Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55159 |
|---|---|
| ensemblid | ENSG00000168411.14 |
| hgncid | 25539 |
| symbol | RFWD3 |
| name | ring finger and WD repeat domain 3 |
| refseq_nuc | NM_018124.4 |
| refseq_prot | NP_060594.3 |
| ensembl_nuc | ENST00000361070.9 |
| ensembl_prot | ENSP00000354361.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 74621399 |
| end | 74666877 |
| strand | - |
| ver | v1.2 |
| region | chr16:74621399-74666877 |
| region5000 | chr16:74616399-74671877 |
| regionname0 | RFWD3_chr16_74621399_74666877 |
| regionname5000 | RFWD3_chr16_74616399_74671877 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 774 | 154 | 27 | 30 | 70 | 3 | 24 | 56 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002 | 0/0 | 774 | 149 | 40 | 21 | 71 | 10 | 7 | 58 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0003 | 1/1 | 774 | 92 | 17 | 21 | 43 | 3 | 6 | 34 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0004 | 0/0 | 774 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0005 | 0/0 | 774 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0006 | 0/0 | 774 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0007 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0008 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0009 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0010 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0011 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0012 | 0/0 | 774 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0013 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0014 | 0/0 | 774 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2325 | 149 | 40 | 21 | 71 | 10 | 7 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0002 | 0/0 | 2325 | 105 | 20 | 11 | 59 | 0 | 15 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0003 | 1/1 | 2325 | 92 | 17 | 21 | 43 | 3 | 6 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0004 | 0/0 | 2325 | 38 | 6 | 15 | 10 | 2 | 5 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0005 | 0/0 | 2325 | 8 | 0 | 3 | 0 | 1 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0006 | 0/0 | 2325 | 5 | 0 | 3 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0007 | 0/0 | 2325 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0008 | 0/0 | 2325 | 2 | 1 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0009 | 0/0 | 2325 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0010 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0011 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0012 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0013 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0014 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0015 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0016 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0017 | 0/0 | 2325 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| c0018 | 0/0 | 2325 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2648 | 112 | 25 | 16 | 56 | 8 | 7 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0002 | 0/0 | 2672 | 89 | 3 | 12 | 59 | 1 | 14 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0003 | 1/0 | 2624 | 70 | 10 | 16 | 38 | 2 | 3 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0004 | 0/0 | 2624 | 24 | 3 | 15 | 0 | 2 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0005 | 0/1 | 2624 | 20 | 7 | 3 | 5 | 1 | 3 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0006 | 0/0 | 2649 | 11 | 6 | 0 | 4 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0007 | 0/0 | 2624 | 8 | 0 | 3 | 0 | 1 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0008 | 0/0 | 2696 | 8 | 0 | 1 | 7 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0009 | 0/0 | 2672 | 6 | 0 | 0 | 6 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0010 | 0/0 | 2648 | 5 | 5 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0011 | 0/0 | 2624 | 4 | 4 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0012 | 0/0 | 2624 | 3 | 0 | 2 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0013 | 0/0 | 2672 | 3 | 2 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0014 | 0/0 | 2648 | 3 | 3 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0015 | 0/0 | 2720 | 2 | 0 | 1 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0016 | 0/0 | 2672 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0017 | 0/0 | 2672 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0018 | 0/0 | 2648 | 2 | 1 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0019 | 0/0 | 2648 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0020 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0021 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0022 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0023 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0024 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0025 | 0/0 | 2720 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0026 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0027 | 0/0 | 2696 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0028 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0029 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0030 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0031 | 0/0 | 2672 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0032 | 0/0 | 2671 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0033 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0034 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0035 | 0/0 | 2672 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0036 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0037 | 0/0 | 2672 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0038 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0039 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0040 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0041 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0042 | 0/0 | 2647 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0043 | 0/0 | 2648 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0044 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0045 | 0/0 | 2648 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0046 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0047 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0048 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0049 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0050 | 0/0 | 2624 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0051 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0052 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0053 | 0/0 | 2693 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0054 | 0/0 | 2648 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0055 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| t0056 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0002 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2325 | 105 | 20 | 11 | 59 | 0 | 15 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004 | 0/0 | 2325 | 38 | 6 | 15 | 10 | 2 | 5 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0005 | 0/0 | 2325 | 8 | 0 | 3 | 0 | 1 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0008 | 0/0 | 2325 | 2 | 1 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0011 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001 | 0/0 | 2325 | 149 | 40 | 21 | 71 | 10 | 7 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0003c0003 | 1/1 | 2325 | 92 | 17 | 21 | 43 | 3 | 6 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0004c0006 | 0/0 | 2325 | 5 | 0 | 3 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0005c0009 | 0/0 | 2325 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0006c0007 | 0/0 | 2325 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0007c0015 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0008c0013 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0009c0010 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0010c0012 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0011c0014 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0012c0017 | 0/0 | 2325 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0013c0016 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0014c0018 | 0/0 | 2325 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 4972 | 4 | 0 | 0 | 4 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0002 | 0/0 | 4996 | 58 | 0 | 7 | 40 | 0 | 11 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0006 | 0/0 | 4973 | 11 | 6 | 0 | 4 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0008 | 0/0 | 5020 | 4 | 0 | 1 | 3 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0011 | 0/0 | 4948 | 4 | 4 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0013 | 0/0 | 4996 | 3 | 2 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0014 | 0/0 | 4972 | 3 | 3 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0015 | 0/0 | 5044 | 2 | 0 | 1 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0016 | 0/0 | 4996 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0026 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0029 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0030 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0031 | 0/0 | 4996 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0032 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0033 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0034 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0035 | 0/0 | 4996 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0036 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0044 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0046 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0049 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0055 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0002t0056 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0004 | 0/0 | 4948 | 24 | 3 | 15 | 0 | 2 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0009 | 0/0 | 4996 | 5 | 0 | 0 | 5 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0017 | 0/0 | 4996 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0021 | 0/0 | 4948 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0023 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0025 | 0/0 | 5044 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0028 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0051 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0052 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0004t0053 | 0/0 | 5017 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0005t0007 | 0/0 | 4948 | 8 | 0 | 3 | 0 | 1 | 4 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0008t0027 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0008t0048 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0001c0011t0002 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0001 | 0/0 | 4972 | 103 | 25 | 13 | 51 | 8 | 6 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0002 | 0/0 | 4996 | 26 | 3 | 5 | 16 | 1 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0008 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0010 | 0/0 | 4972 | 5 | 5 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0012 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0018 | 0/0 | 4972 | 2 | 1 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0024 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0038 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0039 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0040 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0041 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0042 | 0/0 | 4971 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0043 | 0/0 | 4972 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0045 | 0/0 | 4972 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0050 | 0/0 | 4948 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0002c0001t0054 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0003c0003t0003 | 1/0 | 4948 | 70 | 10 | 16 | 38 | 2 | 3 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0003c0003t0005 | 0/1 | 4948 | 19 | 7 | 2 | 5 | 1 | 3 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0003c0003t0012 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0003c0003t0020 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0003c0003t0022 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0004c0006t0001 | 0/0 | 4972 | 4 | 0 | 3 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0004c0006t0019 | 0/0 | 4972 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0005c0009t0008 | 0/0 | 5020 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0006c0007t0002 | 0/0 | 4996 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0007c0015t0002 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0008c0013t0047 | 0/0 | 4972 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0009c0010t0002 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0010c0012t0009 | 0/0 | 4996 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0011c0014t0001 | 0/0 | 4972 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0012c0017t0012 | 0/0 | 4948 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0013c0016t0037 | 0/0 | 4996 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| a0014c0018t0005 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | copy fasta | chr16 | 74616399 | 74671877 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0006g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0008g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0008g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0013g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0014g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0014g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0014g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0015g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0015g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0016g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0016g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0026g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0029g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0030g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0031g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0032g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0033g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0034g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0035g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0036g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0044g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0046g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0049g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0055g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0002t0056g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0017g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0021g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0023g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0025g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0028g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0051g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0052g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0004t0053g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0005t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0008t0027g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0008t0048g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0001c0011t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0010g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0018g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0018g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0024g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0038g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0039g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0040g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0041g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0042g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0043g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0045g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0050g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0002c0001t0054g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0002 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0012g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0020g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0003c0003t0022g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0004c0006t0019g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0005c0009t0008g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0005c0009t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0006c0007t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0006c0007t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0007c0015t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0008c0013t0047g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0009c0010t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0010c0012t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0011c0014t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0012c0017t0012g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0013c0016t0037g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| a0014c0018t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0004 | g0122 | EUR | GBR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00099 | hp2 | a0001 | c0004 | t0004 | g0127 | EUR | GBR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00140 | hp1 | a0001 | c0005 | t0007 | g0045 | EUR | GBR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0337 | EUR | GBR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00280 | hp1 | a0003 | c0003 | t0005 | g0040 | EUR | FIN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00280 | hp2 | a0003 | c0003 | t0003 | g0074 | EUR | FIN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0275 | EUR | FIN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00323 | hp2 | a0002 | c0001 | t0002 | g0164 | EUR | FIN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00408 | hp1 | a0003 | c0003 | t0003 | g0094 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00408 | hp2 | a0001 | c0002 | t0055 | g0385 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0307 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0327 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00544 | hp1 | a0003 | c0003 | t0003 | g0097 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00544 | hp2 | a0002 | c0001 | t0002 | g0163 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0312 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00558 | hp2 | a0001 | c0004 | t0017 | g0013 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0309 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00597 | hp2 | a0003 | c0003 | t0003 | g0046 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0316 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00609 | hp2 | a0003 | c0003 | t0003 | g0007 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0300 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00621 | hp2 | a0003 | c0003 | t0003 | g0071 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00639 | hp1 | a0002 | c0001 | t0002 | g0157 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00639 | hp2 | a0001 | c0004 | t0004 | g0129 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00642 | hp2 | a0003 | c0003 | t0003 | g0026 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00673 | hp1 | a0001 | c0002 | t0006 | g0360 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00673 | hp2 | a0001 | c0002 | t0015 | g0138 | EAS | CHS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0332 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00733 | hp2 | a0001 | c0004 | t0004 | g0001 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00735 | hp1 | a0003 | c0003 | t0003 | g0048 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00735 | hp2 | a0002 | c0001 | t0002 | g0158 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00738 | hp1 | a0001 | c0002 | t0013 | g0166 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00738 | hp2 | a0003 | c0003 | t0005 | g0043 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00741 | hp1 | a0003 | c0003 | t0020 | g0063 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG00741 | hp2 | a0001 | c0004 | t0004 | g0124 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01069 | hp1 | a0002 | c0001 | t0002 | g0011 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01069 | hp2 | a0002 | c0001 | t0001 | g0338 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0308 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01070 | hp2 | a0001 | c0004 | t0004 | g0121 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01071 | hp1 | a0002 | c0001 | t0002 | g0011 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0311 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0289 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01074 | hp2 | a0002 | c0001 | t0002 | g0159 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0278 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01081 | hp2 | a0003 | c0003 | t0022 | g0036 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0264 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01106 | hp2 | a0003 | c0003 | t0003 | g0106 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01109 | hp1 | a0002 | c0001 | t0018 | g0382 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01109 | hp2 | a0002 | c0001 | t0012 | g0057 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0294 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0293 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01169 | hp2 | a0003 | c0003 | t0012 | g0056 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01192 | hp1 | a0003 | c0003 | t0003 | g0053 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01192 | hp2 | a0001 | c0005 | t0007 | g0110 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0326 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01243 | hp2 | a0003 | c0003 | t0003 | g0092 | AMR | PUR | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01255 | hp1 | a0001 | c0004 | t0004 | g0115 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01255 | hp2 | a0003 | c0003 | t0003 | g0076 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01256 | hp1 | a0003 | c0003 | t0003 | g0060 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01256 | hp2 | a0001 | c0002 | t0008 | g0147 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01257 | hp1 | a0003 | c0003 | t0003 | g0002 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01257 | hp2 | a0001 | c0005 | t0007 | g0109 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01261 | hp1 | a0001 | c0002 | t0015 | g0139 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01358 | hp1 | a0001 | c0004 | t0004 | g0134 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0268 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01361 | hp1 | a0003 | c0003 | t0003 | g0025 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01361 | hp2 | a0003 | c0003 | t0005 | g0039 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01433 | hp1 | a0001 | c0005 | t0007 | g0090 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01433 | hp2 | a0004 | c0006 | t0001 | g0276 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0277 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01496 | hp2 | a0001 | c0004 | t0004 | g0135 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0263 | EUR | IBS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01515 | hp2 | a0002 | c0001 | t0050 | g0378 | EUR | IBS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0267 | EUR | IBS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01516 | hp2 | a0002 | c0001 | t0001 | g0245 | EUR | IBS | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0015 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0023 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01928 | hp1 | a0003 | c0003 | t0003 | g0052 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01928 | hp2 | a0001 | c0004 | t0004 | g0120 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01943 | hp1 | a0003 | c0003 | t0003 | g0051 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01952 | hp1 | a0001 | c0004 | t0004 | g0001 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01952 | hp2 | a0001 | c0002 | t0031 | g0206 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01975 | hp1 | a0001 | c0004 | t0004 | g0001 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01975 | hp2 | a0003 | c0003 | t0003 | g0078 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0180 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01978 | hp2 | a0001 | c0004 | t0004 | g0119 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0255 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01981 | hp2 | a0004 | c0006 | t0001 | g0262 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01993 | hp1 | a0001 | c0008 | t0027 | g0140 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01993 | hp2 | a0003 | c0003 | t0003 | g0007 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02004 | hp1 | a0003 | c0003 | t0003 | g0111 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02004 | hp2 | a0001 | c0004 | t0004 | g0001 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02027 | hp1 | a0001 | c0004 | t0025 | g0137 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02027 | hp2 | a0002 | c0001 | t0008 | g0143 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02040 | hp1 | a0003 | c0003 | t0003 | g0067 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0247 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0320 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02080 | hp2 | a0001 | c0004 | t0009 | g0176 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02083 | hp1 | a0003 | c0003 | t0003 | g0103 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02083 | hp2 | a0002 | c0001 | t0002 | g0156 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02132 | hp1 | a0003 | c0003 | t0003 | g0068 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02135 | hp1 | a0003 | c0003 | t0003 | g0059 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02135 | hp2 | a0001 | c0002 | t0032 | g0201 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02145 | hp1 | a0002 | c0001 | t0010 | g0325 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02145 | hp2 | a0002 | c0001 | t0001 | g0350 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02155 | hp1 | a0001 | c0002 | t0026 | g0146 | EAS | CDX | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02155 | hp2 | a0001 | c0002 | t0008 | g0145 | EAS | CDX | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02165 | hp2 | a0001 | c0002 | t0030 | g0192 | EAS | CDX | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02257 | hp1 | a0001 | c0002 | t0034 | g0173 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02257 | hp2 | a0003 | c0003 | t0005 | g0030 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0075 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02258 | hp2 | a0001 | c0002 | t0046 | g0377 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02273 | hp1 | a0003 | c0003 | t0003 | g0113 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02273 | hp2 | a0001 | c0004 | t0004 | g0001 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02280 | hp1 | a0003 | c0003 | t0003 | g0002 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0015 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02293 | hp1 | a0004 | c0006 | t0001 | g0261 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02293 | hp2 | a0003 | c0003 | t0003 | g0077 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02300 | hp1 | a0014 | c0018 | t0005 | g0037 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02300 | hp2 | a0001 | c0004 | t0004 | g0125 | AMR | PEL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02451 | hp1 | a0003 | c0003 | t0005 | g0034 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02451 | hp2 | a0001 | c0002 | t0006 | g0367 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02523 | hp1 | a0002 | c0001 | t0008 | g0141 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | KHV | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02572 | hp1 | a0001 | c0002 | t0006 | g0364 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0291 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02602 | hp1 | a0003 | c0003 | t0005 | g0038 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02602 | hp2 | a0003 | c0003 | t0003 | g0050 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02615 | hp1 | a0002 | c0001 | t0018 | g0383 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0365 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02622 | hp1 | a0001 | c0004 | t0051 | g0380 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02622 | hp2 | a0002 | c0001 | t0001 | g0280 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0348 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0358 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02647 | hp1 | a0003 | c0003 | t0005 | g0029 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0317 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02683 | hp1 | a0003 | c0003 | t0005 | g0041 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02683 | hp2 | a0001 | c0004 | t0004 | g0126 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02698 | hp2 | a0004 | c0006 | t0001 | g0286 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02723 | hp1 | a0001 | c0002 | t0044 | g0335 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0269 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02735 | hp1 | a0003 | c0003 | t0003 | g0002 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0232 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02738 | hp1 | a0003 | c0003 | t0003 | g0081 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02738 | hp2 | a0001 | c0002 | t0016 | g0217 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02809 | hp1 | a0013 | c0016 | t0037 | g0154 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02809 | hp2 | a0002 | c0001 | t0039 | g0288 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02818 | hp1 | a0003 | c0003 | t0003 | g0087 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0020 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02886 | hp1 | a0001 | c0002 | t0014 | g0257 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02886 | hp2 | a0003 | c0003 | t0003 | g0105 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02895 | hp1 | a0003 | c0003 | t0005 | g0031 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02895 | hp2 | a0002 | c0001 | t0002 | g0165 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02896 | hp1 | a0001 | c0004 | t0004 | g0131 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02896 | hp2 | a0003 | c0003 | t0005 | g0032 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02897 | hp1 | a0002 | c0001 | t0002 | g0160 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02897 | hp2 | a0001 | c0004 | t0004 | g0132 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02922 | hp1 | a0002 | c0001 | t0010 | g0343 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02922 | hp2 | a0001 | c0004 | t0023 | g0130 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02970 | hp1 | a0002 | c0001 | t0001 | g0292 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02970 | hp2 | a0001 | c0002 | t0014 | g0357 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02976 | hp1 | a0003 | c0003 | t0005 | g0033 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0270 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03017 | hp1 | a0001 | c0005 | t0007 | g0008 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03017 | hp2 | a0001 | c0002 | t0016 | g0216 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03041 | hp1 | a0002 | c0001 | t0002 | g0161 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0359 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0072 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03098 | hp2 | a0002 | c0001 | t0010 | g0253 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0284 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0273 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03195 | hp1 | a0002 | c0001 | t0040 | g0252 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03195 | hp2 | a0002 | c0001 | t0010 | g0271 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03225 | hp1 | a0008 | c0013 | t0047 | g0323 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03225 | hp2 | a0001 | c0002 | t0011 | g0027 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03453 | hp1 | a0001 | c0002 | t0049 | g0352 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03453 | hp2 | a0003 | c0003 | t0003 | g0096 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0285 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03486 | hp2 | a0001 | c0002 | t0013 | g0152 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03490 | hp2 | a0001 | c0005 | t0007 | g0108 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03492 | hp2 | a0001 | c0005 | t0007 | g0008 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0355 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03516 | hp2 | a0001 | c0002 | t0013 | g0153 | AFR | ESN | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03540 | hp1 | a0002 | c0001 | t0024 | g0136 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03540 | hp2 | a0001 | c0004 | t0052 | g0379 | AFR | GWD | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0347 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0353 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03654 | hp1 | a0002 | c0001 | t0002 | g0162 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03654 | hp2 | a0001 | c0004 | t0021 | g0123 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0339 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0171 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03704 | hp1 | a0001 | c0004 | t0004 | g0117 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03704 | hp2 | a0006 | c0007 | t0002 | g0170 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03710 | hp1 | a0006 | c0007 | t0002 | g0169 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0302 | SAS | PJL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0230 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0299 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0224 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0328 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0210 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03942 | hp2 | a0004 | c0006 | t0019 | g0019 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04115 | hp1 | a0003 | c0003 | t0005 | g0044 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04184 | hp1 | a0002 | c0001 | t0001 | g0272 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0183 | SAS | BEB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04199 | hp1 | a0001 | c0004 | t0004 | g0118 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0212 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04204 | hp1 | a0012 | c0017 | t0012 | g0058 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04204 | hp2 | a0001 | c0004 | t0004 | g0116 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0283 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG04228 | hp2 | a0001 | c0002 | t0006 | g0363 | SAS | STU | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0372 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18522 | hp2 | a0001 | c0002 | t0006 | g0368 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | CHB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0318 | EAS | CHB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18906 | hp1 | a0002 | c0001 | t0038 | g0287 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18906 | hp2 | a0002 | c0001 | t0001 | g0274 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18939 | hp1 | a0003 | c0003 | t0003 | g0100 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0321 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18941 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18942 | hp1 | a0003 | c0003 | t0003 | g0061 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0345 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18944 | hp1 | a0003 | c0003 | t0005 | g0080 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18945 | hp1 | a0001 | c0004 | t0009 | g0187 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0371 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18946 | hp2 | a0005 | c0009 | t0008 | g0148 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0370 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18948 | hp1 | a0003 | c0003 | t0003 | g0098 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18948 | hp2 | a0001 | c0002 | t0036 | g0231 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18949 | hp2 | a0003 | c0003 | t0003 | g0091 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18950 | hp1 | a0001 | c0004 | t0028 | g0144 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0346 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0303 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18954 | hp1 | a0001 | c0002 | t0006 | g0366 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18957 | hp1 | a0001 | c0002 | t0033 | g0227 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0322 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0304 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18960 | hp1 | a0007 | c0015 | t0002 | g0238 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0319 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18962 | hp1 | a0003 | c0003 | t0003 | g0066 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0260 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18963 | hp2 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0256 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18964 | hp2 | a0002 | c0001 | t0002 | g0223 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0297 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18966 | hp1 | a0003 | c0003 | t0003 | g0073 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0369 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0375 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0330 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18968 | hp1 | a0002 | c0001 | t0042 | g0313 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18969 | hp2 | a0003 | c0003 | t0003 | g0064 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0342 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18971 | hp2 | a0009 | c0010 | t0002 | g0193 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18972 | hp1 | a0002 | c0001 | t0001 | g0243 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18972 | hp2 | a0003 | c0003 | t0003 | g0102 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0334 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0258 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18975 | hp1 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0329 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18977 | hp1 | a0003 | c0003 | t0003 | g0085 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18977 | hp2 | a0003 | c0003 | t0005 | g0006 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18978 | hp1 | a0001 | c0004 | t0009 | g0186 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18978 | hp2 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18981 | hp2 | a0003 | c0003 | t0003 | g0112 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0248 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18982 | hp2 | a0001 | c0004 | t0053 | g0381 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18984 | hp1 | a0001 | c0004 | t0009 | g0185 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0301 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18985 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18985 | hp2 | a0001 | c0002 | t0008 | g0142 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18989 | hp1 | a0002 | c0001 | t0001 | g0295 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0310 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0344 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18993 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18993 | hp2 | a0003 | c0003 | t0003 | g0054 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18995 | hp1 | a0003 | c0003 | t0003 | g0101 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0373 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0259 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0315 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA18999 | hp2 | a0003 | c0003 | t0003 | g0084 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19000 | hp2 | a0003 | c0003 | t0003 | g0104 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19001 | hp1 | a0003 | c0003 | t0003 | g0055 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0298 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19002 | hp1 | a0001 | c0002 | t0006 | g0362 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19003 | hp1 | a0010 | c0012 | t0009 | g0221 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19003 | hp2 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19004 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19007 | hp1 | a0003 | c0003 | t0003 | g0099 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19007 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19009 | hp1 | a0003 | c0003 | t0005 | g0006 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19009 | hp2 | a0002 | c0001 | t0002 | g0151 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0082 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0336 | AFR | LWK | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0254 | AFR | LWK | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19055 | hp1 | a0003 | c0003 | t0003 | g0093 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19055 | hp2 | a0011 | c0014 | t0001 | g0331 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19056 | hp1 | a0003 | c0003 | t0003 | g0047 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19056 | hp2 | a0002 | c0001 | t0002 | g0174 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19057 | hp2 | a0003 | c0003 | t0003 | g0107 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19060 | hp1 | a0001 | c0004 | t0009 | g0184 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0249 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19062 | hp1 | a0001 | c0002 | t0056 | g0386 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19063 | hp1 | a0002 | c0001 | t0002 | g0009 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19064 | hp1 | a0003 | c0003 | t0003 | g0022 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19064 | hp2 | a0002 | c0001 | t0002 | g0155 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19065 | hp1 | a0005 | c0009 | t0008 | g0149 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19065 | hp2 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0296 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19066 | hp2 | a0003 | c0003 | t0005 | g0005 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19067 | hp1 | a0002 | c0001 | t0002 | g0167 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19067 | hp2 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0306 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19074 | hp1 | a0002 | c0001 | t0002 | g0182 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19078 | hp1 | a0003 | c0003 | t0003 | g0065 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19078 | hp2 | a0001 | c0002 | t0008 | g0150 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19079 | hp1 | a0002 | c0001 | t0002 | g0009 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19080 | hp1 | a0002 | c0001 | t0002 | g0010 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0250 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19081 | hp1 | a0002 | c0001 | t0002 | g0010 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19082 | hp1 | a0002 | c0001 | t0043 | g0314 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0341 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19085 | hp1 | a0003 | c0003 | t0003 | g0083 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19085 | hp2 | a0001 | c0004 | t0017 | g0013 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0305 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19087 | hp2 | a0001 | c0002 | t0006 | g0361 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19089 | hp1 | a0003 | c0003 | t0003 | g0049 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19090 | hp1 | a0003 | c0003 | t0005 | g0005 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19090 | hp2 | a0001 | c0011 | t0002 | g0215 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19091 | hp1 | a0003 | c0003 | t0003 | g0079 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19240 | hp1 | a0001 | c0002 | t0011 | g0024 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA19240 | hp2 | a0003 | c0003 | t0003 | g0002 | AFR | YRI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20129 | hp1 | a0003 | c0003 | t0003 | g0021 | AFR | ASW | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0265 | AFR | ASW | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0282 | EUR | TSI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0340 | EUR | TSI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20805 | hp1 | a0003 | c0003 | t0003 | g0095 | EUR | TSI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0333 | EUR | TSI | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20905 | hp1 | a0001 | c0002 | t0035 | g0199 | SAS | GIH | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20905 | hp2 | a0001 | c0005 | t0007 | g0089 | SAS | GIH | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01123 | hp1 | a0001 | c0004 | t0004 | g0128 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG01123 | hp2 | a0002 | c0001 | t0045 | g0279 | AMR | CLM | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02109 | hp1 | a0001 | c0002 | t0011 | g0133 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0354 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02486 | hp1 | a0001 | c0002 | t0029 | g0168 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0349 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02559 | hp1 | a0002 | c0001 | t0010 | g0266 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG02559 | hp2 | a0002 | c0001 | t0041 | g0290 | AFR | ACB | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03471 | hp1 | a0001 | c0004 | t0004 | g0114 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG03471 | hp2 | a0001 | c0002 | t0014 | g0356 | AFR | MSL | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG06807 | hp1 | a0003 | c0003 | t0005 | g0035 | AFR | USA | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0324 | AFR | USA | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20300 | hp1 | a0003 | c0003 | t0003 | g0028 | AFR | USA | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA20300 | hp2 | a0002 | c0001 | t0054 | g0384 | AFR | USA | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA21309 | hp1 | a0001 | c0008 | t0048 | g0351 | AFR | LWK | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| NA21309 | hp2 | a0002 | c0001 | t0001 | g0281 | AFR | LWK | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0005 | g0042 | REF | REF | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0003 | g0088 | REF | REF | RFWD3_chr16_74616399_74671877 | RFWD3 | chr16 | 74616399 | 74671877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74623954
|
T | C | 1 | a0012 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2299A>G | p.Met767Val | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2393/4948 | 2299/2325 | 767/774 | chr16 | 74623954 | ||
| chr16:74626549
|
T | A | 1 | a0010 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.1975A>T | p.Asn659Tyr | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/13 | 2069/4948 | 1975/2325 | 659/774 | chr16 | 74626549 | ||
| chr16:74630845
|
T | C | 4 | a0002a0004a0011others(1): Show | 156 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
missense_variant | MODERATE | c.1690A>G | p.Ile564Val | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/13 | 1784/4948 | 1690/2325 | 564/774 | chr16 | 74630845 | ||
| chr16:74632641
|
T | G | 1 | a0005 | 2 | NA18946.hp2 NA19065.hp1 |
missense_variant | MODERATE | c.1459A>C | p.Met487Leu | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/13 | 1553/4948 | 1459/2325 | 487/774 | chr16 | 74632641 | ||
| chr16:74636468
|
T | G | 1 | a0014 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1304A>C | p.Lys435Thr | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/13 | 1398/4948 | 1304/2325 | 435/774 | chr16 | 74636468 | ||
| chr16:74637950
|
A | G | 1 | a0006 | 2 | HG03704.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.1100T>C | p.Met367Thr | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/13 | 1194/4948 | 1100/2325 | 367/774 | chr16 | 74637950 | ||
| chr16:74637968
|
G | A | 1 | a0004 | 5 | HG01433.hp2 HG01981.hp2 HG02293.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.1082C>T | p.Ser361Phe | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/13 | 1176/4948 | 1082/2325 | 361/774 | chr16 | 74637968 | ||
| chr16:74644407
|
