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/13 | 142 | chr16 | 46748335 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:46707951
|
G | A | 5 | a0002c0002t0001g0072a0002c0002t0001g0076a0002c0002t0001g0168others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401-188C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46707951 | ||||||
| chr16:46707953
|
A | ATGAATAT others(3): Show |
5 | a0002c0002t0001g0072a0002c0002t0001g0076a0002c0002t0001g0168others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401-191_2401-190i others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46707953 | ||||||
| chr16:46709214
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2400+325C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46709214 | ||||||
| chr16:46709416
|
T | C | 1 | a0002c0002t0001g0112 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2400+123A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46709416 | ||||||
| chr16:46709443
|
G | GA | 35 | a0002c0002t0001g0008a0002c0002t0001g0065a0002c0002t0001g0066others(32): Show | 36 | HG00099.hp1 HG00621.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2400+95dupT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46709443 | ||||||
| chr16:46709446
|
A | C | 1 | a0001c0001t0002g0027 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2400+93T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 12/12 | chr16 | 46709446 | ||||||
| chr16:46709763
|
G | A | 157 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(154): Show | 159 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2268-92C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/12 | chr16 | 46709763 | ||||||
| chr16:46709796
|
A | G | 2 | a0001c0001t0001g0091a0002c0002t0001g0063 | 2 | NA18955.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2268-125T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/12 | chr16 | 46709796 | ||||||
| chr16:46709857
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2268-186C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/12 | chr16 | 46709857 | ||||||
| chr16:46710135
|
T | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0004c0009t0018g0109 | 3 | HG01884.hp2 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2268-464A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 11/12 | chr16 | 46710135 | ||||||
| chr16:46710926
|
T | C | 2 | a0001c0001t0001g0016a0007c0005t0001g0015 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2115-137A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46710926 | ||||||
| chr16:46711715
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2115-926G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711715 | ||||||
| chr16:46711807
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2114+841A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711807 | ||||||
| chr16:46711962
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2114+686G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711962 | ||||||
| chr16:46711989
|
AT | A | 193 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(190): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.2114+658delA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711989 | ||||||
| chr16:46711989
|
ATT | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0206a0001c0001t0002g0046others(2): Show | 5 | HG02818.hp1 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2114+657_2114+658d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46711989 | ||||||
| chr16:46712172
|
G | T | 1 | a0002c0002t0001g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2114+476C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 10/12 | chr16 | 46712172 | ||||||
| chr16:46713157
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0002g0038 | 2 | HG01106.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1986-381G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713157 | ||||||
| chr16:46713199
|
C | CT | 191 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(188): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1986-424dupA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713199 | ||||||
| chr16:46713245
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1986-469A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713245 | ||||||
| chr16:46713346
|
C | T | 1 | a0001c0001t0003g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1986-570G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713346 | ||||||
| chr16:46713978
|
A | T | 1 | a0001c0001t0015g0203 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1986-1202T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46713978 | ||||||
| chr16:46714007
|
T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0174a0001c0001t0001g0175others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1986-1231A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714007 | ||||||
| chr16:46714085
|
C | T | 1 | a0002c0002t0013g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1986-1309G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714085 | ||||||
| chr16:46714416
|
G | A | 1 | a0002c0002t0001g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1986-1640C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714416 | ||||||
| chr16:46714479
|
C | T | 195 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(192): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1986-1703G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714479 | ||||||
| chr16:46714481
|
C | G | 198 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1986-1705G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714481 | ||||||
| chr16:46714574
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1986-1798C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714574 | ||||||
| chr16:46714656
|
C | T | 1 | a0002c0002t0001g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1986-1880G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714656 | ||||||
| chr16:46714703
|
A | C | 1 | a0002c0002t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1986-1927T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46714703 | ||||||
| chr16:46715077
|
C | T | 1 | a0002c0002t0014g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1986-2301G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715077 | ||||||
| chr16:46715078
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1986-2302C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715078 | ||||||
| chr16:46715286
|
G | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0174a0001c0001t0001g0175others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1986-2510C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715286 | ||||||
| chr16:46715291
|
C | G | 37 | a0002c0002t0001g0008a0002c0002t0001g0065a0002c0002t0001g0066others(34): Show | 38 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1986-2515G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715291 | ||||||
| chr16:46715301
|
A | C | 1 | a0002c0002t0001g0157 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1986-2525T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715301 | ||||||
| chr16:46715462
|
T | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1986-2686A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715462 | ||||||
| chr16:46715500
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1986-2724C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715500 | ||||||
| chr16:46715947
|
