Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5908 |
|---|---|
| ensemblid | ENSG00000127314.18 |
| hgncid | 9857 |
| symbol | RAP1B |
| name | RAP1B, member of RAS oncogene family |
| refseq_nuc | NM_001010942.3 |
| refseq_prot | NP_001010942.1 |
| ensembl_nuc | ENST00000250559.14 |
| ensembl_prot | ENSP00000250559.9 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 68610899 |
| end | 68671901 |
| strand | + |
| ver | v1.2 |
| region | chr12:68610899-68671901 |
| region5000 | chr12:68605899-68676901 |
| regionname0 | RAP1B_chr12_68610899_68671901 |
| regionname5000 | RAP1B_chr12_68605899_68676901 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 184 | 388 | 82 | 66 | 184 | 12 | 42 | 140 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 12826 | 60 | 7 | 14 | 32 | 1 | 5 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0002 | 0/0 | 12824 | 43 | 5 | 11 | 21 | 2 | 4 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0003 | 0/0 | 12823 | 31 | 1 | 0 | 21 | 1 | 8 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0004 | 0/0 | 12824 | 16 | 2 | 2 | 9 | 1 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0005 | 0/0 | 12823 | 14 | 13 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0006 | 0/0 | 12825 | 12 | 0 | 1 | 11 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0007 | 0/0 | 12828 | 10 | 0 | 0 | 10 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0008 | 0/0 | 12823 | 9 | 0 | 1 | 8 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0009 | 0/0 | 12828 | 8 | 8 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0010 | 0/0 | 12828 | 5 | 1 | 1 | 2 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0011 | 0/0 | 12830 | 4 | 0 | 0 | 4 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0012 | 0/0 | 12830 | 4 | 0 | 4 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0013 | 0/0 | 12823 | 4 | 1 | 2 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0014 | 0/0 | 12827 | 4 | 1 | 1 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0015 | 0/0 | 12824 | 4 | 0 | 1 | 2 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0016 | 0/0 | 12820 | 4 | 0 | 4 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0017 | 0/0 | 12826 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0018 | 0/0 | 12827 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0019 | 0/0 | 12828 | 3 | 0 | 2 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0020 | 0/0 | 12825 | 3 | 0 | 1 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0021 | 0/0 | 12825 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0022 | 0/0 | 12823 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0023 | 0/0 | 12823 | 3 | 0 | 1 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0024 | 0/0 | 12824 | 3 | 0 | 1 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0025 | 0/0 | 12823 | 3 | 3 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0026 | 0/0 | 12853 | 2 | 0 | 0 | 0 | 2 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0027 | 0/0 | 12832 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0028 | 0/0 | 12830 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0029 | 0/0 | 12830 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0030 | 0/0 | 12824 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0031 | 0/0 | 12825 | 2 | 0 | 1 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0032 | 0/0 | 12828 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0033 | 0/0 | 12824 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0034 | 0/0 | 12825 | 2 | 0 | 1 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0035 | 0/0 | 12827 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0036 | 0/0 | 12827 | 2 | 0 | 1 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0037 | 0/0 | 12818 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0038 | 0/0 | 12826 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0039 | 0/0 | 12827 | 2 | 1 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0040 | 0/0 | 12825 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0041 | 0/0 | 12823 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0042 | 0/0 | 12822 | 2 | 0 | 0 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0043 | 0/0 | 12823 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0044 | 0/0 | 12825 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0045 | 0/0 | 12824 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0046 | 0/0 | 12823 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0047 | 0/0 | 12826 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0048 | 0/0 | 12851 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0049 | 0/0 | 12812 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0050 | 0/0 | 12825 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0051 | 0/0 | 12831 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0052 | 0/0 | 12828 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0053 | 0/0 | 12832 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0054 | 0/0 | 12832 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0055 | 0/0 | 12833 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0056 | 0/0 | 12830 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0057 | 0/0 | 12831 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0058 | 0/0 | 12830 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0059 | 0/0 | 12830 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0060 | 0/0 | 12830 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0061 | 0/0 | 12827 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0062 | 0/0 | 12825 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0063 | 0/0 | 12827 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0064 | 0/0 | 12825 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0065 | 0/0 | 12826 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0066 | 0/0 | 12828 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0067 | 0/0 | 12827 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0068 | 0/0 | 12828 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0069 | 0/0 | 12828 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0070 | 0/0 | 12828 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0071 | 0/0 | 12828 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0072 | 0/0 | 12827 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0073 | 0/0 | 12827 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0074 | 0/0 | 12828 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0075 | 0/0 | 12827 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0076 | 0/0 | 12826 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0077 | 0/0 | 12826 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0078 | 0/0 | 12826 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0079 | 1/0 | 12824 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0080 | 0/0 | 12826 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0081 | 0/0 | 12826 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0082 | 0/0 | 12826 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0083 | 0/0 | 12826 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0084 | 0/0 | 12825 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0085 | 0/0 | 12826 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0086 | 0/0 | 12828 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0087 | 0/0 | 12826 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0088 | 0/0 | 12818 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0089 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0090 | 0/0 | 12824 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0091 | 0/0 | 12823 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0092 | 0/0 | 12824 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0093 | 0/0 | 12825 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0094 | 0/0 | 12826 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0095 | 0/0 | 12824 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0096 | 0/0 | 12825 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0097 | 0/0 | 12823 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0098 | 0/0 | 12823 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0099 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0100 | 0/0 | 12823 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0101 | 0/0 | 12823 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0102 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0103 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0104 | 0/0 | 12823 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0105 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0106 | 0/0 | 12822 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0107 | 0/0 | 12823 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0108 | 0/0 | 12825 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0109 | 0/0 | 12823 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0110 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0111 | 0/0 | 12823 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0112 | 0/0 | 12823 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0113 | 0/0 | 12822 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0114 | 0/0 | 12824 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0115 | 0/0 | 12821 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0116 | 0/0 | 12822 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0117 | 0/0 | 12825 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0118 | 0/0 | 12822 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0119 | 0/0 | 12823 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0120 | 0/0 | 12824 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0121 | 0/0 | 12819 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0122 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0123 | 0/0 | 12827 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0124 | 0/0 | 12825 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0125 | 0/0 | 12827 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0126 | 0/0 | 12824 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0127 | 0/0 | 12823 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0128 | 0/0 | 12839 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0129 | 0/0 | 12828 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0130 | 0/0 | 12823 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0131 | 0/0 | 12827 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0132 | 0/0 | 12826 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| t0133 | 0/0 | 12823 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 555 | 387 | 82 | 65 | 184 | 12 | 42 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0002 | 0/0 | 555 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 13380 | 60 | 7 | 14 | 32 | 1 | 5 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0002 | 0/0 | 13378 | 43 | 5 | 11 | 21 | 2 | 4 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0003 | 0/0 | 13377 | 31 | 1 | 0 | 21 | 1 | 8 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0004 | 0/0 | 13378 | 16 | 2 | 2 | 9 | 1 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0005 | 0/0 | 13377 | 14 | 13 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0006 | 0/0 | 13379 | 12 | 0 | 1 | 11 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0007 | 0/0 | 13382 | 10 | 0 | 0 | 10 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0008 | 0/0 | 13377 | 9 | 0 | 1 | 8 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0009 | 0/0 | 13382 | 8 | 8 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0010 | 0/0 | 13382 | 5 | 1 | 1 | 2 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0011 | 0/0 | 13384 | 4 | 0 | 0 | 4 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0012 | 0/0 | 13384 | 4 | 0 | 4 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0013 | 0/0 | 13377 | 4 | 1 | 2 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0014 | 0/0 | 13381 | 4 | 1 | 1 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0015 | 0/0 | 13378 | 4 | 0 | 1 | 2 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0016 | 0/0 | 13374 | 4 | 0 | 4 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0017 | 0/0 | 13380 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0018 | 0/0 | 13381 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0019 | 0/0 | 13382 | 3 | 0 | 2 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0020 | 0/0 | 13379 | 3 | 0 | 1 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0021 | 0/0 | 13379 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0022 | 0/0 | 13377 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0023 | 0/0 | 13377 | 3 | 0 | 1 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0024 | 0/0 | 13378 | 2 | 0 | 0 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0025 | 0/0 | 13377 | 3 | 3 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0026 | 0/0 | 13407 | 2 | 0 | 0 | 0 | 2 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0027 | 0/0 | 13386 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0028 | 0/0 | 13384 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0029 | 0/0 | 13384 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0030 | 0/0 | 13378 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0031 | 0/0 | 13379 | 2 | 0 | 1 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0032 | 0/0 | 13382 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0033 | 0/0 | 13378 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0034 | 0/0 | 13379 | 2 | 0 | 1 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0035 | 0/0 | 13381 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0036 | 0/0 | 13381 | 2 | 0 | 1 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0037 | 0/0 | 13372 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0038 | 0/0 | 13380 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0039 | 0/0 | 13381 | 2 | 1 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0040 | 0/0 | 13379 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0041 | 0/0 | 13377 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0042 | 0/0 | 13376 | 2 | 0 | 0 | 0 | 0 | 2 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0043 | 0/0 | 13377 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0044 | 0/0 | 13379 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0045 | 0/0 | 13378 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0046 | 0/0 | 13377 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0047 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0048 | 0/0 | 13405 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0049 | 0/0 | 13366 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0050 | 0/0 | 13379 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0051 | 0/0 | 13385 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0052 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0053 | 0/0 | 13386 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0054 | 0/0 | 13386 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0055 | 0/0 | 13387 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0056 | 0/0 | 13384 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0057 | 0/0 | 13385 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0058 | 0/0 | 13384 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0059 | 0/0 | 13384 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0060 | 0/0 | 13384 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0061 | 0/0 | 13381 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0062 | 0/0 | 13379 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0063 | 0/0 | 13381 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0064 | 0/0 | 13379 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0065 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0066 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0067 | 0/0 | 13381 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0068 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0069 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0070 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0071 | 0/0 | 13382 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0072 | 0/0 | 13381 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0073 | 0/0 | 13381 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0074 | 0/0 | 13382 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0075 | 0/0 | 13381 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0076 | 0/0 | 13380 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0077 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0078 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0079 | 1/0 | 13378 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0080 | 0/0 | 13380 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0081 | 0/0 | 13380 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0082 | 0/0 | 13380 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0083 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0084 | 0/0 | 13379 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0085 | 0/0 | 13380 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0086 | 0/0 | 13382 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0087 | 0/0 | 13380 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0088 | 0/0 | 13372 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0089 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0090 | 0/0 | 13378 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0091 | 0/0 | 13377 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0092 | 0/0 | 13378 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0093 | 0/0 | 13379 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0094 | 0/0 | 13380 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0095 | 0/0 | 13378 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0096 | 0/0 | 13379 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0097 | 0/0 | 13377 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0098 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0099 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0100 | 0/0 | 13377 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0101 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0102 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0103 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0104 | 0/0 | 13377 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0105 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0106 | 0/0 | 13376 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0107 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0108 | 0/0 | 13379 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0109 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0110 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0111 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0112 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0113 | 0/0 | 13376 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0114 | 0/0 | 13378 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0115 | 0/0 | 13375 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0116 | 0/0 | 13376 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0117 | 0/0 | 13379 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0118 | 0/0 | 13376 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0119 | 0/0 | 13377 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0120 | 0/0 | 13378 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0121 | 0/0 | 13373 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0122 | 0/0 | 13378 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0123 | 0/0 | 13381 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0124 | 0/0 | 13379 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0125 | 0/0 | 13381 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0126 | 0/0 | 13378 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0127 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0128 | 0/0 | 13393 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0129 | 0/0 | 13382 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0130 | 0/0 | 13377 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0131 | 0/0 | 13381 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0132 | 0/0 | 13380 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0001t0133 | 0/0 | 13377 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| a0001c0002t0024 | 0/0 | 13378 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | copy fasta | chr12 | 68605899 | 68676901 