C | T | 1 | a0009 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.1034G>A | p.Arg345Gln | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/13 | 1128/4948 | 1034/2325 | 345/774 | chr16 | 74644407 | ||
| chr16:74649149
|
T | C | 1 | a0008 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.775A>G | p.Lys259Glu | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/13 | 869/4948 | 775/2325 | 259/774 | chr16 | 74649149 | ||
| chr16:74660975
|
G | A | 1 | a0011 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.475C>T | p.Arg159Trp | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/13 | 569/4948 | 475/2325 | 159/774 | chr16 | 74660975 | ||
| chr16:74660987
|
C | A | 1 | a0007 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.463G>T | p.Val155Leu | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/13 | 557/4948 | 463/2325 | 155/774 | chr16 | 74660987 | ||
| chr16:74661181
|
G | T | 10 | a0001a0002a0004others(7): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
missense_variant | MODERATE | c.269C>A | p.Thr90Asn | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/13 | 363/4948 | 269/2325 | 90/774 | chr16 | 74661181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74630800
|
A | G | 1 | a0001c0005 | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
synonymous_variant | LOW | c.1735T>C | p.Leu579Leu | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/13 | 1829/4948 | 1735/2325 | 579/774 | chr16 | 74630800 | ||
| chr16:74630912
|
A | T | 11 | a0001c0002a0001c0011a0002c0001others(8): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
synonymous_variant | LOW | c.1623T>A | p.Pro541Pro | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/13 | 1717/4948 | 1623/2325 | 541/774 | chr16 | 74630912 | ||
| chr16:74636560
|
C | T | 10 | a0001c0002a0001c0008a0002c0001others(7): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
synonymous_variant | LOW | c.1212G>A | p.Thr404Thr | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/13 | 1306/4948 | 1212/2325 | 404/774 | chr16 | 74636560 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74621532
|
G | A | 1 | a0001c0004t0052 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2396C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2396 | chr16 | 74621532 | |||||
| chr16:74621636
|
G | A | 3 | a0002c0001t0010a0002c0001t0038a0002c0001t0039 | 7 | HG02145.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2292C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2292 | chr16 | 74621636 | |||||
| chr16:74621663
|
G | A | 1 | a0002c0001t0039 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2265C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2265 | chr16 | 74621663 | |||||
| chr16:74621694
|
T | TG | 43 | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(40): Show | 263 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*2233dupC | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2233 | chr16 | 74621694 | |||||
| chr16:74621699
|
G | GT | 2 | a0001c0002t0006a0002c0001t0041 | 12 | HG00673.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2228dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2228 | chr16 | 74621699 | |||||
| chr16:74621703
|
G | GT | 12 | a0001c0002t0031a0001c0004t0004a0001c0004t0009others(9): Show | 40 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2224dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2224 | chr16 | 74621703 | |||||
| chr16:74621703
|
G | T | 43 | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(40): Show | 263 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*2225C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2225 | chr16 | 74621703 | |||||
| chr16:74621707
|
T | G | 7 | a0002c0001t0012a0003c0003t0005a0003c0003t0012others(4): Show | 25 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2221A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2221 | chr16 | 74621707 | |||||
| chr16:74621736
|
G | C | 59 | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(56): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*2192C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2192 | chr16 | 74621736 | |||||
| chr16:74621754
|
C | T | 12 | a0001c0002t0031a0001c0004t0004a0001c0004t0009others(9): Show | 40 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2174G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2174 | chr16 | 74621754 | |||||
| chr16:74621755
|
G | A | 1 | a0001c0002t0034 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2173C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2173 | chr16 | 74621755 | |||||
| chr16:74621844
|
G | A | 3 | a0001c0002t0006a0001c0002t0013a0002c0001t0040 | 15 | HG00673.hp1 HG00738.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2084C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2084 | chr16 | 74621844 | |||||
| chr16:74621883
|
G | C | 1 | a0001c0002t0035 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2045C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2045 | chr16 | 74621883 | |||||
| chr16:74621926
|
T | C | 1 | a0003c0003t0020 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2002A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 2002 | chr16 | 74621926 | |||||
| chr16:74621950
|
G | A | 59 | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(56): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*1978C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1978 | chr16 | 74621950 | |||||
| chr16:74622024
|
C | A | 2 | a0001c0004t0017a0001c0004t0053 | 3 | HG00558.hp2 NA18982.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1904G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1904 | chr16 | 74622024 | |||||
| chr16:74622034
|
A | G | 1 | a0001c0002t0030 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1894T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1894 | chr16 | 74622034 | |||||
| chr16:74622101
|
T | A | 3 | a0002c0001t0012a0003c0003t0012a0012c0017t0012 | 3 | HG01109.hp2 HG01169.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1827A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1827 | chr16 | 74622101 | |||||
| chr16:74622462
|
CA | C | 57 | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(54): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*1465delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1465 | chr16 | 74622462 | |||||
| chr16:74622509
|
G | A | 2 | a0001c0005t0007a0001c0008t0048 | 9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1419C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1419 | chr16 | 74622509 | |||||
| chr16:74622624
|
A | G | 8 | a0001c0002t0006a0001c0002t0013a0001c0002t0014others(5): Show | 22 | HG00673.hp1 HG00738.hp1 HG02451.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1304T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1304 | chr16 | 74622624 | |||||
| chr16:74622626
|
A | G | 1 | a0001c0002t0029 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1302 | chr16 | 74622626 | |||||
| chr16:74622883
|
T | C | 1 | a0001c0002t0036 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1045A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1045 | chr16 | 74622883 | |||||
| chr16:74622897
|
G | C | 1 | a0001c0004t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1031C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 1031 | chr16 | 74622897 | |||||
| chr16:74622951
|
G | T | 1 | a0001c0002t0046 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*977C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 977 | chr16 | 74622951 | |||||
| chr16:74622979
|
T | C | 1 | a0001c0002t0044 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 949 | chr16 | 74622979 | |||||
| chr16:74623014
|
T | A | 1 | a0002c0001t0045 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 914 | chr16 | 74623014 | |||||
| chr16:74623051
|
G | T | 2 | a0001c0005t0007a0001c0008t0048 | 9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*877C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 877 | chr16 | 74623051 | |||||
| chr16:74623140
|
T | C | 1 | a0008c0013t0047 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 788 | chr16 | 74623140 | |||||
| chr16:74623147
|
G | T | 1 | a0001c0002t0016 | 2 | HG02738.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*781C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 781 | chr16 | 74623147 | |||||
| chr16:74623174
|
G | A | 1 | a0003c0003t0022 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 754 | chr16 | 74623174 | |||||
| chr16:74623350
|
C | A | 2 | a0001c0002t0046a0008c0013t0047 | 2 | HG02258.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*578G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 578 | chr16 | 74623350 | |||||
| chr16:74623394
|
C | T | 1 | a0001c0002t0026 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 534 | chr16 | 74623394 | |||||
| chr16:74623523
|
T | C | 60 | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(57): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 405 | chr16 | 74623523 | |||||
| chr16:74623587
|
A | T | 48 | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(45): Show | 268 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*341T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 341 | chr16 | 74623587 | |||||
| chr16:74623603
|
G | C | 1 | a0001c0002t0049 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 325 | chr16 | 74623603 | |||||
| chr16:74623874
|
C | T | 1 | a0003c0003t0020 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 54 | chr16 | 74623874 | |||||
| chr16:74623885
|
A | G | 3 | a0002c0001t0012a0003c0003t0012a0012c0017t0012 | 3 | HG01109.hp2 HG01169.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*43T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 13/13 | 43 | chr16 | 74623885 | |||||
| chr16:74666819
|
C | CCCGCCGA others(17): Show |
20 | a0001c0002t0001a0001c0002t0006a0001c0002t0014others(17): Show | 144 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
5_prime_UTR_variant | MODIFIER | c.-60_-37dupAGGTAACT others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | |||||
| chr16:74666819
|
C | CCCGCCGA others(41): Show |
21 | a0001c0002t0002a0001c0002t0013a0001c0002t0016others(18): Show | 112 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(109): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-36insAGGTAACT others(40): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | |||||
| chr16:74666819
|
C | CCCGCCGA others(62): Show |
1 | a0001c0004t0053 | 1 | NA18982.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37_-36insTAACTACC others(61): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | |||||
| chr16:74666819
|
C | CCCGCCGA others(65): Show |
6 | a0001c0002t0008a0001c0002t0026a0001c0004t0028others(3): Show | 11 | HG01256.hp2 HG01993.hp1 HG02027.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-36insAGGTAACT others(64): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | |||||
| chr16:74666819
|
C | CCCGCCGA others(89): Show |
2 | a0001c0002t0015a0001c0004t0025 | 3 | HG00673.hp2 HG01261.hp1 HG02027.hp1 |
5_prime_UTR_variant | MODIFIER | c.-37_-36insAGGTAACT others(88): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5371 | chr16 | 74666819 | |||||
| chr16:74666825
|
G | GAAGACTC others(17): Show |
1 | a0002c0001t0024 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43_-42insAGGCGGAG others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5377 | chr16 | 74666825 | |||||
| chr16:74666843
|
T | TCCGCCGA others(17): Show |
2 | a0002c0001t0018a0002c0001t0054 | 3 | HG01109.hp1 HG02615.hp1 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-61_-60insCGGTAACT others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5395 | chr16 | 74666843 | |||||
| chr16:74666844
|
C | CCGCCGAA others(41): Show |
1 | a0001c0002t0055 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62_-61insTAGGTAAC others(40): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5396 | chr16 | 74666844 | |||||
| chr16:74666845
|
G | C | 57 | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(54): Show | 279 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(276): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5396 | chr16 | 74666845 | |||||
| chr16:74666857
|
A | G | 1 | a0004c0006t0019 | 1 | HG03942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5408 | chr16 | 74666857 | |||||
| chr16:74666865
|
T | C | 1 | a0001c0002t0056 | 1 | NA19062.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/13 | 5416 | chr16 | 74666865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74624199
|
C | G | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2182-128G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624199 | ||||||
| chr16:74624285
|
C | T | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-214G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624285 | ||||||
| chr16:74624286
|
T | G | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-215A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624286 | ||||||
| chr16:74624287
|
G | T | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-216C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624287 | ||||||
| chr16:74624420
|
A | T | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-349T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624420 | ||||||
| chr16:74624532
|
A | T | 113 | a0001c0002t0002g0203a0001c0002t0002g0204a0001c0002t0002g0213others(110): Show | 122 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2182-461T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624532 | ||||||
| chr16:74624686
|
C | G | 1 | a0003c0003t0003g0095 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2182-615G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624686 | ||||||
| chr16:74624689
|
G | A | 3 | a0001c0002t0002g0178a0001c0002t0002g0179a0001c0002t0002g0180 | 3 | HG01099.hp1 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2182-618C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624689 | ||||||
| chr16:74624692
|
T | C | 4 | a0002c0001t0001g0268a0002c0001t0001g0277a0002c0001t0001g0293others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2182-621A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624692 | ||||||
| chr16:74624719
|
G | T | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-648C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624719 | ||||||
| chr16:74624821
|
A | T | 296 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(293): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2182-750T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624821 | ||||||
| chr16:74624825
|
A | C | 296 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(293): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2182-754T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624825 | ||||||
| chr16:74624902
|
T | C | 1 | a0002c0001t0001g0283 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2182-831A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624902 | ||||||
| chr16:74624969
|
G | A | 254 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(251): Show | 268 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.2182-898C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624969 | ||||||
| chr16:74624994
|
A | C | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182-923T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74624994 | ||||||
| chr16:74625157
|
A | G | 1 | a0001c0002t0034g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2182-1086T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625157 | ||||||
| chr16:74625199
|
C | CA | 168 | a0001c0002t0002g0191a0001c0002t0002g0212a0001c0002t0006g0358others(165): Show | 178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.2182-1129dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625199 | ||||||
| chr16:74625199
|
C | CAA | 82 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(79): Show | 86 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.2182-1130_2182-112 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625199 | ||||||
| chr16:74625215
|
T | C | 8 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(5): Show | 9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2181+1128A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625215 | ||||||
| chr16:74625239
|
T | TA | 3 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130 | 3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2181+1103dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625239 | ||||||
| chr16:74625241
|
G | C | 20 | a0001c0002t0006g0358a0001c0002t0006g0359a0001c0002t0006g0360others(17): Show | 20 | HG00673.hp1 HG00738.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.2181+1102C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625241 | ||||||
| chr16:74625251
|
T | C | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2181+1092A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625251 | ||||||
| chr16:74625331
|
G | A | 1 | a0001c0008t0048g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2181+1012C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625331 | ||||||
| chr16:74625470
|
C | A | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2181+873G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625470 | ||||||
| chr16:74625514
|
G | GA | 255 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(252): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.2181+828dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625514 | ||||||
| chr16:74625545
|
T | C | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2181+798A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625545 | ||||||
| chr16:74625632
|
C | T | 1 | a0002c0001t0041g0290 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2181+711G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625632 | ||||||
| chr16:74625796
|
A | G | 2 | a0003c0003t0003g0020a0003c0003t0003g0021 | 2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2181+547T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625796 | ||||||
| chr16:74625894
|
A | T | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2181+449T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625894 | ||||||
| chr16:74625934
|
C | T | 6 | a0001c0004t0004g0114a0001c0004t0004g0131a0001c0004t0004g0132others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2181+409G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74625934 | ||||||
| chr16:74626042
|
C | T | 4 | a0002c0001t0001g0256a0002c0001t0001g0329a0002c0001t0001g0330others(1): Show | 4 | NA18964.hp1 NA18967.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181+301G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626042 | ||||||
| chr16:74626199
|
C | T | 1 | a0002c0001t0001g0292 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2181+144G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626199 | ||||||
| chr16:74626263
|
A | G | 4 | a0002c0001t0001g0268a0002c0001t0001g0277a0002c0001t0001g0293others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181+80T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626263 | ||||||
| chr16:74626276
|
G | A | 142 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0017others(139): Show | 152 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.2181+67C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626276 | ||||||
| chr16:74626287
|
C | T | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2181+56G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 12/12 | chr16 | 74626287 | ||||||
| chr16:74626707
|
A | G | 1 | a0002c0001t0041g0290 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1970-153T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626707 | ||||||
| chr16:74626818
|
T | A | 28 | a0001c0004t0004g0001a0001c0004t0004g0115a0001c0004t0004g0116others(25): Show | 33 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1970-264A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626818 | ||||||
| chr16:74626821
|
T | TGAGA | 385 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(382): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.1970-268_1970-267i others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626821 | ||||||
| chr16:74626831
|
C | T | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-277G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626831 | ||||||
| chr16:74626832
|
T | G | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-278A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626832 | ||||||
| chr16:74626833
|
G | C | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-279C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626833 | ||||||
| chr16:74626912
|
T | C | 1 | a0002c0001t0001g0299 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1970-358A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626912 | ||||||
| chr16:74626913
|
T | C | 1 | a0002c0001t0001g0299 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1970-359A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74626913 | ||||||
| chr16:74627095
|
C | A | 285 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(282): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1970-541G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627095 | ||||||
| chr16:74627224
|
T | A | 1 | a0001c0002t0002g0197 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1970-670A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627224 | ||||||
| chr16:74627261
|
T | C | 147 | a0001c0002t0002g0190a0002c0001t0001g0015a0002c0001t0001g0016others(144): Show | 157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1970-707A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627261 | ||||||
| chr16:74627357
|
C | T | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-803G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627357 | ||||||
| chr16:74627359
|
T | C | 1 | a0010c0012t0009g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1970-805A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627359 | ||||||
| chr16:74627521
|
G | A | 1 | a0003c0003t0003g0050 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1969+931C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627521 | ||||||
| chr16:74627575
|
C | A | 2 | a0003c0003t0003g0051a0003c0003t0003g0052 | 2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1969+877G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627575 | ||||||
| chr16:74627682
|
C | T | 385 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(382): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.1969+770G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627682 | ||||||
| chr16:74627702
|
G | A | 1 | a0001c0004t0021g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1969+750C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627702 | ||||||
| chr16:74627746
|
G | A | 1 | a0003c0003t0003g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1969+706C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627746 | ||||||
| chr16:74627840
|
C | A | 8 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(5): Show | 9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1969+612G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627840 | ||||||
| chr16:74627927
|
C | T | 1 | a0002c0001t0001g0328 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1969+525G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74627927 | ||||||
| chr16:74628014
|
G | C | 1 | a0002c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1969+438C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628014 | ||||||
| chr16:74628123
|
T | C | 1 | a0001c0002t0002g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1969+329A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628123 | ||||||
| chr16:74628149
|
A | G | 4 | a0001c0002t0011g0023a0001c0002t0011g0024a0001c0002t0011g0027others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1969+303T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628149 | ||||||
| chr16:74628208
|
G | A | 1 | a0002c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1969+244C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628208 | ||||||
| chr16:74628222
|
C | A | 1 | a0001c0004t0004g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1969+230G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628222 | ||||||
| chr16:74628340
|
G | A | 1 | a0002c0001t0040g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1969+112C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628340 | ||||||
| chr16:74628354
|
G | A | 1 | a0003c0003t0003g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1969+98C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 11/12 | chr16 | 74628354 | ||||||
| chr16:74628699
|
C | T | 143 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(140): Show | 152 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1755-33G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74628699 | ||||||
| chr16:74628816
|
C | A | 2 | a0003c0003t0003g0025a0003c0003t0003g0026 | 2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1755-150G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74628816 | ||||||