A | G | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1986-3171T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46715947 | ||||||
| chr16:46716017
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1986-3241C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716017 | ||||||
| chr16:46716033
|
G | C | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1986-3257C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716033 | ||||||
| chr16:46716045
|
C | T | 3 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0046 | 4 | HG02280.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986-3269G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716045 | ||||||
| chr16:46716077
|
C | T | 1 | a0004c0009t0018g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1986-3301G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716077 | ||||||
| chr16:46716155
|
T | C | 2 | a0001c0001t0008g0032a0001c0001t0008g0033 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1986-3379A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716155 | ||||||
| chr16:46716489
|
GTA | G | 21 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0071others(18): Show | 21 | HG00642.hp2 HG01069.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1986-3715_1986-371 others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716489 | ||||||
| chr16:46716495
|
ATATG | A | 91 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.1986-3723_1986-372 others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716495 | ||||||
| chr16:46716495
|
ATATGTG | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0057a0001c0001t0001g0079others(36): Show | 40 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1986-3725_1986-372 others(10): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716495 | ||||||
| chr16:46716495
|
ATATGTGT others(1): Show |
A | 4 | a0001c0001t0001g0064a0001c0001t0001g0069a0001c0001t0001g0177others(1): Show | 4 | HG00621.hp1 HG02129.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1986-3727_1986-372 others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716495 | ||||||
| chr16:46716495
|
ATATGTGT others(3): Show |
A | 2 | a0002c0002t0001g0138a0002c0002t0005g0118 | 2 | HG02602.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1986-3729_1986-372 others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716495 | ||||||
| chr16:46716497
|
A | ATG | 9 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0019others(6): Show | 11 | HG01515.hp1 HG01517.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1986-3723_1986-372 others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716497 | ||||||
| chr16:46716497
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0003g0049a0002c0002t0013g0122others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986-3721T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716497 | ||||||
| chr16:46716863
|
T | C | 1 | a0002c0002t0009g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1986-4087A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46716863 | ||||||
| chr16:46717530
|
T | TC | 15 | a0001c0001t0001g0056a0001c0001t0002g0001a0001c0001t0002g0002others(12): Show | 18 | HG00099.hp2 HG00733.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1985+3592dupG | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46717530 | ||||||
| chr16:46717540
|
A | G | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1985+3583T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46717540 | ||||||
| chr16:46717556
|
G | A | 2 | a0001c0001t0001g0106a0001c0007t0001g0058 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1985+3567C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46717556 | ||||||
| chr16:46718208
|
A | T | 2 | a0002c0002t0001g0141a0002c0002t0001g0142 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1985+2915T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718208 | ||||||
| chr16:46718408
|
C | T | 2 | a0002c0002t0001g0132a0002c0002t0001g0172 | 2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1985+2715G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718408 | ||||||
| chr16:46718430
|
G | A | 1 | a0002c0002t0001g0154 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1985+2693C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718430 | ||||||
| chr16:46718437
|
A | T | 1 | a0001c0001t0001g0082 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1985+2686T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718437 | ||||||
| chr16:46718522
|
G | C | 37 | a0002c0002t0001g0008a0002c0002t0001g0065a0002c0002t0001g0066others(34): Show | 38 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1985+2601C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46718522 | ||||||
| chr16:46719053
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1985+2070C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719053 | ||||||
| chr16:46719196
|
G | A | 1 | a0002c0002t0001g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1985+1927C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719196 | ||||||
| chr16:46719321
|
G | A | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1985+1802C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719321 | ||||||
| chr16:46719326
|
CA | C | 7 | a0001c0001t0001g0106a0001c0001t0001g0180a0001c0001t0001g0207others(4): Show | 7 | HG01256.hp2 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1985+1796delT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719326 | ||||||
| chr16:46719345
|
A | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0197 | 2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1985+1778T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719345 | ||||||
| chr16:46719376
|
C | T | 1 | a0002c0002t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1985+1747G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46719376 | ||||||
| chr16:46720311
|
C | CA | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0004c0009t0018g0109 | 3 | HG01884.hp2 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1985+811dupT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46720311 | ||||||
| chr16:46720381
|
G | C | 1 | a0002c0002t0001g0157 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1985+742C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46720381 | ||||||
| chr16:46720400
|
G | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1985+723C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46720400 | ||||||
| chr16:46721073
|
C | T | 1 | a0001c0001t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1985+50G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 9/12 | chr16 | 46721073 | ||||||
| chr16:46721301
|
C | G | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1915-108G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721301 | ||||||
| chr16:46721405
|
C | T | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1915-212G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721405 | ||||||
| chr16:46721448
|
T | C | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1915-255A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721448 | ||||||
| chr16:46721573
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1915-380C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721573 | ||||||
| chr16:46721593
|
G | C | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1915-400C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721593 | ||||||
| chr16:46721858
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1915-665T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46721858 | ||||||