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0008g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0009g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0010g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0010g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0010g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0010g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0011g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0012g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0012g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0012g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0012g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0013g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0013g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0013g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0014g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0014g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0014g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0015g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0015g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0015g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0015g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0016g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0016g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0016g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0016g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0017g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0017g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0017g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0018g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0018g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0018g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0019g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0019g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0019g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0020g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0020g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0020g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0021g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0021g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0021g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0022g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0022g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0023g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0023g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0023g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0024g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0024g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0025g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0025g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0026g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0027g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0027g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0028g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0028g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0029g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0029g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0030g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0030g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0031g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0031g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0032g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0032g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0033g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0033g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0034g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0034g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0035g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0035g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0036g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0036g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0037g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0037g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0038g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0038g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0039g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0039g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0040g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0040g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0041g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0041g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0042g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0042g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0043g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0043g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0044g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0044g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0045g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0045g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0046g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0046g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0047g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0048g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0049g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0050g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0051g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0052g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0053g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0054g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0055g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0056g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0057g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0058g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0059g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0060g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0061g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0062g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0063g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0064g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0065g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0066g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0067g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0068g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0069g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0070g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0071g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0072g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0073g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0074g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0075g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0076g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0077g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0078g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0079g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0080g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0081g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0082g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0083g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0084g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0085g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0086g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0087g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0088g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0089g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0090g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0091g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0092g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0093g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0094g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0095g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0096g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0097g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0098g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0099g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0100g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0101g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0102g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0103g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0104g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0105g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0106g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0107g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0108g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0109g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0110g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0111g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0112g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0113g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0114g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0115g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0116g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0117g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0118g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0119g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0120g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0121g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0122g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0123g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0124g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0125g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0126g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0127g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0128g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0129g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0130g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0131g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0132g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0001t0133g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| a0001c0002t0024g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | GBR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00099 | hp2 | a0001 | c0001 | t0028 | g0166 | EUR | GBR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00280 | hp1 | a0001 | c0001 | t0045 | g0111 | EUR | FIN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0315 | EUR | FIN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00323 | hp2 | a0001 | c0001 | t0085 | g0175 | EUR | FIN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00408 | hp2 | a0001 | c0001 | t0030 | g0079 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00438 | hp1 | a0001 | c0001 | t0015 | g0352 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00544 | hp1 | a0001 | c0001 | t0064 | g0047 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00558 | hp1 | a0001 | c0001 | t0033 | g0224 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0081 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0039 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00621 | hp2 | a0001 | c0001 | t0035 | g0230 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00639 | hp1 | a0001 | c0001 | t0080 | g0108 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00639 | hp2 | a0001 | c0001 | t0087 | g0015 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00642 | hp1 | a0001 | c0001 | t0029 | g0297 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00642 | hp2 | a0001 | c0001 | t0015 | g0343 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0066 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00673 | hp2 | a0001 | c0001 | t0010 | g0220 | EAS | CHS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00735 | hp1 | a0001 | c0001 | t0031 | g0035 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00738 | hp1 | a0001 | c0001 | t0023 | g0263 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG00738 | hp2 | a0001 | c0001 | t0100 | g0326 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01069 | hp1 | a0001 | c0001 | t0013 | g0006 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01070 | hp1 | a0001 | c0001 | t0034 | g0014 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01074 | hp2 | a0001 | c0001 | t0013 | g0072 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0368 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01081 | hp2 | a0001 | c0001 | t0106 | g0097 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01106 | hp1 | a0001 | c0001 | t0054 | g0106 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01106 | hp2 | a0001 | c0001 | t0056 | g0367 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01109 | hp1 | a0001 | c0001 | t0012 | g0359 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01109 | hp2 | a0001 | c0001 | t0129 | g0370 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01168 | hp2 | a0001 | c0001 | t0019 | g0122 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01175 | hp1 | a0001 | c0001 | t0119 | g0349 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01192 | hp1 | a0001 | c0001 | t0019 | g0141 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01192 | hp2 | a0001 | c0001 | t0036 | g0215 | AMR | PUR | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01255 | hp1 | a0001 | c0001 | t0016 | g0239 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01255 | hp2 | a0001 | c0001 | t0029 | g0301 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01256 | hp1 | a0001 | c0001 | t0121 | g0248 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01256 | hp2 | a0001 | c0001 | t0020 | g0345 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01258 | hp2 | a0001 | c0001 | t0016 | g0249 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01261 | hp2 | a0001 | c0001 | t0014 | g0176 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01358 | hp1 | a0001 | c0001 | t0016 | g0143 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01358 | hp2 | a0001 | c0001 | t0055 | g0099 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01361 | hp1 | a0001 | c0001 | t0039 | g0260 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01433 | hp1 | a0001 | c0001 | t0012 | g0094 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0034 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01516 | hp1 | a0001 | c0001 | t0057 | g0098 | EUR | IBS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01516 | hp2 | a0001 | c0001 | t0026 | g0013 | EUR | IBS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0076 | EUR | IBS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01517 | hp2 | a0001 | c0001 | t0026 | g0013 | EUR | IBS | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01884 | hp1 | a0001 | c0001 | t0070 | g0295 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01891 | hp1 | a0001 | c0001 | t0058 | g0172 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01978 | hp1 | a0001 | c0001 | t0097 | g0371 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01993 | hp1 | a0001 | c0001 | t0016 | g0195 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02004 | hp1 | a0001 | c0001 | t0012 | g0363 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02004 | hp2 | a0001 | c0001 | t0012 | g0244 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02055 | hp1 | a0001 | c0001 | t0088 | g0262 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0229 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02056 | hp1 | a0001 | c0001 | t0018 | g0084 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02056 | hp2 | a0001 | c0001 | t0131 | g0338 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0337 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02074 | hp2 | a0001 | c0001 | t0017 | g0200 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02083 | hp1 | a0001 | c0001 | t0061 | g0052 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0341 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02132 | hp1 | a0001 | c0001 | t0122 | g0119 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02135 | hp1 | a0001 | c0001 | t0105 | g0121 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02135 | hp2 | a0001 | c0001 | t0086 | g0235 | EAS | KHV | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0266 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02145 | hp2 | a0001 | c0001 | t0128 | g0369 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0354 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CDX | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02155 | hp2 | a0001 | c0001 | t0047 | g0198 | EAS | CDX | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0049 | EAS | CDX | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02257 | hp1 | a0001 | c0001 | t0025 | g0028 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02257 | hp2 | a0001 | c0001 | t0014 | g0181 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02258 | hp1 | a0001 | c0001 | t0068 | g0292 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02293 | hp1 | a0001 | c0002 | t0024 | g0155 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02300 | hp1 | a0001 | c0001 | t0076 | g0258 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02451 | hp1 | a0001 | c0001 | t0069 | g0293 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02451 | hp2 | a0001 | c0001 | t0032 | g0362 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02572 | hp1 | a0001 | c0001 | t0038 | g0237 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02602 | hp1 | a0001 | c0001 | t0096 | g0325 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02602 | hp2 | a0001 | c0001 | t0126 | g0288 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02615 | hp1 | a0001 | c0001 | t0094 | g0185 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02615 | hp2 | a0001 | c0001 | t0072 | g0080 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02622 | hp1 | a0001 | c0001 | t0025 | g0029 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02630 | hp1 | a0001 | c0001 | t0091 | g0083 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02630 | hp2 | a0001 | c0001 | t0081 | g0364 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02647 | hp1 | a0001 | c0001 | t0037 | g0289 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0061 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02698 | hp1 | a0001 | c0001 | t0023 | g0267 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02698 | hp2 | a0001 | c0001 | t0045 | g0110 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02717 | hp1 | a0001 | c0001 | t0044 | g0254 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02735 | hp1 | a0001 | c0001 | t0020 | g0327 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02735 | hp2 | a0001 | c0001 | t0020 | g0285 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02738 | hp1 | a0001 | c0001 | t0108 | g0144 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02738 | hp2 | a0001 | c0001 | t0130 | g0335 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0298 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02809 | hp2 | a0001 | c0001 | t0082 | g0016 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02818 | hp2 | a0001 | c0001 | t0116 | g0169 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02886 | hp1 | a0001 | c0001 | t0039 | g0255 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02895 | hp2 | a0001 | c0001 | t0090 | g0036 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0071 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02922 | hp2 | a0001 | c0001 | t0049 | g0151 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02970 | hp2 | a0001 | c0001 | t0125 | g0168 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02976 | hp1 | a0001 | c0001 | t0067 | g0253 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0303 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03041 | hp1 | a0001 | c0001 | t0104 | g0171 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0299 | AFR | GWD | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03098 | hp1 | a0001 | c0001 | t0060 | g0365 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0300 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03130 | hp1 | a0001 | c0001 | t0117 | g0163 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03130 | hp2 | a0001 | c0001 | t0066 | g0162 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0296 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03209 | hp1 | a0001 | c0001 | t0124 | g0251 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03239 | hp1 | a0001 | c0001 | t0042 | g0347 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03239 | hp2 | a0001 | c0001 | t0034 | g0031 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03453 | hp1 | a0001 | c0001 | t0044 | g0256 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0302 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03486 | hp1 | a0001 | c0001 | t0114 | g0130 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0294 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0360 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03491 | hp1 | a0001 | c0001 | t0019 | g0113 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03491 | hp2 | a0001 | c0001 | t0075 | g0271 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03516 | hp1 | a0001 | c0001 | t0032 | g0366 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03579 | hp1 | a0001 | c0001 | t0059 | g0161 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | MSL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03654 | hp2 | a0001 | c0001 | t0023 | g0287 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03669 | hp1 | a0001 | c0001 | t0028 | g0170 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0062 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03688 | hp2 | a0001 | c0001 | t0120 | g0277 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03704 | hp1 | a0001 | c0001 | t0024 | g0154 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0328 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03710 | hp1 | a0001 | c0001 | t0042 | g0350 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0334 | SAS | PJL | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0357 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03834 | hp2 | a0001 | c0001 | t0024 | g0153 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03927 | hp1 | a0001 | c0001 | t0074 | g0193 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0353 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0342 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04115 | hp1 | a0001 | c0001 | t0073 | g0268 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0346 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04184 | hp2 | a0001 | c0001 | t0015 | g0336 | SAS | BEB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0323 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0329 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0320 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04204 | hp2 | a0001 | c0001 | t0010 | g0093 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04228 | hp1 | a0001 | c0001 | t0113 | g0322 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18522 | hp1 | a0001 | c0001 | t0025 | g0030 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18522 | hp2 | a0001 | c0001 | t0038 | g0184 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CHB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18612 | hp2 | a0001 | c0001 | t0111 | g0242 | EAS | CHB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18747 | hp1 | a0001 | c0001 | t0102 | g0307 | EAS | CHB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0077 | EAS | CHB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18906 | hp1 | a0001 | c0001 | t0037 | g0290 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18906 | hp2 | a0001 | c0001 | t0053 | g0165 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18939 | hp2 | a0001 | c0001 | t0046 | g0313 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18940 | hp1 | a0001 | c0001 | t0063 | g0152 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18944 | hp1 | a0001 | c0001 | t0036 | g0210 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0316 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18946 | hp1 | a0001 | c0001 | t0011 | g0075 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18948 | hp2 | a0001 | c0001 | t0132 | g0190 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18949 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18949 | hp2 | a0001 | c0001 | t0077 | g0219 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18950 | hp1 | a0001 | c0001 | t0101 | g0355 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18951 | hp1 | a0001 | c0001 | t0022 | g0333 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18952 | hp2 | a0001 | c0001 | t0008 | g0321 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18953 | hp1 | a0001 | c0001 | t0015 | g0318 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18953 | hp2 | a0001 | c0001 | t0011 | g0060 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18954 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18957 | hp2 | a0001 | c0001 | t0098 | g0278 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18963 | hp1 | a0001 | c0001 | t0040 | g0136 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18964 | hp2 | a0001 | c0001 | t0109 | g0139 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18965 | hp1 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18966 | hp1 | a0001 | c0001 | t0018 | g0048 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18966 | hp2 | a0001 | c0001 | t0017 | g0197 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0063 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18971 | hp2 | a0001 | c0001 | t0099 | g0314 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18972 | hp1 | a0001 | c0001 | t0014 | g0204 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18973 | hp1 | a0001 | c0001 | t0008 | g0330 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18974 | hp2 | a0001 | c0001 | t0084 | g0304 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18975 | hp1 | a0001 | c0001 | t0007 | g0082 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18975 | hp2 | a0001 | c0001 | t0017 | g0246 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18978 | hp1 | a0001 | c0001 | t0021 | g0123 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18978 | hp2 | a0001 | c0001 | t0065 | g0085 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18980 | hp2 | a0001 | c0001 | t0133 | g0272 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18982 | hp1 | a0001 | c0001 | t0083 | g0206 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18982 | hp2 | a0001 | c0001 | t0051 | g0078 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18983 | hp1 | a0001 | c0001 | t0014 | g0221 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18983 | hp2 | a0001 | c0001 | t0008 | g0344 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18986 | hp2 | a0001 | c0001 | t0093 | g0324 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18989 | hp1 | a0001 | c0001 | t0043 | g0339 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18992 | hp2 | a0001 | c0001 | t0013 | g0046 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18993 | hp1 | a0001 | c0001 | t0062 | g0056 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18994 | hp2 | a0001 | c0001 | t0030 | g0045 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0074 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19002 | hp2 | a0001 | c0001 | t0027 | g0065 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19004 | hp2 | a0001 | c0001 | t0041 | g0275 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19010 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19043 | hp1 | a0001 | c0001 | t0123 | g0250 | AFR | LWK | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19054 | hp1 | a0001 | c0001 | t0078 | g0222 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19056 | hp1 | a0001 | c0001 | t0021 | g0156 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19057 | hp2 | a0001 | c0001 | t0127 | g0309 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19060 | hp1 | a0001 | c0001 | t0010 | g0207 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19062 | hp1 | a0001 | c0001 | t0118 | g0276 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19064 | hp2 | a0001 | c0001 | t0022 | g0012 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19066 | hp1 | a0001 | c0001 | t0103 | g0142 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19068 | hp1 | a0001 | c0001 | t0040 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19068 | hp2 | a0001 | c0001 | t0008 | g0351 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19072 | hp1 | a0001 | c0001 | t0008 | g0332 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19074 | hp1 | a0001 | c0001 | t0033 | g0189 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19077 | hp1 | a0001 | c0001 | t0008 | g0331 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19078 | hp1 | a0001 | c0001 | t0035 | g0212 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19080 | hp1 | a0001 | c0001 | t0011 | g0092 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19082 | hp1 | a0001 | c0001 | t0046 | g0312 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19082 | hp2 | a0001 | c0001 | t0041 | g0308 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19084 | hp1 | a0001 | c0001 | t0022 | g0012 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19085 | hp1 | a0001 | c0001 | t0112 | g0319 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19085 | hp2 | a0001 | c0001 | t0110 | g0116 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19087 | hp2 | a0001 | c0001 | t0031 | g0042 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19089 | hp1 | a0001 | c0001 | t0089 | g0069 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19089 | hp2 | a0001 | c0001 | t0021 | g0203 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19091 | hp1 | a0001 | c0001 | t0018 | g0067 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19091 | hp2 | a0001 | c0001 | t0107 | g0114 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA19240 | hp2 | a0001 | c0001 | t0115 | g0164 | AFR | YRI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ASW | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA20805 | hp1 | a0001 | c0001 | t0048 | g0358 | EUR | TSI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | TSI | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02109 | hp1 | a0001 | c0001 | t0052 | g0265 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02486 | hp1 | a0001 | c0001 | t0092 | g0088 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG02486 | hp2 | a0001 | c0001 | t0050 | g0017 | AFR | ACB | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | USA | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18955 | hp1 | a0001 | c0001 | t0043 | g0311 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA18955 | hp2 | a0001 | c0001 | t0027 | g0064 | EAS | JPT | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | USA | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | USA | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA21309 | hp1 | a0001 | c0001 | t0071 | g0291 | AFR | LWK | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| NA21309 | hp2 | a0001 | c0001 | t0095 | g0158 | AFR | LWK | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0179 | REF | REF | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0079 | g0306 | REF | REF | RAP1B_chr12_68605899_68676901 | RAP1B | chr12 | 68605899 | 68676901 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68654177
|
C | T | 1 | a0001c0002 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.249C>T | p.Ser83Ser | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/8 | 420/13378 | 249/555 | 83/184 | chr12 | 68654177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68610901
|
C | G | 1 | a0001c0001t0133 | 1 | NA18980.hp2 | 5_prime_UTR_variant | MODIFIER | c.-169C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37824 | chr12 | 68610901 | |||||
| chr12:68610914
|
C | T | 1 | a0001c0001t0132 | 1 | NA18948.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-156C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | chr12 | 68610914 | ||||||
| chr12:68610915
|
G | C | 1 | a0001c0001t0047 | 1 | HG02155.hp2 | 5_prime_UTR_variant | MODIFIER | c.-155G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37810 | chr12 | 68610915 | |||||
| chr12:68610963
|
G | C | 2 | a0001c0001t0026a0001c0001t0048 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
5_prime_UTR_variant | MODIFIER | c.-107G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37762 | chr12 | 68610963 | |||||
| chr12:68610996
|
G | A | 1 | a0001c0001t0017 | 3 | HG02074.hp2 NA18966.hp2 NA18975.hp2 |
5_prime_UTR_variant | MODIFIER | c.-74G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37729 | chr12 | 68610996 | |||||
| chr12:68611003
|
GGGGCGAC others(3): Show |
G | 1 | a0001c0001t0049 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64_-55delGCGACGCT others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/8 | 37710 | INFO_REALIGN_3_PRIME | chr12 | 68611003 | ||||
| chr12:68648715
|
A | G | 2 | a0001c0001t0008a0001c0001t0131 | 10 | HG02056.hp2 HG02083.hp2 HG02148.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-10A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/8 | 10 | chr12 | 68648715 | |||||
| chr12:68659457
|
A | C | 1 | a0001c0001t0130 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*208A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 2270 | chr12 | 68659457 | |||||
| chr12:68659838
|
C | T | 6 | a0001c0001t0005a0001c0001t0025a0001c0001t0026others(3): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*589C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 2651 | chr12 | 68659838 | |||||
| chr12:68660165
|
A | G | 2 | a0001c0001t0046a0001c0001t0127 | 3 | NA18939.hp2 NA19057.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*916A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 2978 | chr12 | 68660165 | |||||
| chr12:68660580
|
C | T | 1 | a0001c0001t0126 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 3393 | chr12 | 68660580 | |||||
| chr12:68660777
|
C | T | 6 | a0001c0001t0005a0001c0001t0025a0001c0001t0026others(3): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1528C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 3590 | chr12 | 68660777 | |||||
| chr12:68660847
|
A | C | 1 | a0001c0001t0125 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1598A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 3660 | chr12 | 68660847 | |||||
| chr12:68660954
|
A | G | 1 | a0001c0001t0045 | 2 | HG00280.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1705A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 3767 | chr12 | 68660954 | |||||
| chr12:68661190
|
C | G | 5 | a0001c0001t0024a0001c0001t0049a0001c0001t0123others(2): Show | 6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1941C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4003 | chr12 | 68661190 | |||||
| chr12:68661327
|
G | A | 1 | a0001c0001t0050 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2078G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4140 | chr12 | 68661327 | |||||
| chr12:68661345
|
C | T | 1 | a0001c0001t0122 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2096C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4158 | chr12 | 68661345 | |||||
| chr12:68661569
|
A | G | 3 | a0001c0001t0005a0001c0001t0025a0001c0001t0129 | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2320A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4382 | chr12 | 68661569 | |||||
| chr12:68662008
|
C | CTA | 15 | a0001c0001t0009a0001c0001t0010a0001c0001t0019others(12): Show | 29 | HG00673.hp2 HG01081.hp1 HG01109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2783_*2784dupAT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | ||||
| chr12:68662008
|
C | CTATA | 8 | a0001c0001t0012a0001c0001t0028a0001c0001t0029others(5): Show | 13 | HG00099.hp2 HG00642.hp1 HG01106.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2781_*2784dupATAT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | ||||
| chr12:68662008
|
C | CTATATA | 3 | a0001c0001t0053a0001c0001t0054a0001c0001t0055 | 3 | HG01106.hp1 HG01358.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2779_*2784dupATAT others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | ||||
| chr12:68662008
|
C | CTATATAT others(7): Show |
1 | a0001c0001t0128 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2771_*2784dupATAT others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | ||||
| chr12:68662008
|
C | CTATATAT others(17): Show |
1 | a0001c0001t0048 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2761_*2784dupATAT others(20): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | ||||
| chr12:68662008
|
C | CTATATAT others(19): Show |
1 | a0001c0001t0026 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insATAT others(22): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | ||||
| chr12:68662008
|
CTA | C | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(42): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2783_*2784delAT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4845 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | ||||
| chr12:68662008
|
CTATATA | C | 2 | a0001c0001t0016a0001c0001t0121 | 5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2779_*2784delATAT others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4841 | INFO_REALIGN_3_PRIME | chr12 | 68662008 | ||||
| chr12:68662032
|
ATT | A | 3 | a0001c0001t0024a0001c0001t0049a0001c0002t0024 | 4 | HG02293.hp1 HG02922.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785delTT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4846 | chr12 | 68662032 | |||||
| chr12:68662033
|
T | TA | 1 | a0001c0001t0018 | 3 | HG02056.hp1 NA18966.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662033 | |||||
| chr12:68662033
|
T | TATA | 2 | a0001c0001t0007a0001c0001t0052 | 11 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insATA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662033 | |||||
| chr12:68662033
|
T | TATATA | 1 | a0001c0001t0011 | 4 | NA18946.hp1 NA18953.hp2 NA19010.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insATAT others(1): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662033 | |||||
| chr12:68662033
|
T | TATATATA | 2 | a0001c0001t0027a0001c0001t0051 | 3 | NA18955.hp2 NA18982.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2784_*2785insATAT others(3): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662033 | |||||
| chr12:68662034
|
T | A | 10 | a0001c0001t0004a0001c0001t0006a0001c0001t0013others(7): Show | 41 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2785T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4847 | chr12 | 68662034 | |||||
| chr12:68662035
|
A | AT | 6 | a0001c0001t0007a0001c0001t0011a0001c0001t0018others(3): Show | 21 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2787dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4850 | INFO_REALIGN_3_PRIME | chr12 | 68662035 | ||||
| chr12:68662035
|
A | T | 10 | a0001c0001t0004a0001c0001t0006a0001c0001t0013others(7): Show | 41 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2786A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4848 | chr12 | 68662035 | |||||
| chr12:68662059
|
G | GTA | 3 | a0001c0001t0026a0001c0001t0048a0001c0001t0074 | 4 | HG01516.hp2 HG01517.hp2 HG03927.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2822_*2823dupAT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4886 | INFO_REALIGN_3_PRIME | chr12 | 68662059 | ||||
| chr12:68662103
|
A | G | 1 | a0001c0001t0025 | 3 | HG02257.hp1 HG02622.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2854A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4916 | chr12 | 68662103 | |||||
| chr12:68662113
|
T | C | 1 | a0001c0001t0095 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2864T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 4926 | chr12 | 68662113 | |||||
| chr12:68662206
|
A | G | 3 | a0001c0001t0023a0001c0001t0073a0001c0001t0120 | 5 | HG00738.hp1 HG02698.hp1 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2957A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5019 | chr12 | 68662206 | |||||
| chr12:68662413
|
C | T | 1 | a0001c0001t0052 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3164C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5226 | chr12 | 68662413 | |||||
| chr12:68662454
|
G | T | 2 | a0001c0001t0032a0001c0001t0060 | 3 | HG02451.hp2 HG03098.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3205G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5267 | chr12 | 68662454 | |||||
| chr12:68662492
|
C | T | 1 | a0001c0001t0119 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3243C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5305 | chr12 | 68662492 | |||||
| chr12:68662504
|
T | A | 3 | a0001c0001t0005a0001c0001t0025a0001c0001t0129 | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3255T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5317 | chr12 | 68662504 | |||||
| chr12:68662837
|
A | T | 1 | a0001c0001t0059 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3588A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5650 | chr12 | 68662837 | |||||
| chr12:68662945
|
C | T | 2 | a0001c0001t0039a0001c0001t0044 | 4 | HG01361.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3696C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5758 | chr12 | 68662945 | |||||
| chr12:68662947
|
C | T | 2 | a0001c0001t0038a0001c0001t0094 | 3 | HG02572.hp1 HG02615.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3698C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5760 | chr12 | 68662947 | |||||
| chr12:68663115
|
G | A | 1 | a0001c0001t0074 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3866G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 5928 | chr12 | 68663115 | |||||
| chr12:68663561
|
A | G | 1 | a0001c0001t0118 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4312A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 6374 | chr12 | 68663561 | |||||
| chr12:68664075
|
C | T | 3 | a0001c0001t0022a0001c0001t0043a0001c0001t0093 | 6 | NA18951.hp1 NA18955.hp1 NA18986.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4826C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 6888 | chr12 | 68664075 | |||||
| chr12:68664099
|
C | T | 26 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(23): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*4850C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 6912 | chr12 | 68664099 | |||||
| chr12:68664261
|
G | A | 5 | a0001c0001t0024a0001c0001t0049a0001c0001t0123others(2): Show | 6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5012G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7074 | chr12 | 68664261 | |||||
| chr12:68664570
|
A | G | 1 | a0001c0001t0058 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5321A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7383 | chr12 | 68664570 | |||||
| chr12:68664584
|
C | T | 2 | a0001c0001t0026a0001c0001t0048 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5335C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7397 | chr12 | 68664584 | |||||
| chr12:68664639
|
G | A | 1 | a0001c0001t0043 | 2 | NA18955.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5390G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7452 | chr12 | 68664639 | |||||
| chr12:68664641
|
C | T | 5 | a0001c0001t0039a0001c0001t0044a0001c0001t0115others(2): Show | 7 | HG01361.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5392C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7454 | chr12 | 68664641 | |||||
| chr12:68664703
|
C | CA | 29 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(26): Show | 81 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*5462dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7525 | INFO_REALIGN_3_PRIME | chr12 | 68664703 | ||||
| chr12:68664718
|
G | T | 2 | a0001c0001t0037a0001c0001t0088 | 3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5469G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7531 | chr12 | 68664718 | |||||
| chr12:68664875
|
T | C | 1 | a0001c0001t0047 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5626T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7688 | chr12 | 68664875 | |||||
| chr12:68664895
|
G | A | 2 | a0001c0001t0030a0001c0001t0089 | 3 | HG00408.hp2 NA18994.hp2 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5646G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7708 | chr12 | 68664895 | |||||
| chr12:68664904
|
A | G | 1 | a0001c0001t0101 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5655A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7717 | chr12 | 68664904 | |||||
| chr12:68664923
|
C | G | 1 | a0001c0001t0058 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5674C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7736 | chr12 | 68664923 | |||||
| chr12:68664925
|
G | A | 5 | a0001c0001t0005a0001c0001t0025a0001c0001t0026others(2): Show | 21 | HG01069.hp2 HG01516.hp2 HG01517.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5676G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7738 | chr12 | 68664925 | |||||
| chr12:68665088
|
G | C | 1 | a0001c0001t0068 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5839G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 7901 | chr12 | 68665088 | |||||
| chr12:68665269
|
G | C | 1 | a0001c0001t0076 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6020G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8082 | chr12 | 68665269 | |||||
| chr12:68665296
|
T | TAG | 2 | a0001c0001t0026a0001c0001t0048 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6050_*6051dupAG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8114 | INFO_REALIGN_3_PRIME | chr12 | 68665296 | ||||
| chr12:68665326
|
A | G | 1 | a0001c0001t0128 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6077A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8139 | chr12 | 68665326 | |||||
| chr12:68665858
|
C | CT | 7 | a0001c0001t0025a0001c0001t0036a0001c0001t0055others(4): Show | 10 | HG00639.hp2 HG01192.hp2 HG01358.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6624dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8687 | INFO_REALIGN_3_PRIME | chr12 | 68665858 | ||||
| chr12:68665872
|
T | G | 3 | a0001c0001t0026a0001c0001t0048a0001c0001t0056 | 4 | HG01106.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6623T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8685 | chr12 | 68665872 | |||||
| chr12:68665872
|
T | TG | 2 | a0001c0001t0005a0001c0001t0115 | 15 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6623_*6624insG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8686 | chr12 | 68665872 | |||||
| chr12:68665873
|
T | A | 5 | a0001c0001t0005a0001c0001t0026a0001c0001t0048others(2): Show | 19 | HG01069.hp2 HG01106.hp2 HG01516.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*6624T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8686 | chr12 | 68665873 | |||||
| chr12:68665873
|
T | TGA | 7 | a0001c0001t0009a0001c0001t0029a0001c0001t0068others(4): Show | 15 | HG00642.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6630_*6631dupAG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8694 | INFO_REALIGN_3_PRIME | chr12 | 68665873 | ||||
| chr12:68665920
|
C | T | 1 | a0001c0001t0114 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6671C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8733 | chr12 | 68665920 | |||||
| chr12:68665940
|
G | A | 1 | a0001c0001t0102 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6691G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8753 | chr12 | 68665940 | |||||
| chr12:68666073
|
G | A | 1 | a0001c0001t0077 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6824G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8886 | chr12 | 68666073 | |||||
| chr12:68666147
|
G | T | 1 | a0001c0001t0128 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6898G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 8960 | chr12 | 68666147 | |||||
| chr12:68666206
|
A | C | 1 | a0001c0001t0043 | 2 | NA18955.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6957A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9019 | chr12 | 68666206 | |||||
| chr12:68666286
|
T | C | 4 | a0001c0001t0005a0001c0001t0025a0001c0001t0115others(1): Show | 19 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7037T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9099 | chr12 | 68666286 | |||||
| chr12:68666299
|
T | G | 1 | a0001c0001t0103 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7050T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9112 | chr12 | 68666299 | |||||
| chr12:68666336
|
G | A | 1 | a0001c0001t0059 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7087G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9149 | chr12 | 68666336 | |||||
| chr12:68666422
|
TA | T | 27 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(24): Show | 78 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*7174delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9236 | chr12 | 68666422 | |||||
| chr12:68666423
|
A | T | 1 | a0001c0001t0112 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7174A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9236 | chr12 | 68666423 | |||||
| chr12:68666424
|
C | T | 27 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(24): Show | 78 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*7175C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9237 | chr12 | 68666424 | |||||
| chr12:68666425
|
T | G | 28 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(25): Show | 79 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*7176T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9238 | chr12 | 68666425 | |||||
| chr12:68666993
|
G | C | 1 | a0001c0001t0128 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7744G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 9806 | chr12 | 68666993 | |||||
| chr12:68667214
|
A | G | 4 | a0001c0001t0005a0001c0001t0025a0001c0001t0115others(1): Show | 19 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7965A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10027 | chr12 | 68667214 | |||||
| chr12:68667451
|
G | A | 1 | a0001c0001t0127 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8202G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10264 | chr12 | 68667451 | |||||
| chr12:68667451
|
G | C | 1 | a0001c0001t0062 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8202G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10264 | chr12 | 68667451 | |||||
| chr12:68667459
|
G | A | 1 | a0001c0001t0068 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8210G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10272 | chr12 | 68667459 | |||||
| chr12:68667744
|
G | A | 1 | a0001c0001t0097 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8495G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10557 | chr12 | 68667744 | |||||
| chr12:68667953
|
T | C | 1 | a0001c0001t0069 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8704T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10766 | chr12 | 68667953 | |||||
| chr12:68668076
|