| chr16:74628955
|
A | G | 1 | a0002c0001t0001g0349 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1755-289T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74628955 | ||||||
| chr16:74628991
|
TAAGAA | T | 24 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(21): Show | 28 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1755-330_1755-326d others(7): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74628991 | ||||||
| chr16:74629058
|
C | T | 2 | a0002c0001t0001g0265a0002c0001t0001g0267 | 2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1755-392G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629058 | ||||||
| chr16:74629397
|
G | A | 1 | a0003c0003t0003g0074 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1755-731C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629397 | ||||||
| chr16:74629401
|
G | A | 3 | a0001c0002t0006g0361a0001c0002t0006g0362a0001c0002t0006g0366 | 3 | NA18954.hp1 NA19002.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1755-735C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629401 | ||||||
| chr16:74629422
|
G | C | 1 | a0002c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1755-756C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629422 | ||||||
| chr16:74629478
|
G | T | 3 | a0001c0002t0002g0203a0001c0002t0002g0204a0001c0002t0002g0214 | 3 | NA18959.hp1 NA18969.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1755-812C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629478 | ||||||
| chr16:74629665
|
C | CA | 6 | a0001c0002t0002g0218a0001c0002t0044g0335a0002c0001t0001g0247others(3): Show | 6 | HG02040.hp1 HG02040.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1755-1000dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629665 | ||||||
| chr16:74629665
|
CA | C | 24 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(21): Show | 28 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1755-1000delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629665 | ||||||
| chr16:74629768
|
G | C | 1 | a0002c0001t0012g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1754+1013C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629768 | ||||||
| chr16:74629965
|
C | G | 25 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(22): Show | 29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1754+816G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629965 | ||||||
| chr16:74629978
|
T | C | 8 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(5): Show | 9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1754+803A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74629978 | ||||||
| chr16:74630147
|
G | C | 1 | a0002c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1754+634C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630147 | ||||||
| chr16:74630271
|
T | C | 1 | a0001c0005t0007g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1754+510A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630271 | ||||||
| chr16:74630345
|
G | T | 28 | a0001c0002t0006g0358a0001c0002t0006g0359a0001c0002t0006g0360others(25): Show | 29 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1754+436C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630345 | ||||||
| chr16:74630362
|
T | G | 1 | a0001c0004t0004g0121 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1754+419A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630362 | ||||||
| chr16:74630463
|
G | C | 1 | a0013c0016t0037g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1754+318C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630463 | ||||||
| chr16:74630567
|
T | TACTTGTA others(23): Show |
1 | a0001c0002t0002g0197 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1754+184_1754+213d others(32): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630567 | ||||||
| chr16:74630716
|
G | A | 1 | a0003c0003t0003g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1754+65C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 10/12 | chr16 | 74630716 | ||||||
| chr16:74631064
|
C | G | 1 | a0001c0002t0044g0335 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1578-107G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631064 | ||||||
| chr16:74631071
|
T | A | 289 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(286): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1578-114A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631071 | ||||||
| chr16:74631133
|
A | G | 5 | a0002c0001t0001g0015a0002c0001t0001g0274a0002c0001t0001g0281others(2): Show | 6 | HG01884.hp1 HG02280.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578-176T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631133 | ||||||
| chr16:74631158
|
G | T | 1 | a0001c0002t0002g0197 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1578-201C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631158 | ||||||
| chr16:74631424
|
G | A | 1 | a0014c0018t0005g0037 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1578-467C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631424 | ||||||
| chr16:74631463
|
A | ACTCTCT | 23 | a0001c0002t0006g0360a0001c0002t0006g0361a0001c0002t0006g0362others(20): Show | 23 | HG00673.hp1 HG00738.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1578-512_1578-507d others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | ||||||
| chr16:74631463
|
A | ACTCTCTC others(1): Show |
225 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(222): Show | 237 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1578-514_1578-507d others(10): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | ||||||
| chr16:74631463
|
A | ACTCTCTC others(3): Show |
111 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(108): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1578-516_1578-507d others(12): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | ||||||
| chr16:74631463
|
A | ACTCTCTC others(5): Show |
15 | a0001c0004t0004g0117a0001c0004t0004g0121a0001c0004t0004g0122others(12): Show | 15 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1578-518_1578-507d others(14): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | ||||||
| chr16:74631463
|
A | ACTCTCTC others(7): Show |
8 | a0001c0005t0007g0008a0001c0005t0007g0089a0001c0005t0007g0090others(5): Show | 9 | HG01192.hp2 HG01257.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1578-520_1578-507d others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631463 | ||||||
| chr16:74631734
|
T | C | 8 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(5): Show | 9 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1578-777A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631734 | ||||||
| chr16:74631905
|
C | T | 1 | a0001c0004t0004g0127 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1577+618G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74631905 | ||||||
| chr16:74632004
|
G | A | 2 | a0001c0002t0002g0226a0001c0002t0033g0227 | 2 | NA18957.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1577+519C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632004 | ||||||
| chr16:74632044
|
A | G | 3 | a0002c0001t0001g0259a0002c0001t0001g0260a0002c0001t0001g0303 | 3 | NA18953.hp1 NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1577+479T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632044 | ||||||
| chr16:74632099
|
A | G | 1 | a0003c0003t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1577+424T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632099 | ||||||
| chr16:74632299
|
G | C | 1 | a0001c0002t0029g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1577+224C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632299 | ||||||
| chr16:74632426
|
C | A | 1 | a0001c0002t0006g0359 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1577+97G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632426 | ||||||
| chr16:74632456
|
C | T | 1 | a0002c0001t0001g0245 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1577+67G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632456 | ||||||
| chr16:74632474
|
A | C | 3 | a0002c0001t0001g0248a0002c0001t0001g0249a0002c0001t0001g0251 | 3 | NA18978.hp2 NA18982.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1577+49T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 9/12 | chr16 | 74632474 | ||||||
| chr16:74632736
|
G | C | 291 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(288): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1427-63C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74632736 | ||||||
| chr16:74632821
|
C | G | 1 | a0003c0003t0003g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1427-148G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74632821 | ||||||
| chr16:74633097
|
T | C | 1 | a0001c0004t0004g0125 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1427-424A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633097 | ||||||
| chr16:74633191
|
C | T | 1 | a0001c0002t0031g0206 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1427-518G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633191 | ||||||
| chr16:74633210
|
G | C | 9 | a0003c0003t0003g0028a0003c0003t0003g0049a0003c0003t0003g0054others(6): Show | 9 | NA18972.hp2 NA18981.hp2 NA18993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1427-537C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633210 | ||||||
| chr16:74633212
|
G | A | 3 | a0001c0002t0008g0150a0005c0009t0008g0148a0005c0009t0008g0149 | 3 | NA18946.hp2 NA19065.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1427-539C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633212 | ||||||
| chr16:74633217
|
T | C | 1 | a0001c0002t0002g0211 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1427-544A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633217 | ||||||
| chr16:74633271
|
C | G | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1427-598G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633271 | ||||||
| chr16:74633279
|
G | GA | 250 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(247): Show | 264 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1427-607dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633279 | ||||||
| chr16:74633334
|
A | G | 1 | a0002c0001t0050g0378 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1427-661T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633334 | ||||||
| chr16:74633439
|
G | A | 1 | a0001c0005t0007g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1427-766C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633439 | ||||||
| chr16:74633487
|
G | A | 3 | a0002c0001t0001g0016a0002c0001t0001g0301a0002c0001t0001g0319 | 4 | NA18960.hp2 NA18971.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1427-814C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633487 | ||||||
| chr16:74633536
|
G | A | 1 | a0001c0002t0031g0206 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1427-863C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633536 | ||||||
| chr16:74633565
|
G | A | 1 | a0001c0002t0015g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1427-892C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633565 | ||||||
| chr16:74633881
|
C | T | 83 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(80): Show | 87 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.1427-1208G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633881 | ||||||
| chr16:74633928
|
C | T | 9 | a0001c0002t0002g0172a0001c0002t0002g0177a0001c0002t0002g0207others(6): Show | 9 | HG00642.hp1 HG02135.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1427-1255G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633928 | ||||||
| chr16:74633929
|
G | A | 13 | a0003c0003t0003g0022a0003c0003t0003g0046a0003c0003t0003g0047others(10): Show | 13 | HG00597.hp2 HG00621.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1427-1256C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633929 | ||||||
| chr16:74633966
|
C | T | 289 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(286): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1427-1293G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633966 | ||||||
| chr16:74633984
|
C | CA | 11 | a0001c0002t0002g0172a0001c0002t0002g0207a0001c0002t0002g0208others(8): Show | 11 | HG00642.hp1 HG02155.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1427-1312dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74633984 | ||||||
| chr16:74634033
|
G | T | 3 | a0002c0001t0001g0369a0002c0001t0001g0370a0002c0001t0001g0371 | 3 | NA18946.hp1 NA18947.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1427-1360C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634033 | ||||||
| chr16:74634051
|
A | G | 1 | a0001c0002t0011g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1427-1378T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634051 | ||||||
| chr16:74634080
|
G | A | 1 | a0001c0002t0002g0209 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1427-1407C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634080 | ||||||
| chr16:74634221
|
A | C | 1 | a0002c0001t0001g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1427-1548T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634221 | ||||||
| chr16:74634376
|
C | A | 5 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130others(2): Show | 5 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1427-1703G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634376 | ||||||
| chr16:74634378
|
T | TTATA | 4 | a0003c0003t0003g0072a0003c0003t0003g0087a0003c0003t0003g0096others(1): Show | 4 | HG02818.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1427-1709_1427-170 others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634378 | ||||||
| chr16:74634378
|
TTA | T | 220 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(217): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1427-1707_1427-170 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634378 | ||||||
| chr16:74634548
|
C | T | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1426+1798G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634548 | ||||||
| chr16:74634575
|
G | A | 255 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(252): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1426+1771C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634575 | ||||||
| chr16:74634635
|
C | T | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1426+1711G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634635 | ||||||
| chr16:74634644
|
C | T | 249 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(246): Show | 263 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(260): Show |
intron_variant | MODIFIER | c.1426+1702G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634644 | ||||||
| chr16:74634667
|
T | G | 319 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(316): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1426+1679A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634667 | ||||||
| chr16:74634815
|
A | AG | 3 | a0001c0004t0004g0116a0001c0004t0004g0135a0001c0004t0021g0123 | 3 | HG01496.hp2 HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1426+1530_1426+153 others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634815 | ||||||
| chr16:74634816
|
A | G | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1426+1530T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634816 | ||||||
| chr16:74634823
|
A | G | 322 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(319): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1426+1523T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634823 | ||||||
| chr16:74634962
|
T | C | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1426+1384A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74634962 | ||||||
| chr16:74635003
|
G | A | 1 | a0002c0001t0001g0328 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1426+1343C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635003 | ||||||
| chr16:74635004
|
G | C | 255 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(252): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1426+1342C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635004 | ||||||
| chr16:74635055
|
C | T | 22 | a0003c0003t0003g0020a0003c0003t0003g0021a0003c0003t0005g0005others(19): Show | 24 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1426+1291G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635055 | ||||||
| chr16:74635136
|
T | C | 256 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(253): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1426+1210A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635136 | ||||||
| chr16:74635169
|
A | T | 3 | a0002c0001t0001g0016a0002c0001t0001g0301a0002c0001t0001g0319 | 4 | NA18960.hp2 NA18971.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1426+1177T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635169 | ||||||
| chr16:74635253
|
G | A | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1426+1093C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635253 | ||||||
| chr16:74635331
|
G | A | 1 | a0001c0002t0011g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1426+1015C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635331 | ||||||
| chr16:74635343
|
C | T | 296 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(293): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1426+1003G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635343 | ||||||
| chr16:74635443
|
C | T | 1 | a0003c0003t0003g0022 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1426+903G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635443 | ||||||
| chr16:74635466
|
C | T | 1 | a0003c0003t0003g0077 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1426+880G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635466 | ||||||
| chr16:74635471
|
GA | G | 253 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(250): Show | 267 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.1426+874delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635471 | ||||||
| chr16:74635481
|
A | T | 1 | a0001c0004t0023g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1426+865T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635481 | ||||||
| chr16:74635562
|
CGGACTGG others(3): Show |
C | 1 | a0002c0001t0002g0174 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1426+774_1426+783d others(12): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635562 | ||||||
| chr16:74635568
|
G | A | 1 | a0003c0003t0003g0079 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1426+778C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635568 | ||||||
| chr16:74635929
|
C | A | 3 | a0002c0001t0001g0369a0002c0001t0001g0370a0002c0001t0001g0371 | 3 | NA18946.hp1 NA18947.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1426+417G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74635929 | ||||||
| chr16:74636034
|
C | G | 1 | a0001c0002t0002g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1426+312G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74636034 | ||||||
| chr16:74636094
|
C | T | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1426+252G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74636094 | ||||||
| chr16:74636149
|
T | C | 2 | a0002c0001t0001g0243a0002c0001t0001g0244 | 2 | NA18972.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1426+197A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74636149 | ||||||
| chr16:74636285
|
AAGGAAAT others(4): Show |
A | 1 | a0001c0002t0046g0377 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1426+50_1426+60del others(11): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 8/12 | chr16 | 74636285 | ||||||
| chr16:74636677
|
T | C | 2 | a0001c0004t0004g0116a0001c0004t0004g0118 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1195-100A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636677 | ||||||
| chr16:74636707
|
C | T | 1 | a0001c0002t0049g0352 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1195-130G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636707 | ||||||
| chr16:74636714
|
G | C | 1 | a0001c0004t0004g0121 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1195-137C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636714 | ||||||
| chr16:74636779
|
T | C | 6 | a0002c0001t0001g0273a0002c0001t0001g0347a0002c0001t0001g0348others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195-202A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636779 | ||||||
| chr16:74636923
|
G | A | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1195-346C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74636923 | ||||||
| chr16:74637004
|
C | T | 1 | a0003c0003t0005g0042 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1195-427G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637004 | ||||||
| chr16:74637122
|
T | TA | 51 | a0001c0002t0001g0375a0001c0002t0002g0200a0001c0002t0002g0212others(48): Show | 56 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1195-546dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | ||||||
| chr16:74637122
|
T | TAA | 149 | a0001c0002t0002g0203a0001c0002t0002g0204a0001c0002t0002g0213others(146): Show | 158 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1195-547_1195-546d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | ||||||
| chr16:74637122
|
T | TAAA | 19 | a0001c0002t0006g0363a0001c0002t0006g0366a0001c0002t0011g0027others(16): Show | 20 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1195-548_1195-546d others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | ||||||
| chr16:74637122
|
T | TAAAAAAA others(6): Show |
1 | a0001c0005t0007g0108 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1195-558_1195-546d others(15): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | ||||||
| chr16:74637122
|
T | TAAAAAAA others(7): Show |
2 | a0001c0005t0007g0008a0001c0005t0007g0089 | 3 | HG03017.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1195-559_1195-546d others(16): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | ||||||
| chr16:74637122
|
T | TAAAAAAA others(8): Show |
4 | a0001c0005t0007g0045a0001c0005t0007g0090a0001c0005t0007g0109others(1): Show | 4 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-560_1195-546d others(17): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | ||||||
| chr16:74637122
|
TA | T | 15 | a0001c0002t0002g0205a0001c0002t0002g0232a0001c0002t0002g0236others(12): Show | 15 | HG01081.hp2 HG01256.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.1195-546delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637122 | ||||||
| chr16:74637146
|
C | A | 6 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0090others(3): Show | 7 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195-569G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637146 | ||||||
| chr16:74637201
|
G | T | 1 | a0001c0004t0004g0129 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1195-624C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637201 | ||||||
| chr16:74637423
|
T | C | 1 | a0003c0003t0005g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1194+433A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637423 | ||||||
| chr16:74637443
|
A | G | 1 | a0002c0001t0010g0266 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1194+413T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637443 | ||||||
| chr16:74637501
|
C | T | 15 | a0001c0002t0006g0358a0001c0002t0006g0359a0001c0002t0006g0360others(12): Show | 15 | HG00673.hp1 HG00738.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.1194+355G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637501 | ||||||
| chr16:74637750
|
A | C | 1 | a0001c0004t0023g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1194+106T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 7/12 | chr16 | 74637750 | ||||||
| chr16:74637976
|
G | A | 1 | a0003c0003t0003g0098 | 1 | NA18948.hp1 | splice_region_variant&intron_variant | LOW | c.1080-6C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74637976 | ||||||
| chr16:74638013
|
A | G | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080-43T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638013 | ||||||
| chr16:74638022
|
T | A | 3 | a0001c0002t0013g0152a0001c0002t0013g0153a0001c0002t0013g0166 | 3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1080-52A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638022 | ||||||
| chr16:74638033
|
G | A | 5 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130others(2): Show | 5 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080-63C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638033 | ||||||
| chr16:74638125
|
G | A | 3 | a0002c0001t0001g0255a0002c0001t0001g0308a0002c0001t0001g0311 | 3 | HG01070.hp1 HG01071.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1080-155C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638125 | ||||||