| chr16:46722077
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1915-884G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46722077 | ||||||
| chr16:46722718
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1915-1525C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46722718 | ||||||
| chr16:46722940
|
G | A | 2 | a0002c0002t0001g0120a0002c0002t0007g0061 | 2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1915-1747C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46722940 | ||||||
| chr16:46723207
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1915-2014C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723207 | ||||||
| chr16:46723589
|
A | C | 1 | a0002c0002t0001g0131 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1915-2396T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723589 | ||||||
| chr16:46723616
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1915-2423A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723616 | ||||||
| chr16:46723650
|
C | CT | 167 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(164): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1915-2458dupA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723650 | ||||||
| chr16:46723650
|
C | CTT | 28 | a0001c0001t0001g0096a0001c0011t0001g0179a0002c0002t0001g0059others(25): Show | 28 | HG00738.hp1 HG01106.hp2 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.1915-2459_1915-245 others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723650 | ||||||
| chr16:46723849
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0166a0001c0007t0001g0058 | 3 | HG02818.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1915-2656T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723849 | ||||||
| chr16:46723892
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1915-2699C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723892 | ||||||
| chr16:46723943
|
C | A | 1 | a0001c0001t0007g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1915-2750G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46723943 | ||||||
| chr16:46724173
|
T | G | 6 | a0001c0001t0001g0166a0002c0002t0001g0076a0002c0002t0001g0168others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1915-2980A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724173 | ||||||
| chr16:46724227
|
A | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0174a0001c0001t0001g0175others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+3009T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724227 | ||||||
| chr16:46724260
|
T | C | 1 | a0002c0002t0001g0133 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1914+2976A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724260 | ||||||
| chr16:46724270
|
A | G | 1 | a0001c0001t0006g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1914+2966T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724270 | ||||||
| chr16:46724938
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1914+2298G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46724938 | ||||||
| chr16:46725176
|
T | A | 1 | a0001c0001t0001g0139 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1914+2060A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725176 | ||||||
| chr16:46725565
|
C | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1914+1671G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725565 | ||||||
| chr16:46725862
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1914+1374A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725862 | ||||||
| chr16:46725903
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1914+1333G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725903 | ||||||
| chr16:46725948
|
A | G | 159 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1914+1288T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46725948 | ||||||
| chr16:46726662
|
AAAAAGAA others(6): Show |
A | 2 | a0001c0001t0001g0083a0002c0002t0001g0059 | 2 | HG03654.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1914+561_1914+573d others(15): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726662 | ||||||
| chr16:46726663
|
AAAAGAAA others(7): Show |
A | 21 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0068others(18): Show | 21 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1914+559_1914+572d others(16): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726663 | ||||||
| chr16:46726663
|
AAAAGAAA others(11): Show |
A | 9 | a0001c0001t0001g0081a0001c0001t0001g0103a0001c0001t0001g0202others(6): Show | 9 | HG00558.hp2 HG01175.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1914+555_1914+572d others(20): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726663 | ||||||
| chr16:46726663
|
AAAAGAAA others(15): Show |
A | 7 | a0001c0001t0001g0064a0001c0001t0001g0095a0001c0001t0001g0185others(4): Show | 7 | HG01361.hp1 HG02129.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1914+551_1914+572d others(24): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726663 | ||||||
| chr16:46726663
|
AAAAGAAA others(19): Show |
A | 1 | a0002c0002t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1914+547_1914+572d others(28): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726663 | ||||||
| chr16:46726665
|
AAGAAAGA others(3): Show |
A | 39 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0067others(36): Show | 40 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1914+561_1914+570d others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726665 | ||||||
| chr16:46726669
|
AAGAAAG | A | 28 | a0001c0001t0001g0013a0001c0001t0001g0086a0001c0001t0001g0100others(25): Show | 28 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1914+561_1914+566d others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726669 | ||||||
| chr16:46726673
|
A | T | 2 | a0001c0001t0001g0087a0002c0002t0001g0112 | 2 | NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1914+563T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726673 | ||||||
| chr16:46726673
|
AAG | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0057others(28): Show | 32 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1914+561_1914+562d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726673 | ||||||
| chr16:46726675
|
G | GAA | 19 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0088others(16): Show | 19 | HG00558.hp1 HG01175.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1914+560_1914+561i others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | ||||||
| chr16:46726675
|
G | GAGAA | 17 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0005others(14): Show | 21 | HG00099.hp2 HG00639.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1914+557_1914+560d others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | ||||||
| chr16:46726675
|
G | GAGAAAGA others(1): Show |
11 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0002g0025others(8): Show | 11 | HG01099.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1914+553_1914+560d others(10): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | ||||||
| chr16:46726675
|
G | GAGAAAGA others(5): Show |
3 | a0001c0001t0002g0003a0001c0001t0010g0034a0001c0001t0017g0208 | 4 | HG03139.hp2 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+549_1914+560d others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | ||||||
| chr16:46726675
|
G | GAGAAAGA others(9): Show |