T | C | 2 | a0001c0001t0063a0001c0001t0098 | 2 | NA18940.hp1 NA18957.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8827T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10889 | chr12 | 68668076 | |||||
| chr12:68668078
|
C | A | 1 | a0001c0001t0063 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8829C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10891 | chr12 | 68668078 | |||||
| chr12:68668083
|
G | A | 1 | a0001c0001t0063 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8834G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10896 | chr12 | 68668083 | |||||
| chr12:68668086
|
C | G | 1 | a0001c0001t0063 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8837C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10899 | chr12 | 68668086 | |||||
| chr12:68668089
|
G | T | 1 | a0001c0001t0063 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8840G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10902 | chr12 | 68668089 | |||||
| chr12:68668091
|
C | T | 1 | a0001c0001t0063 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8842C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10904 | chr12 | 68668091 | |||||
| chr12:68668092
|
A | T | 1 | a0001c0001t0063 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8843A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10905 | chr12 | 68668092 | |||||
| chr12:68668160
|
C | G | 1 | a0001c0001t0038 | 2 | HG02572.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8911C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 10973 | chr12 | 68668160 | |||||
| chr12:68668279
|
A | T | 1 | a0001c0001t0062 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9030A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11092 | chr12 | 68668279 | |||||
| chr12:68668386
|
A | T | 1 | a0001c0001t0100 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9137A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11199 | chr12 | 68668386 | |||||
| chr12:68668511
|
A | G | 1 | a0001c0001t0068 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9262A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11324 | chr12 | 68668511 | |||||
| chr12:68668655
|
T | C | 1 | a0001c0001t0104 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9406T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11468 | chr12 | 68668655 | |||||
| chr12:68668924
|
C | T | 2 | a0001c0001t0026a0001c0001t0048 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9675C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11737 | chr12 | 68668924 | |||||
| chr12:68668951
|
A | G | 17 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(14): Show | 63 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*9702A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11764 | chr12 | 68668951 | |||||
| chr12:68669043
|
T | C | 29 | a0001c0001t0003a0001c0001t0008a0001c0001t0015others(26): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*9794T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11856 | chr12 | 68669043 | |||||
| chr12:68669088
|
A | G | 34 | a0001c0001t0001a0001c0001t0010a0001c0001t0012others(31): Show | 114 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*9839A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11901 | chr12 | 68669088 | |||||
| chr12:68669137
|
CTTTATA | C | 2 | a0001c0001t0037a0001c0001t0088 | 3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9895_*9900delTTTA others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 11957 | INFO_REALIGN_3_PRIME | chr12 | 68669137 | ||||
| chr12:68669304
|
A | G | 1 | a0001c0001t0047 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10055A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12117 | chr12 | 68669304 | |||||
| chr12:68669342
|
A | T | 2 | a0001c0001t0026a0001c0001t0048 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10093A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12155 | chr12 | 68669342 | |||||
| chr12:68669395
|
C | T | 1 | a0001c0001t0092 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10146C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12208 | chr12 | 68669395 | |||||
| chr12:68669503
|
T | C | 2 | a0001c0001t0026a0001c0001t0048 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10254T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12316 | chr12 | 68669503 | |||||
| chr12:68669551
|
C | T | 70 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(67): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*10302C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12364 | chr12 | 68669551 | |||||
| chr12:68669585
|
G | A | 1 | a0001c0001t0105 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10336G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12398 | chr12 | 68669585 | |||||
| chr12:68669603
|
C | T | 1 | a0001c0001t0127 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10354C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12416 | chr12 | 68669603 | |||||
| chr12:68669629
|
C | T | 1 | a0001c0001t0088 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10380C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12442 | chr12 | 68669629 | |||||
| chr12:68669765
|
A | C | 2 | a0001c0001t0026a0001c0001t0048 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10516A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12578 | chr12 | 68669765 | |||||
| chr12:68669767
|
T | C | 1 | a0001c0001t0070 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10518T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12580 | chr12 | 68669767 | |||||
| chr12:68669859
|
T | C | 2 | a0001c0001t0082a0001c0001t0087 | 2 | HG00639.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10610T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12672 | chr12 | 68669859 | |||||
| chr12:68669881
|
C | T | 2 | a0001c0001t0005a0001c0001t0115 | 15 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*10632C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12694 | chr12 | 68669881 | |||||
| chr12:68669935
|
C | CT | 34 | a0001c0001t0003a0001c0001t0008a0001c0001t0020others(31): Show | 84 | HG00280.hp2 HG00423.hp2 HG00639.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*10706dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12769 | INFO_REALIGN_3_PRIME | chr12 | 68669935 | ||||
| chr12:68669935
|
C | CTT | 54 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(51): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*10705_*10706dupTT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12769 | INFO_REALIGN_3_PRIME | chr12 | 68669935 | ||||
| chr12:68669935
|
C | CTTT | 9 | a0001c0001t0014a0001c0001t0021a0001c0001t0039others(6): Show | 16 | HG01261.hp2 HG01361.hp1 HG01516.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*10704_*10706dupTT others(1): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12769 | INFO_REALIGN_3_PRIME | chr12 | 68669935 | ||||
| chr12:68669935
|
CTT | C | 3 | a0001c0001t0005a0001c0001t0025a0001c0001t0115 | 18 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*10705_*10706delTT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12767 | INFO_REALIGN_3_PRIME | chr12 | 68669935 | ||||
| chr12:68669947
|
T | C | 1 | a0001c0001t0128 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10698T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12760 | chr12 | 68669947 | |||||
| chr12:68670090
|
C | A | 1 | a0001c0001t0071 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10841C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 12903 | chr12 | 68670090 | |||||
| chr12:68670211
|
C | A | 1 | a0001c0001t0083 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10962C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13024 | chr12 | 68670211 | |||||
| chr12:68670233
|
G | T | 1 | a0001c0001t0085 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10984G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13046 | chr12 | 68670233 | |||||
| chr12:68670819
|
A | G | 1 | a0001c0001t0048 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11570A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13632 | chr12 | 68670819 | |||||
| chr12:68670845
|
G | A | 1 | a0001c0001t0104 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11596G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13658 | chr12 | 68670845 | |||||
| chr12:68671016
|
G | A | 2 | a0001c0001t0041a0001c0001t0118 | 3 | NA19004.hp2 NA19062.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11767G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13829 | chr12 | 68671016 | |||||
| chr12:68671027
|
T | TA | 11 | a0001c0001t0006a0001c0001t0018a0001c0001t0035others(8): Show | 25 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*11799dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13862 | INFO_REALIGN_3_PRIME | chr12 | 68671027 | ||||
| chr12:68671027
|
TA | T | 13 | a0001c0001t0013a0001c0001t0026a0001c0001t0042others(10): Show | 18 | HG01069.hp1 HG01074.hp2 HG01256.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*11799delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13861 | INFO_REALIGN_3_PRIME | chr12 | 68671027 | ||||
| chr12:68671181
|
C | T | 1 | a0001c0001t0064 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11932C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 13994 | chr12 | 68671181 | |||||
| chr12:68671198
|
C | T | 19 | a0001c0001t0002a0001c0001t0019a0001c0001t0021others(16): Show | 67 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*11949C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 14011 | chr12 | 68671198 | |||||
| chr12:68671415
|
T | C | 2 | a0001c0001t0123a0001c0001t0124 | 2 | HG03209.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12166T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 14228 | chr12 | 68671415 | |||||
| chr12:68671551
|
G | A | 1 | a0001c0001t0074 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12302G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 8/8 | 14364 | chr12 | 68671551 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68611086
|
GCGGCCGC others(14): Show |
G | 1 | a0001c0001t0097g0371 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-27+48_-27+68delCG others(19): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68611086 | |||||
| chr12:68611095
|
CG | C | 18 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(15): Show | 20 | HG00639.hp2 HG01069.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-27+56delG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68611095 | |||||
| chr12:68611170
|
G | A | 1 | a0001c0001t0034g0031 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-27+127G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611170 | ||||||
| chr12:68611188
|
G | A | 65 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(62): Show | 65 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-27+145G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611188 | ||||||
| chr12:68611225
|
C | G | 34 | a0001c0001t0001g0014a0001c0001t0001g0360a0001c0001t0001g0361others(31): Show | 37 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-27+182C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611225 | ||||||
| chr12:68611291
|
C | T | 1 | a0001c0001t0002g0357 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-27+248C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611291 | ||||||
| chr12:68611346
|
A | T | 55 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0310others(52): Show | 58 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-27+303A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611346 | ||||||
| chr12:68611697
|
T | C | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(370): Show | 386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.-27+654T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611697 | ||||||
| chr12:68611892
|
C | T | 2 | a0001c0001t0006g0090a0001c0001t0006g0091 | 2 | NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-27+849C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68611892 | ||||||
| chr12:68612081
|
G | T | 1 | a0001c0001t0003g0356 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-27+1038G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612081 | ||||||
| chr12:68612164
|
C | G | 1 | a0001c0001t0084g0304 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-27+1121C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612164 | ||||||
| chr12:68612198
|
T | C | 2 | a0001c0001t0006g0090a0001c0001t0006g0091 | 2 | NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-27+1155T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612198 | ||||||
| chr12:68612208
|
G | A | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+1165G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612208 | ||||||
| chr12:68612263
|
C | T | 179 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(176): Show | 185 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-27+1220C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612263 | ||||||
| chr12:68612624
|
T | G | 1 | a0001c0001t0010g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-27+1581T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612624 | ||||||
| chr12:68612699
|
T | C | 1 | a0001c0001t0012g0094 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-27+1656T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612699 | ||||||
| chr12:68612723
|
T | C | 2 | a0001c0001t0005g0004a0001c0001t0005g0018 | 3 | HG02818.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-27+1680T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612723 | ||||||
| chr12:68612734
|
T | C | 1 | a0001c0001t0097g0371 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-27+1691T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612734 | ||||||
| chr12:68612755
|
ATAGTCTT others(61): Show |
A | 1 | a0001c0001t0088g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27+1781_-27+1848d others(70): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68612755 | |||||
| chr12:68612905
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-27+1862A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68612905 | ||||||
| chr12:68613030
|
C | G | 1 | a0001c0001t0129g0370 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-27+1987C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613030 | ||||||
| chr12:68613088
|
T | C | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+2045T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613088 | ||||||
| chr12:68613294
|
T | C | 2 | a0001c0001t0002g0095a0001c0001t0002g0096 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27+2251T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613294 | ||||||
| chr12:68613389
|
T | TA | 133 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0107others(130): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-27+2365dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68613389 | |||||
| chr12:68613389
|
T | TAA | 18 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(15): Show | 19 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+2364_-27+2365d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68613389 | |||||
| chr12:68613389
|
TA | T | 11 | a0001c0001t0001g0257a0001c0001t0001g0259a0001c0001t0004g0089others(8): Show | 11 | HG01081.hp1 HG01361.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.-27+2365delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68613389 | |||||
| chr12:68613424
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-27+2381A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613424 | ||||||
| chr12:68613502
|
T | C | 12 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(9): Show | 14 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27+2459T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613502 | ||||||
| chr12:68613684
|
A | C | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+2641A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613684 | ||||||
| chr12:68613798
|
T | C | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+2755T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613798 | ||||||
| chr12:68613842
|
T | C | 2 | a0001c0001t0004g0033a0001c0001t0006g0034 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-27+2799T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68613842 | ||||||
| chr12:68614172
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-27+3129C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614172 | ||||||
| chr12:68614284
|
C | T | 2 | a0001c0001t0123g0250a0001c0001t0124g0251 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+3241C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614284 | ||||||
| chr12:68614291
|
A | G | 1 | a0001c0001t0126g0288 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-27+3248A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614291 | ||||||
| chr12:68614299
|
A | G | 1 | a0001c0001t0023g0287 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-27+3256A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614299 | ||||||
| chr12:68614492
|
T | C | 1 | a0001c0001t0031g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-27+3449T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614492 | ||||||
| chr12:68614621
|
A | AG | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+3580dupG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68614621 | |||||
| chr12:68614862
|
C | T | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+3819C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68614862 | ||||||
| chr12:68615186
|
A | C | 2 | a0001c0001t0016g0249a0001c0001t0121g0248 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-27+4143A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615186 | ||||||
| chr12:68615193
|
A | AT | 8 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(5): Show | 8 | HG02015.hp2 HG02027.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27+4153dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68615193 | |||||
| chr12:68615332
|
C | T | 1 | a0001c0001t0008g0354 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-27+4289C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615332 | ||||||
| chr12:68615875
|
C | A | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+4832C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615875 | ||||||
| chr12:68615936
|
C | A | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+4893C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615936 | ||||||
| chr12:68615967
|
AT | A | 256 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(253): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-27+4938delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68615967 | |||||
| chr12:68615982
|
G | A | 3 | a0001c0001t0023g0263a0001c0001t0023g0267a0001c0001t0073g0268 | 3 | HG00738.hp1 HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-27+4939G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68615982 | ||||||
| chr12:68616027
|
G | A | 1 | a0001c0001t0090g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+4984G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616027 | ||||||
| chr12:68616242
|
G | A | 1 | a0001c0001t0058g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-27+5199G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616242 | ||||||
| chr12:68616251
|
T | C | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+5208T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616251 | ||||||
| chr12:68616273
|
G | T | 1 | a0001c0001t0104g0171 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-27+5230G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616273 | ||||||
| chr12:68616330
|
G | A | 1 | a0001c0001t0031g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-27+5287G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616330 | ||||||
| chr12:68616438
|
A | AT | 40 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0238others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.-27+5421dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | |||||
| chr12:68616438
|
AT | A | 66 | a0001c0001t0001g0173a0001c0001t0001g0261a0001c0001t0001g0360others(63): Show | 69 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-27+5421delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | |||||
| chr12:68616438
|
ATT | A | 45 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0284others(42): Show | 48 | HG00280.hp2 HG00438.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-27+5420_-27+5421d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | |||||
| chr12:68616438
|
ATTT | A | 21 | a0001c0001t0003g0264a0001c0001t0003g0269a0001c0001t0003g0270others(18): Show | 21 | HG00738.hp1 HG02602.hp2 HG02698.hp1 others(18): Show |
intron_variant | MODIFIER | c.-27+5419_-27+5421d others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | |||||
| chr12:68616438
|
ATTTTTTT others(3): Show |
A | 25 | a0001c0001t0004g0040a0001c0001t0004g0041a0001c0001t0004g0043others(22): Show | 25 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-27+5412_-27+5421d others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | |||||
| chr12:68616438
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0004g0037a0001c0001t0006g0038 | 2 | NA18949.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-27+5411_-27+5421d others(13): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68616438 | |||||
| chr12:68616577
|
G | A | 4 | a0001c0001t0024g0153a0001c0001t0024g0154a0001c0001t0049g0151others(1): Show | 4 | HG02293.hp1 HG02922.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+5534G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616577 | ||||||
| chr12:68616583
|
A | C | 2 | a0001c0001t0002g0138a0001c0001t0109g0139 | 2 | NA18964.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-27+5540A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616583 | ||||||
| chr12:68616719
|
C | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+5676C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616719 | ||||||
| chr12:68616781
|
A | G | 1 | a0001c0001t0051g0078 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-27+5738A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616781 | ||||||
| chr12:68616851
|
C | T | 1 | a0001c0001t0007g0077 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-27+5808C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68616851 | ||||||
| chr12:68617094
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-27+6051C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617094 | ||||||
| chr12:68617481
|
A | G | 1 | a0001c0001t0041g0308 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-27+6438A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617481 | ||||||
| chr12:68617581
|
A | G | 1 | a0001c0001t0053g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-27+6538A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617581 | ||||||
| chr12:68617719
|
A | G | 4 | a0001c0001t0009g0266a0001c0001t0009g0298a0001c0001t0009g0299others(1): Show | 4 | HG02145.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+6676A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617719 | ||||||
| chr12:68617735
|
G | A | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+6692G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617735 | ||||||
| chr12:68617747
|
AACCATAA others(14): Show |
A | 4 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(1): Show | 4 | NA18951.hp2 NA18972.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+6705_-27+6725d others(23): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617747 | ||||||
| chr12:68617774
|
A | AT | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(18): Show | 24 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27+6742dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68617774 | |||||
| chr12:68617839
|
C | T | 2 | a0001c0001t0009g0302a0001c0001t0009g0303 | 2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-27+6796C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617839 | ||||||
| chr12:68617910
|
C | A | 1 | a0001c0001t0028g0166 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-27+6867C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68617910 | ||||||
| chr12:68618025
|
A | G | 2 | a0001c0001t0028g0166a0001c0001t0028g0170 | 2 | HG00099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-27+6982A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618025 | ||||||