| chr16:74638170
|
C | G | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1080-200G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638170 | ||||||
| chr16:74638218
|
A | T | 3 | a0001c0002t0002g0207a0001c0002t0002g0208a0001c0002t0002g0209 | 3 | NA18943.hp2 NA18945.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1080-248T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638218 | ||||||
| chr16:74638243
|
C | T | 4 | a0002c0001t0001g0334a0002c0001t0001g0344a0002c0001t0001g0345others(1): Show | 4 | NA18943.hp1 NA18950.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-273G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638243 | ||||||
| chr16:74638244
|
G | C | 1 | a0001c0002t0002g0172 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1080-274C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638244 | ||||||
| chr16:74638303
|
G | A | 297 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(294): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1080-333C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638303 | ||||||
| chr16:74638329
|
G | A | 1 | a0001c0002t0049g0352 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1080-359C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638329 | ||||||
| chr16:74638343
|
A | G | 4 | a0001c0002t0011g0023a0001c0002t0011g0024a0001c0002t0011g0027others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-373T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638343 | ||||||
| chr16:74638346
|
TA | T | 3 | a0001c0002t0013g0152a0001c0002t0013g0153a0001c0002t0013g0166 | 3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1080-377delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638346 | ||||||
| chr16:74638450
|
T | C | 1 | a0001c0002t0002g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1080-480A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638450 | ||||||
| chr16:74638453
|
C | T | 1 | a0002c0001t0001g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1080-483G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638453 | ||||||
| chr16:74638592
|
T | C | 2 | a0006c0007t0002g0169a0006c0007t0002g0170 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1080-622A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638592 | ||||||
| chr16:74638593
|
TGGAAAAG others(4): Show |
T | 1 | a0003c0003t0003g0094 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1080-634_1080-624d others(13): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638593 | ||||||
| chr16:74638605
|
A | T | 1 | a0003c0003t0003g0094 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1080-635T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638605 | ||||||
| chr16:74638606
|
G | T | 1 | a0003c0003t0003g0094 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1080-636C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638606 | ||||||
| chr16:74638607
|
C | T | 1 | a0003c0003t0003g0094 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1080-637G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638607 | ||||||
| chr16:74638663
|
T | A | 3 | a0001c0002t0013g0152a0001c0002t0013g0153a0001c0002t0013g0166 | 3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1080-693A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638663 | ||||||
| chr16:74638997
|
T | C | 1 | a0002c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1080-1027A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74638997 | ||||||
| chr16:74639002
|
C | A | 256 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(253): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1080-1032G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639002 | ||||||
| chr16:74639003
|
T | A | 256 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(253): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1080-1033A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639003 | ||||||
| chr16:74639036
|
C | CT | 8 | a0001c0004t0009g0186a0003c0003t0003g0025a0003c0003t0003g0050others(5): Show | 8 | HG00741.hp1 HG01243.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080-1067dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639036 | ||||||
| chr16:74639036
|
CT | C | 7 | a0001c0002t0002g0189a0001c0002t0002g0240a0001c0002t0002g0241others(4): Show | 7 | HG00408.hp2 NA18747.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080-1067delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639036 | ||||||
| chr16:74639036
|
CTT | C | 96 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(93): Show | 100 | HG00642.hp1 HG00673.hp2 HG01099.hp1 others(97): Show |
intron_variant | MODIFIER | c.1080-1068_1080-106 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639036 | ||||||
| chr16:74639036
|
CTTT | C | 154 | a0001c0002t0002g0204a0001c0002t0006g0359a0001c0002t0006g0360others(151): Show | 164 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1080-1069_1080-106 others(7): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639036 | ||||||
| chr16:74639041
|
T | C | 2 | a0002c0001t0001g0310a0002c0001t0001g0312 | 2 | HG00558.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1080-1071A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639041 | ||||||
| chr16:74639063
|
G | A | 1 | a0002c0001t0001g0372 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1080-1093C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639063 | ||||||
| chr16:74639127
|
C | G | 3 | a0001c0002t0013g0152a0001c0002t0013g0153a0001c0002t0013g0166 | 3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1080-1157G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639127 | ||||||
| chr16:74639161
|
C | T | 10 | a0001c0002t0001g0374a0001c0002t0001g0375a0001c0002t0001g0376others(7): Show | 10 | NA18946.hp2 NA18952.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1080-1191G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639161 | ||||||
| chr16:74639282
|
C | G | 4 | a0001c0002t0011g0023a0001c0002t0011g0024a0001c0002t0011g0027others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080-1312G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639282 | ||||||
| chr16:74639634
|
A | C | 1 | a0002c0001t0001g0336 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1080-1664T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639634 | ||||||
| chr16:74639662
|
G | A | 1 | a0001c0008t0048g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1080-1692C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639662 | ||||||
| chr16:74639724
|
T | C | 1 | a0001c0002t0002g0188 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1080-1754A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639724 | ||||||
| chr16:74639908
|
T | C | 2 | a0002c0001t0018g0382a0002c0001t0018g0383 | 2 | HG01109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1080-1938A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639908 | ||||||
| chr16:74639963
|
T | C | 2 | a0001c0002t0002g0191a0001c0002t0034g0173 | 2 | HG01168.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1080-1993A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639963 | ||||||
| chr16:74639982
|
A | AT | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080-2013dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74639982 | ||||||
| chr16:74640002
|
G | A | 1 | a0003c0003t0003g0064 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1080-2032C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640002 | ||||||
| chr16:74640109
|
G | C | 33 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0116others(30): Show | 38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1080-2139C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640109 | ||||||
| chr16:74640110
|
G | A | 54 | a0002c0001t0001g0016a0002c0001t0001g0017a0002c0001t0001g0018others(51): Show | 62 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1080-2140C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640110 | ||||||
| chr16:74640145
|
AT | A | 282 | a0001c0002t0001g0373a0001c0002t0001g0375a0001c0002t0001g0376others(279): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1080-2176delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640145 | ||||||
| chr16:74640145
|
ATT | A | 7 | a0001c0002t0001g0374a0001c0002t0002g0242a0001c0002t0006g0368others(4): Show | 7 | HG01168.hp1 HG01256.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1080-2177_1080-217 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640145 | ||||||
| chr16:74640229
|
G | A | 1 | a0006c0007t0002g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1080-2259C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640229 | ||||||
| chr16:74640336
|
C | G | 288 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(285): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1080-2366G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640336 | ||||||
| chr16:74640344
|
T | C | 1 | a0001c0002t0011g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1080-2374A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640344 | ||||||
| chr16:74640373
|
C | T | 295 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(292): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1080-2403G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640373 | ||||||
| chr16:74640644
|
A | T | 1 | a0002c0001t0001g0336 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1080-2674T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640644 | ||||||
| chr16:74640665
|
C | T | 1 | a0002c0001t0054g0384 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1080-2695G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640665 | ||||||
| chr16:74640677
|
T | A | 3 | a0003c0003t0003g0055a0003c0003t0003g0069a0003c0003t0003g0085 | 3 | NA18977.hp1 NA19001.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1080-2707A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640677 | ||||||
| chr16:74640774
|
C | A | 1 | a0001c0002t0011g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1080-2804G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640774 | ||||||
| chr16:74640822
|
T | C | 318 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(315): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1080-2852A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640822 | ||||||
| chr16:74640955
|
A | G | 375 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(372): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.1080-2985T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640955 | ||||||
| chr16:74640985
|
C | CT | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080-3016dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74640985 | ||||||
| chr16:74641028
|
G | C | 1 | a0002c0001t0054g0384 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1080-3058C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641028 | ||||||
| chr16:74641212
|
G | C | 3 | a0002c0001t0018g0382a0002c0001t0018g0383a0002c0001t0054g0384 | 3 | HG01109.hp1 HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1079+3150C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641212 | ||||||
| chr16:74641221
|
G | A | 3 | a0001c0004t0004g0127a0001c0004t0004g0128a0001c0004t0004g0129 | 3 | HG00099.hp2 HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1079+3141C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641221 | ||||||
| chr16:74641259
|
T | A | 1 | a0004c0006t0001g0286 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1079+3103A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641259 | ||||||
| chr16:74641288
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1079+3074C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641288 | ||||||
| chr16:74641295
|
T | G | 1 | a0002c0001t0001g0336 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1079+3067A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641295 | ||||||
| chr16:74641306
|
G | A | 1 | a0002c0001t0054g0384 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1079+3056C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641306 | ||||||
| chr16:74641351
|
T | A | 1 | a0001c0004t0009g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1079+3011A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641351 | ||||||
| chr16:74641385
|
A | C | 255 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(252): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1079+2977T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641385 | ||||||
| chr16:74641469
|
GATTA | G | 255 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(252): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1079+2889_1079+289 others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641469 | ||||||
| chr16:74641655
|
T | C | 1 | a0002c0001t0008g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1079+2707A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641655 | ||||||
| chr16:74641706
|
C | T | 33 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0116others(30): Show | 38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1079+2656G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641706 | ||||||
| chr16:74641769
|
A | C | 1 | a0001c0002t0002g0234 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1079+2593T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641769 | ||||||
| chr16:74641810
|
C | T | 27 | a0001c0004t0004g0001a0001c0004t0004g0116a0001c0004t0004g0117others(24): Show | 32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1079+2552G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641810 | ||||||
| chr16:74641928
|
C | CA | 40 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(37): Show | 42 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.1079+2433dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | ||||||
| chr16:74641928
|
CA | C | 80 | a0001c0002t0002g0171a0001c0002t0002g0181a0001c0002t0002g0188others(77): Show | 84 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1079+2433delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | ||||||
| chr16:74641928
|
CAA | C | 148 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0376others(145): Show | 158 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1079+2432_1079+243 others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | ||||||
| chr16:74641928
|
CAAA | C | 30 | a0001c0002t0002g0197a0001c0002t0002g0198a0001c0002t0006g0358others(27): Show | 30 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1079+2431_1079+243 others(7): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | ||||||
| chr16:74641928
|
CAAAA | C | 26 | a0001c0002t0014g0356a0001c0002t0014g0357a0001c0004t0004g0001others(23): Show | 31 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.1079+2430_1079+243 others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74641928 | ||||||
| chr16:74642017
|
A | T | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1079+2345T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642017 | ||||||
| chr16:74642135
|
A | T | 288 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(285): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1079+2227T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642135 | ||||||
| chr16:74642143
|
C | G | 295 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(292): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1079+2219G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642143 | ||||||
| chr16:74642160
|
T | C | 1 | a0003c0003t0003g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1079+2202A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642160 | ||||||
| chr16:74642209
|
G | A | 1 | a0001c0002t0001g0373 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1079+2153C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642209 | ||||||
| chr16:74642272
|
A | G | 1 | a0001c0005t0007g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1079+2090T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642272 | ||||||
| chr16:74642283
|
C | T | 1 | a0008c0013t0047g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1079+2079G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642283 | ||||||
| chr16:74642361
|
C | T | 1 | a0003c0003t0003g0022 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1079+2001G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642361 | ||||||
| chr16:74642398
|
T | G | 2 | a0003c0003t0005g0039a0003c0003t0005g0040 | 2 | HG00280.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1079+1964A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642398 | ||||||
| chr16:74642502
|
T | C | 1 | a0001c0002t0002g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1079+1860A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642502 | ||||||
| chr16:74642525
|
G | A | 1 | a0001c0002t0011g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1079+1837C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642525 | ||||||
| chr16:74642652
|
C | T | 295 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(292): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1079+1710G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642652 | ||||||
| chr16:74642672
|
T | C | 1 | a0001c0002t0002g0210 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1079+1690A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642672 | ||||||
| chr16:74642705
|
C | T | 1 | a0001c0004t0052g0379 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1079+1657G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642705 | ||||||
| chr16:74642740
|
G | C | 4 | a0002c0001t0002g0003a0002c0001t0002g0009a0002c0001t0002g0010others(1): Show | 9 | NA18941.hp2 NA18985.hp1 NA19004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1079+1622C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642740 | ||||||
| chr16:74642788
|
C | T | 1 | a0001c0002t0002g0175 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1079+1574G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642788 | ||||||
| chr16:74642970
|
A | T | 1 | a0001c0002t0013g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1079+1392T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74642970 | ||||||
| chr16:74643066
|
T | C | 150 | a0001c0002t0002g0203a0001c0002t0002g0204a0001c0002t0002g0213others(147): Show | 160 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1079+1296A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643066 | ||||||
| chr16:74643112
|
C | G | 3 | a0001c0002t0002g0178a0001c0002t0002g0179a0001c0002t0002g0180 | 3 | HG01099.hp1 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1079+1250G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643112 | ||||||
| chr16:74643249
|
G | A | 1 | a0001c0002t0001g0376 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1079+1113C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643249 | ||||||
| chr16:74643414
|
T | C | 6 | a0001c0004t0004g0114a0001c0004t0004g0131a0001c0004t0004g0132others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079+948A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643414 | ||||||
| chr16:74643669
|
G | GC | 221 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0376others(218): Show | 233 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1079+692_1079+693i others(3): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | ||||||
| chr16:74643669
|
G | GCT | 43 | a0001c0002t0001g0375a0001c0002t0002g0014a0001c0002t0002g0178others(40): Show | 45 | HG00597.hp1 HG01070.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.1079+692_1079+693i others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | ||||||
| chr16:74643669
|
G | GCTT | 3 | a0001c0002t0002g0226a0002c0001t0001g0344a0002c0001t0001g0346 | 3 | NA18950.hp2 NA18981.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1079+692_1079+693i others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | ||||||
| chr16:74643669
|
GT | G | 20 | a0001c0004t0004g0114a0001c0004t0004g0131a0001c0004t0023g0130others(17): Show | 21 | HG00140.hp1 HG00280.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1079+692delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | ||||||
| chr16:74643669
|
GTTTTTTT others(6): Show |
G | 27 | a0001c0004t0004g0001a0001c0004t0004g0116a0001c0004t0004g0117others(24): Show | 32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1079+680_1079+692d others(15): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643669 | ||||||
| chr16:74643670
|
T | C | 70 | a0001c0002t0002g0204a0001c0002t0006g0367a0001c0004t0004g0115others(67): Show | 76 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1079+692A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643670 | ||||||
| chr16:74643671
|
T | C | 20 | a0001c0004t0004g0114a0001c0004t0004g0131a0001c0004t0023g0130others(17): Show | 21 | HG00140.hp1 HG00280.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1079+691A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643671 | ||||||
| chr16:74643672
|
T | C | 1 | a0001c0004t0004g0132 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1079+690A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643672 | ||||||
| chr16:74643683
|
T | C | 27 | a0001c0004t0004g0001a0001c0004t0004g0116a0001c0004t0004g0117others(24): Show | 32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1079+679A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643683 | ||||||
| chr16:74643699
|
G | A | 254 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(251): Show | 268 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.1079+663C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643699 | ||||||
| chr16:74643822
|
T | C | 2 | a0001c0002t0002g0183a0001c0002t0002g0224 | 2 | HG03927.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1079+540A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643822 | ||||||
| chr16:74643837
|
G | A | 1 | a0001c0002t0002g0212 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1079+525C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643837 | ||||||
| chr16:74643852
|
AT | A | 6 | a0001c0002t0002g0212a0001c0002t0036g0231a0001c0002t0056g0386others(3): Show | 6 | HG04199.hp2 NA18948.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1079+509delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643852 | ||||||
| chr16:74643878
|
C | T | 1 | a0002c0001t0001g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1079+484G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643878 | ||||||
| chr16:74643898
|
T | C | 9 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(6): Show | 10 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1079+464A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643898 | ||||||
| chr16:74643912
|
T | C | 1 | a0002c0001t0001g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1079+450A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643912 | ||||||
| chr16:74643965
|
C | T | 1 | a0001c0002t0011g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1079+397G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643965 | ||||||
| chr16:74643987
|
T | C | 1 | a0003c0003t0003g0061 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1079+375A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74643987 | ||||||
| chr16:74644165
|
C | T | 27 | a0001c0004t0004g0001a0001c0004t0004g0116a0001c0004t0004g0117others(24): Show | 32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1079+197G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74644165 | ||||||
| chr16:74644260
|
T | A | 20 | a0001c0002t0006g0358a0001c0002t0006g0359a0001c0002t0006g0360others(17): Show | 20 | HG00673.hp1 HG00738.hp1 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.1079+102A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 6/12 | chr16 | 74644260 | ||||||
| chr16:74644823
|
CA | C | 89 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(86): Show | 93 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.793-89delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74644823 | ||||||
| chr16:74645184
|
G | A | 1 | a0002c0001t0054g0384 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.793-449C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645184 | ||||||
| chr16:74645248
|
A | G | 1 | a0001c0004t0004g0120 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.793-513T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645248 | ||||||
| chr16:74645346
|
C | A | 115 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(112): Show | 119 | HG00408.hp2 HG00642.hp1 HG00673.hp1 others(116): Show |
intron_variant | MODIFIER | c.793-611G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645346 | ||||||
| chr16:74645364
|
A | T | 3 | a0001c0004t0009g0184a0001c0004t0009g0187a0010c0012t0009g0221 | 3 | NA18945.hp1 NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.793-629T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645364 | ||||||
| chr16:74645418
|
C | T | 20 | a0003c0003t0005g0005a0003c0003t0005g0006a0003c0003t0005g0029others(17): Show | 22 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.793-683G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645418 | ||||||