3 | a0001c0001t0002g0026a0001c0001t0003g0010a0001c0001t0003g0050 | 3 | HG01081.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1914+545_1914+560d others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | ||||||
| chr16:46726675
|
GAGAA | G | 4 | a0001c0001t0002g0028a0001c0001t0002g0036a0001c0001t0002g0037others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1914+557_1914+560d others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | ||||||
| chr16:46726675
|
GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0006g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1914+549_1914+560d others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726675 | ||||||
| chr16:46726733
|
GA | G | 4 | a0001c0001t0001g0082a0001c0001t0001g0191a0001c0001t0002g0035others(1): Show | 4 | HG00733.hp1 HG02280.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1914+502delT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726733 | ||||||
| chr16:46726737
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1914+499T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726737 | ||||||
| chr16:46726738
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1914+498C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726738 | ||||||
| chr16:46726744
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1914+492C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726744 | ||||||
| chr16:46726748
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1914+488C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726748 | ||||||
| chr16:46726752
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0190 | 2 | HG01884.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1914+484T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726752 | ||||||
| chr16:46726762
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1914+474T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726762 | ||||||
| chr16:46726763
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1914+473C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726763 | ||||||
| chr16:46726763
|
G | GAAAGAGA others(14): Show |
1 | a0001c0001t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1914+472_1914+473i others(23): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726763 | ||||||
| chr16:46726803
|
G | T | 159 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1914+433C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726803 | ||||||
| chr16:46726883
|
G | A | 155 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1914+353C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46726883 | ||||||
| chr16:46727177
|
G | A | 1 | a0002c0002t0004g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1914+59C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 8/12 | chr16 | 46727177 | ||||||
| chr16:46727538
|
T | G | 1 | a0002c0002t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1773-161A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46727538 | ||||||
| chr16:46727579
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1773-202A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46727579 | ||||||
| chr16:46727609
|
C | T | 1 | a0001c0001t0006g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1773-232G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46727609 | ||||||
| chr16:46727813
|
C | T | 1 | a0001c0001t0010g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1773-436G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46727813 | ||||||
| chr16:46728446
|
T | A | 1 | a0001c0001t0003g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1772+578A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46728446 | ||||||
| chr16:46728454
|
C | T | 1 | a0001c0001t0006g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1772+570G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46728454 | ||||||
| chr16:46728818
|
G | A | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1772+206C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46728818 | ||||||
| chr16:46729000
|
G | A | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0017g0208 | 3 | HG01884.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1772+24C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46729000 | ||||||
| chr16:46729004
|
G | A | 8 | a0002c0002t0001g0059a0002c0002t0001g0108a0002c0002t0001g0117others(5): Show | 8 | HG02698.hp2 HG02738.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.1772+20C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 7/12 | chr16 | 46729004 | ||||||
| chr16:46729261
|
C | T | 1 | a0002c0002t0007g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1663-128G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 6/12 | chr16 | 46729261 | ||||||
| chr16:46730042
|
G | T | 1 | a0001c0001t0002g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1569-355C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730042 | ||||||
| chr16:46730383
|
G | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1568+210C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730383 | ||||||
| chr16:46730439
|
A | C | 1 | a0002c0002t0001g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1568+154T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730439 | ||||||
| chr16:46730462
|
C | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(37): Show | 41 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1568+131G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730462 | ||||||
| chr16:46730488
|
G | C | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1568+105C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730488 | ||||||
| chr16:46730570
|
A | C | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1568+23T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 5/12 | chr16 | 46730570 | ||||||
| chr16:46730980
|
A | G | 2 | a0002c0002t0001g0066a0002c0002t0001g0149 | 2 | HG01175.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1463-282T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46730980 | ||||||
| chr16:46730988
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1463-290C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46730988 | ||||||
| chr16:46731203
|
A | G | 1 | a0001c0001t0001g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1463-505T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731203 | ||||||
| chr16:46731207
|
C | T | 1 | a0002c0002t0001g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1463-509G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731207 | ||||||
| chr16:46731234
|
G | A | 159 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1463-536C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731234 | ||||||
| chr16:46731351
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1463-653A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731351 | ||||||
| chr16:46731596
|
AG | A | 3 | a0002c0003t0001g0146a0002c0003t0001g0147a0002c0003t0001g0161 | 3 | HG01109.hp2 HG01243.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1462+611delC | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731596 | ||||||
| chr16:46731771
|
G | C | 1 | a0001c0001t0015g0203 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1462+437C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731771 | ||||||
| chr16:46731789
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1462+419G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731789 | ||||||
| chr16:46731803
|