| chr12:68618082
|
A | G | 1 | a0001c0001t0119g0349 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-27+7039A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618082 | ||||||
| chr12:68618086
|
C | CT | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(167): Show | 176 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.-27+7068dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | |||||
| chr12:68618086
|
C | CTT | 23 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0245others(20): Show | 23 | HG00621.hp2 HG00735.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.-27+7067_-27+7068d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | |||||
| chr12:68618086
|
C | CTTT | 14 | a0001c0001t0001g0233a0001c0001t0003g0010a0001c0001t0003g0269others(11): Show | 15 | HG01106.hp2 HG01109.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-27+7066_-27+7068d others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | |||||
| chr12:68618086
|
C | CTTTT | 51 | a0001c0001t0003g0011a0001c0001t0003g0270a0001c0001t0003g0273others(48): Show | 52 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.-27+7065_-27+7068d others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | |||||
| chr12:68618086
|
C | CTTTTT | 19 | a0001c0001t0003g0264a0001c0001t0003g0279a0001c0001t0003g0280others(16): Show | 20 | HG00423.hp2 HG01175.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.-27+7064_-27+7068d others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | |||||
| chr12:68618086
|
CTTTTTTT others(2): Show |
C | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+7060_-27+7068d others(11): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618086 | |||||
| chr12:68618150
|
C | T | 2 | a0001c0001t0002g0131a0001c0001t0108g0144 | 2 | HG02258.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-27+7107C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618150 | ||||||
| chr12:68618174
|
G | GC | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+7132dupC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618174 | |||||
| chr12:68618204
|
A | G | 1 | a0001c0001t0006g0038 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-27+7161A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618204 | ||||||
| chr12:68618280
|
G | A | 2 | a0001c0001t0006g0090a0001c0001t0006g0091 | 2 | NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-27+7237G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618280 | ||||||
| chr12:68618310
|
G | A | 1 | a0001c0001t0126g0288 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-27+7267G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618310 | ||||||
| chr12:68618315
|
C | T | 1 | a0001c0001t0011g0092 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-27+7272C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618315 | ||||||
| chr12:68618683
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-27+7640G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68618683 | ||||||
| chr12:68618698
|
CTGTCCTA others(8): Show |
C | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+7659_-27+7673d others(17): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618698 | |||||
| chr12:68618740
|
ATTT | A | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+7704_-27+7706d others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68618740 | |||||
| chr12:68619040
|
C | T | 1 | a0001c0001t0019g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-27+7997C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619040 | ||||||
| chr12:68619055
|
G | A | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+8012G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619055 | ||||||
| chr12:68619361
|
G | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0100a0001c0001t0002g0101others(58): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-27+8318G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619361 | ||||||
| chr12:68619466
|
GAA | G | 7 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(4): Show | 7 | HG00558.hp1 HG02027.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+8425_-27+8426d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68619466 | |||||
| chr12:68619550
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-27+8507A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619550 | ||||||
| chr12:68619637
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-27+8594G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619637 | ||||||
| chr12:68619661
|
T | C | 1 | a0001c0001t0101g0355 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-27+8618T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619661 | ||||||
| chr12:68619894
|
A | G | 2 | a0001c0001t0063g0152a0001c0001t0078g0222 | 2 | NA18940.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-27+8851A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619894 | ||||||
| chr12:68619895
|
T | C | 1 | a0001c0001t0099g0314 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-27+8852T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619895 | ||||||
| chr12:68619943
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-27+8900C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68619943 | ||||||
| chr12:68620032
|
T | C | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+8989T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620032 | ||||||
| chr12:68620036
|
T | C | 1 | a0001c0001t0127g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-27+8993T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620036 | ||||||
| chr12:68620055
|
A | G | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+9012A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620055 | ||||||
| chr12:68620111
|
G | C | 4 | a0001c0001t0004g0006a0001c0001t0004g0061a0001c0001t0004g0062others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+9068G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620111 | ||||||
| chr12:68620207
|
T | A | 67 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-27+9164T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620207 | ||||||
| chr12:68620450
|
T | G | 24 | a0001c0001t0003g0264a0001c0001t0003g0269a0001c0001t0003g0270others(21): Show | 24 | HG00738.hp1 HG02074.hp1 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27+9407T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620450 | ||||||
| chr12:68620502
|
C | G | 1 | a0001c0001t0114g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-27+9459C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620502 | ||||||
| chr12:68620606
|
C | CT | 77 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(74): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.-27+9577dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68620606 | |||||
| chr12:68620825
|
C | T | 1 | a0001c0001t0006g0091 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-27+9782C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620825 | ||||||
| chr12:68620878
|
G | A | 1 | a0001c0001t0033g0224 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-27+9835G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620878 | ||||||
| chr12:68620951
|
G | A | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+9908G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68620951 | ||||||
| chr12:68621105
|
A | T | 1 | a0001c0001t0088g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27+10062A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621105 | ||||||
| chr12:68621130
|
A | C | 18 | a0001c0001t0004g0051a0001c0001t0004g0087a0001c0001t0006g0038others(15): Show | 18 | HG00544.hp1 HG00621.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+10087A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621130 | ||||||
| chr12:68621132
|
G | A | 1 | a0001c0001t0126g0288 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-27+10089G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621132 | ||||||
| chr12:68621232
|
C | T | 1 | a0001c0001t0014g0221 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-27+10189C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621232 | ||||||
| chr12:68621253
|
ATAAT | A | 63 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(60): Show | 63 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.-27+10214_-27+1021 others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68621253 | |||||
| chr12:68621280
|
A | G | 1 | a0001c0001t0015g0336 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-27+10237A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621280 | ||||||
| chr12:68621349
|
CACTGACT others(3): Show |
C | 1 | a0001c0001t0104g0171 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-27+10308_-27+1031 others(14): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68621349 | |||||
| chr12:68621558
|
G | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+10515G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621558 | ||||||
| chr12:68621875
|
T | C | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+10832T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68621875 | ||||||
| chr12:68622139
|
C | T | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+11096C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622139 | ||||||
| chr12:68622227
|
A | G | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+11184A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622227 | ||||||
| chr12:68622294
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-27+11251C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622294 | ||||||
| chr12:68622453
|
C | A | 1 | a0001c0001t0003g0270 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-27+11410C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622453 | ||||||
| chr12:68622584
|
A | G | 1 | a0001c0001t0003g0264 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-27+11541A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622584 | ||||||
| chr12:68622622
|
C | T | 4 | a0001c0001t0039g0255a0001c0001t0039g0260a0001c0001t0044g0254others(1): Show | 4 | HG01361.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+11579C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622622 | ||||||
| chr12:68622734
|
A | T | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+11691A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622734 | ||||||
| chr12:68622736
|
C | G | 1 | a0001c0001t0007g0077 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-27+11693C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68622736 | ||||||
| chr12:68623016
|
A | G | 1 | a0001c0001t0034g0031 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-27+11973A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623016 | ||||||
| chr12:68623030
|
A | G | 2 | a0001c0001t0003g0334a0001c0001t0130g0335 | 2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-27+11987A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623030 | ||||||
| chr12:68623065
|
C | T | 1 | a0001c0001t0010g0220 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-27+12022C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623065 | ||||||
| chr12:68623144
|
A | C | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+12101A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623144 | ||||||
| chr12:68623199
|
T | G | 80 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(77): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+12156T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623199 | ||||||
| chr12:68623266
|
G | A | 1 | a0001c0001t0114g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-27+12223G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623266 | ||||||
| chr12:68623361
|
A | C | 1 | a0001c0001t0062g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-27+12318A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623361 | ||||||
| chr12:68623497
|
T | G | 1 | a0001c0001t0092g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-27+12454T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623497 | ||||||
| chr12:68623629
|
G | A | 185 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(182): Show | 191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-27+12586G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623629 | ||||||
| chr12:68623781
|
G | A | 1 | a0001c0001t0001g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-27+12738G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623781 | ||||||
| chr12:68623838
|
C | T | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+12795C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623838 | ||||||
| chr12:68623839
|
G | A | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+12796G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623839 | ||||||
| chr12:68623877
|
C | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+12834C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623877 | ||||||
| chr12:68623973
|
A | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+12930A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623973 | ||||||
| chr12:68623975
|
T | C | 350 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(347): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.-27+12932T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68623975 | ||||||
| chr12:68624038
|
A | AG | 2 | a0001c0001t0022g0012a0001c0001t0022g0333 | 3 | NA18951.hp1 NA19064.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-27+12995_-27+1299 others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624038 | ||||||
| chr12:68624445
|
C | A | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+13402C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624445 | ||||||
| chr12:68624457
|
A | G | 1 | a0001c0001t0097g0371 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-27+13414A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624457 | ||||||
| chr12:68624618
|
C | G | 1 | a0001c0001t0002g0129 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-27+13575C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624618 | ||||||
| chr12:68624653
|
T | TA | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+13615dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68624653 | |||||
| chr12:68624661
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-27+13618T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624661 | ||||||
| chr12:68624703
|
C | G | 3 | a0001c0001t0010g0207a0001c0001t0010g0220a0001c0001t0111g0242 | 3 | HG00673.hp2 NA18612.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-27+13660C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624703 | ||||||
| chr12:68624721
|
A | G | 1 | a0001c0001t0010g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-27+13678A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624721 | ||||||
| chr12:68624746
|
C | G | 1 | a0001c0001t0042g0347 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-27+13703C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624746 | ||||||
| chr12:68624856
|
A | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+13813A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624856 | ||||||
| chr12:68624943
|
G | T | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+13900G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68624943 | ||||||
| chr12:68625014
|
C | T | 1 | a0001c0001t0003g0346 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-27+13971C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625014 | ||||||
| chr12:68625158
|
C | T | 3 | a0001c0001t0050g0017a0001c0001t0082g0016a0001c0001t0087g0015 | 3 | HG00639.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-27+14115C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625158 | ||||||
| chr12:68625254
|
G | T | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+14211G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625254 | ||||||
| chr12:68625299
|
C | G | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+14256C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625299 | ||||||
| chr12:68625327
|
T | A | 1 | a0001c0001t0002g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-27+14284T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625327 | ||||||
| chr12:68625570
|
A | G | 1 | a0001c0001t0008g0332 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-27+14527A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625570 | ||||||
| chr12:68625624
|
T | A | 1 | a0001c0001t0011g0060 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-27+14581T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625624 | ||||||
| chr12:68625625
|
T | A | 1 | a0001c0001t0011g0060 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-27+14582T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625625 | ||||||
| chr12:68625668
|
C | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+14625C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625668 | ||||||
| chr12:68625685
|
C | T | 2 | a0001c0001t0008g0330a0001c0001t0008g0331 | 2 | NA18973.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-27+14642C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625685 | ||||||
| chr12:68625751
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-27+14708G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625751 | ||||||
| chr12:68625778
|
C | T | 1 | a0001c0001t0083g0206 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-27+14735C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625778 | ||||||
| chr12:68625791
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-27+14748G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625791 | ||||||
| chr12:68625848
|
G | A | 1 | a0001c0001t0127g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-27+14805G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625848 | ||||||
| chr12:68625876
|
C | T | 66 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(63): Show | 66 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-27+14833C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625876 | ||||||
| chr12:68625899
|
C | T | 3 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0103 | 3 | HG01496.hp1 HG02300.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-27+14856C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68625899 | ||||||
| chr12:68625920
|
CA | C | 20 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(17): Show | 22 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+14892delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68625920 | |||||
| chr12:68626075
|
A | G | 1 | a0001c0001t0115g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-27+15032A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626075 | ||||||
| chr12:68626142
|
A | C | 1 | a0001c0001t0129g0370 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-27+15099A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626142 | ||||||
| chr12:68626178
|
C | T | 1 | a0001c0001t0006g0058 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-27+15135C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626178 | ||||||
| chr12:68626213
|
A | G | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27+15170A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626213 | ||||||
| chr12:68626227
|
G | C | 1 | a0001c0001t0066g0162 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-27+15184G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626227 | ||||||
| chr12:68626705
|
C | T | 12 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(9): Show | 14 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27+15662C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626705 | ||||||
| chr12:68626723
|
C | T | 3 | a0001c0001t0032g0362a0001c0001t0032g0366a0001c0001t0060g0365 | 3 | HG02451.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-27+15680C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626723 | ||||||
| chr12:68626785
|
GTTGT | G | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+15761_-27+1576 others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68626785 | |||||
| chr12:68626872
|
A | T | 3 | a0001c0001t0016g0143a0001c0001t0016g0249a0001c0001t0121g0248 | 3 | HG01256.hp1 HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-27+15829A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626872 | ||||||
| chr12:68626929
|
G | A | 2 | a0001c0001t0007g0063a0001c0001t0027g0064 | 2 | NA18955.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-27+15886G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626929 | ||||||
| chr12:68626963
|
C | G | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+15920C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626963 | ||||||
| chr12:68626971
|
C | A | 2 | a0001c0001t0123g0250a0001c0001t0124g0251 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+15928C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68626971 | ||||||
| chr12:68627031
|
G | C | 1 | a0001c0001t0003g0315 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-27+15988G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627031 | ||||||
| chr12:68627173
|
G | C | 1 | a0001c0001t0064g0047 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-27+16130G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627173 | ||||||
| chr12:68627263
|
CATACA | C | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+16227_-27+1623 others(9): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68627263 | |||||
| chr12:68627467
|
T | A | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-27+16424T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627467 | ||||||
| chr12:68627479
|
A | G | 3 | a0001c0001t0037g0289a0001c0001t0037g0290a0001c0001t0088g0262 | 3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-27+16436A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627479 | ||||||
| chr12:68627503
|
G | A | 1 | a0001c0001t0004g0040 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-27+16460G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627503 | ||||||
| chr12:68627576
|
T | C | 2 | a0001c0001t0123g0250a0001c0001t0124g0251 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-27+16533T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627576 | ||||||
| chr12:68627693
|
G | A | 1 | a0001c0001t0106g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-27+16650G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627693 | ||||||
| chr12:68627946
|
T | A | 1 | a0001c0001t0001g0179 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-27+16903T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627946 | ||||||
| chr12:68627947
|
A | T | 4 | a0001c0001t0020g0345a0001c0001t0026g0013a0001c0001t0042g0347others(1): Show | 5 | HG01256.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+16904A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627947 | ||||||
| chr12:68627957
|
A | G | 1 | a0001c0001t0014g0221 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-27+16914A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627957 | ||||||
| chr12:68627984
|
A | G | 1 | a0001c0001t0090g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+16941A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68627984 | ||||||
| chr12:68628416
|
C | G | 3 | a0001c0001t0002g0146a0001c0001t0002g0148a0001c0001t0002g0150 | 3 | HG02027.hp1 HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-27+17373C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628416 | ||||||
| chr12:68628449
|
G | T | 3 | a0001c0001t0053g0165a0001c0001t0059g0161a0001c0001t0067g0253 | 3 | HG02976.hp1 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-27+17406G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628449 | ||||||
| chr12:68628516
|
C | G | 69 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(66): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-27+17473C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628516 | ||||||
| chr12:68628660
|
T | A | 266 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(263): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-27+17617T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628660 | ||||||
| chr12:68628876
|