| chr16:74645501
|
T | G | 1 | a0003c0003t0003g0094 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.793-766A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645501 | ||||||
| chr16:74645554
|
T | C | 1 | a0001c0002t0016g0217 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.793-819A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645554 | ||||||
| chr16:74645644
|
C | T | 1 | a0004c0006t0019g0019 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.793-909G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645644 | ||||||
| chr16:74645726
|
T | G | 15 | a0001c0002t0006g0358a0001c0002t0006g0359a0001c0002t0006g0360others(12): Show | 15 | HG00673.hp1 HG00738.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.793-991A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645726 | ||||||
| chr16:74645745
|
C | CT | 33 | a0001c0004t0004g0001a0001c0004t0004g0115a0001c0004t0004g0116others(30): Show | 38 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.793-1011dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645745 | ||||||
| chr16:74645745
|
C | CTT | 10 | a0001c0004t0004g0118a0001c0004t0004g0119a0001c0004t0004g0131others(7): Show | 10 | HG01358.hp1 HG01978.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-1012_793-1011d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645745 | ||||||
| chr16:74645745
|
CT | C | 231 | a0001c0002t0001g0373a0001c0002t0001g0376a0001c0002t0002g0004others(228): Show | 246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.793-1011delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645745 | ||||||
| chr16:74645745
|
CTT | C | 9 | a0001c0002t0001g0374a0001c0002t0002g0191a0001c0002t0002g0236others(6): Show | 9 | HG00323.hp2 HG01168.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-1012_793-1011d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645745 | ||||||
| chr16:74645746
|
T | C | 1 | a0003c0003t0003g0095 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.793-1011A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645746 | ||||||
| chr16:74645751
|
T | C | 1 | a0008c0013t0047g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793-1016A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645751 | ||||||
| chr16:74645754
|
T | C | 1 | a0002c0001t0001g0304 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.793-1019A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645754 | ||||||
| chr16:74645789
|
G | A | 1 | a0001c0002t0006g0368 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.793-1054C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645789 | ||||||
| chr16:74645813
|
C | G | 2 | a0003c0003t0003g0075a0003c0003t0003g0076 | 2 | HG01255.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.793-1078G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645813 | ||||||
| chr16:74645815
|
G | C | 324 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(321): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.793-1080C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645815 | ||||||
| chr16:74645837
|
C | T | 1 | a0002c0001t0001g0270 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.793-1102G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645837 | ||||||
| chr16:74645913
|
C | T | 1 | a0001c0002t0002g0179 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.793-1178G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645913 | ||||||
| chr16:74645939
|
G | A | 2 | a0003c0003t0003g0049a0003c0003t0003g0073 | 2 | NA18966.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.793-1204C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645939 | ||||||
| chr16:74645985
|
C | T | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.793-1250G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645985 | ||||||
| chr16:74645987
|
A | C | 1 | a0002c0001t0001g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.793-1252T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74645987 | ||||||
| chr16:74646069
|
T | C | 1 | a0001c0002t0002g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.793-1334A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646069 | ||||||
| chr16:74646081
|
A | T | 1 | a0001c0002t0030g0192 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.793-1346T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646081 | ||||||
| chr16:74646162
|
C | A | 1 | a0001c0004t0004g0115 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.793-1427G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646162 | ||||||
| chr16:74646176
|
A | G | 67 | a0002c0001t0001g0016a0002c0001t0001g0017a0002c0001t0001g0018others(64): Show | 75 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.793-1441T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646176 | ||||||
| chr16:74646180
|
G | A | 1 | a0001c0002t0002g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.793-1445C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646180 | ||||||
| chr16:74646207
|
C | T | 290 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.793-1472G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646207 | ||||||
| chr16:74646354
|
G | A | 1 | a0003c0003t0003g0074 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.793-1619C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646354 | ||||||
| chr16:74646388
|
T | C | 1 | a0002c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.793-1653A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646388 | ||||||
| chr16:74646408
|
G | C | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-1673C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646408 | ||||||
| chr16:74646454
|
G | A | 3 | a0001c0002t0002g0014a0001c0002t0002g0241a0001c0002t0002g0242 | 4 | NA18949.hp1 NA18968.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1719C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646454 | ||||||
| chr16:74646569
|
T | C | 1 | a0003c0003t0005g0039 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.793-1834A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646569 | ||||||
| chr16:74646602
|
A | C | 3 | a0001c0002t0002g0178a0001c0002t0002g0179a0001c0002t0002g0180 | 3 | HG01099.hp1 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.793-1867T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646602 | ||||||
| chr16:74646614
|
C | T | 1 | a0001c0002t0011g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.793-1879G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646614 | ||||||
| chr16:74646615
|
G | A | 2 | a0001c0002t0015g0138a0001c0008t0048g0351 | 2 | HG00673.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.793-1880C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646615 | ||||||
| chr16:74646659
|
G | A | 1 | a0001c0002t0011g0133 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.793-1924C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646659 | ||||||
| chr16:74646774
|
T | C | 1 | a0002c0001t0001g0255 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.793-2039A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646774 | ||||||
| chr16:74646794
|
C | G | 88 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(85): Show | 92 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.793-2059G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646794 | ||||||
| chr16:74646847
|
C | T | 1 | a0001c0002t0008g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.793-2112G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646847 | ||||||
| chr16:74646903
|
TCAA | T | 32 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(29): Show | 37 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.793-2171_793-2169d others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646903 | ||||||
| chr16:74646903
|
TCAACAA | T | 3 | a0003c0003t0003g0075a0003c0003t0003g0076a0003c0003t0003g0107 | 3 | HG01255.hp2 HG02258.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.793-2174_793-2169d others(8): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646903 | ||||||
| chr16:74646903
|
TCAACAAC others(5): Show |
T | 257 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(254): Show | 271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.793-2180_793-2169d others(14): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646903 | ||||||
| chr16:74646903
|
TCAACAAC others(8): Show |
T | 1 | a0002c0001t0001g0307 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.793-2183_793-2169d others(17): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646903 | ||||||
| chr16:74646994
|
G | C | 3 | a0001c0002t0014g0257a0001c0002t0014g0356a0001c0002t0014g0357 | 3 | HG02886.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.792+2138C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74646994 | ||||||
| chr16:74647085
|
C | CA | 10 | a0001c0002t0002g0209a0001c0002t0013g0166a0001c0002t0014g0257others(7): Show | 11 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.792+2046dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647085 | ||||||
| chr16:74647100
|
A | C | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+2032T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647100 | ||||||
| chr16:74647232
|
G | A | 1 | a0001c0002t0044g0335 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.792+1900C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647232 | ||||||
| chr16:74647554
|
C | G | 2 | a0003c0003t0003g0064a0003c0003t0003g0093 | 2 | NA18969.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.792+1578G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647554 | ||||||
| chr16:74647580
|
G | A | 1 | a0001c0002t0002g0190 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.792+1552C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647580 | ||||||
| chr16:74647583
|
C | T | 3 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130 | 3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.792+1549G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647583 | ||||||
| chr16:74647584
|
GGCC | G | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+1545_792+1547d others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647584 | ||||||
| chr16:74647609
|
T | C | 4 | a0001c0002t0002g0205a0001c0002t0002g0220a0001c0002t0015g0139others(1): Show | 4 | HG00642.hp1 HG01261.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+1523A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647609 | ||||||
| chr16:74647652
|
C | T | 2 | a0003c0003t0003g0075a0003c0003t0003g0076 | 2 | HG01255.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.792+1480G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647652 | ||||||
| chr16:74647683
|
C | T | 1 | a0001c0002t0002g0222 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.792+1449G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647683 | ||||||
| chr16:74647734
|
T | G | 257 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(254): Show | 271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.792+1398A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647734 | ||||||
| chr16:74647737
|
G | A | 1 | a0002c0001t0001g0317 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.792+1395C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647737 | ||||||
| chr16:74647756
|
TA | T | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+1375delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647756 | ||||||
| chr16:74647779
|
A | G | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.792+1353T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647779 | ||||||
| chr16:74647788
|
C | T | 1 | a0002c0001t0002g0174 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.792+1344G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647788 | ||||||
| chr16:74647793
|
T | C | 1 | a0002c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.792+1339A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647793 | ||||||
| chr16:74647822
|
C | A | 1 | a0001c0002t0006g0363 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.792+1310G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647822 | ||||||
| chr16:74647945
|
T | C | 1 | a0001c0008t0048g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.792+1187A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74647945 | ||||||
| chr16:74648046
|
A | C | 6 | a0001c0004t0004g0114a0001c0004t0004g0131a0001c0004t0004g0132others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1086T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648046 | ||||||
| chr16:74648071
|
A | G | 6 | a0001c0004t0004g0114a0001c0004t0004g0131a0001c0004t0004g0132others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1061T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648071 | ||||||
| chr16:74648528
|
T | C | 3 | a0002c0001t0001g0268a0002c0001t0001g0282a0002c0001t0050g0378 | 3 | HG01358.hp2 HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.792+604A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648528 | ||||||
| chr16:74648539
|
G | A | 1 | a0001c0002t0002g0232 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.792+593C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648539 | ||||||
| chr16:74648546
|
G | A | 1 | a0003c0003t0005g0040 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.792+586C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648546 | ||||||
| chr16:74648598
|
C | T | 256 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(253): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.792+534G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648598 | ||||||
| chr16:74648645
|
G | C | 1 | a0001c0004t0004g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.792+487C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648645 | ||||||
| chr16:74648711
|
A | G | 297 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(294): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.792+421T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648711 | ||||||
| chr16:74648784
|
G | A | 1 | a0001c0002t0001g0375 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.792+348C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648784 | ||||||
| chr16:74648792
|
A | G | 1 | a0001c0002t0011g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.792+340T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648792 | ||||||
| chr16:74648837
|
A | G | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.792+295T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648837 | ||||||
| chr16:74648851
|
C | T | 3 | a0003c0003t0003g0050a0003c0003t0003g0092a0003c0003t0020g0063 | 3 | HG00741.hp1 HG01243.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.792+281G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648851 | ||||||
| chr16:74648854
|
G | A | 13 | a0001c0004t0004g0001a0001c0004t0004g0115a0001c0004t0004g0117others(10): Show | 17 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+278C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648854 | ||||||
| chr16:74648883
|
C | T | 3 | a0001c0004t0004g0127a0001c0004t0004g0128a0001c0004t0004g0129 | 3 | HG00099.hp2 HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.792+249G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74648883 | ||||||
| chr16:74649104
|
G | A | 6 | a0001c0002t0002g0172a0001c0002t0002g0207a0001c0002t0002g0208others(3): Show | 6 | HG02155.hp2 NA18943.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+28C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74649104 | ||||||
| chr16:74649112
|
T | A | 1 | a0003c0003t0003g0050 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.792+20A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74649112 | ||||||
| chr16:74649113
|
A | T | 1 | a0005c0009t0008g0148 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.792+19T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 4/12 | chr16 | 74649113 | ||||||
| chr16:74649205
|
G | A | 1 | a0001c0002t0002g0220 | 1 | HG00642.hp1 | splice_region_variant&intron_variant | LOW | c.722-3C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649205 | ||||||
| chr16:74649206
|
C | A | 1 | a0001c0002t0002g0220 | 1 | HG00642.hp1 | splice_region_variant&intron_variant | LOW | c.722-4G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649206 | ||||||
| chr16:74649255
|
T | C | 1 | a0003c0003t0005g0041 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.722-53A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649255 | ||||||
| chr16:74649335
|
G | C | 1 | a0001c0002t0002g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.722-133C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649335 | ||||||
| chr16:74649468
|
A | G | 1 | a0002c0001t0001g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.722-266T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649468 | ||||||
| chr16:74649839
|
T | C | 256 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(253): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.722-637A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649839 | ||||||
| chr16:74649839
|
T | G | 1 | a0002c0001t0001g0322 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.722-637A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649839 | ||||||
| chr16:74649884
|
G | T | 1 | a0002c0001t0001g0269 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.722-682C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74649884 | ||||||
| chr16:74650039
|
C | G | 1 | a0002c0001t0001g0306 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.722-837G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650039 | ||||||
| chr16:74650098
|
G | A | 3 | a0001c0002t0013g0152a0001c0002t0013g0153a0001c0002t0013g0166 | 3 | HG00738.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.722-896C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650098 | ||||||
| chr16:74650117
|
G | T | 1 | a0002c0001t0018g0382 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.722-915C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650117 | ||||||
| chr16:74650296
|
C | T | 1 | a0001c0002t0016g0217 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.722-1094G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650296 | ||||||
| chr16:74650356
|
T | C | 2 | a0002c0001t0001g0354a0002c0001t0001g0355 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.722-1154A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650356 | ||||||
| chr16:74650420
|
G | T | 11 | a0001c0002t0006g0358a0001c0002t0006g0359a0001c0002t0006g0360others(8): Show | 11 | HG00673.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.722-1218C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650420 | ||||||
| chr16:74650628
|
G | A | 1 | a0002c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.721+1292C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650628 | ||||||
| chr16:74650792
|
G | A | 25 | a0002c0001t0001g0245a0002c0001t0001g0246a0002c0001t0001g0247others(22): Show | 26 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.721+1128C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650792 | ||||||
| chr16:74650904
|
C | A | 1 | a0001c0002t0002g0172 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.721+1016G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650904 | ||||||
| chr16:74650998
|
G | GT | 257 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(254): Show | 271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.721+921dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74650998 | ||||||
| chr16:74651016
|
T | C | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.721+904A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651016 | ||||||
| chr16:74651061
|
A | T | 2 | a0004c0006t0001g0261a0004c0006t0001g0262 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.721+859T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651061 | ||||||
| chr16:74651254
|
A | G | 2 | a0002c0001t0001g0284a0002c0001t0001g0285 | 2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.721+666T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651254 | ||||||
| chr16:74651425
|
C | T | 1 | a0002c0001t0001g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.721+495G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651425 | ||||||
| chr16:74651426
|
G | A | 1 | a0002c0001t0001g0289 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.721+494C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651426 | ||||||
| chr16:74651691
|
C | T | 296 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(293): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.721+229G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651691 | ||||||
| chr16:74651909
|
A | G | 2 | a0002c0001t0001g0296a0002c0001t0001g0305 | 2 | NA19066.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.721+11T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 3/12 | chr16 | 74651909 | ||||||
| chr16:74652192
|
T | C | 1 | a0001c0004t0004g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.519-70A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652192 | ||||||
| chr16:74652268
|
G | A | 255 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(252): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.519-146C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652268 | ||||||
| chr16:74652335
|
C | A | 1 | a0002c0001t0001g0346 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.519-213G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652335 | ||||||
| chr16:74652626
|
G | A | 2 | a0003c0003t0003g0075a0003c0003t0003g0076 | 2 | HG01255.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.519-504C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652626 | ||||||
| chr16:74652788
|
A | G | 1 | a0001c0002t0001g0376 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.519-666T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652788 | ||||||
| chr16:74652789
|
C | T | 1 | a0001c0002t0029g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.519-667G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652789 | ||||||
| chr16:74652792
|
G | A | 289 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(286): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.519-670C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652792 | ||||||
| chr16:74652877
|
T | C | 1 | a0001c0002t0011g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.519-755A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652877 | ||||||
| chr16:74652923
|
C | T | 3 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130 | 3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.519-801G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74652923 | ||||||
| chr16:74653129
|
A | C | 3 | a0001c0002t0014g0257a0001c0002t0014g0356a0001c0002t0014g0357 | 3 | HG02886.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.519-1007T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653129 | ||||||
| chr16:74653151
|
T | G | 89 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(86): Show | 93 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.519-1029A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653151 | ||||||
| chr16:74653226
|
C | T | 2 | a0003c0003t0003g0047a0003c0003t0003g0062 | 2 | NA19056.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.519-1104G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653226 | ||||||
| chr16:74653353
|
A | G | 6 | a0002c0001t0001g0327a0002c0001t0001g0328a0002c0001t0001g0344others(3): Show | 6 | HG00423.hp2 HG03927.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.519-1231T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653353 | ||||||
| chr16:74653490
|
CA | C | 33 | a0001c0002t0002g0191a0001c0004t0004g0001a0001c0004t0004g0114others(30): Show | 38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.519-1369delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653490 | ||||||
| chr16:74653704
|
T | C | 94 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(91): Show | 98 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.519-1582A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653704 | ||||||
| chr16:74653816
|
T | C | 1 | a0002c0001t0001g0334 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.519-1694A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653816 | ||||||
| chr16:74653906
|
C | T | 288 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(285): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.519-1784G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653906 | ||||||
| chr16:74653909
|
A | T | 1 | a0002c0001t0002g0160 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.519-1787T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74653909 | ||||||
| chr16:74654008
|
A | G | 256 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(253): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.519-1886T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654008 | ||||||
| chr16:74654024
|
T | C | 2 | a0002c0001t0001g0259a0002c0001t0001g0260 | 2 | NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.519-1902A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654024 | ||||||