C | T | 37 | a0002c0002t0001g0008a0002c0002t0001g0065a0002c0002t0001g0066others(34): Show | 38 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1462+405G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 4/12 | chr16 | 46731803 | ||||||
| chr16:46732850
|
C | T | 1 | a0001c0001t0003g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1002-182G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46732850 | ||||||
| chr16:46732880
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1002-212C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46732880 | ||||||
| chr16:46732956
|
G | A | 1 | a0002c0002t0009g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1002-288C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46732956 | ||||||
| chr16:46732979
|
C | T | 1 | a0002c0002t0001g0120 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1002-311G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46732979 | ||||||
| chr16:46733340
|
G | A | 1 | a0001c0001t0006g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-672C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46733340 | ||||||
| chr16:46733452
|
C | T | 1 | a0002c0002t0001g0108 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1002-784G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46733452 | ||||||
| chr16:46733495
|
C | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1002-827G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46733495 | ||||||
| chr16:46733817
|
G | A | 1 | a0002c0002t0016g0148 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1002-1149C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46733817 | ||||||
| chr16:46734030
|
C | T | 1 | a0001c0001t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1002-1362G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46734030 | ||||||
| chr16:46734123
|
C | T | 1 | a0001c0001t0010g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1002-1455G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46734123 | ||||||
| chr16:46734702
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1002-2034T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46734702 | ||||||
| chr16:46735003
|
T | C | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1002-2335A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735003 | ||||||
| chr16:46735089
|
C | T | 3 | a0002c0002t0001g0060a0002c0002t0005g0118a0002c0002t0005g0119 | 3 | NA18942.hp1 NA18968.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1002-2421G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735089 | ||||||
| chr16:46735354
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1001+2357G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735354 | ||||||
| chr16:46735355
|
G | A | 39 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(36): Show | 45 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1001+2356C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735355 | ||||||
| chr16:46735368
|
G | A | 1 | a0002c0002t0001g0157 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1001+2343C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735368 | ||||||
| chr16:46735592
|
C | T | 1 | a0002c0002t0001g0140 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1001+2119G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735592 | ||||||
| chr16:46735693
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1001+2018T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735693 | ||||||
| chr16:46735791
|
G | C | 9 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0068others(6): Show | 9 | HG00621.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1001+1920C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46735791 | ||||||
| chr16:46736044
|
G | T | 1 | a0002c0002t0001g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1001+1667C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736044 | ||||||
| chr16:46736055
|
T | C | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1001+1656A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736055 | ||||||
| chr16:46736366
|
C | A | 2 | a0002c0002t0001g0168a0002c0002t0001g0171 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1001+1345G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736366 | ||||||
| chr16:46736424
|
C | G | 155 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1001+1287G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736424 | ||||||
| chr16:46736485
|
T | G | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001+1226A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736485 | ||||||
| chr16:46736868
|
G | A | 3 | a0001c0001t0001g0106a0001c0007t0001g0058a0002c0002t0001g0065 | 3 | HG01106.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1001+843C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736868 | ||||||
| chr16:46736892
|
G | GA | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001+818_1001+819i others(3): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736892 | ||||||
| chr16:46736893
|
C | G | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1001+818G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46736893 | ||||||
| chr16:46737068
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1001+643G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737068 | ||||||
| chr16:46737300
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1001+411C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737300 | ||||||
| chr16:46737343
|
G | A | 2 | a0001c0001t0001g0106a0001c0007t0001g0058 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1001+368C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737343 | ||||||
| chr16:46737561
|
C | A | 1 | a0001c0001t0017g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1001+150G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737561 | ||||||
| chr16:46737588
|
C | T | 1 | a0001c0001t0011g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1001+123G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 3/12 | chr16 | 46737588 | ||||||
| chr16:46738162
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.569-19C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738162 | ||||||
| chr16:46738187
|
G | C | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569-44C>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738187 | ||||||
| chr16:46738321
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0011g0014 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.569-178G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738321 | ||||||
| chr16:46738419
|
T | C | 1 | a0002c0002t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.569-276A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738419 | ||||||
| chr16:46738516
|
C | T | 1 | a0001c0001t0006g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.569-373G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738516 | ||||||
| chr16:46738517
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.569-374C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738517 | ||||||
| chr16:46738881
|
C | T | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569-738G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46738881 | ||||||
| chr16:46739168
|
A | G | 159 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.568+889T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739168 | ||||||
| chr16:46739212
|
C | G | 45 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(42): Show | 46 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.568+845G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739212 | ||||||
| chr16:46739233