A | G | 1 | a0001c0001t0006g0055 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-27+17833A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628876 | ||||||
| chr12:68628925
|
A | G | 3 | a0001c0001t0011g0060a0001c0001t0011g0075a0001c0001t0011g0092 | 3 | NA18946.hp1 NA18953.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-27+17882A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628925 | ||||||
| chr12:68628988
|
C | G | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+17945C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68628988 | ||||||
| chr12:68629013
|
A | ATCTG | 74 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(71): Show | 77 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-27+17986_-27+1798 others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68629013 | |||||
| chr12:68629013
|
A | ATCTGTCT others(1): Show |
3 | a0001c0001t0041g0308a0001c0001t0046g0312a0001c0001t0046g0313 | 3 | NA18939.hp2 NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-27+17982_-27+1798 others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68629013 | |||||
| chr12:68629018
|
T | G | 69 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(66): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-27+17975T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629018 | ||||||
| chr12:68629039
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-27+17996A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629039 | ||||||
| chr12:68629247
|
A | G | 2 | a0001c0001t0009g0296a0001c0001t0070g0295 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-27+18204A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629247 | ||||||
| chr12:68629269
|
G | C | 1 | a0001c0001t0008g0332 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-27+18226G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629269 | ||||||
| chr12:68629319
|
C | G | 1 | a0001c0001t0020g0285 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-27+18276C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629319 | ||||||
| chr12:68629494
|
G | A | 1 | a0001c0001t0090g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+18451G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629494 | ||||||
| chr12:68629680
|
T | C | 1 | a0001c0001t0086g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-27+18637T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629680 | ||||||
| chr12:68629682
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0241 | 2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-27+18639C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68629682 | ||||||
| chr12:68630111
|
C | G | 1 | a0001c0001t0129g0370 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-26-18588C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630111 | ||||||
| chr12:68630331
|
C | T | 1 | a0001c0001t0025g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-26-18368C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630331 | ||||||
| chr12:68630487
|
T | C | 3 | a0001c0001t0003g0010a0001c0001t0003g0310a0001c0001t0015g0352 | 4 | HG00438.hp1 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-18212T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630487 | ||||||
| chr12:68630608
|
G | A | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-18091G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630608 | ||||||
| chr12:68630746
|
C | T | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-17953C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630746 | ||||||
| chr12:68630764
|
A | G | 1 | a0001c0001t0104g0171 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26-17935A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630764 | ||||||
| chr12:68630778
|
A | G | 4 | a0001c0001t0039g0255a0001c0001t0039g0260a0001c0001t0044g0254others(1): Show | 4 | HG01361.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-17921A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630778 | ||||||
| chr12:68630915
|
G | A | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-17784G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630915 | ||||||
| chr12:68630932
|
G | GT | 11 | a0001c0001t0002g0001a0001c0001t0002g0125a0001c0001t0002g0126others(8): Show | 12 | HG02486.hp2 HG02622.hp1 NA18968.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-17757dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68630932 | |||||
| chr12:68630932
|
G | T | 1 | a0001c0001t0008g0344 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-26-17767G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630932 | ||||||
| chr12:68630936
|
T | C | 1 | a0001c0001t0125g0168 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26-17763T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630936 | ||||||
| chr12:68630962
|
G | A | 1 | a0001c0001t0020g0285 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-26-17737G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68630962 | ||||||
| chr12:68631045
|
C | G | 2 | a0001c0001t0003g0328a0001c0001t0003g0329 | 2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-26-17654C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631045 | ||||||
| chr12:68631046
|
C | T | 1 | a0001c0001t0004g0076 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-26-17653C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631046 | ||||||
| chr12:68631279
|
T | C | 1 | a0001c0001t0119g0349 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-26-17420T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631279 | ||||||
| chr12:68631577
|
C | T | 2 | a0001c0001t0123g0250a0001c0001t0124g0251 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-26-17122C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631577 | ||||||
| chr12:68631620
|
A | C | 1 | a0001c0001t0002g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-26-17079A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631620 | ||||||
| chr12:68631841
|
G | T | 1 | a0001c0001t0006g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-26-16858G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68631841 | ||||||
| chr12:68632035
|
A | G | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-16664A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632035 | ||||||
| chr12:68632050
|
GT | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-16639delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632050 | |||||
| chr12:68632086
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-26-16613A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632086 | ||||||
| chr12:68632128
|
T | G | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-16571T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632128 | ||||||
| chr12:68632129
|
G | GT | 27 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(24): Show | 27 | HG00438.hp1 HG01361.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.-26-16554dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632129 | |||||
| chr12:68632129
|
G | T | 2 | a0001c0001t0043g0311a0001c0001t0043g0339 | 2 | NA18955.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-26-16570G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632129 | ||||||
| chr12:68632129
|
GT | G | 10 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0205others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-16554delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632129 | |||||
| chr12:68632132
|
T | G | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-16567T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632132 | ||||||
| chr12:68632137
|
T | TTG | 6 | a0001c0001t0005g0004a0001c0001t0005g0018a0001c0001t0005g0021others(3): Show | 7 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-16561_-26-1656 others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632137 | |||||
| chr12:68632138
|
T | G | 2 | a0001c0001t0020g0285a0001c0001t0045g0110 | 2 | HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-26-16561T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632138 | ||||||
| chr12:68632138
|
T | TG | 9 | a0001c0001t0005g0005a0001c0001t0005g0019a0001c0001t0005g0020others(6): Show | 10 | HG01069.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-26-16561_-26-1656 others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632138 | ||||||
| chr12:68632140
|
T | G | 8 | a0001c0001t0001g0223a0001c0001t0024g0153a0001c0001t0024g0154others(5): Show | 8 | HG00639.hp2 HG02293.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-16559T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632140 | ||||||
| chr12:68632141
|
T | G | 11 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0205others(8): Show | 11 | HG00738.hp1 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26-16558T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632141 | ||||||
| chr12:68632142
|
T | G | 83 | a0001c0001t0001g0225a0001c0001t0001g0232a0001c0001t0001g0245others(80): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.-26-16557T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632142 | ||||||
| chr12:68632143
|
T | G | 2 | a0001c0001t0041g0308a0001c0001t0046g0312 | 2 | NA19082.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-26-16556T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632143 | ||||||
| chr12:68632143
|
TTTGTTTG | T | 67 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-26-16553_-26-1654 others(11): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632143 | |||||
| chr12:68632144
|
TTGTTTG | T | 13 | a0001c0001t0004g0037a0001c0001t0004g0040a0001c0001t0004g0089others(10): Show | 13 | HG00597.hp1 HG02040.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-26-16553_-26-1654 others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68632144 | |||||
| chr12:68632145
|
T | G | 10 | a0001c0001t0001g0179a0001c0001t0003g0280a0001c0001t0010g0093others(7): Show | 10 | HG00639.hp2 HG02293.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-26-16554T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632145 | ||||||
| chr12:68632146
|
G | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(134): Show | 145 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.-26-16553G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632146 | ||||||
| chr12:68632150
|
G | T | 27 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0205others(24): Show | 29 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.-26-16549G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632150 | ||||||
| chr12:68632151
|
T | G | 10 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0205others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-16548T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632151 | ||||||
| chr12:68632154
|
T | G | 3 | a0001c0001t0002g0167a0001c0001t0002g0247a0001c0001t0057g0098 | 3 | HG01516.hp1 HG02040.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-26-16545T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632154 | ||||||
| chr12:68632155
|
T | G | 5 | a0001c0001t0003g0286a0001c0001t0024g0153a0001c0001t0024g0154others(2): Show | 5 | HG02293.hp1 HG02922.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26-16544T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632155 | ||||||
| chr12:68632156
|
T | G | 1 | a0001c0001t0001g0209 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-26-16543T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632156 | ||||||
| chr12:68632160
|
T | C | 80 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(77): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-16539T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632160 | ||||||
| chr12:68632505
|
C | T | 1 | a0001c0001t0011g0060 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-26-16194C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632505 | ||||||
| chr12:68632526
|
A | G | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-16173A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632526 | ||||||
| chr12:68632577
|
G | C | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-16122G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632577 | ||||||
| chr12:68632700
|
A | G | 1 | a0001c0001t0003g0283 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-26-15999A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632700 | ||||||
| chr12:68632934
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-26-15765G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632934 | ||||||
| chr12:68632947
|
T | C | 1 | a0001c0001t0028g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-26-15752T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68632947 | ||||||
| chr12:68633029
|
T | A | 1 | a0001c0001t0125g0168 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26-15670T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633029 | ||||||
| chr12:68633050
|
A | T | 1 | a0001c0001t0003g0264 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-26-15649A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633050 | ||||||
| chr12:68633132
|
G | A | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-15567G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633132 | ||||||
| chr12:68633148
|
A | G | 1 | a0001c0001t0003g0337 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-26-15551A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633148 | ||||||
| chr12:68633153
|
A | T | 1 | a0001c0001t0031g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-26-15546A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633153 | ||||||
| chr12:68633173
|
A | G | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-15526A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633173 | ||||||
| chr12:68633389
|
A | G | 5 | a0001c0001t0028g0166a0001c0001t0028g0170a0001c0001t0053g0165others(2): Show | 5 | HG00099.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-15310A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633389 | ||||||
| chr12:68633461
|
G | A | 1 | a0001c0001t0003g0270 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-26-15238G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633461 | ||||||
| chr12:68633943
|
G | A | 1 | a0001c0001t0036g0210 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-26-14756G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68633943 | ||||||
| chr12:68634093
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0360a0001c0001t0001g0361others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-26-14606C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634093 | ||||||
| chr12:68634309
|
T | G | 3 | a0001c0001t0090g0036a0001c0001t0091g0083a0001c0001t0092g0088 | 3 | HG02486.hp1 HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-26-14390T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634309 | ||||||
| chr12:68634319
|
A | G | 1 | a0001c0001t0010g0220 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-26-14380A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634319 | ||||||
| chr12:68634327
|
A | G | 3 | a0001c0001t0004g0040a0001c0001t0004g0044a0001c0001t0065g0085 | 3 | NA18961.hp1 NA18978.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-26-14372A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634327 | ||||||
| chr12:68634349
|
C | T | 1 | a0001c0001t0112g0319 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-26-14350C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634349 | ||||||
| chr12:68634391
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-26-14308A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634391 | ||||||
| chr12:68634450
|
C | T | 5 | a0001c0001t0028g0166a0001c0001t0028g0170a0001c0001t0053g0165others(2): Show | 5 | HG00099.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-14249C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634450 | ||||||
| chr12:68634582
|
A | AT | 3 | a0001c0001t0005g0020a0001c0001t0026g0013a0001c0001t0048g0358 | 4 | HG01516.hp2 HG01517.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-14115dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68634582 | |||||
| chr12:68634585
|
A | AT | 8 | a0001c0001t0001g0180a0001c0001t0004g0044a0001c0001t0010g0220others(5): Show | 8 | HG00673.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26-14103dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68634585 | |||||
| chr12:68634585
|
A | ATT | 61 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-26-14104_-26-1410 others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68634585 | |||||
| chr12:68634585
|
A | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 20 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26-14114A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634585 | ||||||
| chr12:68634629
|
T | TA | 4 | a0001c0001t0024g0153a0001c0001t0024g0154a0001c0001t0049g0151others(1): Show | 4 | HG02293.hp1 HG02922.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-14064dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68634629 | |||||
| chr12:68634781
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-26-13918A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634781 | ||||||
| chr12:68634811
|
C | T | 1 | a0001c0001t0034g0031 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-26-13888C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634811 | ||||||
| chr12:68634824
|
A | G | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-13875A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634824 | ||||||
| chr12:68634912
|
G | C | 1 | a0001c0001t0003g0320 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-26-13787G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68634912 | ||||||
| chr12:68635126
|
A | G | 1 | a0001c0001t0004g0043 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-26-13573A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635126 | ||||||
| chr12:68635158
|
A | C | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-13541A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635158 | ||||||
| chr12:68635192
|
G | A | 1 | a0001c0001t0025g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-26-13507G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635192 | ||||||
| chr12:68635213
|
G | A | 2 | a0001c0001t0003g0328a0001c0001t0003g0329 | 2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-26-13486G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635213 | ||||||
| chr12:68635555
|
A | G | 1 | a0001c0001t0003g0282 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-26-13144A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635555 | ||||||
| chr12:68635622
|
A | G | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-13077A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635622 | ||||||
| chr12:68635643
|
C | T | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-13056C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635643 | ||||||
| chr12:68635657
|
A | G | 1 | a0001c0001t0100g0326 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-26-13042A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635657 | ||||||
| chr12:68635682
|
T | A | 1 | a0001c0001t0003g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-26-13017T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635682 | ||||||
| chr12:68635882
|
T | TGCA | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-12816_-26-1281 others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68635882 | |||||
| chr12:68635885
|
A | AGAG | 167 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(164): Show | 170 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.-26-12814_-26-1281 others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635885 | ||||||
| chr12:68635885
|
A | G | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-12814A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635885 | ||||||
| chr12:68635902
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-26-12797G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635902 | ||||||
| chr12:68635918
|
G | A | 1 | a0001c0001t0119g0349 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-26-12781G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68635918 | ||||||
| chr12:68636027
|
C | T | 1 | a0001c0001t0104g0171 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26-12672C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636027 | ||||||
| chr12:68636044
|
A | AT | 7 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0159others(4): Show | 8 | HG01516.hp2 HG01517.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-12643dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68636044 | |||||
| chr12:68636068
|
A | G | 2 | a0001c0001t0004g0043a0001c0001t0013g0046 | 2 | NA18992.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-26-12631A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636068 | ||||||
| chr12:68636165
|
A | G | 2 | a0001c0001t0004g0073a0001c0001t0004g0089 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-26-12534A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636165 | ||||||
| chr12:68636356
|
A | G | 3 | a0001c0001t0025g0028a0001c0001t0025g0029a0001c0001t0025g0030 | 3 | HG02257.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-26-12343A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636356 | ||||||
| chr12:68636407
|
A | C | 1 | a0001c0001t0096g0325 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-26-12292A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636407 | ||||||
| chr12:68636574
|
T | C | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-12125T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636574 | ||||||
| chr12:68636725
|
G | GT | 78 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(75): Show | 81 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-26-11965dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68636725 | |||||
| chr12:68636725
|
G | GTT | 18 | a0001c0001t0003g0337a0001c0001t0005g0004a0001c0001t0005g0005others(15): Show | 20 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26-11966_-26-1196 others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68636725 | |||||
| chr12:68636778
|
G | T | 2 | a0001c0001t0116g0169a0001c0001t0117g0163 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-26-11921G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636778 | ||||||
| chr12:68636816
|
G | A | 1 | a0001c0001t0129g0370 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-26-11883G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636816 | ||||||
| chr12:68636915
|
A | G | 2 | a0001c0001t0123g0250a0001c0001t0124g0251 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-26-11784A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68636915 | ||||||
| chr12:68637490
|
G | A | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-11209G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637490 | ||||||
| chr12:68637577
|
T | C | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(292): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-26-11122T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637577 | ||||||
| chr12:68637599
|
C | CA | 47 | a0001c0001t0001g0177a0001c0001t0001g0187a0001c0001t0001g0188others(44): Show | 47 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.-26-11071dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | |||||
| chr12:68637599
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0024g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26-11085_-26-1107 others(19): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | |||||
| chr12:68637599
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0024g0154 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-26-11086_-26-1107 others(20): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | |||||
| chr12:68637599
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0024g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-26-11087_-26-1107 others(21): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | |||||
| chr12:68637599
|
CA | C | 61 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0183others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.-26-11071delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | |||||
| chr12:68637599
|