| chr16:74654028
|
G | GT | 9 | a0002c0001t0001g0256a0002c0001t0001g0259a0002c0001t0001g0260others(6): Show | 9 | HG01074.hp2 NA18953.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.519-1907dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654028 | ||||||
| chr16:74654096
|
T | C | 2 | a0003c0003t0005g0043a0003c0003t0005g0044 | 2 | HG00738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.519-1974A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654096 | ||||||
| chr16:74654111
|
A | G | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-1989T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654111 | ||||||
| chr16:74654171
|
T | C | 1 | a0001c0002t0013g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.519-2049A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654171 | ||||||
| chr16:74654260
|
C | G | 1 | a0001c0002t0014g0357 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.519-2138G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654260 | ||||||
| chr16:74654321
|
C | T | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-2199G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654321 | ||||||
| chr16:74654379
|
T | C | 1 | a0001c0002t0011g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.519-2257A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654379 | ||||||
| chr16:74654433
|
T | A | 1 | a0001c0002t0034g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.519-2311A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654433 | ||||||
| chr16:74654542
|
A | G | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-2420T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654542 | ||||||
| chr16:74654585
|
A | G | 4 | a0002c0001t0001g0291a0002c0001t0001g0292a0002c0001t0024g0136others(1): Show | 4 | HG02559.hp2 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.519-2463T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654585 | ||||||
| chr16:74654610
|
G | C | 2 | a0001c0004t0051g0380a0001c0004t0052g0379 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.519-2488C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654610 | ||||||
| chr16:74654755
|
A | G | 4 | a0002c0001t0002g0157a0002c0001t0002g0158a0002c0001t0002g0162others(1): Show | 4 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-2633T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654755 | ||||||
| chr16:74654796
|
T | C | 1 | a0001c0008t0048g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.519-2674A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654796 | ||||||
| chr16:74654925
|
G | A | 1 | a0002c0001t0002g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.519-2803C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654925 | ||||||
| chr16:74654939
|
T | C | 3 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130 | 3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.519-2817A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74654939 | ||||||
| chr16:74655050
|
T | G | 257 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(254): Show | 271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.519-2928A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655050 | ||||||
| chr16:74655155
|
G | T | 1 | a0002c0001t0001g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.519-3033C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655155 | ||||||
| chr16:74655284
|
G | A | 33 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0116others(30): Show | 38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.519-3162C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655284 | ||||||
| chr16:74655364
|
C | T | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-3242G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655364 | ||||||
| chr16:74655388
|
C | T | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-3266G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655388 | ||||||
| chr16:74655494
|
G | A | 2 | a0003c0003t0003g0087a0003c0003t0003g0105 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.519-3372C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655494 | ||||||
| chr16:74655506
|
C | T | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-3384G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655506 | ||||||
| chr16:74655619
|
GCTCT | G | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-3501_519-3498d others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655619 | ||||||
| chr16:74655626
|
CTCTT | C | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.519-3508_519-3505d others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655626 | ||||||
| chr16:74655921
|
T | C | 1 | a0002c0001t0010g0266 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.519-3799A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74655921 | ||||||
| chr16:74656164
|
G | C | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-4042C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656164 | ||||||
| chr16:74656213
|
G | A | 27 | a0003c0003t0003g0007a0003c0003t0003g0028a0003c0003t0003g0051others(24): Show | 28 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.519-4091C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656213 | ||||||
| chr16:74656305
|
T | C | 297 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(294): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.519-4183A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656305 | ||||||
| chr16:74656308
|
C | CA | 110 | a0001c0002t0002g0183a0001c0002t0002g0210a0001c0002t0002g0211others(107): Show | 116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.519-4187dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656308 | ||||||
| chr16:74656308
|
C | CAA | 22 | a0001c0002t0011g0027a0001c0002t0056g0386a0001c0005t0007g0008others(19): Show | 23 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.519-4188_519-4187d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656308 | ||||||
| chr16:74656308
|
CA | C | 35 | a0001c0002t0002g0190a0001c0004t0004g0001a0001c0004t0004g0114others(32): Show | 40 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.519-4187delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656308 | ||||||
| chr16:74656308
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0001t0001g0254 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.519-4197_519-4187d others(13): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656308 | ||||||
| chr16:74656324
|
A | G | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.519-4202T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656324 | ||||||
| chr16:74656327
|
A | G | 2 | a0001c0002t0002g0225a0001c0002t0006g0361 | 2 | NA18947.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.519-4205T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656327 | ||||||
| chr16:74656328
|
A | G | 1 | a0001c0002t0002g0233 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.519-4206T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656328 | ||||||
| chr16:74656457
|
T | C | 2 | a0002c0001t0001g0284a0002c0001t0001g0285 | 2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.519-4335A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656457 | ||||||
| chr16:74656534
|
G | A | 1 | a0002c0001t0001g0302 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.518+4398C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656534 | ||||||
| chr16:74656536
|
G | A | 1 | a0002c0001t0001g0372 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.518+4396C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656536 | ||||||
| chr16:74656661
|
T | C | 1 | a0001c0002t0029g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.518+4271A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656661 | ||||||
| chr16:74656716
|
C | G | 1 | a0008c0013t0047g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.518+4216G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656716 | ||||||
| chr16:74656733
|
T | C | 118 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(115): Show | 122 | HG00408.hp2 HG00642.hp1 HG00673.hp1 others(119): Show |
intron_variant | MODIFIER | c.518+4199A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656733 | ||||||
| chr16:74656771
|
T | C | 1 | a0003c0003t0003g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.518+4161A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656771 | ||||||
| chr16:74656933
|
T | C | 3 | a0003c0003t0003g0085a0003c0003t0005g0005a0003c0003t0005g0006 | 5 | NA18977.hp1 NA18977.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.518+3999A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74656933 | ||||||
| chr16:74657046
|
GA | G | 5 | a0001c0005t0007g0008a0001c0005t0007g0090a0001c0005t0007g0108others(2): Show | 6 | HG01192.hp2 HG01257.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+3885delT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657046 | ||||||
| chr16:74657100
|
G | C | 1 | a0001c0002t0011g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.518+3832C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657100 | ||||||
| chr16:74657137
|
A | G | 2 | a0001c0004t0051g0380a0001c0004t0052g0379 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.518+3795T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657137 | ||||||
| chr16:74657149
|
C | A | 1 | a0002c0001t0001g0318 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.518+3783G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657149 | ||||||
| chr16:74657294
|
T | C | 1 | a0002c0001t0001g0250 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.518+3638A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657294 | ||||||
| chr16:74657366
|
T | C | 256 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(253): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.518+3566A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657366 | ||||||
| chr16:74657464
|
C | T | 256 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(253): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.518+3468G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657464 | ||||||
| chr16:74657474
|
TTTTC | T | 27 | a0001c0004t0004g0001a0001c0004t0004g0115a0001c0004t0004g0116others(24): Show | 32 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.518+3454_518+3457d others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657474 | ||||||
| chr16:74657478
|
C | CTT | 239 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(236): Show | 253 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.518+3452_518+3453d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657478 | ||||||
| chr16:74657478
|
C | CTTT | 15 | a0001c0002t0006g0360a0001c0002t0049g0352a0002c0001t0001g0302others(12): Show | 15 | HG00323.hp2 HG00639.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.518+3451_518+3453d others(5): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657478 | ||||||
| chr16:74657498
|
C | T | 1 | a0002c0001t0001g0347 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518+3434G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657498 | ||||||
| chr16:74657559
|
T | C | 13 | a0001c0004t0004g0001a0001c0004t0004g0115a0001c0004t0004g0117others(10): Show | 17 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.518+3373A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657559 | ||||||
| chr16:74657636
|
C | T | 2 | a0002c0001t0001g0301a0002c0001t0001g0319 | 2 | NA18960.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.518+3296G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657636 | ||||||
| chr16:74657758
|
G | A | 1 | a0001c0004t0004g0114 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.518+3174C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657758 | ||||||
| chr16:74657763
|
T | C | 8 | a0003c0003t0005g0029a0003c0003t0005g0030a0003c0003t0005g0031others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.518+3169A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657763 | ||||||
| chr16:74657791
|
A | G | 1 | a0001c0004t0004g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.518+3141T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657791 | ||||||
| chr16:74657894
|
T | G | 2 | a0003c0003t0012g0056a0012c0017t0012g0058 | 2 | HG01169.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.518+3038A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657894 | ||||||
| chr16:74657930
|
C | T | 1 | a0001c0002t0002g0175 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.518+3002G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657930 | ||||||
| chr16:74657940
|
T | C | 6 | a0001c0002t0006g0360a0001c0002t0006g0361a0001c0002t0006g0362others(3): Show | 6 | HG00673.hp1 HG01993.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+2992A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74657940 | ||||||
| chr16:74658207
|
G | C | 3 | a0001c0002t0002g0219a0001c0002t0016g0216a0001c0002t0016g0217 | 3 | HG02738.hp2 HG03017.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.518+2725C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658207 | ||||||
| chr16:74658320
|
G | A | 3 | a0002c0001t0010g0253a0002c0001t0038g0287a0002c0001t0039g0288 | 3 | HG02809.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.518+2612C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658320 | ||||||
| chr16:74658446
|
T | C | 1 | a0001c0002t0049g0352 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.518+2486A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658446 | ||||||
| chr16:74658528
|
C | T | 290 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.518+2404G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658528 | ||||||
| chr16:74658555
|
C | T | 290 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.518+2377G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658555 | ||||||
| chr16:74658694
|
C | T | 2 | a0002c0001t0001g0245a0002c0001t0001g0332 | 2 | HG00733.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.518+2238G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658694 | ||||||
| chr16:74658698
|
C | G | 2 | a0001c0004t0009g0184a0010c0012t0009g0221 | 2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.518+2234G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658698 | ||||||
| chr16:74658702
|
T | C | 10 | a0001c0004t0009g0176a0001c0004t0009g0184a0001c0004t0009g0185others(7): Show | 11 | HG00558.hp2 HG02027.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.518+2230A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658702 | ||||||
| chr16:74658724
|
C | T | 4 | a0002c0001t0001g0297a0002c0001t0001g0298a0002c0001t0001g0299others(1): Show | 4 | HG00621.hp1 HG03831.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.518+2208G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658724 | ||||||
| chr16:74658766
|
A | AT | 13 | a0001c0002t0002g0189a0001c0002t0011g0023a0002c0001t0001g0268others(10): Show | 13 | HG01358.hp2 HG01515.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.518+2165dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658766 | ||||||
| chr16:74658766
|
AT | A | 15 | a0001c0002t0002g0175a0001c0002t0002g0177a0001c0002t0002g0218others(12): Show | 15 | HG01106.hp2 HG01192.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.518+2165delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658766 | ||||||
| chr16:74658766
|
ATT | A | 33 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(30): Show | 38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.518+2164_518+2165d others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658766 | ||||||
| chr16:74658800
|
T | G | 1 | a0001c0004t0009g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.518+2132A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658800 | ||||||
| chr16:74658817
|
G | T | 1 | a0002c0001t0001g0340 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.518+2115C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658817 | ||||||
| chr16:74658834
|
C | A | 1 | a0002c0001t0001g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.518+2098G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658834 | ||||||
| chr16:74658863
|
G | A | 6 | a0001c0002t0006g0360a0001c0002t0006g0361a0001c0002t0006g0362others(3): Show | 6 | HG00673.hp1 HG01993.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+2069C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658863 | ||||||
| chr16:74658924
|
C | G | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.518+2008G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658924 | ||||||
| chr16:74658939
|
T | C | 1 | a0002c0001t0008g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.518+1993A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658939 | ||||||
| chr16:74658979
|
C | T | 5 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130others(2): Show | 5 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.518+1953G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658979 | ||||||
| chr16:74658980
|
G | A | 2 | a0003c0003t0003g0054a0003c0003t0003g0112 | 2 | NA18981.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.518+1952C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74658980 | ||||||
| chr16:74659032
|
T | C | 5 | a0001c0005t0007g0008a0001c0005t0007g0090a0001c0005t0007g0108others(2): Show | 6 | HG01192.hp2 HG01257.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+1900A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659032 | ||||||
| chr16:74659040
|
G | T | 1 | a0001c0002t0029g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.518+1892C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659040 | ||||||
| chr16:74659171
|
T | C | 1 | a0003c0003t0003g0113 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.518+1761A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659171 | ||||||
| chr16:74659197
|
G | A | 1 | a0001c0002t0002g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.518+1735C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659197 | ||||||
| chr16:74659209
|
C | T | 1 | a0001c0002t0044g0335 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.518+1723G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659209 | ||||||
| chr16:74659510
|
G | A | 2 | a0002c0001t0001g0289a0002c0001t0001g0326 | 2 | HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.518+1422C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659510 | ||||||
| chr16:74659577
|
A | G | 1 | a0003c0003t0003g0046 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.518+1355T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659577 | ||||||
| chr16:74659590
|
T | A | 1 | a0002c0001t0054g0384 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.518+1342A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659590 | ||||||
| chr16:74659601
|
C | CA | 250 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(247): Show | 264 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.518+1330dupT | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659601 | ||||||
| chr16:74659703
|
T | A | 2 | a0001c0002t0006g0364a0001c0002t0006g0365 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.518+1229A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659703 | ||||||
| chr16:74659791
|
T | C | 1 | a0001c0002t0001g0376 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.518+1141A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659791 | ||||||
| chr16:74659818
|
C | T | 3 | a0002c0001t0001g0297a0002c0001t0001g0298a0002c0001t0001g0299 | 3 | HG03831.hp2 NA18965.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.518+1114G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74659818 | ||||||
| chr16:74660010
|
G | C | 10 | a0002c0001t0001g0245a0002c0001t0001g0246a0002c0001t0001g0247others(7): Show | 10 | HG00733.hp1 HG01516.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.518+922C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660010 | ||||||
| chr16:74660029
|
T | TG | 34 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0115others(31): Show | 39 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.518+902dupC | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660029 | ||||||
| chr16:74660075
|
C | G | 292 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(289): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.518+857G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660075 | ||||||
| chr16:74660160
|
T | G | 257 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(254): Show | 271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.518+772A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660160 | ||||||
| chr16:74660577
|
A | G | 2 | a0001c0002t0011g0023a0001c0002t0011g0133 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.518+355T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660577 | ||||||
| chr16:74660686
|
C | G | 298 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(295): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.518+246G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660686 | ||||||
| chr16:74660794
|
T | C | 137 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0017others(134): Show | 147 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.518+138A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660794 | ||||||
| chr16:74660817
|
G | T | 1 | a0001c0002t0029g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.518+115C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660817 | ||||||
| chr16:74660833
|
C | A | 33 | a0001c0004t0004g0001a0001c0004t0004g0114a0001c0004t0004g0116others(30): Show | 38 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.518+99G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660833 | ||||||
| chr16:74660849
|
C | T | 1 | a0002c0001t0001g0263 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.518+83G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660849 | ||||||
| chr16:74660876
|
A | G | 2 | a0002c0001t0002g0167a0002c0001t0002g0182 | 2 | NA19067.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.518+56T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660876 | ||||||
| chr16:74660880
|
T | G | 4 | a0002c0001t0001g0291a0002c0001t0001g0292a0002c0001t0024g0136others(1): Show | 4 | HG02559.hp2 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.518+52A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 2/12 | chr16 | 74660880 | ||||||
| chr16:74661660
|
C | T | 1 | a0002c0001t0001g0296 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-2-209G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661660 | ||||||
| chr16:74661691
|
G | A | 1 | a0001c0004t0052g0379 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-2-240C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661691 | ||||||
| chr16:74661701
|
G | A | 1 | a0001c0004t0009g0187 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-2-250C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661701 | ||||||
| chr16:74661887
|
GATAA | G | 3 | a0001c0002t0014g0257a0001c0002t0014g0356a0001c0002t0014g0357 | 3 | HG02886.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-2-440_-2-437delTT others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661887 | ||||||
| chr16:74661915
|
C | A | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-464G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74661915 | ||||||
| chr16:74662007
|
T | A | 2 | a0002c0001t0001g0293a0002c0001t0001g0294 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-2-556A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662007 | ||||||
| chr16:74662027
|
CCAT | C | 72 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(69): Show | 76 | HG00408.hp2 HG00642.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.-2-579_-2-577delAT others(1): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662027 | ||||||
| chr16:74662101
|
T | C | 1 | a0001c0002t0015g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-2-650A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662101 | ||||||
| chr16:74662147
|
AAAT | A | 19 | a0002c0001t0001g0245a0002c0001t0001g0246a0002c0001t0001g0247others(16): Show | 20 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2-699_-2-697delAT others(1): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662147 | ||||||
| chr16:74662279
|
G | A | 1 | a0002c0001t0010g0253 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2-828C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662279 | ||||||
| chr16:74662374
|
T | C | 1 | a0002c0001t0001g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-2-923A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662374 | ||||||
| chr16:74662463
|
A | C | 1 | a0001c0002t0006g0366 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-2-1012T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662463 | ||||||
| chr16:74662491
|
A | C | 1 | a0003c0003t0012g0056 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-2-1040T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662491 | ||||||
| chr16:74662549