|
T | C | 1 | a0001c0001t0007g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.568+824A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739233 | ||||||
| chr16:46739482
|
G | A | 1 | a0001c0001t0006g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.568+575C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739482 | ||||||
| chr16:46739549
|
C | T | 159 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.568+508G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739549 | ||||||
| chr16:46739638
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.568+419A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739638 | ||||||
| chr16:46739840
|
G | T | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.568+217C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739840 | ||||||
| chr16:46739935
|
A | T | 1 | a0002c0002t0004g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.568+122T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739935 | ||||||
| chr16:46739937
|
A | C | 2 | a0002c0002t0001g0129a0002c0002t0001g0133 | 2 | HG02300.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.568+120T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739937 | ||||||
| chr16:46739985
|
G | A | 1 | a0002c0002t0004g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.568+72C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 2/12 | chr16 | 46739985 | ||||||
| chr16:46740389
|
C | T | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.478-242G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740389 | ||||||
| chr16:46740520
|
T | C | 1 | a0001c0001t0017g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478-373A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740520 | ||||||
| chr16:46740526
|
T | C | 1 | a0002c0002t0001g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.478-379A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740526 | ||||||
| chr16:46740530
|
T | C | 1 | a0002c0002t0012g0073 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.478-383A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740530 | ||||||
| chr16:46740536
|
C | CAT | 83 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(80): Show | 84 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.478-391_478-390dup others(2): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740536 | ||||||
| chr16:46740536
|
C | CATAT | 29 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 30 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.478-393_478-390dup others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740536 | ||||||
| chr16:46740536
|
C | CATATAT | 2 | a0001c0001t0001g0176a0003c0010t0001g0085 | 2 | NA19076.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.478-395_478-390dup others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740536 | ||||||
| chr16:46740536
|
C | T | 1 | a0001c0011t0001g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478-389G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740536 | ||||||
| chr16:46740540
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.478-393A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740540 | ||||||
| chr16:46740551
|
A | ATAT | 30 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(27): Show | 35 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.478-405_478-404ins others(3): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740551 | ||||||
| chr16:46740552
|
T | TA | 5 | a0002c0002t0001g0063a0002c0002t0001g0123a0002c0002t0001g0124others(2): Show | 5 | HG01167.hp1 HG01496.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-406_478-405ins others(1): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740552 | ||||||
| chr16:46740552
|
T | TATA | 41 | a0001c0001t0001g0101a0001c0001t0001g0106a0001c0001t0001g0177others(38): Show | 42 | HG00738.hp1 HG01074.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.478-406_478-405ins others(3): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740552 | ||||||
| chr16:46740552
|
T | TATATA | 7 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(4): Show | 7 | HG02723.hp1 HG03471.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-406_478-405ins others(5): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740552 | ||||||
| chr16:46740553
|
T | A | 100 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(97): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.478-406A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740553 | ||||||
| chr16:46740554
|
T | A | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0106others(11): Show | 14 | HG00280.hp1 HG02630.hp1 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.478-407A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740554 | ||||||
| chr16:46740555
|
T | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0097others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.478-408A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740555 | ||||||
| chr16:46740557
|
T | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0207a0008c0004t0001g0009 | 3 | HG02622.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.478-410A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740557 | ||||||
| chr16:46740766
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.478-619C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740766 | ||||||
| chr16:46740797
|
C | T | 5 | a0002c0002t0001g0076a0002c0002t0001g0168a0002c0002t0001g0169others(2): Show | 5 | HG02145.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-650G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740797 | ||||||
| chr16:46740847
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.478-700G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740847 | ||||||
| chr16:46740919
|
C | T | 2 | a0001c0001t0008g0032a0001c0001t0008g0033 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.478-772G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46740919 | ||||||
| chr16:46741030
|
G | A | 4 | a0002c0002t0001g0059a0002c0002t0001g0108a0002c0002t0001g0117others(1): Show | 4 | HG03490.hp1 HG03654.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-883C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741030 | ||||||
| chr16:46741037
|
T | C | 3 | a0002c0002t0001g0060a0002c0002t0005g0118a0002c0002t0005g0119 | 3 | NA18942.hp1 NA18968.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.478-890A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741037 | ||||||
| chr16:46741150
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.478-1003C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741150 | ||||||
| chr16:46741638
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.478-1491T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741638 | ||||||
| chr16:46741731
|
G | A | 159 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(156): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.478-1584C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741731 | ||||||
| chr16:46741770
|
AT | A | 188 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.478-1624delA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741770 | ||||||
| chr16:46741770
|
ATT | A | 6 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0182others(3): Show | 6 | HG01081.hp1 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1625_478-1624d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741770 | ||||||
| chr16:46741934
|