CAA | C | 115 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(112): Show | 120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-26-11072_-26-1107 others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | |||||
| chr12:68637599
|
CAAA | C | 10 | a0001c0001t0002g0124a0001c0001t0002g0127a0001c0001t0020g0327others(7): Show | 12 | HG01070.hp2 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-11073_-26-1107 others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68637599 | |||||
| chr12:68637610
|
A | C | 1 | a0001c0001t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-26-11089A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637610 | ||||||
| chr12:68637616
|
A | C | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-11083A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637616 | ||||||
| chr12:68637618
|
A | C | 1 | a0001c0001t0069g0293 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-26-11081A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637618 | ||||||
| chr12:68637851
|
C | T | 1 | a0001c0001t0020g0285 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-26-10848C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68637851 | ||||||
| chr12:68638016
|
T | C | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-10683T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638016 | ||||||
| chr12:68638057
|
G | T | 14 | a0001c0001t0009g0266a0001c0001t0009g0294a0001c0001t0009g0296others(11): Show | 14 | HG00642.hp1 HG01255.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-10642G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638057 | ||||||
| chr12:68638133
|
G | A | 9 | a0001c0001t0002g0107a0001c0001t0002g0112a0001c0001t0002g0124others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26-10566G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638133 | ||||||
| chr12:68638283
|
CT | C | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-10413delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68638283 | |||||
| chr12:68638337
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-26-10362G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638337 | ||||||
| chr12:68638473
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-26-10226T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638473 | ||||||
| chr12:68638579
|
T | G | 1 | a0001c0001t0050g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-26-10120T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638579 | ||||||
| chr12:68638647
|
A | G | 3 | a0001c0001t0010g0207a0001c0001t0010g0220a0001c0001t0111g0242 | 3 | HG00673.hp2 NA18612.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-26-10052A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638647 | ||||||
| chr12:68638683
|
A | C | 1 | a0001c0001t0108g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-26-10016A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638683 | ||||||
| chr12:68638696
|
G | C | 1 | a0001c0001t0019g0113 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-26-10003G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638696 | ||||||
| chr12:68638722
|
G | A | 1 | a0001c0001t0035g0212 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-26-9977G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638722 | ||||||
| chr12:68638771
|
C | T | 20 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0003g0273others(17): Show | 20 | HG00738.hp1 HG02074.hp1 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26-9928C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638771 | ||||||
| chr12:68638818
|
A | G | 266 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(263): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-26-9881A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638818 | ||||||
| chr12:68638955
|
C | A | 1 | a0001c0001t0125g0168 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26-9744C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68638955 | ||||||
| chr12:68639065
|
A | C | 1 | a0001c0001t0075g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-26-9634A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639065 | ||||||
| chr12:68639122
|
T | A | 6 | a0001c0001t0039g0255a0001c0001t0039g0260a0001c0001t0044g0254others(3): Show | 6 | HG01361.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26-9577T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639122 | ||||||
| chr12:68639206
|
C | A | 1 | a0001c0001t0001g0209 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-26-9493C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639206 | ||||||
| chr12:68639362
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-26-9337A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639362 | ||||||
| chr12:68639366
|
A | G | 6 | a0001c0001t0024g0153a0001c0001t0024g0154a0001c0001t0049g0151others(3): Show | 6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-9333A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639366 | ||||||
| chr12:68639457
|
G | A | 2 | a0001c0001t0006g0090a0001c0001t0006g0091 | 2 | NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-26-9242G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639457 | ||||||
| chr12:68639843
|
A | AT | 13 | a0001c0001t0001g0208a0001c0001t0001g0245a0001c0001t0003g0264others(10): Show | 14 | HG01516.hp2 HG01517.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-8841dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68639843 | |||||
| chr12:68639859
|
G | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-8840G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68639859 | ||||||
| chr12:68640127
|
C | A | 1 | a0001c0002t0024g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26-8572C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640127 | ||||||
| chr12:68640201
|
AAATTT | A | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-26-8494_-26-8490d others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68640201 | |||||
| chr12:68640310
|
T | C | 1 | a0001c0001t0033g0189 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-26-8389T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640310 | ||||||
| chr12:68640392
|
G | C | 2 | a0001c0001t0024g0153a0001c0001t0024g0154 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-26-8307G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640392 | ||||||
| chr12:68640672
|
G | A | 3 | a0001c0001t0029g0297a0001c0001t0029g0301a0001c0001t0071g0291 | 3 | HG00642.hp1 HG01255.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-26-8027G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640672 | ||||||
| chr12:68640836
|
A | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(65): Show | 69 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-26-7863A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640836 | ||||||
| chr12:68640936
|
A | G | 1 | a0001c0001t0009g0294 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-26-7763A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640936 | ||||||
| chr12:68640955
|
C | T | 3 | a0001c0001t0012g0359a0001c0001t0026g0013a0001c0001t0048g0358 | 4 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-7744C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640955 | ||||||
| chr12:68640957
|
G | T | 1 | a0001c0001t0102g0307 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-26-7742G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68640957 | ||||||
| chr12:68641006
|
A | G | 2 | a0001c0001t0002g0138a0001c0001t0109g0139 | 2 | NA18964.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-26-7693A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641006 | ||||||
| chr12:68641020
|
G | A | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-7679G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641020 | ||||||
| chr12:68641110
|
G | A | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-7589G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641110 | ||||||
| chr12:68641171
|
T | G | 11 | a0001c0001t0002g0001a0001c0001t0002g0115a0001c0001t0002g0125others(8): Show | 12 | NA18612.hp1 NA18968.hp2 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-7528T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641171 | ||||||
| chr12:68641220
|
G | A | 291 | a0001c0001t0001g0014a0001c0001t0001g0182a0001c0001t0001g0183others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-26-7479G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641220 | ||||||
| chr12:68641279
|
G | T | 12 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(9): Show | 14 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-26-7420G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641279 | ||||||
| chr12:68641310
|
T | A | 1 | a0001c0001t0019g0113 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-26-7389T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641310 | ||||||
| chr12:68641501
|
G | C | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-7198G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641501 | ||||||
| chr12:68641604
|
T | C | 3 | a0001c0001t0037g0289a0001c0001t0037g0290a0001c0001t0088g0262 | 3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-26-7095T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641604 | ||||||
| chr12:68641745
|
T | C | 2 | a0001c0001t0082g0016a0001c0001t0087g0015 | 2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-26-6954T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641745 | ||||||
| chr12:68641792
|
T | TA | 23 | a0001c0001t0003g0269a0001c0001t0003g0270a0001c0001t0003g0273others(20): Show | 23 | HG00738.hp1 HG02074.hp1 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.-26-6895dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68641792 | |||||
| chr12:68641792
|
T | TAA | 53 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(50): Show | 56 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-26-6896_-26-6895d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68641792 | |||||
| chr12:68641792
|
TA | T | 18 | a0001c0001t0001g0177a0001c0001t0005g0004a0001c0001t0005g0005others(15): Show | 21 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.-26-6895delA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68641792 | |||||
| chr12:68641807
|
G | C | 1 | a0001c0001t0025g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-26-6892G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641807 | ||||||
| chr12:68641986
|
A | C | 1 | a0001c0001t0013g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-26-6713A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68641986 | ||||||
| chr12:68642062
|
G | A | 1 | a0001c0001t0104g0171 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26-6637G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642062 | ||||||
| chr12:68642086
|
G | C | 27 | a0001c0001t0002g0001a0001c0001t0002g0105a0001c0001t0002g0115others(24): Show | 28 | HG01099.hp2 HG01975.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-26-6613G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642086 | ||||||
| chr12:68642364
|
A | G | 1 | a0001c0001t0068g0292 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-26-6335A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642364 | ||||||
| chr12:68642814
|
G | A | 3 | a0001c0001t0037g0289a0001c0001t0037g0290a0001c0001t0088g0262 | 3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-26-5885G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642814 | ||||||
| chr12:68642831
|
C | A | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-5868C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642831 | ||||||
| chr12:68642844
|
C | T | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-5855C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642844 | ||||||
| chr12:68642983
|
C | T | 1 | a0001c0001t0047g0198 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-26-5716C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68642983 | ||||||
| chr12:68643009
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-26-5690C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643009 | ||||||
| chr12:68643010
|
G | A | 2 | a0001c0001t0123g0250a0001c0001t0124g0251 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-26-5689G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643010 | ||||||
| chr12:68643029
|
C | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(65): Show | 69 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-26-5670C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643029 | ||||||
| chr12:68643066
|
T | A | 3 | a0001c0001t0003g0010a0001c0001t0003g0310a0001c0001t0015g0352 | 4 | HG00438.hp1 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-5633T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643066 | ||||||
| chr12:68643292
|
G | A | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-5407G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643292 | ||||||
| chr12:68643346
|
C | G | 1 | a0001c0001t0020g0327 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-26-5353C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643346 | ||||||
| chr12:68643701
|
G | A | 1 | a0001c0001t0009g0300 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-26-4998G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643701 | ||||||
| chr12:68643918
|
T | C | 2 | a0001c0001t0028g0166a0001c0001t0028g0170 | 2 | HG00099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-26-4781T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68643918 | ||||||
| chr12:68644039
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-26-4660A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644039 | ||||||
| chr12:68644099
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-26-4600T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644099 | ||||||
| chr12:68644121
|
A | G | 1 | a0001c0001t0048g0358 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-26-4578A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644121 | ||||||
| chr12:68644292
|
T | A | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-4407T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644292 | ||||||
| chr12:68644667
|
A | T | 18 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(15): Show | 20 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-26-4032A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644667 | ||||||
| chr12:68644686
|
C | CT | 75 | a0001c0001t0001g0234a0001c0001t0002g0127a0001c0001t0003g0010others(72): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-3993dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68644686 | |||||
| chr12:68644686
|
C | CTT | 11 | a0001c0001t0003g0323a0001c0001t0003g0329a0001c0001t0015g0343others(8): Show | 12 | HG00642.hp2 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-3994_-26-3993d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68644686 | |||||
| chr12:68644686
|
CT | C | 7 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(4): Show | 7 | HG00558.hp1 HG02486.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26-3993delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68644686 | |||||
| chr12:68644770
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-26-3929C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644770 | ||||||
| chr12:68644950
|
C | T | 2 | a0001c0001t0004g0073a0001c0001t0004g0089 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-26-3749C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644950 | ||||||
| chr12:68644979
|
G | A | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26-3720G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68644979 | ||||||
| chr12:68645514
|
AC | A | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-3184delC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68645514 | ||||||
| chr12:68645831
|
T | G | 1 | a0001c0001t0015g0352 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-26-2868T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68645831 | ||||||
| chr12:68645957
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-26-2742A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68645957 | ||||||
| chr12:68645978
|
G | A | 1 | a0001c0001t0061g0052 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-26-2721G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68645978 | ||||||
| chr12:68646029
|
A | G | 2 | a0001c0001t0063g0152a0001c0001t0078g0222 | 2 | NA18940.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-26-2670A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646029 | ||||||
| chr12:68646050
|
T | A | 2 | a0001c0001t0116g0169a0001c0001t0117g0163 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-26-2649T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646050 | ||||||
| chr12:68646072
|
G | C | 1 | a0001c0001t0002g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-26-2627G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646072 | ||||||
| chr12:68646225
|
T | G | 6 | a0001c0001t0024g0153a0001c0001t0024g0154a0001c0001t0049g0151others(3): Show | 6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-2474T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646225 | ||||||
| chr12:68646275
|
G | A | 266 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(263): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-26-2424G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646275 | ||||||
| chr12:68646303
|
T | G | 1 | a0001c0001t0119g0349 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-26-2396T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646303 | ||||||
| chr12:68646373
|
G | A | 1 | a0001c0001t0008g0351 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-26-2326G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646373 | ||||||
| chr12:68646493
|
A | G | 2 | a0001c0001t0004g0033a0001c0001t0006g0034 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-26-2206A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646493 | ||||||
| chr12:68646631
|
T | C | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-26-2068T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646631 | ||||||
| chr12:68646903
|
T | C | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-1796T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68646903 | ||||||
| chr12:68647170
|
G | A | 2 | a0001c0001t0004g0076a0001c0001t0031g0035 | 2 | HG00735.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-26-1529G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647170 | ||||||
| chr12:68647299
|
C | T | 1 | a0001c0001t0013g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-26-1400C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647299 | ||||||
| chr12:68647313
|
T | A | 4 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(1): Show | 4 | NA18951.hp2 NA18972.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-1386T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647313 | ||||||
| chr12:68647335
|
C | T | 3 | a0001c0001t0003g0323a0001c0001t0003g0342a0001c0001t0003g0346 | 3 | HG03942.hp2 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-26-1364C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647335 | ||||||
| chr12:68647387
|
G | GC | 40 | a0001c0001t0002g0101a0001c0001t0002g0128a0001c0001t0002g0135others(37): Show | 40 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-26-1295dupC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | |||||
| chr12:68647387
|
G | GCC | 21 | a0001c0001t0002g0102a0001c0001t0002g0109a0001c0001t0004g0044others(18): Show | 21 | HG00597.hp1 HG01192.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-26-1296_-26-1295d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | |||||
| chr12:68647387
|
G | GCCCCCCC others(5): Show |
1 | a0001c0001t0124g0251 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-26-1306_-26-1295d others(14): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | |||||
| chr12:68647387
|
GC | G | 47 | a0001c0001t0002g0096a0001c0001t0002g0104a0001c0001t0002g0107others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.-26-1295delC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | |||||
| chr12:68647387
|
GCC | G | 56 | a0001c0001t0001g0183a0001c0001t0001g0236a0001c0001t0002g0117others(53): Show | 58 | HG00423.hp2 HG00438.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-26-1296_-26-1295d others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | |||||
| chr12:68647387
|
GCCC | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(72): Show | 81 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-26-1297_-26-1295d others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | |||||
| chr12:68647387
|
GCCCC | G | 51 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0174others(48): Show | 52 | HG00323.hp2 HG00673.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.-26-1298_-26-1295d others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | |||||
| chr12:68647387
|
GCCCCC | G | 16 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0217others(13): Show | 19 | HG01069.hp2 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-1299_-26-1295d others(7): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 68647387 | |||||
| chr12:68647389
|
C | G | 1 | a0001c0001t0073g0268 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-26-1310C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647389 | ||||||
| chr12:68647396
|
C | A | 1 | a0001c0001t0010g0220 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-26-1303C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647396 | ||||||
| chr12:68647403
|
C | A | 1 | a0001c0001t0130g0335 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-26-1296C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647403 | ||||||
| chr12:68647403
|
C | G | 4 | a0001c0001t0015g0343a0001c0001t0020g0327a0001c0001t0020g0345others(1): Show | 4 | HG00642.hp2 HG01256.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-1296C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647403 | ||||||
| chr12:68647404
|
C | A | 1 | a0001c0001t0005g0023 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-26-1295C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647404 | ||||||
| chr12:68647405
|
A | C | 1 | a0001c0001t0088g0262 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-26-1294A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647405 | ||||||
| chr12:68647621
|
C | T | 1 | a0001c0001t0125g0168 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26-1078C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647621 | ||||||
| chr12:68647659
|
A | G | 1 | a0001c0001t0115g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-26-1040A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68647659 | ||||||
| chr12:68648265
|
T | C | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(4): Show | 7 | HG01192.hp2 HG01981.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26-434T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648265 | ||||||
| chr12:68648328
|
A | G | 4 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0159others(1): Show | 4 | HG02717.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-371A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648328 | ||||||
| chr12:68648409
|
G | A | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-290G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648409 | ||||||
| chr12:68648552
|
A | G | 1 | a0001c0001t0075g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-26-147A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648552 | ||||||
| chr12:68648614
|
A | G | 1 | a0001c0002t0024g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26-85A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648614 | ||||||
| chr12:68648647
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-26-52C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | chr12 | 68648647 | ||||||
| chr12:68648910
|
T | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0095a0001c0001t0002g0096others(63): Show | 67 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.57+129T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68648910 | ||||||
| chr12:68649246
|
A | G | 1 | a0001c0001t0128g0369 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.57+465A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649246 | ||||||