|
T | C | 1 | a0008c0013t0047g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-2-1098A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662549 | ||||||
| chr16:74662575
|
G | C | 2 | a0004c0006t0001g0261a0004c0006t0001g0262 | 2 | HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-2-1124C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662575 | ||||||
| chr16:74662627
|
G | A | 3 | a0001c0002t0006g0364a0001c0002t0006g0365a0001c0002t0006g0368 | 3 | HG02572.hp1 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-2-1176C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662627 | ||||||
| chr16:74662903
|
GCTT | G | 5 | a0002c0001t0001g0347a0002c0001t0001g0348a0002c0001t0001g0349others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-1455_-2-1453del others(3): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662903 | ||||||
| chr16:74662904
|
C | T | 1 | a0001c0002t0002g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-2-1453G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662904 | ||||||
| chr16:74662907
|
C | CT | 6 | a0002c0001t0001g0324a0002c0001t0001g0341a0003c0003t0003g0091others(3): Show | 6 | HG01981.hp2 HG02293.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-1457dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662907 | ||||||
| chr16:74662907
|
CT | C | 8 | a0001c0002t0002g0222a0001c0002t0049g0352a0002c0001t0001g0245others(5): Show | 8 | HG00323.hp2 HG01168.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-1457delA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662907 | ||||||
| chr16:74662932
|
T | C | 1 | a0001c0002t0029g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2-1481A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662932 | ||||||
| chr16:74662943
|
T | C | 3 | a0001c0004t0004g0127a0001c0004t0004g0128a0001c0004t0004g0129 | 3 | HG00099.hp2 HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-2-1492A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74662943 | ||||||
| chr16:74663061
|
C | T | 263 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(260): Show | 278 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.-2-1610G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663061 | ||||||
| chr16:74663068
|
C | A | 1 | a0002c0001t0002g0223 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-2-1617G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663068 | ||||||
| chr16:74663072
|
T | C | 1 | a0003c0003t0003g0107 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-2-1621A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663072 | ||||||
| chr16:74663121
|
G | C | 14 | a0002c0001t0012g0057a0003c0003t0005g0005a0003c0003t0005g0006others(11): Show | 16 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-2-1670C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663121 | ||||||
| chr16:74663281
|
A | G | 1 | a0001c0002t0002g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-2-1830T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663281 | ||||||
| chr16:74663290
|
G | C | 1 | a0001c0002t0029g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2-1839C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663290 | ||||||
| chr16:74663340
|
T | C | 25 | a0001c0002t0011g0133a0001c0004t0004g0001a0001c0004t0004g0114others(22): Show | 29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-1889A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663340 | ||||||
| chr16:74663377
|
G | A | 4 | a0002c0001t0001g0243a0002c0001t0001g0244a0002c0001t0001g0341others(1): Show | 4 | NA18970.hp1 NA18972.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1926C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663377 | ||||||
| chr16:74663406
|
T | C | 1 | a0002c0001t0001g0321 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-2-1955A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663406 | ||||||
| chr16:74663523
|
C | T | 297 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(294): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-2-2072G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663523 | ||||||
| chr16:74663674
|
C | T | 3 | a0002c0001t0001g0295a0002c0001t0002g0155a0002c0001t0002g0156 | 3 | HG02083.hp2 NA18989.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-2-2223G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663674 | ||||||
| chr16:74663774
|
A | T | 25 | a0001c0002t0011g0133a0001c0004t0004g0001a0001c0004t0004g0114others(22): Show | 29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-2323T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663774 | ||||||
| chr16:74663884
|
A | G | 1 | a0008c0013t0047g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-2-2433T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663884 | ||||||
| chr16:74663984
|
G | A | 1 | a0001c0008t0048g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2-2533C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74663984 | ||||||
| chr16:74664101
|
ATGTGAGA others(86): Show |
A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2592_-2-2651del others(93): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664101 | ||||||
| chr16:74664153
|
G | A | 1 | a0002c0001t0001g0322 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-3+2633C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664153 | ||||||
| chr16:74664198
|
G | C | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2588C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664198 | ||||||
| chr16:74664199
|
C | T | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2587G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664199 | ||||||
| chr16:74664204
|
G | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2582C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664204 | ||||||
| chr16:74664206
|
C | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2580G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664206 | ||||||
| chr16:74664207
|
T | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2579A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664207 | ||||||
| chr16:74664209
|
C | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2577G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664209 | ||||||
| chr16:74664213
|
A | C | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2573T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664213 | ||||||
| chr16:74664215
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2571A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664215 | ||||||
| chr16:74664216
|
G | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2570C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664216 | ||||||
| chr16:74664217
|
C | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2569G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664217 | ||||||
| chr16:74664218
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2568A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664218 | ||||||
| chr16:74664219
|
G | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2567C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664219 | ||||||
| chr16:74664223
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2563A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664223 | ||||||
| chr16:74664224
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2562A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664224 | ||||||
| chr16:74664226
|
C | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2560G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664226 | ||||||
| chr16:74664228
|
G | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2558C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664228 | ||||||
| chr16:74664232
|
T | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2554A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664232 | ||||||
| chr16:74664235
|
G | GATCTCTC others(4): Show |
1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2550_-3+2551ins others(11): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664235 | ||||||
| chr16:74664237
|
T | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2549A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664237 | ||||||
| chr16:74664240
|
T | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2546A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664240 | ||||||
| chr16:74664241
|
G | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2545C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664241 | ||||||
| chr16:74664244
|
G | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2542C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664244 | ||||||
| chr16:74664246
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2540A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664246 | ||||||
| chr16:74664248
|
C | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2538G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664248 | ||||||
| chr16:74664249
|
C | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2537G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664249 | ||||||
| chr16:74664250
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2536A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664250 | ||||||
| chr16:74664253
|
C | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2533G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664253 | ||||||
| chr16:74664254
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2532A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664254 | ||||||
| chr16:74664260
|
C | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2526G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664260 | ||||||
| chr16:74664261
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2525A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664261 | ||||||
| chr16:74664262
|
T | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2524A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664262 | ||||||
| chr16:74664263
|
T | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2523A>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664263 | ||||||
| chr16:74664264
|
T | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2522A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664264 | ||||||
| chr16:74664265
|
A | G | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2521T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664265 | ||||||
| chr16:74664268
|
G | C | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2518C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664268 | ||||||
| chr16:74664270
|
T | C | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2516A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664270 | ||||||
| chr16:74664273
|
T | TCTCATCA others(71): Show |
1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2512_-3+2513ins others(78): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664273 | ||||||
| chr16:74664277
|
G | A | 1 | a0003c0003t0003g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-3+2509C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664277 | ||||||
| chr16:74664354
|
A | T | 49 | a0002c0001t0001g0015a0002c0001t0001g0263a0002c0001t0001g0264others(46): Show | 50 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+2432T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664354 | ||||||
| chr16:74664365
|
C | G | 137 | a0002c0001t0001g0015a0002c0001t0001g0016a0002c0001t0001g0017others(134): Show | 147 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-3+2421G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664365 | ||||||
| chr16:74664426
|
T | C | 1 | a0001c0002t0029g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3+2360A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664426 | ||||||
| chr16:74664489
|
G | A | 25 | a0001c0002t0011g0133a0001c0004t0004g0001a0001c0004t0004g0114others(22): Show | 29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-3+2297C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664489 | ||||||
| chr16:74664521
|
C | A | 2 | a0003c0003t0005g0005a0003c0003t0005g0006 | 4 | NA18977.hp2 NA19009.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+2265G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664521 | ||||||
| chr16:74664530
|
G | T | 385 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(382): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.-3+2256C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664530 | ||||||
| chr16:74664537
|
A | G | 3 | a0001c0002t0002g0178a0001c0002t0002g0179a0001c0002t0002g0180 | 3 | HG01099.hp1 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-3+2249T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664537 | ||||||
| chr16:74664549
|
C | T | 2 | a0002c0001t0001g0259a0002c0001t0001g0260 | 2 | NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-3+2237G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664549 | ||||||
| chr16:74664599
|
A | T | 2 | a0001c0002t0002g0228a0001c0002t0002g0229 | 2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-3+2187T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664599 | ||||||
| chr16:74664654
|
C | A | 1 | a0001c0002t0002g0229 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-3+2132G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664654 | ||||||
| chr16:74664671
|
C | T | 1 | a0003c0003t0003g0059 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-3+2115G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664671 | ||||||
| chr16:74664678
|
A | G | 290 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-3+2108T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664678 | ||||||
| chr16:74664755
|
G | A | 1 | a0002c0001t0001g0245 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-3+2031C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664755 | ||||||
| chr16:74664755
|
G | GAAA | 23 | a0002c0001t0012g0057a0003c0003t0003g0020a0003c0003t0003g0021others(20): Show | 25 | HG00280.hp1 HG00738.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3+2028_-3+2030dup others(3): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664755 | ||||||
| chr16:74664755
|
G | GAAAA | 295 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(292): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-3+2027_-3+2030dup others(4): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664755 | ||||||
| chr16:74664818
|
A | C | 290 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-3+1968T>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664818 | ||||||
| chr16:74664845
|
G | C | 10 | a0002c0001t0001g0245a0002c0001t0001g0246a0002c0001t0001g0247others(7): Show | 10 | HG00733.hp1 HG01516.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+1941C>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664845 | ||||||
| chr16:74664864
|
C | T | 3 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130 | 3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-3+1922G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664864 | ||||||
| chr16:74664937
|
A | G | 1 | a0001c0004t0009g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-3+1849T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664937 | ||||||
| chr16:74664992
|
T | C | 2 | a0003c0003t0005g0043a0003c0003t0005g0044 | 2 | HG00738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-3+1794A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74664992 | ||||||
| chr16:74665104
|
G | A | 2 | a0002c0001t0010g0325a0002c0001t0010g0343 | 2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-3+1682C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665104 | ||||||
| chr16:74665203
|
CTGAAATG others(29): Show |
C | 1 | a0001c0002t0002g0224 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-3+1547_-3+1582del others(36): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665203 | ||||||
| chr16:74665395
|
T | C | 266 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(263): Show | 281 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.-3+1391A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665395 | ||||||
| chr16:74665421
|
T | C | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0033g0227 | 3 | NA18947.hp1 NA18957.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.-3+1365A>G | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665421 | ||||||
| chr16:74665589
|
G | A | 1 | a0001c0002t0049g0352 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-3+1197C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665589 | ||||||
| chr16:74665628
|
G | A | 2 | a0001c0002t0002g0228a0001c0002t0002g0229 | 2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-3+1158C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665628 | ||||||
| chr16:74665636
|
G | T | 1 | a0001c0002t0008g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-3+1150C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665636 | ||||||
| chr16:74665685
|
G | A | 25 | a0001c0002t0011g0133a0001c0004t0004g0001a0001c0004t0004g0114others(22): Show | 29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-3+1101C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665685 | ||||||
| chr16:74665707
|
C | T | 11 | a0002c0001t0001g0327a0002c0001t0001g0328a0002c0001t0001g0344others(8): Show | 12 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+1079G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665707 | ||||||
| chr16:74665749
|
TTTC | T | 21 | a0001c0002t0006g0358a0001c0002t0006g0359a0001c0002t0006g0360others(18): Show | 21 | HG00673.hp1 HG00738.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-3+1034_-3+1036del others(3): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665749 | ||||||
| chr16:74665752
|
C | CT | 129 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(126): Show | 138 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-3+1033dupA | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665752 | ||||||
| chr16:74665756
|
C | T | 295 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(292): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-3+1030G>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665756 | ||||||
| chr16:74665849
|
C | G | 2 | a0001c0002t0002g0175a0002c0001t0002g0174 | 2 | NA19056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-3+937G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74665849 | ||||||
| chr16:74666082
|
G | A | 25 | a0002c0001t0001g0245a0002c0001t0001g0246a0002c0001t0001g0247others(22): Show | 26 | HG00423.hp2 HG00733.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-3+704C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666082 | ||||||
| chr16:74666159
|
CATAG | C | 7 | a0001c0005t0007g0008a0001c0005t0007g0045a0001c0005t0007g0089others(4): Show | 8 | HG00140.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+623_-3+626delCT others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666159 | ||||||
| chr16:74666182
|
T | TTAGA | 22 | a0001c0005t0007g0008a0001c0005t0007g0108a0001c0005t0007g0109others(19): Show | 24 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3+600_-3+603dupTC others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | ||||||
| chr16:74666182
|
T | TTAGATAG others(1): Show |
3 | a0003c0003t0003g0111a0003c0003t0003g0112a0003c0003t0003g0113 | 3 | HG02004.hp1 HG02273.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-3+596_-3+603dupTC others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | ||||||
| chr16:74666182
|
TTAGA | T | 43 | a0001c0002t0002g0012a0001c0002t0002g0014a0001c0002t0002g0171others(40): Show | 45 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-3+600_-3+603delTC others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | ||||||
| chr16:74666182
|
TTAGATAG others(1): Show |
T | 21 | a0001c0004t0052g0379a0001c0005t0007g0045a0003c0003t0003g0028others(18): Show | 23 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-3+596_-3+603delTC others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | ||||||
| chr16:74666182
|
TTAGATAG others(5): Show |
T | 18 | a0001c0004t0004g0001a0001c0004t0004g0115a0001c0004t0004g0116others(15): Show | 22 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.-3+592_-3+603delTC others(10): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666182 | ||||||
| chr16:74666212
|
A | T | 6 | a0002c0001t0001g0246a0002c0001t0001g0247a0002c0001t0001g0248others(3): Show | 6 | HG02040.hp2 NA18963.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+574T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666212 | ||||||
| chr16:74666216
|
A | AGATT | 26 | a0001c0002t0013g0166a0001c0002t0044g0335a0002c0001t0001g0243others(23): Show | 32 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-3+569_-3+570insAA others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666216 | ||||||
| chr16:74666216
|
A | T | 114 | a0001c0002t0013g0152a0001c0002t0013g0153a0001c0002t0014g0257others(111): Show | 118 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.-3+570T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666216 | ||||||
| chr16:74666220
|
A | AGATAGAT others(5): Show |
5 | a0001c0002t0001g0375a0001c0002t0001g0376a0001c0002t0002g0239others(2): Show | 5 | NA18952.hp1 NA18967.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+565_-3+566insAA others(10): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | ||||||
| chr16:74666220
|
A | AGATAGAT others(1): Show |
3 | a0001c0002t0011g0027a0005c0009t0008g0148a0005c0009t0008g0149 | 3 | HG03225.hp2 NA18946.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-3+565_-3+566insAA others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | ||||||
| chr16:74666220
|
A | AGATAGAT others(5): Show |
2 | a0001c0002t0011g0023a0001c0002t0011g0024 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-3+565_-3+566insAA others(10): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | ||||||
| chr16:74666220
|
A | AGATT | 10 | a0001c0002t0001g0374a0001c0002t0002g0232a0001c0002t0002g0233others(7): Show | 10 | HG00642.hp2 HG02258.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+562_-3+565dupAA others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | ||||||
| chr16:74666220
|
A | AGATTGAT others(1): Show |
5 | a0001c0002t0049g0352a0001c0008t0048g0351a0002c0001t0001g0353others(2): Show | 5 | HG02109.hp2 HG03453.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+558_-3+565dupAA others(6): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | ||||||
| chr16:74666220
|
A | T | 239 | a0001c0002t0001g0373a0001c0002t0002g0004a0001c0002t0002g0012others(236): Show | 253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.-3+566T>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | ||||||
| chr16:74666220
|
AGATT | A | 3 | a0001c0004t0004g0131a0001c0004t0004g0132a0001c0004t0023g0130 | 3 | HG02896.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-3+562_-3+565delAA others(2): Show |
RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666220 | ||||||
| chr16:74666224
|
T | A | 1 | a0001c0002t0011g0133 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-3+562A>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666224 | ||||||
| chr16:74666238
|
G | T | 1 | a0002c0001t0001g0245 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-3+548C>A | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666238 | ||||||
| chr16:74666266
|
TG | T | 3 | a0002c0001t0002g0003a0002c0001t0002g0009a0002c0001t0002g0151 | 7 | NA18941.hp2 NA18985.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+519delC | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666266 | ||||||
| chr16:74666267
|
G | A | 1 | a0002c0001t0001g0372 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-3+519C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666267 | ||||||
| chr16:74666342
|
C | A | 100 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(97): Show | 105 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.-3+444G>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666342 | ||||||
| chr16:74666502
|
G | A | 1 | a0001c0002t0046g0377 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-3+284C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666502 | ||||||
| chr16:74666548
|
C | G | 1 | a0003c0003t0003g0022 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-3+238G>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666548 | ||||||
| chr16:74666686
|
G | A | 2 | a0001c0004t0004g0134a0001c0004t0004g0135 | 2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-3+100C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666686 | ||||||
| chr16:74666730
|
G | A | 285 | a0001c0002t0001g0373a0001c0002t0001g0374a0001c0002t0001g0375others(282): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.-3+56C>T | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666730 | ||||||
| chr16:74666754
|
A | G | 2 | a0003c0003t0003g0020a0003c0003t0003g0021 | 2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-3+32T>C | RFWD3 | ENSG00000168411.14 | transcript | ENST00000361070.9 | protein_coding | 1/12 | chr16 | 74666754 |