C | G | 38 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(35): Show | 44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.478-1787G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741934 | ||||||
| chr16:46741959
|
T | C | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.478-1812A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46741959 | ||||||
| chr16:46742006
|
T | G | 38 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(35): Show | 44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.478-1859A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742006 | ||||||
| chr16:46742227
|
G | GA | 113 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(110): Show | 114 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.478-2081dupT | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742227 | ||||||
| chr16:46742244
|
G | A | 1 | a0002c0002t0001g0105 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.478-2097C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742244 | ||||||
| chr16:46742323
|
G | A | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.478-2176C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742323 | ||||||
| chr16:46742333
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.478-2186A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742333 | ||||||
| chr16:46742417
|
G | A | 1 | a0002c0002t0012g0073 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.478-2270C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742417 | ||||||
| chr16:46742442
|
G | GCACACAC others(9): Show |
1 | a0006c0006t0001g0080 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.478-2296_478-2295i others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742442 | ||||||
| chr16:46742443
|
CAA | C | 4 | a0002c0002t0004g0075a0002c0002t0004g0162a0002c0002t0004g0163others(1): Show | 4 | HG03654.hp2 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-2298_478-2297d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742443 | ||||||
| chr16:46742445
|
A | AAC | 19 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0071others(16): Show | 20 | HG00280.hp1 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | AACAC | 28 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(25): Show | 28 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(6): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | AACACAC | 9 | a0001c0001t0001g0098a0001c0001t0001g0180a0001c0001t0001g0202others(6): Show | 9 | HG02572.hp1 HG02602.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | AACACACA others(1): Show |
34 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0057others(31): Show | 34 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(10): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | AACACACA others(3): Show |
20 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0114others(17): Show | 20 | HG00738.hp1 HG02630.hp1 HG02738.hp1 others(17): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | AACACACA others(5): Show |
8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0087others(5): Show | 8 | HG01258.hp2 HG01361.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-2299_478-2298i others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | AACACACA others(7): Show |
3 | a0001c0001t0001g0084a0001c0001t0001g0176a0003c0010t0001g0085 | 3 | HG04199.hp1 NA19076.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.478-2299_478-2298i others(16): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | AACACACA others(9): Show |
1 | a0001c0001t0001g0083 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.478-2299_478-2298i others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | AACACACA others(11): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.478-2299_478-2298i others(20): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | ACACACAC others(2): Show |
2 | a0001c0001t0001g0089a0001c0001t0001g0204 | 2 | HG01433.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.478-2299_478-2298i others(11): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | ACACACAC others(4): Show |
2 | a0001c0001t0001g0086a0001c0001t0001g0174 | 2 | HG00642.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.478-2299_478-2298i others(13): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | ACACACAC others(6): Show |
1 | a0002c0002t0001g0108 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.478-2299_478-2298i others(15): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
A | C | 4 | a0001c0001t0001g0079a0002c0002t0001g0107a0002c0002t0001g0165others(1): Show | 4 | HG00558.hp1 HG02738.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.478-2298T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
AAAACAC | A | 5 | a0002c0002t0001g0076a0002c0002t0001g0168a0002c0002t0001g0169others(2): Show | 5 | HG02145.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-2304_478-2299d others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
AAAACACA others(7): Show |
A | 1 | a0002c0002t0001g0172 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.478-2312_478-2299d others(16): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742445
|
AAAACACA others(9): Show |
A | 1 | a0001c0001t0001g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.478-2314_478-2299d others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742445 | ||||||
| chr16:46742447
|
A | AACACACA others(9): Show |
1 | a0004c0009t0018g0109 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.478-2316_478-2301d others(18): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | ||||||
| chr16:46742447
|
A | C | 140 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(137): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.478-2300T>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | ||||||
| chr16:46742447
|
AACACAC | A | 5 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0054others(2): Show | 5 | HG02109.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-2306_478-2301d others(8): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | ||||||
| chr16:46742447
|
AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0006g0194 | 3 | HG01884.hp2 HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.478-2308_478-2301d others(10): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | ||||||
| chr16:46742447
|
AACACACA others(3): Show |
A | 2 | a0001c0001t0002g0001a0001c0001t0002g0024 | 3 | HG01515.hp1 HG01517.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.478-2310_478-2301d others(12): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | ||||||
| chr16:46742447
|
AACACACA others(5): Show |
A | 8 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0025others(5): Show | 10 | HG00099.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.478-2312_478-2301d others(14): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | ||||||
| chr16:46742447
|
AACACACA others(7): Show |
A | 28 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(25): Show | 31 | HG00639.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.478-2314_478-2301d others(16): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | ||||||
| chr16:46742447
|
AACACACA others(11): Show |
A | 2 | a0001c0001t0003g0010a0001c0001t0003g0055 | 2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.478-2318_478-2301d others(20): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742447 | ||||||
| chr16:46742493
|
G | A | 1 | a0002c0002t0001g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.478-2346C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742493 | ||||||