| chr12:68649373
|
G | A | 1 | a0001c0001t0042g0350 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.57+592G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649373 | ||||||
| chr12:68649393
|
T | C | 2 | a0001c0001t0004g0062a0001c0001t0019g0113 | 2 | HG03491.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.57+612T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649393 | ||||||
| chr12:68649441
|
T | C | 1 | a0001c0001t0013g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.57+660T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649441 | ||||||
| chr12:68649693
|
A | G | 3 | a0001c0001t0009g0296a0001c0001t0069g0293a0001c0001t0070g0295 | 3 | HG01884.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.58-707A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68649693 | ||||||
| chr12:68650389
|
T | A | 1 | a0001c0001t0104g0171 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.58-11T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 2/7 | chr12 | 68650389 | ||||||
| chr12:68650501
|
G | T | 15 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(12): Show | 17 | HG01069.hp2 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.126+33G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68650501 | ||||||
| chr12:68650514
|
ATACT | A | 3 | a0001c0001t0050g0017a0001c0001t0082g0016a0001c0001t0087g0015 | 3 | HG00639.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.126+49_126+52delCT others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 68650514 | |||||
| chr12:68650662
|
T | A | 1 | a0001c0001t0003g0270 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.126+194T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68650662 | ||||||
| chr12:68650696
|
T | G | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+228T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68650696 | ||||||
| chr12:68650954
|
A | G | 1 | a0001c0001t0050g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126+486A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68650954 | ||||||
| chr12:68651126
|
C | T | 77 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(74): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.126+658C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651126 | ||||||
| chr12:68651330
|
G | A | 3 | a0001c0001t0037g0289a0001c0001t0037g0290a0001c0001t0088g0262 | 3 | HG02055.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.127-665G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651330 | ||||||
| chr12:68651662
|
G | A | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-333G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651662 | ||||||
| chr12:68651685
|
T | G | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.127-310T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651685 | ||||||
| chr12:68651780
|
C | T | 1 | a0001c0001t0052g0265 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127-215C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 3/7 | chr12 | 68651780 | ||||||
| chr12:68652088
|
T | G | 6 | a0001c0001t0028g0166a0001c0001t0028g0170a0001c0001t0053g0165others(3): Show | 6 | HG00099.hp2 HG02976.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+37T>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652088 | ||||||
| chr12:68652170
|
T | A | 1 | a0001c0001t0003g0317 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.183+119T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652170 | ||||||
| chr12:68652330
|
C | T | 2 | a0001c0001t0018g0084a0001c0001t0062g0056 | 2 | HG02056.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.183+279C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652330 | ||||||
| chr12:68652536
|
C | T | 1 | a0001c0001t0099g0314 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.183+485C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652536 | ||||||
| chr12:68652614
|
A | G | 1 | a0001c0001t0115g0164 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.183+563A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652614 | ||||||
| chr12:68652668
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.183+617A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652668 | ||||||
| chr12:68652675
|
G | T | 5 | a0001c0001t0028g0166a0001c0001t0028g0170a0001c0001t0053g0165others(2): Show | 5 | HG00099.hp2 HG02976.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+624G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652675 | ||||||
| chr12:68652677
|
G | T | 1 | a0001c0001t0001g0305 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.183+626G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652677 | ||||||
| chr12:68652708
|
C | G | 1 | a0001c0001t0031g0042 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.183+657C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652708 | ||||||
| chr12:68652814
|
G | A | 1 | a0001c0001t0108g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.183+763G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652814 | ||||||
| chr12:68652858
|
A | G | 6 | a0001c0001t0005g0004a0001c0001t0005g0018a0001c0001t0005g0019others(3): Show | 7 | HG01069.hp2 HG01891.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+807A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652858 | ||||||
| chr12:68652880
|
A | G | 1 | a0001c0001t0050g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.183+829A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652880 | ||||||
| chr12:68652926
|
G | C | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.183+875G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68652926 | ||||||
| chr12:68653208
|
C | G | 1 | a0001c0001t0097g0371 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.184-904C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653208 | ||||||
| chr12:68653251
|
A | G | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.184-861A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653251 | ||||||
| chr12:68653370
|
G | GTTACCTT others(3): Show |
80 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(77): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.184-741_184-732dup others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 68653370 | |||||
| chr12:68653397
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.184-715A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653397 | ||||||
| chr12:68653429
|
C | G | 76 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(73): Show | 79 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.184-683C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653429 | ||||||
| chr12:68653495
|
C | T | 80 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(77): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.184-617C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653495 | ||||||
| chr12:68653516
|
A | G | 53 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0286others(50): Show | 56 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.184-596A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653516 | ||||||
| chr12:68653556
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.184-556T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653556 | ||||||
| chr12:68653622
|
G | A | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.184-490G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653622 | ||||||
| chr12:68653694
|
C | T | 3 | a0001c0001t0003g0317a0001c0001t0003g0337a0001c0001t0015g0318 | 3 | HG02071.hp2 HG02080.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.184-418C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653694 | ||||||
| chr12:68653818
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.184-294C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653818 | ||||||
| chr12:68653883
|
G | A | 95 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0264others(92): Show | 101 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.184-229G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | chr12 | 68653883 | ||||||
| chr12:68653929
|
C | CA | 7 | a0001c0001t0026g0013a0001c0001t0028g0166a0001c0001t0028g0170others(4): Show | 8 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.184-172dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 68653929 | |||||
| chr12:68654351
|
T | TG | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(274): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.324+109dupG | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68654351 | |||||
| chr12:68654351
|
T | TGG | 41 | a0001c0001t0001g0187a0001c0001t0001g0199a0001c0001t0001g0227others(38): Show | 41 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.324+108_324+109dup others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68654351 | |||||
| chr12:68654354
|
G | GA | 4 | a0001c0001t0002g0157a0001c0001t0002g0167a0001c0001t0021g0123others(1): Show | 4 | NA18963.hp1 NA18978.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+102_324+103ins others(1): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654354 | ||||||
| chr12:68654358
|
G | A | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.324+106G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654358 | ||||||
| chr12:68654359
|
G | T | 1 | a0001c0001t0037g0290 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.324+107G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654359 | ||||||
| chr12:68654543
|
G | A | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.324+291G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654543 | ||||||
| chr12:68654603
|
G | A | 1 | a0001c0001t0008g0354 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.324+351G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654603 | ||||||
| chr12:68654719
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.324+467C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654719 | ||||||
| chr12:68654752
|
T | TAAAG | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.324+501_324+504dup others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68654752 | |||||
| chr12:68654831
|
C | T | 3 | a0001c0001t0001g0238a0001c0001t0014g0221a0001c0001t0086g0235 | 3 | HG02135.hp2 NA18983.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.324+579C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68654831 | ||||||
| chr12:68655156
|
T | A | 94 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0205others(91): Show | 97 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.324+904T>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655156 | ||||||
| chr12:68655316
|
C | G | 1 | a0001c0001t0015g0336 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.325-990C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655316 | ||||||
| chr12:68655535
|
C | CT | 81 | a0001c0001t0001g0196a0001c0001t0001g0226a0001c0001t0001g0232others(78): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.325-753dupT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68655535 | |||||
| chr12:68655535
|
CT | C | 23 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(20): Show | 26 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.325-753delT | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68655535 | |||||
| chr12:68655558
|
C | T | 1 | a0001c0001t0061g0052 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.325-748C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655558 | ||||||
| chr12:68655643
|
C | G | 1 | a0001c0001t0065g0085 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.325-663C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655643 | ||||||
| chr12:68655727
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.325-579G>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655727 | ||||||
| chr12:68655732
|
C | T | 1 | a0001c0001t0081g0364 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325-574C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655732 | ||||||
| chr12:68655895
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.325-411C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68655895 | ||||||
| chr12:68655960
|
T | TTTCTCAA others(3): Show |
1 | a0001c0001t0117g0163 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.325-343_325-334dup others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 68655960 | |||||
| chr12:68656081
|
A | T | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.325-225A>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 5/7 | chr12 | 68656081 | ||||||
| chr12:68656455
|
G | A | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
splice_region_variant&intron_variant | LOW | c.468+6G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | chr12 | 68656455 | ||||||
| chr12:68656554
|
TGATGTTA others(3): Show |
T | 1 | a0001c0001t0117g0163 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.468+107_468+116del others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 68656554 | |||||
| chr12:68656566
|
C | CA | 7 | a0001c0001t0002g0145a0001c0001t0004g0032a0001c0001t0006g0049others(4): Show | 7 | HG01255.hp2 HG02015.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+129dupA | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 68656566 | |||||
| chr12:68656581
|
C | T | 3 | a0001c0001t0002g0146a0001c0001t0002g0148a0001c0001t0002g0150 | 3 | HG02027.hp1 HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.468+132C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | chr12 | 68656581 | ||||||
| chr12:68656609
|
TAAAC | T | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+163_468+166del others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 68656609 | |||||
| chr12:68656859
|
A | G | 1 | a0001c0001t0033g0189 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.469-242A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | chr12 | 68656859 | ||||||
| chr12:68656949
|
G | A | 3 | a0001c0001t0009g0296a0001c0001t0069g0293a0001c0001t0070g0295 | 3 | HG01884.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.469-152G>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | chr12 | 68656949 | ||||||
| chr12:68656981
|
G | GC | 17 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(14): Show | 19 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.469-119dupC | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 68656981 | |||||
| chr12:68657231
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.*30+14T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657231 | ||||||
| chr12:68657321
|
A | G | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.*30+104A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657321 | ||||||
| chr12:68657364
|
C | G | 3 | a0001c0001t0038g0184a0001c0001t0038g0237a0001c0001t0094g0185 | 3 | HG02572.hp1 HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.*30+147C>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657364 | ||||||
| chr12:68657447
|
C | A | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.*30+230C>A | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657447 | ||||||
| chr12:68657565
|
C | T | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.*30+348C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657565 | ||||||
| chr12:68657723
|
AAAACACA others(5): Show |
A | 1 | a0001c0001t0042g0350 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*30+508_*30+519del others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657723 | |||||
| chr12:68657724
|
AAACACAC others(4): Show |
A | 1 | a0001c0001t0008g0354 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.*30+509_*30+519del others(11): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657724 | |||||
| chr12:68657725
|
A | AAC | 43 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0177others(40): Show | 45 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.*30+555_*30+556dup others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
A | AACAC | 19 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0191others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.*30+553_*30+556dup others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
A | AACACAC | 15 | a0001c0001t0001g0179a0001c0001t0001g0213a0001c0001t0002g0095others(12): Show | 15 | HG01099.hp2 HG01975.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.*30+551_*30+556dup others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
A | AACACACA others(1): Show |
13 | a0001c0001t0002g0001a0001c0001t0002g0105a0001c0001t0002g0125others(10): Show | 14 | HG02132.hp1 HG02135.hp1 HG03041.hp1 others(11): Show |
intron_variant | MODIFIER | c.*30+549_*30+556dup others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
A | AACACACA others(3): Show |
3 | a0001c0001t0021g0156a0001c0001t0021g0203a0001c0001t0108g0144 | 3 | HG02738.hp1 NA19056.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.*30+547_*30+556dup others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
A | AACACACA others(5): Show |
3 | a0001c0001t0002g0137a0001c0001t0084g0304a0001c0001t0114g0130 | 3 | HG03486.hp1 HG03688.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.*30+545_*30+556dup others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
A | AACACACA others(7): Show |
2 | a0001c0001t0002g0131a0001c0001t0107g0114 | 2 | HG02258.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.*30+543_*30+556dup others(14): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
A | ACAC | 3 | a0001c0001t0001g0234a0001c0001t0002g0109a0001c0001t0002g0149 | 3 | HG02027.hp2 HG04228.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.*30+508_*30+509ins others(3): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | ||||||
| chr12:68657725
|
A | ACACAC | 4 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0036g0215others(1): Show | 4 | HG01192.hp2 HG02647.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.*30+508_*30+509ins others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | ||||||
| chr12:68657725
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0110g0116 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.*30+508_*30+509ins others(11): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | ||||||
| chr12:68657725
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0002g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.*30+508_*30+509ins others(13): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | ||||||
| chr12:68657725
|
A | C | 3 | a0001c0001t0012g0244a0001c0001t0012g0363a0001c0001t0117g0163 | 3 | HG02004.hp1 HG02004.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.*30+508A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657725 | ||||||
| chr12:68657725
|
AAC | A | 30 | a0001c0001t0001g0173a0001c0001t0001g0196a0001c0001t0001g0202others(27): Show | 30 | HG00544.hp2 HG00673.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.*30+555_*30+556del others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACAC | A | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0182others(33): Show | 38 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.*30+553_*30+556del others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACAC | A | 54 | a0001c0001t0002g0102a0001c0001t0003g0264a0001c0001t0003g0273others(51): Show | 54 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.*30+551_*30+556del others(6): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACACA others(1): Show |
A | 29 | a0001c0001t0002g0147a0001c0001t0003g0274a0001c0001t0003g0284others(26): Show | 29 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.*30+549_*30+556del others(8): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACACA others(3): Show |
A | 29 | a0001c0001t0001g0205a0001c0001t0001g0236a0001c0001t0001g0241others(26): Show | 32 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.*30+547_*30+556del others(10): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACACA others(5): Show |
A | 21 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0103others(18): Show | 22 | HG00438.hp1 HG01175.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.*30+545_*30+556del others(12): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACACA others(7): Show |
A | 4 | a0001c0001t0002g0104a0001c0001t0009g0300a0001c0001t0027g0064others(1): Show | 4 | HG00099.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*30+543_*30+556del others(14): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACACA others(11): Show |
A | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01891.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.*30+539_*30+556del others(18): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACACA others(13): Show |
A | 6 | a0001c0001t0024g0153a0001c0001t0024g0154a0001c0001t0049g0151others(3): Show | 6 | HG02293.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.*30+537_*30+556del others(20): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACACA others(17): Show |
A | 1 | a0001c0001t0003g0334 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.*30+533_*30+556del others(24): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657725
|
AACACACA others(19): Show |
A | 1 | a0001c0001t0130g0335 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.*30+531_*30+556del others(26): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657725 | |||||
| chr12:68657752
|
ACACACAC others(19): Show |
A | 1 | a0001c0001t0129g0370 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*30+537_*30+562del others(26): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657752 | |||||
| chr12:68657779
|
C | T | 1 | a0001c0001t0003g0269 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.*30+562C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657779 | ||||||
| chr12:68657811
|
C | CCT | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.*30+594_*30+595ins others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657811 | ||||||
| chr12:68657825
|
A | AAC | 11 | a0001c0001t0001g0223a0001c0001t0007g0007a0001c0001t0007g0063others(8): Show | 11 | HG00597.hp1 HG03942.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.*30+627_*30+628dup others(2): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657825 | |||||
| chr12:68657825
|
A | AACAC | 2 | a0001c0001t0026g0013a0001c0001t0048g0358 | 3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.*30+625_*30+628dup others(4): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68657825 | |||||
| chr12:68657906
|
T | C | 1 | a0001c0001t0037g0290 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*30+689T>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68657906 | ||||||
| chr12:68658018
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.*30+801G>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658018 | ||||||
| chr12:68658044
|
A | G | 1 | a0001c0001t0015g0343 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.*30+827A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658044 | ||||||
| chr12:68658063
|
C | T | 279 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0205others(276): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.*30+846C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658063 | ||||||
| chr12:68658079
|
A | G | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.*30+862A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658079 | ||||||
| chr12:68658466
|
A | G | 19 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(16): Show | 22 | HG01069.hp2 HG01109.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.*31-814A>G | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68658466 | ||||||
| chr12:68658669
|
TAATAG | T | 9 | a0001c0001t0002g0107a0001c0001t0002g0112a0001c0001t0002g0124others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.*31-607_*31-603del others(5): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 68658669 | |||||
| chr12:68659115
|
A | C | 2 | a0001c0001t0045g0110a0001c0001t0045g0111 | 2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.*31-165A>C | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68659115 | ||||||
| chr12:68659214
|
C | T | 16 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0018others(13): Show | 18 | HG01069.hp2 HG01109.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.*31-66C>T | RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 7/7 | chr12 | 68659214 |