| chr16:46742814
|
C | G | 2 | a0001c0001t0001g0106a0001c0007t0001g0058 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.478-2667G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742814 | ||||||
| chr16:46742837
|
A | G | 1 | a0001c0001t0003g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.478-2690T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742837 | ||||||
| chr16:46742884
|
T | C | 1 | a0002c0002t0001g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.478-2737A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46742884 | ||||||
| chr16:46743149
|
G | A | 3 | a0001c0001t0006g0192a0001c0001t0006g0193a0001c0001t0006g0194 | 3 | HG02970.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.478-3002C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743149 | ||||||
| chr16:46743151
|
C | T | 38 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(35): Show | 44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.478-3004G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743151 | ||||||
| chr16:46743168
|
G | A | 1 | a0002c0002t0001g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.478-3021C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743168 | ||||||
| chr16:46743252
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.478-3105A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743252 | ||||||
| chr16:46743370
|
A | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.478-3223T>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743370 | ||||||
| chr16:46743405
|
G | T | 38 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(35): Show | 44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.478-3258C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743405 | ||||||
| chr16:46743501
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.478-3354A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743501 | ||||||
| chr16:46743501
|
T | G | 1 | a0001c0001t0001g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.478-3354A>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743501 | ||||||
| chr16:46743541
|
C | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.478-3394G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743541 | ||||||
| chr16:46743564
|
C | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.478-3417G>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743564 | ||||||
| chr16:46743589
|
A | G | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.478-3442T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743589 | ||||||
| chr16:46743772
|
C | T | 1 | a0002c0002t0001g0105 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.478-3625G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46743772 | ||||||
| chr16:46744158
|
G | A | 45 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(42): Show | 46 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.477+3559C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744158 | ||||||
| chr16:46744159
|
G | T | 1 | a0001c0001t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.477+3558C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744159 | ||||||
| chr16:46744177
|
T | C | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.477+3540A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744177 | ||||||
| chr16:46744234
|
A | G | 1 | a0002c0002t0001g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.477+3483T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744234 | ||||||
| chr16:46744275
|
G | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.477+3442C>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744275 | ||||||
| chr16:46744330
|
C | CT | 38 | a0001c0001t0001g0188a0001c0001t0001g0207a0001c0001t0002g0001others(35): Show | 44 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.477+3386dupA | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744330 | ||||||
| chr16:46744330
|
C | CTT | 105 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0023others(102): Show | 106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.477+3385_477+3386d others(4): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744330 | ||||||
| chr16:46744330
|
C | CTTT | 53 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(50): Show | 54 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.477+3384_477+3386d others(5): Show |
MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744330 | ||||||
| chr16:46744364
|
T | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.477+3353A>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744364 | ||||||
| chr16:46744491
|
G | A | 2 | a0001c0001t0001g0207a0008c0004t0001g0009 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.477+3226C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744491 | ||||||
| chr16:46744769
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.477+2948C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744769 | ||||||
| chr16:46744815
|
T | C | 1 | a0002c0002t0001g0198 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.477+2902A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46744815 | ||||||
| chr16:46745336
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.477+2381T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46745336 | ||||||
| chr16:46745363
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.477+2354C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46745363 | ||||||
| chr16:46745608
|
T | C | 3 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG00642.hp2 HG01069.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.477+2109A>G | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46745608 | ||||||
| chr16:46745837
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.477+1880C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46745837 | ||||||
| chr16:46746056
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0011g0014 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.477+1661C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746056 | ||||||
| chr16:46746283
|
A | G | 39 | a0001c0001t0001g0023a0001c0001t0002g0001a0001c0001t0002g0002others(36): Show | 45 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.477+1434T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746283 | ||||||
| chr16:46746355
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0204a0001c0001t0001g0205others(5): Show | 8 | HG01433.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+1362C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746355 | ||||||
| chr16:46746393
|
A | G | 2 | a0001c0001t0001g0016a0007c0005t0001g0015 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.477+1324T>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746393 | ||||||
| chr16:46746398
|
G | A | 1 | a0001c0001t0017g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.477+1319C>T | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746398 | ||||||
| chr16:46746613
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0011g0014 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.477+1104G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46746613 | ||||||
| chr16:46747100
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.477+617G>A | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46747100 | ||||||
| chr16:46747218
|
C | G | 1 | a0001c0001t0003g0010 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.477+499G>C | MYLK3 | ENSG00000140795.13 | transcript | ENST00000394809.9 | protein_coding | 1/12 | chr16 | 46747218 |